Non invasive high resolution in vivo imaging of alpha-naphthylisothiocyanate
(ANIT) induced hepatobiliary toxicity in STII medaka
Ron Hardman∗, Seth Kullman, Bonny Yuen, David E. Hinton
Duke University, Nicholas School of the Environment and Earth Sciences, Durham, NC 27708, United States
DOI:10.21276/ijlssr.2016.2.4.20
ABSTRACT- The present investigation was carried out to the effect of dimethoate on histopathological changes in
kidney of freshwater fish, Garra mullya. Fishes was exposed to sub lethal concentration of dimethoate (0.0238ppm of
96hrs.) for 7, 14, 21 days. Fishes exposed to dimethoate were characterized by loosening of haemopoietic tissue,
uriniferous tubules have lost their original appearance, vacuolated cytoplasm, degeneration in the epithelial cells of renal
tubule, narrowing of the tubular lumen and damaged glomeruli. The lesions in the vital organ might have resulted in
physiological and metabolical dysregulations. In chronic treatment of dimethoate exposure may pose serious threat to fish
health and affect their population. Key-words- Dimethoate, Histopathology, Kidney, Garra mullya
botanic gardens, meta-analysis, use of networks in ecology, conservation of biodiversity, species-people correlation, sudden oak death, Phytophthora ramorum, network epidemiology, geographical genetics, scale-dependence of the species-people correlation, invasion of plant pathogens, plant health and global change, sustainability,
ABSTRACT- The present study was conducted to investigate the effect of cadmium chloride on Histoarchiteceture of head kidney of fresh water fish Heteropneustes fossilis. The fishes were exposed to 0.5 ppm of cadmium chloride for 21 days. The most remarkable changes in head kidney, due to cadmium chloride were lysed condition of interrenal and chromaffin cells. The traces of cytoplasm had dark brown to black coloured cytoplasm. Most of cells are deformed and necrotic condition. Their size was significant at (P< 0.01 and 0.001) increased after cadmium chloride. All these changes will be recovered by herbal compound i.e. Ashwagandha. The damaged tissues were recovered in already treated group.
Key-words- Ashwagandha, Cadmium chloride, Chromaffin cells, Heteropneustes fossilis, Histopathology, Interrenal cells
Spermatotoxic impact of bonny light crude oil (BLCO) ingestion on adult male ...lukeman Joseph Ade shittu
Increasing concern has been expressed about the possible declining trend in the sperm quality and sperm count of man as a result of exposure to environmental estrogenic agents in the past few years now. There is a general paucity of knowledge of BLCO ingestion on the reproductive effect. Hence, we aim to evaluate the impact of sub-lethal dose of BLCO ingestion on semen parameters of adult male mice. Initial acute toxicity study was carried out to determine the lethal dose of BLCO, which was calculated to be 37.4 mg/Kg body wt. A sub-lethal dose of 20 mg/Kg bwt /day of BLCO were then given to 8 male mice in the experimental group. While, the control group of 7 animals received equal volume of 0.9% normal saline via oral garvage for 2 weeks. Data were analysed using SPSS 12 statistical software with P < 0.05 considered statistically significant. There was a significant (P < 0.05) weight gain in the treated group with a significant (P < 0.05) reduction in sperm motility in the treated compared with control. The sperm density of treated and control were 14.5 x 106 /ml and 20.5 x 106 /ml respectively. However, there were also no significant difference in the relative testicular weight and sperm density of treated from that of the control respectively. Thus, it was concluded that BLCO ingestion is spermatotoxic in the adult male Swiss mice
DOI:10.21276/ijlssr.2016.2.4.20
ABSTRACT- The present investigation was carried out to the effect of dimethoate on histopathological changes in
kidney of freshwater fish, Garra mullya. Fishes was exposed to sub lethal concentration of dimethoate (0.0238ppm of
96hrs.) for 7, 14, 21 days. Fishes exposed to dimethoate were characterized by loosening of haemopoietic tissue,
uriniferous tubules have lost their original appearance, vacuolated cytoplasm, degeneration in the epithelial cells of renal
tubule, narrowing of the tubular lumen and damaged glomeruli. The lesions in the vital organ might have resulted in
physiological and metabolical dysregulations. In chronic treatment of dimethoate exposure may pose serious threat to fish
health and affect their population. Key-words- Dimethoate, Histopathology, Kidney, Garra mullya
botanic gardens, meta-analysis, use of networks in ecology, conservation of biodiversity, species-people correlation, sudden oak death, Phytophthora ramorum, network epidemiology, geographical genetics, scale-dependence of the species-people correlation, invasion of plant pathogens, plant health and global change, sustainability,
ABSTRACT- The present study was conducted to investigate the effect of cadmium chloride on Histoarchiteceture of head kidney of fresh water fish Heteropneustes fossilis. The fishes were exposed to 0.5 ppm of cadmium chloride for 21 days. The most remarkable changes in head kidney, due to cadmium chloride were lysed condition of interrenal and chromaffin cells. The traces of cytoplasm had dark brown to black coloured cytoplasm. Most of cells are deformed and necrotic condition. Their size was significant at (P< 0.01 and 0.001) increased after cadmium chloride. All these changes will be recovered by herbal compound i.e. Ashwagandha. The damaged tissues were recovered in already treated group.
Key-words- Ashwagandha, Cadmium chloride, Chromaffin cells, Heteropneustes fossilis, Histopathology, Interrenal cells
Spermatotoxic impact of bonny light crude oil (BLCO) ingestion on adult male ...lukeman Joseph Ade shittu
Increasing concern has been expressed about the possible declining trend in the sperm quality and sperm count of man as a result of exposure to environmental estrogenic agents in the past few years now. There is a general paucity of knowledge of BLCO ingestion on the reproductive effect. Hence, we aim to evaluate the impact of sub-lethal dose of BLCO ingestion on semen parameters of adult male mice. Initial acute toxicity study was carried out to determine the lethal dose of BLCO, which was calculated to be 37.4 mg/Kg body wt. A sub-lethal dose of 20 mg/Kg bwt /day of BLCO were then given to 8 male mice in the experimental group. While, the control group of 7 animals received equal volume of 0.9% normal saline via oral garvage for 2 weeks. Data were analysed using SPSS 12 statistical software with P < 0.05 considered statistically significant. There was a significant (P < 0.05) weight gain in the treated group with a significant (P < 0.05) reduction in sperm motility in the treated compared with control. The sperm density of treated and control were 14.5 x 106 /ml and 20.5 x 106 /ml respectively. However, there were also no significant difference in the relative testicular weight and sperm density of treated from that of the control respectively. Thus, it was concluded that BLCO ingestion is spermatotoxic in the adult male Swiss mice
Wagner College Forum for Undergraduate Research, Vol 12 No 1Wagner College
The Fall 2013 issue contains 15 abstracts of papers and posters presented at the 67th Annual Eastern Colleges Science Conference held in Providence, R.I. on April 20, 2013. The student authors were Faiz Abed, Samar Alwani, Joseph Biggica, Daniel Cimilluca, Janna Denisenko, Leonid Denisenko, Corey Gaylets, Basil Hussain, Vincent Lombardo, Pakinam Mekki, Sandra Minchala, Alisa Ndokaj, Holly Santapaga, Juliana Schipani, Eden Stark, Lynn Tay and Elaina Tsimbikos. The remainder of the Fall 2013 issue consists of eight full-length research papers by James Alicea, Kiana Balacich, Michael Chicolo, Leobardo Dominguez, Michelle Greenough, Stephanie Lombardo, Caroline Mauduy, Carley Nicoletti, Adam Rizzuti and Carly Schmidt.
New Spectrophotometric Determination of Tenofovir Disoproxil Fumaratein Bulk ...IOSRJAC
Two new, selective and sensitive visible spectrophotometric methods (method A and B) have been developed for the estimation of Tenofovir disoproxil fumaratein bulk and in pharmaceutical preparations. Method ‘A’ is based on the reaction with wool fast blue, in the presence of buffer at PH 1.5 to form a colored species with a λmax 590nm. Method B is based on the reaction with tropaeoline -00 dye under acidic condition with a λ max 410nm. Beer’s law is obeyed in the concentration range of 50 to 250µg/ml for both the methods. The methods were extended to pharmaceutical formulations and there was no interference form any common pharmaceutical excepients and diluents. The result of analysis has been validated statistically and by recovery studies.
PhD confirmation - ecology of estuarine sharks & rayssharonle
This is a ppt that was used in my confirmation for candidature. It describes how I will use stable isotope and fatty acid analysis to determine what estuarine sharks and rays eat and which areas of the South Alligator River, (NT, Aus) they utilise. This will then inform environmental managers of which areas are critical to the survival of these species.
Molecular and cytogenetic phylogeography of h. malabaricuscmvolcker
Claudio Michael Völcker
Jorge A. Dergam
Molecular and karyotypic phylogeography in the Neotropical Hoplias malabaricus (Erythrinidae) fish in eastern Brazil
Developmental Anomalies and Oxidative Stress Responses in Zebrafish (Danio Re...Premier Publishers
The discharge of human pharmaceuticals via wastewater treatment plants represents a major threat to non-target aquatic organisms since they are continually exposed throughout their lifespan. The individual effects of the anaesthetic, lidocaine; the cytostatics, ifosfamide and cyclophosphamide; and the antimicrobials, sulfamethoxazole, amoxicillin and erythromycin on 24 hpf (hours post fertilization) zebrafish (Danio rerio) following a 96-h exposure was investigated by evaluating embryonic development, catalase (CAT) enzyme activity, and the gene expressions of CAT, cytosolic superoxide dismutase (SOD1), and mitochondrial superoxide dismutase (SOD2). Lidocaine, cyclophosphamide and sulfamethoxazole induced neurotoxicity (scoliosis, tail malformation) and cardiotoxicity (pericardial edema, bradycardia) in the zebrafish which correlate with their adverse effects in mammals. These observations were linked to oxidative stress as indicated by the significant alteration of CAT activity and amounts of transcripts of SOD1, SOD2, and CAT. The CAT activity and gene expressions of the antioxidants were significantly upregulated at sublethal and levels of ifosfamide, lidocaine, cyclophosphamide, and erythromycin non-toxic to embryonic development in this study which suggest that these antioxidants may play a role in the prevention of teratogenicity in the larvae. The multi-level effect approach adopted in this study provides a better understanding of the mechanisms of toxicity employed by lidocaine, cyclophosphamide and sulfamethoxazole towards zebrafish. This study shows the importance of evaluating stress biomarkers and emphasizes the need for chronic studies in assessing pharmaceutical effects on aquatic organisms.
Microplastic uptake and retention in Perna perna (L.); Tripneustes gratilla (...MACE Lab
Gemma Gerber, Thembani Mkhize, Robertson-Andersson, Gan Moodley. Presented at the ninth Scientific Symposium of the Western Indian Ocean Marine Science Association (WIOMSA) 2015.
An In Vivo Look at Vertebrate Liver Architecture: Three-Dimensional Reconstructions from Medaka (Oryzias latipes)
RON C. HARDMAN,* DAVE C. VOLZ, SETH W. KULLMAN, AND DAVID E. HINTON
Duke University, Nicholas School of the Environment and Earth Sciences,
Durham, North Carolina
Wagner College Forum for Undergraduate Research, Vol 12 No 1Wagner College
The Fall 2013 issue contains 15 abstracts of papers and posters presented at the 67th Annual Eastern Colleges Science Conference held in Providence, R.I. on April 20, 2013. The student authors were Faiz Abed, Samar Alwani, Joseph Biggica, Daniel Cimilluca, Janna Denisenko, Leonid Denisenko, Corey Gaylets, Basil Hussain, Vincent Lombardo, Pakinam Mekki, Sandra Minchala, Alisa Ndokaj, Holly Santapaga, Juliana Schipani, Eden Stark, Lynn Tay and Elaina Tsimbikos. The remainder of the Fall 2013 issue consists of eight full-length research papers by James Alicea, Kiana Balacich, Michael Chicolo, Leobardo Dominguez, Michelle Greenough, Stephanie Lombardo, Caroline Mauduy, Carley Nicoletti, Adam Rizzuti and Carly Schmidt.
New Spectrophotometric Determination of Tenofovir Disoproxil Fumaratein Bulk ...IOSRJAC
Two new, selective and sensitive visible spectrophotometric methods (method A and B) have been developed for the estimation of Tenofovir disoproxil fumaratein bulk and in pharmaceutical preparations. Method ‘A’ is based on the reaction with wool fast blue, in the presence of buffer at PH 1.5 to form a colored species with a λmax 590nm. Method B is based on the reaction with tropaeoline -00 dye under acidic condition with a λ max 410nm. Beer’s law is obeyed in the concentration range of 50 to 250µg/ml for both the methods. The methods were extended to pharmaceutical formulations and there was no interference form any common pharmaceutical excepients and diluents. The result of analysis has been validated statistically and by recovery studies.
PhD confirmation - ecology of estuarine sharks & rayssharonle
This is a ppt that was used in my confirmation for candidature. It describes how I will use stable isotope and fatty acid analysis to determine what estuarine sharks and rays eat and which areas of the South Alligator River, (NT, Aus) they utilise. This will then inform environmental managers of which areas are critical to the survival of these species.
Molecular and cytogenetic phylogeography of h. malabaricuscmvolcker
Claudio Michael Völcker
Jorge A. Dergam
Molecular and karyotypic phylogeography in the Neotropical Hoplias malabaricus (Erythrinidae) fish in eastern Brazil
Developmental Anomalies and Oxidative Stress Responses in Zebrafish (Danio Re...Premier Publishers
The discharge of human pharmaceuticals via wastewater treatment plants represents a major threat to non-target aquatic organisms since they are continually exposed throughout their lifespan. The individual effects of the anaesthetic, lidocaine; the cytostatics, ifosfamide and cyclophosphamide; and the antimicrobials, sulfamethoxazole, amoxicillin and erythromycin on 24 hpf (hours post fertilization) zebrafish (Danio rerio) following a 96-h exposure was investigated by evaluating embryonic development, catalase (CAT) enzyme activity, and the gene expressions of CAT, cytosolic superoxide dismutase (SOD1), and mitochondrial superoxide dismutase (SOD2). Lidocaine, cyclophosphamide and sulfamethoxazole induced neurotoxicity (scoliosis, tail malformation) and cardiotoxicity (pericardial edema, bradycardia) in the zebrafish which correlate with their adverse effects in mammals. These observations were linked to oxidative stress as indicated by the significant alteration of CAT activity and amounts of transcripts of SOD1, SOD2, and CAT. The CAT activity and gene expressions of the antioxidants were significantly upregulated at sublethal and levels of ifosfamide, lidocaine, cyclophosphamide, and erythromycin non-toxic to embryonic development in this study which suggest that these antioxidants may play a role in the prevention of teratogenicity in the larvae. The multi-level effect approach adopted in this study provides a better understanding of the mechanisms of toxicity employed by lidocaine, cyclophosphamide and sulfamethoxazole towards zebrafish. This study shows the importance of evaluating stress biomarkers and emphasizes the need for chronic studies in assessing pharmaceutical effects on aquatic organisms.
Microplastic uptake and retention in Perna perna (L.); Tripneustes gratilla (...MACE Lab
Gemma Gerber, Thembani Mkhize, Robertson-Andersson, Gan Moodley. Presented at the ninth Scientific Symposium of the Western Indian Ocean Marine Science Association (WIOMSA) 2015.
An In Vivo Look at Vertebrate Liver Architecture: Three-Dimensional Reconstructions from Medaka (Oryzias latipes)
RON C. HARDMAN,* DAVE C. VOLZ, SETH W. KULLMAN, AND DAVID E. HINTON
Duke University, Nicholas School of the Environment and Earth Sciences,
Durham, North Carolina
Summary review of the aquatic toxicology of munitions constituentsGeoffrey Carton
Military munitions are present in waters around the world, including those waters located at current and former Department of Defense sites. This report provides a review of the aquatic ecotoxicology of munitions constituents (MC), including nitroaromatics (2,4,6-trinitrotoluene (TNT),
dinitrotoluenes (DNTs), 1,3,5-trinitrobenzene (TNB), 2,4,6-
trinitrophenylmethylnitramine (tetryl) and ,4,6-trinitrophenol (picric acid)); nitrate esters (nitrocellulose (NC), pentaerythritoltetranitrate (PETN), nitroglycerine (NG)); and nitramines (hexahydro-1,3,5- trinitro-1,3,5-triazine
(RDX), and octahydro-1,3,5,7-tetranitro-1,3,5,7-tetrazocine (HMX)). The major focus of this report is on the fate and effects of MC in the marine environment. Most MC observed in this study rapidly degraded in aqueous
exposure systems and nitroaromatics showed a significant binding affinity with organic matter.
Artificial intelligence (AI) is everywhere, promising self-driving cars, medical breakthroughs, and new ways of working. But how do you separate hype from reality? How can your company apply AI to solve real business problems?
Here’s what AI learnings your business should keep in mind for 2017.
Renal Toxicity Studies of Albino Rats Exposed to Common Emulsion Paint SolutionPremier Publishers
Emulsion paint solutions (EPS) are constantly used to decorate and protect different materials in the environment. The occupational exposure of professional painters and paint factory workers to EPS may predispose them to systemic toxicity. This work investigated the effects of EPS exposure on renal function indices in albino rats to assess potential renal toxicity. Twenty male albino rats weighing between 120-140g were collected and divided into four groups. Two groups were exposed to periodic intraperitoneal administration of 2.5mg/kg body weight (bw) of the EPS for 14days while the other two groups received the same dose of distilled water and served as control. The rats were sacrificed after 7and14days respectively, and their blood collected and analyzed for heavy metals, urea, creatinine and electrolytes, using standard methods. The rat kidneys were also excised, weighed and analyzed for total protein and histopathology. Results showed that bw, kidney weight, serum creatinine, urea and electrolytes decreased significantly(p<0.05) in the exposed groups compared to control. However, urea and Na+ increased significantly(p<0.05) after the initial 7days exposure. Kidney total protein increased by 20.83% and Pb, Ni, and Cd were detected in the exposed rats. Results of kidney histopathology showed intact renal tubules and glomeruli. These results suggest that exposure of albino rats to EPS caused significant alterations in the steady-state levels of renal function biomarkers. Therefore, prolonged exposure may exert deleterious effects on renal function.
E-screen assay validation: evaluation of estrogenic activity by MCF7 cell cul...Agriculture Journal IJOEAR
— Natural and synthetic estrogens have been detected in rivers, lakes and estuaries in many parts of the world. Primary sources of these compounds are domestic and industrial effluents, which are not deleted after the water treatment. Estrogen has been the endocrine disruptor most researched to be very active biologically and be the etiologic agent of diverse types of cancer and other conditions such as endometriosis, precocious puberty, feminization, masculinization, sterility. In this context, we use water of 36 natural reservoirs or dams, in a bioassay to characterize their estrogenicity in culture of MCF7 cells and obtained high concentration of estrogen in samples taken in Ibiúna and Equestrian Santo Amaro / SP. However, certain concentration in our samples for most water samples from different regions was very close to the limit of quantification by bioassay and estrogen was in fmol. It has been shown that e-screen assay with MCF7 cells is a sensitive and stable tool for quantitative analysis of estrogenicity of water and can easily be developed and implemented for routine for estrogen quantification also in animal food and man, aqueous and plastics etc. Keywords— endocrine disrupters, estrogen, breast cancer cells, (MCF7) bioassay: E-screen assay
Effects of Fenitrothion on some histo-architecture of freshwater fish Channa ...IOSR Journals
The presence of insecticide in the environment, due to extensive use in agriculture is of potential toxicological concern for fish. Histotoxicological studies have been widely used as biomarkes in the evaluation of the health of fish exposed to the pesticides studies. In the present study the hazardous effect of the organophosphate insecticide, Fenitrothion on the histology of the fresh water fish (Channa punctatus) after exposure for 21 days was investigated. Fish used in the experiment was nearly similar weight and length. The treated groups were compared with the control group for the histological changes in the selected tissue (kidney, liver and heart) and marked changes were observed.
IOSR Journal of Pharmacy and Biological Sciences(IOSR-JPBS) is an open access international journal that provides rapid publication (within a month) of articles in all areas of Pharmacy and Biological Science. The journal welcomes publications of high quality papers on theoretical developments and practical applications in Pharmacy and Biological Science. Original research papers, state-of-the-art reviews, and high quality technical notes are invited for publications.
Biometric Assessment of Bacteriological Profile of Borehole Water in Relation...Premier Publishers
Borehole water is a major water source in some parts of the world and human health depends largely on the quality of water consumed. Hence, bacteriological assessment of borehole water in relation to distance and age of septic tanks in nine student’s hostels in Ikot Udota was investigated using standard scientific methods. The organisms isolated were: Escherichia coli, Klebsiella spp, Bacillus spp Pseudomonas spp, Streptococcus spp, Enterobacter spp, Salmonella typhi, Vibrio cholerae, and Proteus vulgaris. The result revealed that the total bacteria counts of the samples ranged from 30cfu/ml in Ario house, 246 cfu/ml in Macdone. However, Macdone’s lodge had the highest faecal coliform count with 2 (66.6%), while Anthonys’ had the lowest faecal coliform count with 1 (33.3%). Correlation analysis signaled that there is a significant (p<0.05) likelihood that contaminants enrichment grossly emanated from a point source seeing that 72.2% of TBC and 73.5% of FCC were associated with short distances from septic tanks. Also, 28.5% of TBC and 15.4% of FCC were associated with borehole age. Conclusively, boreholes should be situated far from refuse/sewage disposal units and routine treatment of old borehole water sources is a necessity.
Operation “Blue Star” is the only event in the history of Independent India where the state went into war with its own people. Even after about 40 years it is not clear if it was culmination of states anger over people of the region, a political game of power or start of dictatorial chapter in the democratic setup.
The people of Punjab felt alienated from main stream due to denial of their just demands during a long democratic struggle since independence. As it happen all over the word, it led to militant struggle with great loss of lives of military, police and civilian personnel. Killing of Indira Gandhi and massacre of innocent Sikhs in Delhi and other India cities was also associated with this movement.
Synthetic Fiber Construction in lab .pptxPavel ( NSTU)
Synthetic fiber production is a fascinating and complex field that blends chemistry, engineering, and environmental science. By understanding these aspects, students can gain a comprehensive view of synthetic fiber production, its impact on society and the environment, and the potential for future innovations. Synthetic fibers play a crucial role in modern society, impacting various aspects of daily life, industry, and the environment. ynthetic fibers are integral to modern life, offering a range of benefits from cost-effectiveness and versatility to innovative applications and performance characteristics. While they pose environmental challenges, ongoing research and development aim to create more sustainable and eco-friendly alternatives. Understanding the importance of synthetic fibers helps in appreciating their role in the economy, industry, and daily life, while also emphasizing the need for sustainable practices and innovation.
Welcome to TechSoup New Member Orientation and Q&A (May 2024).pdfTechSoup
In this webinar you will learn how your organization can access TechSoup's wide variety of product discount and donation programs. From hardware to software, we'll give you a tour of the tools available to help your nonprofit with productivity, collaboration, financial management, donor tracking, security, and more.
The Roman Empire A Historical Colossus.pdfkaushalkr1407
The Roman Empire, a vast and enduring power, stands as one of history's most remarkable civilizations, leaving an indelible imprint on the world. It emerged from the Roman Republic, transitioning into an imperial powerhouse under the leadership of Augustus Caesar in 27 BCE. This transformation marked the beginning of an era defined by unprecedented territorial expansion, architectural marvels, and profound cultural influence.
The empire's roots lie in the city of Rome, founded, according to legend, by Romulus in 753 BCE. Over centuries, Rome evolved from a small settlement to a formidable republic, characterized by a complex political system with elected officials and checks on power. However, internal strife, class conflicts, and military ambitions paved the way for the end of the Republic. Julius Caesar’s dictatorship and subsequent assassination in 44 BCE created a power vacuum, leading to a civil war. Octavian, later Augustus, emerged victorious, heralding the Roman Empire’s birth.
Under Augustus, the empire experienced the Pax Romana, a 200-year period of relative peace and stability. Augustus reformed the military, established efficient administrative systems, and initiated grand construction projects. The empire's borders expanded, encompassing territories from Britain to Egypt and from Spain to the Euphrates. Roman legions, renowned for their discipline and engineering prowess, secured and maintained these vast territories, building roads, fortifications, and cities that facilitated control and integration.
The Roman Empire’s society was hierarchical, with a rigid class system. At the top were the patricians, wealthy elites who held significant political power. Below them were the plebeians, free citizens with limited political influence, and the vast numbers of slaves who formed the backbone of the economy. The family unit was central, governed by the paterfamilias, the male head who held absolute authority.
Culturally, the Romans were eclectic, absorbing and adapting elements from the civilizations they encountered, particularly the Greeks. Roman art, literature, and philosophy reflected this synthesis, creating a rich cultural tapestry. Latin, the Roman language, became the lingua franca of the Western world, influencing numerous modern languages.
Roman architecture and engineering achievements were monumental. They perfected the arch, vault, and dome, constructing enduring structures like the Colosseum, Pantheon, and aqueducts. These engineering marvels not only showcased Roman ingenuity but also served practical purposes, from public entertainment to water supply.
The Art Pastor's Guide to Sabbath | Steve ThomasonSteve Thomason
What is the purpose of the Sabbath Law in the Torah. It is interesting to compare how the context of the law shifts from Exodus to Deuteronomy. Who gets to rest, and why?
Students, digital devices and success - Andreas Schleicher - 27 May 2024..pptxEduSkills OECD
Andreas Schleicher presents at the OECD webinar ‘Digital devices in schools: detrimental distraction or secret to success?’ on 27 May 2024. The presentation was based on findings from PISA 2022 results and the webinar helped launch the PISA in Focus ‘Managing screen time: How to protect and equip students against distraction’ https://www.oecd-ilibrary.org/education/managing-screen-time_7c225af4-en and the OECD Education Policy Perspective ‘Students, digital devices and success’ can be found here - https://oe.cd/il/5yV
Instructions for Submissions thorugh G- Classroom.pptxJheel Barad
This presentation provides a briefing on how to upload submissions and documents in Google Classroom. It was prepared as part of an orientation for new Sainik School in-service teacher trainees. As a training officer, my goal is to ensure that you are comfortable and proficient with this essential tool for managing assignments and fostering student engagement.
How to Make a Field invisible in Odoo 17Celine George
It is possible to hide or invisible some fields in odoo. Commonly using “invisible” attribute in the field definition to invisible the fields. This slide will show how to make a field invisible in odoo 17.
How to Split Bills in the Odoo 17 POS ModuleCeline George
Bills have a main role in point of sale procedure. It will help to track sales, handling payments and giving receipts to customers. Bill splitting also has an important role in POS. For example, If some friends come together for dinner and if they want to divide the bill then it is possible by POS bill splitting. This slide will show how to split bills in odoo 17 POS.
This is a presentation by Dada Robert in a Your Skill Boost masterclass organised by the Excellence Foundation for South Sudan (EFSS) on Saturday, the 25th and Sunday, the 26th of May 2024.
He discussed the concept of quality improvement, emphasizing its applicability to various aspects of life, including personal, project, and program improvements. He defined quality as doing the right thing at the right time in the right way to achieve the best possible results and discussed the concept of the "gap" between what we know and what we do, and how this gap represents the areas we need to improve. He explained the scientific approach to quality improvement, which involves systematic performance analysis, testing and learning, and implementing change ideas. He also highlighted the importance of client focus and a team approach to quality improvement.
The Indian economy is classified into different sectors to simplify the analysis and understanding of economic activities. For Class 10, it's essential to grasp the sectors of the Indian economy, understand their characteristics, and recognize their importance. This guide will provide detailed notes on the Sectors of the Indian Economy Class 10, using specific long-tail keywords to enhance comprehension.
For more information, visit-www.vavaclasses.com
Ethnobotany and Ethnopharmacology:
Ethnobotany in herbal drug evaluation,
Impact of Ethnobotany in traditional medicine,
New development in herbals,
Bio-prospecting tools for drug discovery,
Role of Ethnopharmacology in drug evaluation,
Reverse Pharmacology.
2. Author's personal copy
R. Hardman et al. / Aquatic Toxicology 86 (2008) 20–37 21
Relevant to the findings presented here is a brief synopsis of 2. Materials and methods
what is known about the piscine biliary system. Previous studies
from this laboratory have shown the hepatobiliary systems 2.1. STII medaka
of channel catfish (Ictalurus punctatus), trout (Oncorhynchus
mykiss), and medaka (Oryzias latipes) to exhibit numerous For decades various color mutant strains of medaka (O.
transitional biliary passageways, termed bile preductules, latipes), acquired from natural and commercially available pop-
between hepatocellular canaliculi and biliary epithelial cell ulations, have been maintained in the Laboratory of Freshwater
(BEC) delimited bile ductules (Hampton et al., 1988; Hardman Fish Stocks at Nagoya University, Japan. Cross breeding from
et al., 2007b; Okihiro and Hinton, 2000). These transitional these stocks was used to produce a stable “transparent” strain of
biliary passageways, first described in the mammalian liver by medaka. See-through (STII) medaka are homozygous recessive
Steiner and Carruthers (1961), are anatomically associated with for all four pigments (iridophores, leucophores, xanthophores,
peri-portal canals of Hering and oval cells in the mammalian melanophores). Exhibiting no expression of leucophores and
liver (Fausto, 2000; Fausto and Campbell, 2003; Golding et al., melanophores, and minimal expression of xanthophores and
1996; Theise et al., 1999). iridiophores, STII medaka are essentially transparent through-
More recent in vivo investigations in STII medaka that out their life cycle (Wakamatsu et al., 2001), and allow high
elucidated structure/function relationships in both 2 and 3 resolution (<1 m) non invasive in vivo imaging of internal
dimensional contexts revealed medaka livers to be replete with organs and tissues at the subcellular level (Fig. 1) (Hardman
bile preductular epithelial cells (BPDECs), and the transitional et al., 2007a,b; Hinton et al., 2004). Our STII medaka colony,
biliary passageways (bile preductules, BPDs) associated with maintained at Duke University since 2002, was first cultured
them (Hardman et al., 2007a,b). These investigations revealed with stock obtained from Prof. Y. Wakamatsu (Nagoya Uni-
that the intrahepatic biliary system in medaka is largely an inter- versity). Medaka were housed in a charcoal filtrated, UV
connected network of equidiameter (1–2 m) canaliculi and bile treated re-circulating system (City of Durham, NC, water) main-
preductules, organized through a polyhedral (hexagonal) struc- tained at 25 ± 0.5 ◦ C. Water chemistries were maintained at: pH
tural motif, that occupies the majority of the liver corpus (∼95%) (7.0–7.4), dissolved oxygen (6–7 ppm), ammonia (0–0.5 ppm),
uniformly. Larger bile ductules and ducts were predominantly nitrite (0–0.5 ppm) and nitrate (0–10 ppm). A diel cycle of
found in the hilar and peri-hilar region of the liver, and it follows, 16:8 h light:dark was employed. Medaka larvae were fed ground
an arborizing biliary tree (as described in mammals) was absent, (pressed through a 60 m sieve) Otohime diet (Ashby Aquat-
seen only in the rudimentary branching of intrahepatic ducts ics, West Chester, PA) via an automatic feeder seven times per
from the hilar hepatic duct. From prior investigations we rec- day. Because Otohime has been shown to be free of estro-
ognized injury to BPDECs may serve to distort bile preductular genic complications (Inudo et al., 2004), we considered it an
lumina and result in transient or longer alterations to intrahep- optimal fish food. In addition, all brood stock fish diets were sup-
atic bile flow, and that attention to BPDECs/BPDs, and their plemented daily with Artemia nauplia (hatched brine shrimp).
relationship to the interconnected intrahepatic biliary network, Egg clusters, collected daily, were cleaned in embryo rearing
is essential to understanding the spectrum of responses of the medium (ERM), and individual fertilized eggs were separated
piscine hepatobiliary system to xenobiotics that target this organ and maintained in ERM at 25 ◦ C. Unconsumed diet, detritus
system. and associated algal material were removed from rearing and
With a better comparative understanding of the medaka hep- brood stock tanks daily. Care and maintenance of medaka were in
atobiliary system established in prior studies, and normalcy accordance with protocols approved by the Institutional Animal
characterized, we were then able to investigate response of Care and Use Committee (IACUC; A117-07-04; A141-06-04;
the hepatobiliary system to xenobiotics in vivo. To do so A173-03-05).
we used -naphthylisothiocyanate (ANIT), a well described
hepatotoxicant that induces hallmark responses in the mam- 2.2. Xenobiotic exposures
malian biliary system, namely: cytotoxicity in biliary epithelium
of bile ductules and ducts, cholestasis (Hill and Roth, 1998; Studies were designed to evaluate hepatobiliary struc-
Orsler et al., 1999; Waters et al., 2002; Woolley et al., 1979), ture/function during the onset, progression, and recovery from
and biliary tree arborization (biliary epithelial cell hyperpla- ANIT exposure. Multiple cohorts of STII medaka (10–30 fish)
sia) (Alpini et al., 1992; Connolly et al., 1988; Masyuk et were exposed to the reference toxicant -naphthylisothiocyanate
al., 2003). Because biliary toxicity and cholestasis are poorly (ANIT) to target hepatocytes and biliary epithelia for toxic
understood in piscine species, and because we now under- response. Acute and chronic aqueous bath exposures were
stand the medaka hepatobiliary system to be more similar carried out from 3 to 60 days post fertilization (dpf). Con-
to mammalian liver architecture than previously considered trols consisted of untreated medaka, and medaka treated with
(Hardman et al., 2007b), we considered ANIT a good toxicant dimethyl sulfoxide (DMSO; ANIT solvent). All exposures were
for investigation of comparative hepatology. The goals of these carried out in 750 ml wide-bottom glass rearing beakers at
investigations were to determine the cellular targets of ANIT in 25 ◦ C, using a 16 h light/8 h dark cycle. Aqueous bath expo-
medaka and to characterize toxic response, relative to what is sure medium consisted of ERM:de-ionized water (1:3). Acute
known regarding ANIT induced hepatotoxicity in mammalian exposures: medaka cohorts were reared in aqueous baths that
liver. were given a single aliquot of ANIT to achieve exposure con-
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22 R. Hardman et al. / Aquatic Toxicology 86 (2008) 20–37
Fig. 1. Non invasive in vivo imaging of hepatic parenchyma and blood to bile transport. (A) Brightfield microscopy, STII medaka, 30 dpf, left lateral view. The
liver (L), gall bladder (GB) and associated organs are observable through the abdominal wall. (A1) Widefield fluorescence microscopy of region of interest (gray
square) in frame A, illustrating in vivo imaging of -Bodipy C5 phosphocholine fluorescence (green) transport through intrahepatic biliary passageways (IHBPs)
of the liver, and gall bladder. (B1) Confocal DIC image, single optical section. STII medaka, 9 dpf. Two rows of hepatocytes in longitudinal section characterize
parenchymal architecture (muralium). Hepatic nuclei (HN). Red blood cells in circulation through sinusoids (S/r) appear as stacked ovate structures. (B2) Same as B1,
illustrating concentrative transport of -Bodipy C5 phosphocholine (FITC, green fluorescence) from sinusoids (S/r) to IHBPs. Imaged acquired in vivo 30 min post
administration of fluorophore in aqueous bath. (B3) Composite of B1 (DIC) and B2 (FITC) localizing fluorophore transport to the area between apical membranes of
adjacent hepatocytes. (C) Surface map of region of interest (white square) in B2 illustrating concentration of the fluorophore in IHBPs. (D) Semi-quantitative analysis
of fluorescence profile across an 18.3 m section (white rectangle in frame C) of the parenchyma from sinusoid (S) to IHBP, showed an increase in fluorescence,
from sinusoid to canaliculus (IHBP), of ∼20-fold.
centrations ranging from 0.25 M to 10 M ANIT. Chronic anesthetized fish 7 days after the 2nd ANIT injection, placed in
exposures: medaka were serially exposed every 3 days or once 4% paraformaldehyde overnight at 4 ◦ C, dehydrated in graded
weekly (static renewal) for the duration of study using the same ethanol solutions, cleared with xylene, and paraffin embedded
concentrations given for acute exposure. At given time points at 60 ◦ C. A 200 mg/kg ANIT dose was employed because: our
during exposure regimes (e.g. at 5 min, 15 min. . . 3, 6, 12, 24, preliminary studies in medaka showed 200 mg/kg ANIT to be
48, 72 and 96 h, and day 7, 10, 20, 30, 40 and 60 post expo- the LD50 (96 h) for IP injection; an LD50 of 200 mg/kg of ANIT
sure) subpopulations of medaka were removed from a cohort has been reported in rats following oral exposure (McLean and
for in vivo and ex vivo studies (histological, immunohistochem- Rees, 1958); and biliary epithelial cell proliferation has been
ical, and transmission electron microscopy) of the hepatobiliary observed in rats treated with a single oral dose of 150 mg/kg of
system. ANIT (Kossor et al., 1995). While embryo, larval and juvenile
Adult STII medaka (>90 dpf) were anesthetized with medaka were subjected to waterborne ANIT exposures, IP injec-
0.1 g/L tricane methanesulfonate (MS-222) and twice injected tions were employed in adult fish for comparison to published
(intraperitoneal; IP) with 200 mg/kg ANIT, with a 7-day depu- ANIT studies in rodent animal models, and to investigate the
ration period between injections. Livers were removed from sensitivity of medaka to both routes of exposure.
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R. Hardman et al. / Aquatic Toxicology 86 (2008) 20–37 23
2.3. In vivo imaging Table 1
Fluorescent probes employed for in vivo investigations
Prior studies (Fig. 1) described the utility of fluorophores Probe Exposure concentration
such as -Bodipy C5 phosphocholine and fluorescein isothio- 7 BR: 7-benzyloxyresorufin 10–50 M
cyanate in elucidating the intra- and extrahepatic biliary system -Bodipy C5-HPC [BODIPY® 581/591 C5-HPC 30 nM–10 M
of STII medaka, and the application of exogenous fluorophores (2-(4,4-difluoro-5-(4-phenyl-1,3-butadienyl)-4-
for in vivo evaluation of blood to bile transport (Hardman et al., bora-3a,4a-diaza-s-indacene-3-pentanoyl)-1-
2007a,b). Briefly, fluorescent probes were administered to con- hexadecanoyl-sn-glycero-3-phosphocholine)
Bodipy FL C5-ceramide 500 nM–5 M
trol and ANIT treated STII medaka, via aqueous bath, prior [N-(4,4-difluoro-5,7-dimethyl-4-bora-3a,4a-
to in vivo imaging to aid in elucidation of biological struc- diaza-s-indacene-3-pentanoyl)
ture/function and interpretation of normalcy and toxic response. sphingosine]
Time points for in vivo investigations varied from 10 min to 2 h FITC: fluorescein isothiocyanate 1 nM–50 M
post fluorophore administration, dependent on the fluorescent DAPI [4 ,6-diamidino-2-phenylindole, 0.3–3.0 M
dihydrochloride], *1 mM solution in DMSO
probe employed, and the portion of the hepatobiliary system YO-PRO® -1 iodide (491/509) 1 M
being studied. By example; Bodipy C5 HPC and fluorescein
isothiocyanate accumulation in the hepatic parenchyma was first
observed at ∼10 min post fluorophore exposure, with saturation
(peak fluorescence; proxy for equilibrium of fluorophore uptake Photoshop (Adobe, Inc.), Amira 3D (Mercury Computer Sys-
and excretion) of the fluorophores in the hepatic parenchyma tems, Berlin), ImageJ (V1.32j), IP Lab software (Scanalytics,
occurring at ∼40 min. In contrast, Bodipy C5 ceramide satura- Inc., version 3.55), and Zeiss Image Browser (Carl Zeiss). All
tion was commonly observed at ∼70 min. The majority of in vivo transmission electron microscopy (TEM) was performed at the
observations were made between 15 and 50 min post fluorophore Laboratory for Advanced Electron and Light Optical Methods
exposure. In addition to the use of exogenous fluorophores, aut- (LAELOM), College of Veterinary Medicine, North Carolina
ofluorescence was also employed for in vivo elucidation of cell State University. For TEM investigations individual medaka
and tissue morphology, and xenobiotic response. were anesthetized and fixed in 4F:1G fixative (4% formalde-
After fluorophore exposure medaka embryos, larvae and hyde and 1% glutaraldehyde in a monobasic phosphate buffer
juveniles (treated and untreated), at various stages of devel- with a final pH of 7.2–7.4 and a final osmolality of 176 mosmol).
opment, and at the time-points described, were sedated with Following processing and embedment thin sections (Spurr resin
10 M tricaine-methane sulfonate (MS-222) in accordance with embedded) were made and examined using a FEI/Philips EM
IACUC approved animal protocols. Once sedated, medaka were 208S Transmission Electron Microscope.
mounted in a solution of de-ionized water:ERM (3:1) on depres-
sion well glass slides, oriented in the desired the anatomical
2.5. Fluorescent probes
position, and glass slides sealed with a cover slip. Medaka were
then imaged live with brightfield, widefield and/or laser scan-
Fluorescent probes employed are listed in Table 1. Fluo-
ning confocal fluorescence microscopy (LSCM). With widefield
rophores were acquired through Invitrogen/Molecular Probes
and LSCM salient features of the organ system such as canali-
(Carlsbad, CA). All fluorescent probes were administered to
culi, space of Disse, endothelial cells, biliary epithelial cells,
STII medaka via aqueous bath at the exposure concentration
red blood cells, and hepatocytes and their nuclei, were clearly
ranges given, under dark conditions, at room temperature.
resolved. Confocal stacks from in vivo imaging (LSCM) of the
hepatobiliary system were used for 3D reconstructions, and from
these, architectural, morphometric and volumetric analyses were 2.6. Chemicals
made.
-Naphthyliosthiocyanate (Sigma, N4525), tricaine-
2.4. Imaging systems methane sulfonate (Sigma, E10521), dimethyl sulfoxide
(DMSO) (Sigma, 276855), and Pronase (streptococcal
Confocal fluorescence microscopy was performed on a Zeiss protease, Sigma).
510 Meta system with Zeiss LSM 5 Axiovision image acquisi-
tion software, Argon and HeNe laser, Carl Zeiss C-apochromatic 2.7. Immunohistochemistry
40×/1.2, and C-apochromatic 10×/0.45. Widefield fluores-
cence microscopy was performed on a Zeiss Axioskopp Cytokeratins were localized on paraffin sections of medaka
with DAPI/TRITC/FITC filter cube set. Excitation/emission liver using mouse pan-cytokeratin (AE1/AE3, 1:200 dilution)
parameters for widefield microscopy were: DAPI/UV (Ex antibody (Zymed, CA, USA) and visualized with the DAKO
360–380 nm/Em All Vis >400 nm); FITC (Ex 450-490 nm/Em EnvisionTM+System (Dako, CA, USA). In brief; after de-
515–565 nm); TRITC (Ex 528–552 nm/Em 578–632 nm). For waxing and rehydration of paraffin sections, heat induced
brightfield microscopy a Nikon SZM 1500 dissecting micro- epitope retrieval was carried out prior to immuno-labeling.
scope with a Nikon DXM 1200 digital capture system was Endogenous peroxidase activity was blocked by incubating sec-
employed. Software used: EclipseNet (Nikon, USA), Adobe tions with 0.03% hydrogen peroxide and non-specific labeling
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24 R. Hardman et al. / Aquatic Toxicology 86 (2008) 20–37
was reduced by blocking sections with 5% normal goat serum for
20 min. Sections were incubated with AE1/AE3 (0.01 M phos-
phate buffer saline at pH 7.4, 0.1% Tween 20, 0.1% sodium azide
and 1% BSA) at 4 ◦ C overnight. After rinsing in PBS sections
were incubated with secondary antibody (peroxidase labeled
polymer conjugated goat anti-mouse immunoglobulin (IgG))
at room temperature for 30 min. Sections were rinsed a sec-
ond time with PBS, visualized with diaminobenzidine (DAB),
counterstained with Harris’ hematoxylin and observed/imaged
with brightfield microscopy. Negative controls were pre-
pared by substituting primary antibody with non immune
serum.
After fixation of anaesthetized medaka in 10% formalin for
24 h whole mount paraffin sections were prepared and assayed
Fig. 2. Overview: responses of the medaka hepatobiliary system to aqueous
with proliferating cell nuclear antigen (PCNA; Biogenics, San ANIT.
Ramon, CA) by the histopathology laboratory in the College of
Veterinary Medicine at North Carolina State University. As a
positive control, PCNA labeling of the gut was evaluated. 3.2. Canalicular attenuation and dilation and bile
preductular lesions
2.8. Statistics
Medaka cohorts exposed to 1–5 M aqueous ANIT exhibited
distinct alterations to the intrahepatic biliary system, to include
Differences in fluorescence intensity in digital image cap-
canalicular attenuation and dilation (acute exposure), and bile
tures were analyzed statistically using ImageJ (NIH, (V1.32j)
preductular lesions (chronic exposure). In vivo investigations in
and Statview software (SAS institute, Cary, NC). Two way
acutely exposed medaka revealed a simultaneous attenuation
ANOVA with Fisher’s T-test was employed to assess statistically
and dilation of bile canaliculi, first observed 4 h post ANIT
significant differences in fluorescence intensity. Background
exposure (1–3 M, Fig. 3). Canalicular attenuation/dilation
fluorescence and autofluorescence were accounted for in statis-
appeared relatively uniformly throughout the parenchyma, and
tical analyses. Descriptive statistics were used for volumetric
persisted for 96–120 h post acute exposure. Both attenuated and
and morphometric analyses. Pearson’s correlation coefficient
dilated canaliculi occurred in close spatial proximity (e.g. within
was used for comparison of calculated versus measured mor-
20 m); where one bile segment, or canaliculus, was observed
phometric values in vivo. Equality of variance F-test was
to be attenuated, the adjacent connected branching bile segment
used for assessment of blood to bile transport; temporal
was observed to be dilated. Dilated canaliculi, which ranged
evaluation of fluorescence intensities across sinusoid, hepato-
between ∼3 and 4 m, were found to be up to ∼3 times normal
cytic cytosol and canalicular spaces. All quantitative analyses
diameter (1.3 ± 0.4 m). Attenuated canaliculi were distinct,
were performed on unaltered (no deconvolution), or normal-
appearing as fine sinuous passageways 0.4–0.8 m in diameter
ized, single optical sections from in vivo confocal image
(Fig. 3A and B).
captures.
Where acute exposure to 1–3 M aqueous ANIT resulted in
canalicular dilation/attenuation, chronic exposures to 2–5 M
3. Results aqueous ANIT (>3 days) resulted in foci of alteration that
appeared more consistent with changes to bile preductule
3.1. Overview (BPD) structural integrity. Where normal (control) canali-
culi and bile preductules appeared as equidiameter tubular
Exposure of medaka to ANIT resulted in distinct concentra- passageways (1.3 ± 0.4 m), altered bile preductules exhib-
tion dependent responses, summarized in Fig. 2. These included: ited marked irregularities in lumen morphology and increased
(1) canalicular attenuation and dilation in response to 1–3 M lumen diameter (Fig. 4B, C, E and F), suggesting loss of
acute aqueous ANIT exposure; (2) bile preductular lesions integrity of hepatocellular/bile preductular epithelial cell junc-
in response to 2–5 M chronic ANIT exposure; (3) hydropic tions. Foci of alteration were frequently associated with changes
vacuolation, at ANIT concentrations of 2–8 M ANIT, which to bile preductular epithelia cell (BPDEC) morphology. Trans-
resulted in a distinct “pebbling” of the liver when evaluated mission electron micrographs (TEM) of livers from medaka
in vivo; and (4) chronic passive hepatic congestion, an end cohorts exposed to 2–5 M aqueous ANIT typically showed
stage response of the liver associated with high mortality, at BPDECs with an increased cytosolic area, cytosolic vacuo-
6–8 M ANIT. In vivo observations were correlated with ex lation, and altered cell membrane integrity (Fig. 4E and F).
vivo histological and electron microscopic studies to aid in When lesions were reconstructed and examined in 3 dimen-
interpretation of in vivo findings and to verify affected cell sions (Fig. 4D and E) altered BPDs were often found to
types. These responses are described in detail in the following terminate in blind ends, unconnected to surrounding canali-
sections. culi/bile preductules. It follows that the majority of lesions
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Fig. 3. Phenotypic responses of the medaka hepatobiliary system: canalicular attenuation and dilation. (A and B) STII medaka, 24 dpf, 2.5 M aqueous ANIT
(48 h, acute exposure): LSCM in vivo imaging illustrating dilated (black arrowheads) and attenuated bile canaliculi (white arrowheads). IHBPs (green fluorescence)
elucidated with fluorescein isothiocyanate (FITC). Epithelium is largely non-fluorescent, aside from weak fluorescence of surrounding hepatocellular cytosol and
nucleus (HN, gray arrowhead). Frame B is same as frame A, in a different plane of section in the liver. Example diameters of IHBPs are given. (C) STII medaka control,
30 dpf, showing typical morphological appearance of IHBPs in vivo. Normalcy finds canaliculi and bile preductules equidiameter throughout the liver, averaging
1.3 m (±0.3 m), also see blue arrowhead in frame (B). (D) TEM, STII medaka, 30 dpf, 48 h post exposure to 1 M ANIT. Ultrastructure suggested hepatocellular
swelling (HN, hepatocyte nuclei) to be associated with canalicular attenuation/dilation (white and black arrowheads). Normal morphological appearance of a bile
preductular epithelial cell indicated by green arrowhead.
appeared to be localized to BPDEC/hepatocellular junctional exhibited no such phenotype when allowed to recover for 7 days
complexes (bile preductules); unique morphological complexes in an ANIT free bath.
described by Hampton et al. (1988) and Hardman et al.
(2007b). 3.3. Hydropic vacuolation
BPD lesions were observed in all fish chronically exposed
to 2–5 M aqueous ANIT. Onset of lesions appeared approx- Acute and chronic aqueous exposures to 2–8 M ANIT
imately 48 h post ANIT exposure, and a higher incidence of resulted in a distinct “pebbling” of the liver, a phenotypic
lesions was associated with increased exposure duration. By response consistently evident by 24 h post ANIT exposure
example; at 10 days of chronic ANIT exposure approximately (Fig. 5), which was not observed in DMSO or untreated
10% of bile preductular complexes (transitional biliary passage- medaka, nor readily apparent at lower or higher ANIT expo-
ways) appeared to be affected. BPD lesions persisted for the sure concentrations. Non invasive in vivo imaging (Fig. 5C
duration of chronic exposure studies (e.g. out to 60 days), and and E) revealed intracellular ovate structures within hepato-
foci of alteration appeared randomly distributed in the livers cytes and biliary epithelia, which, when viewed at the organ
examined. BPD lesions, like canalicular attenuation/dilation, level of organization (Fig. 5A and B), manifested as a “peb-
were observed to be a reversible form of injury, as medaka bling” of the hepatic parenchyma. This phenotype was observed
withdrawn from chronic exposures (2–5 M aqueous ANIT) with the aid of autofluorescence (Fig. 5A and B) and/or
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26 R. Hardman et al. / Aquatic Toxicology 86 (2008) 20–37
Fig. 4. Phenotypic responses of the medaka hepatobiliary system: bile preductular lesions. (A) STII medaka control, 23 dpf: LSCM, in vivo, single optical section.
Sinusoids (S), bile preductules (BPD), hepatocellular nuclei (HN). Parenchyma elucidated with Bodipy C5 Ceramide. (B) STII medaka, 30 dpf: LSCM, in vivo, single
optical section, 10 days chronic exposure to 2.5 M aqueous ANIT illustrating BDP lesions (orange arrowheads). White arrows indicate BPDECs. Sinusoid with red
blood cell (S/r). (C) STII medaka, 28 dpf: LSCM, in vivo, single optical section, 3 days chronic exposure to 5 M ANIT, illustrating appearance of dilated BPDs
(gray arrowheads) and mild BDPEC cytomegaly (white arrows). (D) STII medaka control, 30 dpf: example of 3D reconstruction of IHBPs (green) and surrounding
sinusoids (S, red). (E) STII medaka, 30 dpf, 10 days chronic exposure to 2.5 M ANIT, reconstruction of terminal BPD lesion (IHBPs). (F) TEM: STII medaka, 26
dpf, 5 M ANIT, illustrating alterations to BPDECs associated with BPD lesions. Inset illustrates normal BPDEC morphology, scale bar = 2 m.
differential interference microscopy (DIC) alone (Fig. 5E). aqueous ANIT concentrations from 1–6 M. HV was observed
The application of exogenous fluorophores was not neces- to be most prevalent in the livers of medaka exposed to 4–6 M
sary for elucidating/imaging this phenotypic response (Fig. 5A ANIT, and occurred throughout the hepatic parenchyma, affect-
and B). ing ∼95% of the area of livers examined (Fig. 5B). Vacuoles
ANIT exposed medaka exhibiting a “pebbling” phenotype were first observed in response to 1 M ANIT, and of low preva-
were treated with the nuclear stain DAPI (via aqueous bath) lence, affecting ∼10% of observed areas of the liver. Vacuoles
to investigate whether intracellular ovate structures were asso- were also of lower prevalence at ANIT concentrations exceeding
ciated with nuclei. Ovate structures did not label with DAPI, 6 M (ranging from 5 to 20% of the area of the liver examined).
were distinguishable from hepatocyte and biliary epithelial cell Hence, a concentration dependent increase in HV was observed
nuclei, and were localized to the cytosol of affected cell types from 1 to 6 M ANIT, and decrease observed from 6 to 10 M.
(Fig. 5C). Medaka exhibiting this phenotypic response showed no overt
Ultrastructural investigations (TEM) revealed the alterations signs of impaired health, exhibiting normal swimming and feed-
to be membrane-less cytosolic structures ranging in diameter ing behavior. HV was not observed in the livers of DMSO control
from 2–10 m, which contained moderate to dense granular medaka.
infiltrates of low electron density (Fig. 5D); features con- In the majority of livers studied hepatocytes and biliary
sistent with hydropic vacuolation (symptomatic cell injury epithelia affected by HV appeared throughout the liver corpus,
and swelling, the result of the intracellular accumulation of with no apparent zonation; an observation enabled by the ability
water). Hydropic vacuoles (HV) occurred in both hepato- to observe/image internal liver structure at various depths (e.g.
cytes and BPDECs (Fig. 5D and E), and were observed up to 200 m from the liver surface with confocal microscopy).
to displace, and in some instances wrap themselves around, Hydropic vacuoles were found to be a reversible form of ANIT
cell nuclei. Vacuoles appeared as early as 6 h post ANIT induced cell injury; not observed in any cell type following
exposure, and were consistently marked by 24 h post expo- recovery from ANIT exposure. By example, medaka exposed
sure. to 3–6 M ANIT for 3 days, and subsequently reared in an
Formation of HVs was concentration dependent, with ANIT free bath for 7 days, showed no signs of HV in vivo or in
increasing prevalence of vacuolation associated with increasing ultrastructure (TEM) studies.
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R. Hardman et al. / Aquatic Toxicology 86 (2008) 20–37 27
Fig. 5. Phenotypic responses of the medaka hepatobiliary system: hydropic vacuolation. (A) STII medaka control, 20 dpf, ventral view, widefield fluorescence
microscopy, autofluorescence (DAPI/UV excitation). Inset scale bar = 100 m. Gill (GI), ventral aorta (VA), heart atrium (Ha), heart ventricle (Hv), liver (L), gall
bladder (GB), gut (Gt). (B) Pebbling phenotype: STII medaka, 20 dpf, ventral view, 4 M ANIT, 48 h of exposure, widefield fluorescence microscopy (autoflu-
orescence; FITC-DAPI/UV composite). Inset scale bar = 20 m. (C) STII medaka, 29 dpf, 4 M ANIT, 48 h of exposure. DAPI labeling (blue) differentiating
intracellular ovate structures from nuclei. (D) TEM: STII medaka, 28 dpf, 4 M ANIT, 24 h of exposure. Hydropic vacuolation in hepatocytes (black arrowheads)
and bile preductular epithelia (inset). (E) STII medaka, 29 dpf, 4 M ANIT, 24 h of exposure: In vivo confocal image (DIC and TRITC composite) of YO-PRO-1
labeling (green). Hydropic vacuoles (black arrowhead).
3.4. In vivo investigation of apoptosis promised membrane integrity. YO-PRO-1 fluorescent cells were
not observed in DMSO controls, and were only observed in tan-
Preliminary studies suggest it is possible to detect cells with dem with the development of hydropic vacuoles, typically within
compromised cell membranes in vivo. While these observa- 24–72 h post ANIT exposure. Due to the staining characteristics
tions are not conclusive, they merit mention. Putative apoptotic, of YO-PRO-1, which primarily labeled nuclei, and the fact that
or necrotic cells with compromised cell membranes were labeled cells also exhibited loss of normal cell morphology, it
detected/imaged in vivo using confocal microscopy and the flu- was difficult to differentiate affected cell types.
orescent probes SYTO® 16 green and YO-PRO-1, both of which
are established in vitro nucleic acid stains used for detection of 3.5. Biliary epithelial cell proliferation
apoptosis (the cationic fluorophores only enter cells with com-
promised cell membrane integrity) (Al-Gubory, 2005; Santos et In vivo and immunohistochemical analyses (AE1/AE3 and
al., 2006; Wlodkowic et al., 2007). Of these, YO-PRO-1 was PCNA), used to assess proliferation of BPDECs, BECs (cells
the fluorophore of choice for in vivo studies (Fig. 5E). Cells lining bile ductules and ducts) and hepatocytes in response to
incorporating YO-PRO-1 were observed in the livers of medaka ANIT, suggest biliary epithelial cells are early responders to
exposed to 3–6 M ANIT as early as 6 h post exposure. In the ANIT, with hepatocytic changes occurring subsequently (Fig. 6).
fields of liver observed in vivo, ∼3% of cells fluoresced as a BEC hyperplasia was first observed at 5 days of chronic expo-
result of YO-PRO-1 incorporation, indicative of cells with com- sure to 2–6 M ANIT, and remained apparent out to 60 days
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28 R. Hardman et al. / Aquatic Toxicology 86 (2008) 20–37
Fig. 6. Phenotypic responses of the medaka hepatobiliary system: biliary and bile preductular epithelial cells (A and A1) AE1/AE3 immunohistochemistry: STII
medaka DMSO control, ∼9 months of age. (A2) AE1/AE3 immunohistochemistry: STII medaka, ∼9 months of age, 72 h post injection 200 mg/kg ANIT, illustrating
denser BEC AE1/AE3 labeling and BEC cytomegaly. (B) TEM: STII medaka, 31 dpf, 5 days post exposure to 1 M ANIT, illustrating BPDEC alterations (red
arrowheads) and associated BPDs (orange arrows). Inset: normal BPD and BPDEC (arrowhead) morphology, 26 dpf, scale bar = 2 m. (B1) TEM: STII medaka,
34 dpf, 5 M ANIT, 24 h of acute exposure, illustrating BEC cytotoxicity (red arrowhead) and associated dilated bile passageway (black arrowhead). Lipid vesicles
(gray arrowhead), hydropic vacuolation (white arrowhead). Inset (scale bar = 5 m) illustrates normal appearance of BECs (gray arrowheads) and associated bile
passageway. (C) LSCM, in vivo, single optical section, STII medaka, 80 dpf, 60 days 2.5 M ANIT exposure. Under chronic exposure BPDECs (red arrowheads)
appeared enlarged and more numerous (contiguously) per unit area of liver examined, as compared to controls. (C1) STII medaka control illustrating normal in
vivo appearance of BPDs/BPDECs (red arrowheads). Hepatocytes (white arrowhead), sinusoid (gray arrowhead). (D) STII medaka, DMSO control, 55 dpf: six of
eight control livers exhibited no or minimal PCNA staining throughout the liver (L). Gall bladder (GB), Gut (Gt). (D1) STII medaka, 55 dpf, 2.5 M ANIT, 30 days
of chronic exposure: ANIT treated medaka exhibited stronger and more prevalent PCNA staining in the hilar and peri-hilar regions of the liver (circled areas in D
and D1).
during chronic exposure studies. The majority of proliferating clearly resolved in immunohistochemical preparations due to
cell nuclear antigen (PCNA) positive cells were localized to the their small size (3–8 m), and relatively low density compared
hilar and peri-hilar region of the livers examined, suggesting to hepatocytes and biliary epithelial cells (per unit volume of
BECs were the most responsive (hyperplastic) cell type (Fig. 6D liver). While BPDEC proliferation was not evidenced by PCNA
and D1). PCNA staining was occasionally observed in more dis- analyses, qualitative in vivo observations suggested changes to
tal regions of the liver in small cuboidal biliary epithelia of bile BPDECs consistent with mild BPDEC cytomegaly, and hyper-
ductules/ducts (see Fig. 7A for these cell types), though this plasia. In chronically exposed medaka BPDECs consistently
observation was infrequent, and encountered in livers of mature appeared, in vivo, more numerous, contiguous, and larger, as
medaka, older than 120 days (not shown in figures). PCNA pos- opposed to control livers (Fig. 6C).
itive hepatocytes, BECs, and BPDECs were not evident in acute Immunohistochemical studies with the pan cytokeratin stain
ANIT exposures, or chronic exposures exceeding 6 M ANIT. AE1/AE3, used to detect in biliary epithelial and hepatocytic
While PCNA positive BPDECs were not apparent in any expo- cytokeratins, also suggest BECs to be early responders to ANIT.
sure regime, it is possible that BPDECs, if labeled, were not In adult medaka injected with 200 mg/kg ANIT, BECs exhibited
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R. Hardman et al. / Aquatic Toxicology 86 (2008) 20–37 29
Fig. 7. Bile duct cystic vacuolation in response to aqueous ANIT. (A) STII medaka control, 40 dpf, H&E, showing normal morphology of an intrahepatic bile duct
and associated biliary epithelial cells (square and enlarged inset). (B) STII medaka, 40 dpf, H&E, 40 days of chronic exposure to 3 M ANIT. Cystic formations
(black arrowhead) were observed in bile ducts of the liver hilus. Cysts often contained inspissated bile or proteinaceous material. An enlarged vessel filled with red
blood cells (gray arrowhead), likely an early branch of the hepatic portal vein, can be seen below and left of the biliary cyst.
cytomegaly, as compared to DMSO (vehicle/solvent) controls 3.8. Volumetric studies on ANIT induced biliary changes
(Fig. 6A, A1 and A2). BECs lining bile ductules and ducts in
ANIT treated livers also appeared to label more heavily with While altered blood to bile transport was not evident via quan-
the AE1/AE3 cytokeratin antibodies, suggesting greater density, titative in vivo studies with FITC and Bodipy C5 Ceramide,
and perhaps, proliferation of these cell types. Modest vascular volumetric analyses (which can be considered a proxy for
endothelial staining with AE1/AE3 was also observed, though intrahepatic bile flow) from 3D in vivo investigations suggest dif-
with less consistency and intensity. ferences in intrahepatic biliary volume in ANIT treated versus
untreated medaka. Quantitative morphometric and volumetric
3.6. ANIT associated biliary cystic vacuolation analyses were performed on 3D reconstructions from two ANIT
treated medaka and three controls (Table 2). Volumetric indices
Chronic exposures to 3 M ANIT resulted in cystic vacuola- of an individual medaka (40 dpf) from a cohort exposed to
tion of larger bile ducts of the liver hilus, with accompanied 2.5 M ANIT for 30 days suggest a reduction in canalicular
hepatocellular changes; responses consistent with spongiosis lumen volume of ∼50% (Table 2). A second evaluation of an
hepatis, a probable degenerative lesion (Brown-Peterson et al., individual medaka from a cohort exposed to 1 M ANIT for 48 h
1999) (Fig. 7B). In histological preparations (H&E) cysts were volumetric indices suggested an increase in intrahepatic biliary
distinct, ranged from 40 to 100 m in diameter, and often con- volume. Relative to liver volume, biliary volume was found to
tained material consistent with inspissated bile or proteinaceous be 1.18%, versus a mean of 0.95% (±0.08) in control livers
material. Evident in the same livers were smaller hepatocellu- (Table 2). In both cases volumes of vasculature, parenchyma
lar vacuoles consistent with hydropic vacuolation (Section 3.3). and hepatocellular space, relative to total liver volume exam-
Cystic formations of this nature were encountered only during ined, remained well conserved across ANIT treated and control
chronic exposures, and were not observed in livers of acutely fish, from 8 to 40 dpf, indices which serve as controls, and which
exposed medaka (<3 days), regardless of ANIT concentration. can be used to assess precision across individual 3D volumetric
studies (Table 2).
3.7. Hepatobiliary transport
3.9. Cardiovascular changes
STII medaka exposed to 0.25– 8 M aqueous ANIT were
treated with the fluorophores FITC and Bodipy C5 Ceramide Aqueous ANIT concentrations of 4–8 M resulted in phe-
and examined for altered hepatobiliary transport at 6, 8, 12, notypic changes consistent with passive hepatic congestion. In
24, 48, and 96 h (Fig. 1, Fig. 8). In vivo confocal image cap- vivo investigations revealed a marked cardiovascular response,
tures (single optical sections) were measured (random repeated where all liver vasculature, afferent and efferent vessels, showed
measures) for fluorescence intensity in sinusoid, cytosol and increasing dilation in response to increasing ANIT concentra-
canalicular spaces. No impairment of blood to bile transport was tions (Fig. 9). Dilation of sinusoids, hepatic vein, and hepatic
detected for either fluorophore in response to 0.25–6 M aque- portal vein, were all observed. Sinusoid diameter was observed
ous ANIT exposures (Fig. 8). Loss of hepatobiliary transport to increase ∼2-fold at ANIT concentrations approaching the
function (for both FITC and Bodipy C5 Ceramide) was only LC100 (8 M). Where control sinusoids averaged 7.4 m in
observed in vivo at ANIT exposure concentrations exceeding diameter, sinusoid diameter averaged 15.3 m (±4.1, n = 18) at
6 M, ANIT concentrations also associated with vasodilation 8 M ANIT, 48 h post exposure (Fig. 9). Vasodilation of hepatic
and decreased cardiac output (discussed following). vasculature was observed in tandem with a concentration depen-
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30 R. Hardman et al. / Aquatic Toxicology 86 (2008) 20–37
Fig. 8. In vivo evaluations of altered hepatobiliary transport function in response to ANIT. (A) STII medaka control, 40 dpf, LSCM, single optical section, illustrating
normal appearance of FITC (green fluorescence) transport from blood to bile, through IHBPs of the liver (see also Fig. 1). (B) STII medaka, 40 dpf, LSCM, single
optical section of medaka liver 48 h post exposure to 6 M ANIT, illustrating reduced fluorescence of FITC in IHBPs and hepatocellular cytosol. Note increased
FITC fluorescence in blood plasma (gray arrowhead), but not in hepatocyte cytosol, and minimal fluorescence in IHBPs. Such an altered fluorescence profile would
be consistent with decreased hepatocellular uptake of fluorophore from blood plasma. (C) STII medaka, 20 dpf, quantitative analysis of blood to bile transport. The
statistical means of fluorescence intensity (n = 30) are given. No statistically significant difference in fluorophore transport was observed between controls and ANIT
treated animals (in vivo), at ANIT concentrations below 6 M.
dent decrease in heart rate and motility, observed in all medaka 4. Discussion
(n = 18) exposed to 4 M to 8 M ANIT (acute and chronic
exposures). By example: where control heart rates averaged 134 Results of this study suggest cells of medaka intrahepatic
(±9) beats per minute (bpm), medaka exposed to 8 M ANIT biliary system respond to ANIT, and that responses, both cellu-
exhibited heart rates of 118 (±12) bpm at 6 h post exposure, 73 lar and system level, are similar to those described in rodents
(±13) bpm at 24 h post exposure, and 61 (± 7) bpm at 48 h post (Alpini et al., 2001; Carpenter-Deyo et al., 1991; Connolly
exposure. Hence, the magnitude of both the vasodilation and et al., 1988; Hill et al., 1999; Kossor et al., 1993; Lesage et
heart rate responses were concentration (ANIT) dependent, and al., 2001; Orsler et al., 1999; Waters et al., 2001). Changes
appeared to be coupled. observed in vivo, and confirmed with ex-vivo analyses (histolog-
Table 2
Volumetric indices from 3D reconstructions: ANIT treated vs. untreated medaka
Compartment Control (%) ANIT treated (%)
8 dpf 12 dpf 30 dpf Mean (%) (S.D.): 8–12 dpf 2.5 M ANIT 30 dpf 1 M ANIT 30 dpf
IHBPs 1.03 0.86 1.01 0.97 (0.09) 0.50 1.18
Vasculature 6.33 8.60 7.60 7.51 (1.14) 7.30 7.92
Parenchyma 93.67 91.40 92.40 92.49 (1.14) 92.70 92.08
Hepatocellular 92.64 90.54 91.39 91.52 (1.06) 92.20 92.15
Volumetric comparisons between two ANIT treated and three untreated medaka. Individual indices, statistical mean and standard deviation (S.D.) of volumetric
analyses from control (untreated) livers at 8, 12, and 30 dpf are given. Indices are % volumes relative to volume of liver examined.
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R. Hardman et al. / Aquatic Toxicology 86 (2008) 20–37 31
Fig. 9. Phenotypic responses of the medaka hepatobiliary system: passive hepatic congestion. (A) STII medaka control (DMSO), 20 dpf, 24 h post exposure,
widefield fluorescence (DAPI/UV autofluorescence). Vasculature (V) appears non fluorescent (dark), epithelia of hepatic parenchyma appears light gray. Inset scale
bar = 100 m. Ventral aorta (Va), heart ventricle (Hv), heart atrium (Ha), liver (L). (B &C) STII medaka, 18 dpf, 4 M ANIT, 24 h post exposure: widefield fluorescence
(DAPI/UV autofluorescence) illustrating moderate dilation of hepatic vasculature (V). Inset scale bar = 100 m. Gill (Gl), sinus venosus (SV), gall bladder (GB). (C)
Widefield fluorescence (DAPI/TRITC composite) illustrating FITC (white arrows) in transport through the hepatic parenchyma (gray arrowhead), in the presence
of ANIT induced vasodilation (white arrowhead, also indicating red cells in circulation (S/r)). (D) STII medaka, 17 dpf, 8 M ANIT, 24 h, widefield microscopy
(DAPI/UV). (E) STII medaka, 24 dpf, 8 M ANIT, 48 h post exposure: In vivo LSCM confirmed dilation of intrahepatic vasculature occurred uniformly throughout
the liver. Vasculature lumena (white arrowheads), replete with red blood cells, appears dark gray, parenchyma fluoresces green (Bodipy C5 ceramide). (F) TEM: STII
medaka, 8 M ANIT, 20 dpf, 48 h post exposure: intrahepatic vessel showing abnormal (attenuated) endothelial cell membrane morphology (gray arrowhead), and
vasodilation (V). Endothelial cell nucleus (black arrowhead). Graph: ANIT dose-duration relationship of heart rate to sinusoid diameter. Indices are mean, ±S.E.
ical, immunohistochemical, ultrastructural), were; attenuation Of interest, canalicular dilation/attenuation was only dis-
and dilation of bile canaliculi, bile preductular lesions, hydropic tinct in vivo. Were in vivo observations not made, it is
vacuolation of hepatocytes and BPDECs, BPDEC cytomegaly, questionable whether this phenotypic response would have
and hyperplasia of BECs in the hilar and peri-hilar region of been detected simply employing histological or ultrastructural
the liver. While in vivo evaluations revealed no alterations to studies alone. Even knowing what to look for from in vivo
bile transport, volumetric analyses of 3D reconstructions from observations, attenuated/dilated canaliculi could not be clearly
ANIT treated medaka suggest a reduction in intrahepatic bil- discerned in histological preparations. In fixed tissue sections
iary passageway volume at 2.5 M ANIT (cholestasis?), and an canaliculi were often indistinct. It is also possible that tissue
increase in intrahepatic biliary passageway volume (choleresis?) processing may alter canalicular lumen diameter. Hence, even
at 1 M ANIT, with no changes to other volumetric liver indices when resolved/identified, histological observations of canaliculi
(Table 2). may have proven inaccurate. Likewise, canalicular attenua-
tion/dilation may have gone undetected in TEM investigations
4.1. Canalicular attenuation and dilation were the response not previously well recognized in vivo
(Fig. 3). Hence, in vivo observations were not only important
Canalicular dilation/attenuation, frequently observed in to elucidation of this phenotypic response, but elucidated this
response to 1–3 M aqueous ANIT, and evaluated both in vivo change in ways ex vivo techniques were not, we found, well
and via 3D reconstructions, appeared to be more consistent with suited.
an adaptive response of the intrahepatic biliary system, as no What may explain canalicular dilation/attenuation? Bear-
clear alteration to overall canalicular integrity or loss of func- ing in mind that hepatocytes have been observed to contribute
tion was observed in association with this change, nor were to 1 to 3 canaliculi, in both mammals and medaka (Arias,
mortality or morbidity observed. Apical hepatocyte membrane 1988; Hardman et al., 2007b; Motta, 1975), canalicular atten-
integrity in dilated canaliculi appeared to be maintained, and uation/dilation could result from two sources: (1) a contractile
canalicular lumens appeared uniform and smooth, equidiame- regulatory problem at the pericanalicular region of hepatocytes
ter in dimension, as observed in the hepatocytes (canaliculi) of involving cytoskeletal and tight junctional elements, or (2) it may
normal livers. In short, altered canalicular lumen diameter was result from the swelling of hepatocytes (or BPDECs, while atten-
the only observed change as compared to untreated livers. This uation/dilation of intrahepatic biliary passageways appeared to
type of canalicular response (e.g. mosaic of normal and abnor- be largely associated with canaliculi, bile preductules cannot be
mal canaliculi; either dilated canaliculi, or in some instances, ruled out). In the latter case, hepatocellular swelling could pre-
collapsed canaliculi of reduced diameter) is often observed dur- clude or diminish bile flow via reduction of canalicular lumen
ing cholestasis in the mammalian liver (Arias, 1988; Thung and diameter. If bile secretory rates remained unchanged, canalicu-
Gerber, 1992). lar attenuation would force bile to take alternate routes through
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32 R. Hardman et al. / Aquatic Toxicology 86 (2008) 20–37
the interconnected intrahepatic biliary network, which, in the governed by cytoskeletal proteins and actin filaments in the
event bile volume is conserved, would necessitate the occur- pericanalicular region of hepatocytes, it is possible the canalic-
rence of dilated canaliculi in other portions of the intrahepatic ular changes observed may be attributable to ANIT induced
canaliculo-preductular network. Dilated canaliculi may reflect (either direct or indirect) cytoskeletal alterations in hepatocytes.
locally redirected bile from attenuated passageways (i.e. alter- Cytoskeletal derangements resulting from ANIT exposure have
nate routes of flow). This structural change may comprise an been observed in isolated rat hepatocyte couplets (Orsler et al.,
adaptive/functional response of the liver to maintain bile secre- 1999), and in vivo (Furuta et al., 2004; Kan and Coleman,
tory/transport functions in the presence of impaired bile flow, 1986; Lowe et al., 1985). Hence, mammalian studies suggest
and may illustrate one of the underlying attributes of an intercon- ANIT induced cytoskeletal alterations a plausible mechanism by
nected, polyhedral based, canaliculo-bile preductular network; which the observed canalicular attenuation/dilation in medaka
in that it provides alternate routes of bile flow for continu- may manifest. We have to date not fully explored ANIT associ-
ous secretion of hepatocellular bile (Hardman et al., 2007a,b). ated cytoskeletal changes in medaka, though future studies aim
Because diminished/precluded canalicular transport of bile may to incorporate assessment of cytoskeletal integrity in medaka
result in hepatocellular toxicity by reducing or inhibiting elimi- hepatocytes and biliary epithelia pre and post ANIT exposure.
nation of potentially toxic cytosolic solutes (from intracellular to While canalicular dilation/attenuation was distinct, there did
canalicular lumen), an interconnected network of canaliculi and not appear to be any loss of canalicular (bile) transport of
preductules would allow alternate/multiple routes of elimination the fluorophores Bodipy FL C5 Ceramide, -Bodipy C5-HPC
(transport) of bile solutes away from hepatocytes for export to the or fluorescein isothiocyanate associated with this phenotypic
gall bladder and elimination via the gut, circumventing potential response. The only qualitative and quantitative changes in
hepatotoxicity (bile retention) in the event of impaired/precluded bile transport observed were, perhaps not surprisingly, a mod-
bile flow in portions of intrahepatic biliary passageways. Hence, est increase in fluorescence in dilated canaliculi (a proxy for
because hepatocytes synthesize and secret bile, and may con- increased bile volume), and decrease in fluorescence in attenu-
tribute bile to one to three individual canaliculi, it is possible ated canaliculi (a proxy for decreased bile volume). While these
that simultaneous attenuation/dilation of canaliculi is reflective local changes were apparent, overall transport of fluorophores
of an adaptive response of the liver to maintain flow of total bile from IHBPs to extrahepatic bile ducts and gall bladder did not
volume (homeostasis of bile synthesis and secretion). appear qualitatively or quantitatively different than that observed
While attributing canalicular dilation/attenuation to swollen in control fish. Hence, in vivo investigations into hepatobiliary
hepatocytes is not definitively supported by the findings pre- transport suggest the intrahepatic biliary system, due to its inter-
sented, it can be hypothesized this is a feasible mechanism connected network of canaliculi and bile preductules, was able
by which lumen attenuation/dilation could be occurring. Com- to maintain overall bile transport from intrahepatic to extrahep-
panion TEMs showing altered hepatocytes, in conjunction with atic bile passageways at the time canalicular attenuation/dilation
associated dilated/attenuated canaliculi, support this conjecture was observed.
(Figs. 3–6 Figs. 3D, 4F, 5D and 6B, B1), and studies in rodents
describe ANIT induced cytotoxicity in hepatocytes, and biliary 4.2. Bile preductular epithelial cell toxicity
epithelium (Alpini et al., 1992; Connolly et al., 1988; Leonard
et al., 1981; Lesage et al., 2001). Because in vivo techniques The cause of bile preductular (BPD) lesions is perhaps
focused on elucidation of IHBPs via application of FITC and more clear. In vivo and ex vivo investigations suggest the
Bodipy HPC fluorophores (excellent for elucidation of intra- observed BPD lesions are likely attributable to BPDEC
and extrahepatic bile passageways, not optimal for elucidat- swelling/cytotoxicity, as opposed to hepatocellular injury. BPD
ing cell cytosol or organelles), swollen hepatocytes and BECs lesions (as opposed to attenuated/dilated canaliculi) were
could not be consistently evaluated in vivo in livers exhibit- commonly associated with changes in BPDEC morphology,
ing dilated/attenuated canaliculi. It is possible to co-administer observed in vivo, and in TEM investigations (Figs. 4 and 5
Bodipy C5 ceramide (good for elucidating intracellular mor- Figs. 4C, F and 5D). 3D reconstructions also help affirm the
phology) with either of the aforementioned fluorophores to hypothesis that BDPEC cytotoxicity contributed to altered bile
simultaneously elucidate both intrahepatic bile passageways and preductule morphology (Fig. 4D and E), and may in part be
cell morphology in vivo. However, we were not able to ade- responsible for observed alterations to bile flow/transport (dis-
quately refine this in vivo procedure during the course of the cussion follows). Hence, in vivo and ex vivo findings together
ANIT studies. In summary, results from in vivo and ex vivo anal- suggest BPDEC toxicity to be a likely candidate for the BPD
yses suggest hepatocellular swelling may be responsible for the lesions observed.
dilated/attenuated canaliculi observed, a phenotypic response Relevant to BPDEC cytotoxicity discussed here are prior
to ANIT that merits further study in medaka and other piscine studies investigating carcinogenesis in medaka (Okihiro and
species, particularly in regard to the effect of xenobiotics on bile Hinton, 1999), which revealed that larval medaka exposed to
synthesis and transport. diethyl nitrosamine (DEN) exhibited a higher prevalence of bil-
An alternate hypothesis is that ANIT induced cytoskeletal iary tumors (46.4% of all tumors in larval-exposed medaka were
derangements may be responsible for the altered canalicu- biliary versus 8.1% in adult-exposed fish), as opposed to hepa-
lar morphology (e.g. constriction/dilation regulation). Because tocellular carcinomas, which were the prevalent neoplasm when
canaliculi are contractile structures, the function of which is medaka were exposed as adults (100% of hepatocellular tumors
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R. Hardman et al. / Aquatic Toxicology 86 (2008) 20–37 33
in adult-exposed medaka were malignant, while only 51.5% of cal and biochemical investigations have shown that cytoplasmic
larval hepatocellular tumors were malignant). These findings, vacuolation of hepatocytes following low doses of CCL4 was
describing a differential response to DEN, depending on the due to excess accumulation of glycogen, predominantly of the
life stage at which exposure occurred, may reflect differences in monoparticulate form. Low dose CCL4 exposed cells lacked
cell populations during development (e.g. presence and preva- features of degeneration or regeneration, and were much less sus-
lence of BPDECs), and perhaps the role of these cell types on ceptible to injury by larger subsequent CCl4 doses, as assessed
growth and differentiation of tumors in embryonic and adult by structural and serum enzyme analyses (Nayak et al., 1996).
livers. Given: (1) the findings discussed here, (2) that previ- The occurrence of HV in medaka was found to be con-
ous findings show the livers of early life stage medaka, at least centration dependent, with increasing prevalence up to 6 M
up to 40 days post fertilization, to be replete with BPDECs ANIT (LC50 = 5 M), beyond which HV prevalence declined.
(Hardman et al., 2007b; Okihiro and Hinton, 2000), and (3) While electron dense particulates, which may represent glyco-
that these cell types are putative bipotent/pluripotent stem-like gen deposits, where observed sporadically in HVs, we did not
cells, akin to mammalian oval cells (Farber, 1956; Fausto and attempt to further characterize this response, and cannot elabo-
Campbell, 2003; Golding et al., 1996; Okihiro and Hinton, rate on whether HV was an adaptive versus toxic response. The
1999; Theise et al., 1999); it is possible that BPDEC toxicity in vivo findings presented do however yield a clearer under-
may be responsible for the age dependent differences in the standing of the morphology of this response at the cellular and
types of liver tumors observed by Okihiro and Hinton (1999) system level of organization.
(e.g. stem cell hypothesis of carcinogenesis). Although anatom-
ical variations between mammalian and medaka liver exist (e.g. 4.4. Biliary epithelial cell proliferation and biliary tree
while BPDECs are located throughout the hepatic parenchyma arborization
of medaka, mammalian oval cells are localized to the peri-portal
canals of Hering) (Hardman et al., 2007b; Hinton et al., 2007), While several of the structural and functional changes
response of BPDECs to ANIT is intriguing in the presence of observed in ANIT treated medaka are consistent with a
our current understanding of ANIT induced changes in progen- cholestatic response, relatively well described in rodents and
itor cells of the mammalian liver (Alpini et al., 1992; Faa et al., humans, such as a mosaic of either dilated or collapsed canali-
1998; Roskams et al., 1998, 2003). It follows that BPDECs may culi and BEC toxicity (Anwer, 2004; Muller and Jansen, 1998;
play important roles in further elucidating comparative struc- Trauner et al., 2005), arborization of the biliary tree (hyperpla-
ture/function relationships, and toxic response, in piscine and sia of biliary epithelia of bile ductules and ducts), a common
mammalian livers. response observed during chronic cholestasis in the mammalian
liver (Alpini et al., 1989; Lesage et al., 2001; Masyuk et al.,
4.3. Hydropic vacuolation 2003), was not observed in STII medaka in response to ANIT.
While arborization appeared to be absent, examination of the
Hydropic vacuolation (HV), the result of the intracellu- liver hilus revealed BEC proliferation, suggesting a biliary tree
lar accumulation of water and symptomatic of cell swelling, “arborization-like” response in medaka liver, as compared with
has been employed as a biomarker of exposure to assess the its mammalian counterparts. Lack of biliary tree arborization (as
response of wild fishes to environmental contaminants, particu- compared to rodent) may be due to at least two important fac-
larly polynuclear aromatic hydrocarbons, halogenated aromatic tors: (1) biliary tree arborization described in mammalian livers
hydrocarbons, and pesticides (Bodammer and Murchelano, is a function of proliferation of biliary epithelia of bile ductules
1990; Gardner and Pruell, 1988; Moore et al., 1996, 2005; and ducts, which are largely localized to portal tracts, and (2)
Murchelano and Wolke, 1985; Myers et al., 1998a,b). By exam- because larger bile ducts in medaka are found predominantly in
ple, winter flounder (Pleuronectes americanus) were annually the hilar/peri-hilar region of liver, arborization of the biliary tree
surveyed for trends in hepatotoxicity and chemical body bur- in medaka would be localized primarily to liver hilus. These two
den to evaluate water quality and effluent treatment efficacy points are discussed in the following.
in Boston Harbor, with HV employed as a key indicator of First, in vivo and ex vivo (histological, immunohisto-
hepatic injury (Moore et al., 2005). HV as a biomarker of chemical, TEM) analyses presented show ANIT induces
environmental stress has also been employed on the U.S. West specific changes in the medaka hepatobiliary system involv-
coast to monitor contaminated coastal environments (Bodammer ing hepatocytes (vacuolation, cytomegaly), biliary epithelial
and Murchelano, 1990; Gardner and Pruell, 1988; Moore et cells (hyperplasia, vacuolation, cytomegaly) and BPDECs
al., 1996, 2005), and was most commonly observed in biliary (cytomegaly, vacuolation). AE1/AE3 staining suggests response
epithelial cells and hepatocytes in starry flounder (Platichthys BECs of the intrahepatic biliary passageways, and PCNA analy-
stellatus), white croaker (Genyonemus lineatus) and rock sole ses suggest BEC proliferation in the hilar and peri-hilar region of
(Lepidopsetta bilineata).Of interest, Nayak et al. (1996) sug- the liver, in response to chronic ANIT exposure (Figs. 4–6 Figs.
gest HV may reflect an adaptive, as opposed to toxic, cellular 4C, F, 5D, E and 6). These findings, particularly BEC hyperpla-
response. Observations in animal and human livers suggest sia in the hilar/peri-hilar region of the liver, are consistent with
vacuolated hepatocytes observed during liver injury are cells prior observations correlating medaka and mammalian hepato-
adaptively altered to resist further insult, as opposed to cells biliary structure/function relationships (Hardman et al., 2007b),
undergoing hydropic degeneration. By example, morphologi- and suggest the hepatobiliary system of medaka responds to
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34 R. Hardman et al. / Aquatic Toxicology 86 (2008) 20–37
ANIT in a manner consistent with that observed in the mam- tocellular transport mechanisms (e.g. ATP binding cassette of
malian liver. Previously investigations suggested that the liver of transmembrane transporters). At 8 M ANIT STII medaka were
medaka, in total, can be considered the structural and functional non-motile by 6 h of exposure and exhibited passive hepatic con-
analogue of an individual mammalian lobule, with both livers gestion in tandem with decreased heart rate (determined by rate
(medaka and mammalian) sharing a common functional unit. of ventricular contraction). Reduced heart rate was likely asso-
However, in medaka, “arborization” of the biliary tree would ciated with reduced cardiac output. Given the apparent systemic
be localized to the liver hilus, the sole region of medaka liver toxicity at 6 M ANIT and above, the observed decrease in
distinctly akin to the mammalian portal tract. Because the mam- fluorophore transport could have resulted from: (1) decreased
malian liver is comprised of numerous lobules, with portal tracts respiratory (branchial) uptake of the fluorophores (which in
containing bile ductules and small ducts at the lobule periphery vivo observations suggest is via gill uptake mechanisms), (2)
(which, structurally, yields a biliary tree), arborization occurs a decrease in intrahepatic circulation (reduced heart rate, sinu-
throughout the mammalian liver. In contrast, bile ductules and soidal flow rates, reduced fluorophore availability over time)
ducts of the medaka liver are largely found near or within the and/or (3) from general systemic toxicity not characterized in
liver hilus (single lobule hypothesis). Hence, while arborization these studies. Because impaired transport function was asso-
of the biliary tree occurs in medaka and mammals, this response, ciated with cardiovascular changes and overall morbidity, it
as suggested earlier (Hardman et al., 2007b), and reconfirmed is likely that the loss of transport function observed (in vivo)
hererin, will be different in pattern, site and amount. at ANIT concentrations >6 M was symptomatic of general
Importantly, because of the comparative anatomical arrange- systemic toxicity, rather than ANIT mediated disruption of hepa-
ment of mammalian and medaka biliary systems, there will be tocellular and biliary epithelial cell transmembrane transporters,
differences as to the interpretation of responses of these livers which play key roles in bile transport and cholestasis.
to insult, though the response may, fundamentally, be similar. In contrast to in vivo transport studies with fluorescent probes,
Lack of distinct “biliary tree arborization” throughout the liver volumetric analyses of 3D reconstructions, while performed in
corpus of medaka, and localization of BEC proliferation to the only two 2 ANIT treated medaka and three control livers, sug-
hilar region of the liver, is illustrative of this concept and an gest modest cholestatic and choleretic responses. The finding
important comparative finding given arborization of portal tracts are noteworthy given; (1) 3D analyses from 3 control livers at
(BECs) in rodents is a hallmark response to reduced bile flow 8, 12, and 30 dpf yielded average intrahepatic biliary (canalic-
and BEC injury. By example, studies by Masyuk et al. (2003) ular, bile preductular) volumes of 0.97% (±0.09) relative to
found total biliary tree volume (one measure of arborization) in the volume of liver examined, and (2) in hepatobiliary met-
ANIT treated rats to increase 18 times above controls. In con- rics were consistent across 2D and 3D in vivo analyses, and
junction, hepatic artery volume and portal vein volume increased ex vivo evaluations, revealing accuracy of in vivo and ex vivo
4 times and 3 times that of control animals, respectively, while quantitative assessments. Where the volumes of sinusoidal, hep-
bile duct diameter between ANIT treated and control rodents atocellular, and parenchymal space, relative to total liver volume
remained unchanged. Note: Arborization of the biliary tree has examined, remained unchanged in ANIT treated medaka, bile
also recently been described in three dimensions in the human canalicular volume was found to be diminished (cholestasis?) at
liver (Ludwig et al., 1998). low ANIT concentrations, and increased (choleresis?) at higher
It follows from the above discussion, and previous findings concentrations (Table 2). Assuming 3D reconstructions from
(Hardman et al., 2007b), that arborization of the biliary “tree” in in vivo imaging accurately represent physiological change, the
medaka, in response to proliferative agents, would likely be less results are of interest given prior studies describing an adaptive
pronounced than that observed in the mammalian liver, given choleretic response reported at non-toxic doses of ANIT (Alpini
medaka can be considered to possess a single portal tract (the et al., 1999), and altered intrahepatic biliary volume (Masyuk
liver hilus), as opposed to mammals, which possess myriad por- et al., 2003), in rodent livers. While statistical analyses are not
tal tracts throughout the liver corpus. It should be noted the possible, the changes in biliary volume suggested in volumetric
findings presented here were be no means all inclusive in terms analyses are perhaps representative of real physiological change
of investigation of BEC proliferation in response to ANIT, and in response to ANIT, and may illustrate the ability to perform
it is interesting to consider that, upon chronic ANIT exposure volumetric analyses in vivo in STII medaka.
extending for months, one may see BEC proliferation infiltrate What can explain the discrepancy between volumetric and
more distal regions of the liver (relative to hilus), with an increase in vivo fluorophore transport studies? Foremost, bile trans-
in intrahepatic ductules and ducts. port in mammals is a multi-phasic process (bi-directional
apical and basal membrane transport) governed in part by a
4.5. Hepatobiliary transport suite of transmembrane transporters such as; the basolateral
Na+ /taurocholate cotransporter (NTCP), organic anion trans-
No impairment of blood to bile transport of the fluorophores porting proteins (OATPs), apical bile salt export pump (BSEP),
FITC, Bodipy HPC and Bodipy C5 Ceramide was observed at and the multidrug resistant family of transporters (MDR/MRP)
ANIT concentrations <6 M. The only observed impairment of (see reviews by (Boyer, 1996a,b; Trauner and Boyer, 2003;
hepatobiliary transport function in vivo was at aqueous ANIT Trauner et al., 2000)). Because fluorophore physico-chemical
concentrations >6 M, which approached the LC100 (10 M, properties determine transporter substrate specificity, it is pos-
48 h), which cannot be necessarily attributed to altered hepa- sible that the fluorophores employed were not substrates for
16. Author's personal copy
R. Hardman et al. / Aquatic Toxicology 86 (2008) 20–37 35
affected transporters (if affected by ANIT exposure). By exam- while BECs, and their associated bile ductules and ducts, are
ple, FITC, an organic anion, is a potential candidate for OATP largely localized to the liver hilus.
transport on the basal membrane, and MRP2 on the apical These findings, which describe similarities and differences
membrane, neither of which may be affected by ANIT (no between mammalian and medaka hepatobiliary systems in
information on the effects of ANIT on transporter proteins in response to a reference hepatotoxicant (ANIT), in conjunction
fish exists). Hence, while no loss of fluorophore transport was with prior in vivo work characterizing normalcy (Hampton et
observed in vivo, it is important to recognize that: (1) being the al., 1988, 1989; Hardman et al., 2007b; Hinton et al., 2004,
first in vivo transport studies of their kind, these studies were 2007; and others), illustrate the importance of our compara-
of a screening nature, and (2) we did not attempt to elucidate tive understanding of the vertebrate liver, and the significance
which transporters the employed fluorophores were substrates of this understanding on the interpretation and communication
for, nor did we evaluate other fluorophores that may have proved of xenobiotic induced injury in piscine livers. From these and
better substrates for the variety of transporters present (as under- previous findings it is apparent that appreciating the spectrum
stood in the mammalian liver). Given these factors discrepancies of responses of the piscine liver to xenobiotics that target this
between volumetric and in vivo fluorophore transport studies are organ system, particularly in a comparative sense, requires more
not altogether surprising, and more refined study designs will attention to bile preductular epithelial cells, bile preductules,
be required to elucidate the mechanisms of altered fluorophore and their relationship to the interconnected intrahepatic biliary
transport in vivo. network. This is becoming increasingly important given that
toxicity screening in embryos and eleutheroembryos is a key
4.6. Cholestasis factor in the regulatory evaluation of chemicals of environmental
concern (e.g. REACh protocol; regulatory framework for Regis-
While we have been reluctant to use the term cholesta- tration, Evaluation, Authorization and Restriction of Chemicals)
sis here, we feel discussion of this response important, given (ECHA, 2007), and that the liver is a key target organ of toxicity.
its lack of description in piscine species. Cholestasis, a hall- The findings presented have also shown for the first time
mark response of the mammalian liver to injury and insult, in vivo evaluation of toxicity in the STII medaka hepatobiliary
is a complex response that involves not only the hepatobil- system, and demonstrate the ability to study and image, with high
iary system but many other organ systems (e.g. gastrointestinal resolution, normalcy and toxicity in living medaka; a valuable
tract, kidney, cardiovascular system, endocrine system) as well. diagnostic and investigatory tool. Given the described coupling
Because a variety of pharmaceuticals and environmental con- of in vivo and ex vivo investigations, this suggests the future
taminants have been shown to alter bile transport in mammals ability to integrate molecular mechanisms of disease and toxicity
(Chang and Schiano, 2007; Mohi-ud-din and Lewis, 2004; with system level phenotypes, a current research aim in this
Sakurai et al., 2007), in vivo models and methodologies, as laboratory.
described here, may prove valuable for investigation of altered
bile transport in piscine species. Evaluation of this response in Acknowledgments
the piscine liver is important given the relevance of this type
of hepatic injury/adaptation to ecotoxicological considerations, Thanks to Dr. David Miller, Laboratory of Pharmacology
for instance; the effects of antibacterial agents, pesticides, and and Chemistry, National Institute of Environmental Health Sci-
hormones employed in aquaculture, and other environmental ences, Research Triangle Park, for providing access to their laser
contaminants, on fish reproduction, fitness and population health scanning confocal microscopy facility, and to the Duke Uni-
(Alderman and Hastings, 1998; Cabello, 2006; Goldburg and versity Integrated Toxicology Program. This publication was
Naylor, 2005; Rhodes et al., 2000). In short, understanding a made possible by Grant Number 1 RO1 RR018583-02 from the
cholestatic type response in fish is imperative to more fully National Center for Research Resources (NCRR), a component
elucidating the effects of environmental contaminants and pro- of the National Institutes of Health (NIH), and Grant Number
phylactic substances on hepatobiliary metabolic and transport R21CA106084-01A1 from the National Cancer Institute (NCI),
function, and health of the individual. also a component of NIH. Its contents are solely the responsi-
bility of the authors and do not necessarily represent the official
5. Conclusions views of NCRR or NIH.
While the responses described are largely morphological in
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