By the end of this presentation we’ll be able to learn about- -Geographical distribution of leishmania parasites- Know the different stages of leishmania parasites and their morphology.-Describe the lifecycle of leishmania.-Causes and pathogenesis of leishmania -Preventive measures of leishmaniasis
By the end of this presentation we’ll be able to learn about- -Geographical distribution of leishmania parasites- Know the different stages of leishmania parasites and their morphology.-Describe the lifecycle of leishmania.-Causes and pathogenesis of leishmania -Preventive measures of leishmaniasis
Clonorchis sinensis
Prepared by:
Shafqat Hussain
Taxonomy
Kingdome : Animalia
Phylum : Platyhelminths
Class : Trematoda
Order : Opisthorchiida
Family : Opisthorchiidae
Genus : Clonorchis
Species : C. sinensis
Introduction
•
Clonorchis is also known as the Chinese or oriental liver fluke.
Clonorchis is a liver fluke parasite (trematode or worm) that can
infect the liver, gallbladder, and bile duct.
food born parasite
Host
Definitive Hosts
First intermediate host must always be a snail, mainly
Parafossarulus manchouricus
Life cycle
•
Clonorchis sinensis eggs are discharged in the biliary ducts and in
the stool in an embryonated state
Eggs are ingested by a suitable snail (P. manchouricus)
intermediate host
Eggs release miracidia
which go through several developmental stages (sporocysts, rediae, and
cercariae).
The cercariae are released from the snail and, after a short period
of free-swimming time in water, they come in contact and
penetrate the flesh of freshwater fish, where they encyst as
metacercariae
Infection of humans occurs by ingestion of under cooked, salted,
pickled, or smoked freshwater fish
After ingestion, the metacercariae excyst in the duodenum
and ascend the biliary tract through the ampulla of Vater
Maturation takes approximately one month. The adult flukes
(measuring 10 to 25 mm by 3 to 5 mm) reside in small and
medium sized biliary ducts.
they lay eggs in intestine
the embryonated eggs release in stool.
The eggs are embryonated and contain the larvae called miracidia.
The sporocyst resembles a hollow and simple sac.
Oftentimes, the developing rediae are visible inside the sac.
Redia - At this larval stage, it retains a very simple worm structure.
In some ways, it still resembles a sac.
Pathogenesis
Liver flukes infect the liver, gallbladder, and bile duct in humans.
inflammation in biliary epithelium
Laboratory Findings
Blood routine test: eosinophilia, anemia in severe infection
Echinococcus granulosus, also called hydatid worm belongs to class Cestoda
It causes cystic echinococcosis in livestock and humans being intermediate hosts and parasitize the small intestines of adult canids
It is a zoonotic disease
Definitive hosts are carnivorous predators like dogs, wolves, foxes and lions. While sheep, goat, cattle, pigs and rodents are intermediate hosts. Birds and arthropods act as mechanical vectors
Everything you wanna know about Chagas disease and Trypanosoma cruzi in a nutshell, including the morphology and life-cycle of the parasite ,diagnosis treatment and prophylaxis of Chagas disease.
nd invade the genital ridges in the sixth week of
development. here they form primitive sex cords. in
the absence of tdf, medullary cords disappear and
get replaced by a vascular stroma (ovarian medulla).
cortical cords develop and surround one or more
primitive germ cells. the germ cells subsequently
develop into oogonia, while the surrounding epithelial
cells form the follicular cells. this differentiates
undifferentiated gonads into ovaries. stroma of ovary
develops from basal mesenchyme. granulosa and theca
cells develop from celomic epithelium.
development of genital ducts
development of genital duct system and the external
genitalia occurs under the influence of hormones
circulating in the fetus. sertoli cells in the fetal testes
produce a nonsteroidal substance known as müllerian
inhibiting substance (mis) that causes regression of
müllerian ducts. androgen from the fetal testes causes
masculinization of external genitalia. in the absence of
mis, müllerian ducts develop and mesonephric duct
system regresses. in the absence of androgen, external
genitalia differentiate into female phenotype. the
müllerian duct develops between the fifth and sixth
weeks lateral to intermediate cell mass and wolffian
duct. the müllerian duct has the following three parts:
•cranial vertical portion that opens into celomic
cavity. later it differentiates into fallopian tubes.
•horizontal part crosses the mesonephric duct.
•caudal vertical part that fuses with its partner
from opposite side. this fused part later differ
entiates into uterus, cervix, and upper one-third
of the vagina.
the dorsal celomic epithelium (which forms
müllerian duct) remains open at its site of origin and
ultimately forms the fimbriated ends of the fallopian
tubes. at their point of origin, each of the müllerian
ducts forms a solid bud. each bud penetrates the
mesenchyme lateral and parallel to the wolffian duct.
as the solid buds elongate, a lumen appears in the
cranial part, beginning at each celomic opening. the
caudal end of each müllerian duct crosses the way
Clonorchis sinensis
Prepared by:
Shafqat Hussain
Taxonomy
Kingdome : Animalia
Phylum : Platyhelminths
Class : Trematoda
Order : Opisthorchiida
Family : Opisthorchiidae
Genus : Clonorchis
Species : C. sinensis
Introduction
•
Clonorchis is also known as the Chinese or oriental liver fluke.
Clonorchis is a liver fluke parasite (trematode or worm) that can
infect the liver, gallbladder, and bile duct.
food born parasite
Host
Definitive Hosts
First intermediate host must always be a snail, mainly
Parafossarulus manchouricus
Life cycle
•
Clonorchis sinensis eggs are discharged in the biliary ducts and in
the stool in an embryonated state
Eggs are ingested by a suitable snail (P. manchouricus)
intermediate host
Eggs release miracidia
which go through several developmental stages (sporocysts, rediae, and
cercariae).
The cercariae are released from the snail and, after a short period
of free-swimming time in water, they come in contact and
penetrate the flesh of freshwater fish, where they encyst as
metacercariae
Infection of humans occurs by ingestion of under cooked, salted,
pickled, or smoked freshwater fish
After ingestion, the metacercariae excyst in the duodenum
and ascend the biliary tract through the ampulla of Vater
Maturation takes approximately one month. The adult flukes
(measuring 10 to 25 mm by 3 to 5 mm) reside in small and
medium sized biliary ducts.
they lay eggs in intestine
the embryonated eggs release in stool.
The eggs are embryonated and contain the larvae called miracidia.
The sporocyst resembles a hollow and simple sac.
Oftentimes, the developing rediae are visible inside the sac.
Redia - At this larval stage, it retains a very simple worm structure.
In some ways, it still resembles a sac.
Pathogenesis
Liver flukes infect the liver, gallbladder, and bile duct in humans.
inflammation in biliary epithelium
Laboratory Findings
Blood routine test: eosinophilia, anemia in severe infection
Echinococcus granulosus, also called hydatid worm belongs to class Cestoda
It causes cystic echinococcosis in livestock and humans being intermediate hosts and parasitize the small intestines of adult canids
It is a zoonotic disease
Definitive hosts are carnivorous predators like dogs, wolves, foxes and lions. While sheep, goat, cattle, pigs and rodents are intermediate hosts. Birds and arthropods act as mechanical vectors
Everything you wanna know about Chagas disease and Trypanosoma cruzi in a nutshell, including the morphology and life-cycle of the parasite ,diagnosis treatment and prophylaxis of Chagas disease.
nd invade the genital ridges in the sixth week of
development. here they form primitive sex cords. in
the absence of tdf, medullary cords disappear and
get replaced by a vascular stroma (ovarian medulla).
cortical cords develop and surround one or more
primitive germ cells. the germ cells subsequently
develop into oogonia, while the surrounding epithelial
cells form the follicular cells. this differentiates
undifferentiated gonads into ovaries. stroma of ovary
develops from basal mesenchyme. granulosa and theca
cells develop from celomic epithelium.
development of genital ducts
development of genital duct system and the external
genitalia occurs under the influence of hormones
circulating in the fetus. sertoli cells in the fetal testes
produce a nonsteroidal substance known as müllerian
inhibiting substance (mis) that causes regression of
müllerian ducts. androgen from the fetal testes causes
masculinization of external genitalia. in the absence of
mis, müllerian ducts develop and mesonephric duct
system regresses. in the absence of androgen, external
genitalia differentiate into female phenotype. the
müllerian duct develops between the fifth and sixth
weeks lateral to intermediate cell mass and wolffian
duct. the müllerian duct has the following three parts:
•cranial vertical portion that opens into celomic
cavity. later it differentiates into fallopian tubes.
•horizontal part crosses the mesonephric duct.
•caudal vertical part that fuses with its partner
from opposite side. this fused part later differ
entiates into uterus, cervix, and upper one-third
of the vagina.
the dorsal celomic epithelium (which forms
müllerian duct) remains open at its site of origin and
ultimately forms the fimbriated ends of the fallopian
tubes. at their point of origin, each of the müllerian
ducts forms a solid bud. each bud penetrates the
mesenchyme lateral and parallel to the wolffian duct.
as the solid buds elongate, a lumen appears in the
cranial part, beginning at each celomic opening. the
caudal end of each müllerian duct crosses the way
Leishmaniasis dates back to the 1st century AD. It was initially known as “Dum dum” fever and later “Kal- Azar.” It is a neglected disease that affects 700 000 to 1 million new cases that occur annually (WHO, 2021).
Massive Splenomegaly By Dr Bashir Ahmed Dar Chinkipora Sopore Kashmir Associa...Prof Dr Bashir Ahmed Dar
Dr.Bashir Ahmed Dar Chinkipora Sopore Kashmir India,Associate Prof of medicine presently working in malaysia is a keen teacher, educator and takes pride in his clinical and research accomplishments. His interests include publishing articles related to health issues.Email drbashir123@gmail.com
Adv. biopharm. APPLICATION OF PHARMACOKINETICS : TARGETED DRUG DELIVERY SYSTEMSAkankshaAshtankar
MIP 201T & MPH 202T
ADVANCED BIOPHARMACEUTICS & PHARMACOKINETICS : UNIT 5
APPLICATION OF PHARMACOKINETICS : TARGETED DRUG DELIVERY SYSTEMS By - AKANKSHA ASHTANKAR
Title: Sense of Smell
Presenter: Dr. Faiza, Assistant Professor of Physiology
Qualifications:
MBBS (Best Graduate, AIMC Lahore)
FCPS Physiology
ICMT, CHPE, DHPE (STMU)
MPH (GC University, Faisalabad)
MBA (Virtual University of Pakistan)
Learning Objectives:
Describe the primary categories of smells and the concept of odor blindness.
Explain the structure and location of the olfactory membrane and mucosa, including the types and roles of cells involved in olfaction.
Describe the pathway and mechanisms of olfactory signal transmission from the olfactory receptors to the brain.
Illustrate the biochemical cascade triggered by odorant binding to olfactory receptors, including the role of G-proteins and second messengers in generating an action potential.
Identify different types of olfactory disorders such as anosmia, hyposmia, hyperosmia, and dysosmia, including their potential causes.
Key Topics:
Olfactory Genes:
3% of the human genome accounts for olfactory genes.
400 genes for odorant receptors.
Olfactory Membrane:
Located in the superior part of the nasal cavity.
Medially: Folds downward along the superior septum.
Laterally: Folds over the superior turbinate and upper surface of the middle turbinate.
Total surface area: 5-10 square centimeters.
Olfactory Mucosa:
Olfactory Cells: Bipolar nerve cells derived from the CNS (100 million), with 4-25 olfactory cilia per cell.
Sustentacular Cells: Produce mucus and maintain ionic and molecular environment.
Basal Cells: Replace worn-out olfactory cells with an average lifespan of 1-2 months.
Bowman’s Gland: Secretes mucus.
Stimulation of Olfactory Cells:
Odorant dissolves in mucus and attaches to receptors on olfactory cilia.
Involves a cascade effect through G-proteins and second messengers, leading to depolarization and action potential generation in the olfactory nerve.
Quality of a Good Odorant:
Small (3-20 Carbon atoms), volatile, water-soluble, and lipid-soluble.
Facilitated by odorant-binding proteins in mucus.
Membrane Potential and Action Potential:
Resting membrane potential: -55mV.
Action potential frequency in the olfactory nerve increases with odorant strength.
Adaptation Towards the Sense of Smell:
Rapid adaptation within the first second, with further slow adaptation.
Psychological adaptation greater than receptor adaptation, involving feedback inhibition from the central nervous system.
Primary Sensations of Smell:
Camphoraceous, Musky, Floral, Pepperminty, Ethereal, Pungent, Putrid.
Odor Detection Threshold:
Examples: Hydrogen sulfide (0.0005 ppm), Methyl-mercaptan (0.002 ppm).
Some toxic substances are odorless at lethal concentrations.
Characteristics of Smell:
Odor blindness for single substances due to lack of appropriate receptor protein.
Behavioral and emotional influences of smell.
Transmission of Olfactory Signals:
From olfactory cells to glomeruli in the olfactory bulb, involving lateral inhibition.
Primitive, less old, and new olfactory systems with different path
Lung Cancer: Artificial Intelligence, Synergetics, Complex System Analysis, S...Oleg Kshivets
RESULTS: Overall life span (LS) was 2252.1±1742.5 days and cumulative 5-year survival (5YS) reached 73.2%, 10 years – 64.8%, 20 years – 42.5%. 513 LCP lived more than 5 years (LS=3124.6±1525.6 days), 148 LCP – more than 10 years (LS=5054.4±1504.1 days).199 LCP died because of LC (LS=562.7±374.5 days). 5YS of LCP after bi/lobectomies was significantly superior in comparison with LCP after pneumonectomies (78.1% vs.63.7%, P=0.00001 by log-rank test). AT significantly improved 5YS (66.3% vs. 34.8%) (P=0.00000 by log-rank test) only for LCP with N1-2. Cox modeling displayed that 5YS of LCP significantly depended on: phase transition (PT) early-invasive LC in terms of synergetics, PT N0—N12, cell ratio factors (ratio between cancer cells- CC and blood cells subpopulations), G1-3, histology, glucose, AT, blood cell circuit, prothrombin index, heparin tolerance, recalcification time (P=0.000-0.038). Neural networks, genetic algorithm selection and bootstrap simulation revealed relationships between 5YS and PT early-invasive LC (rank=1), PT N0—N12 (rank=2), thrombocytes/CC (3), erythrocytes/CC (4), eosinophils/CC (5), healthy cells/CC (6), lymphocytes/CC (7), segmented neutrophils/CC (8), stick neutrophils/CC (9), monocytes/CC (10); leucocytes/CC (11). Correct prediction of 5YS was 100% by neural networks computing (area under ROC curve=1.0; error=0.0).
CONCLUSIONS: 5YS of LCP after radical procedures significantly depended on: 1) PT early-invasive cancer; 2) PT N0--N12; 3) cell ratio factors; 4) blood cell circuit; 5) biochemical factors; 6) hemostasis system; 7) AT; 8) LC characteristics; 9) LC cell dynamics; 10) surgery type: lobectomy/pneumonectomy; 11) anthropometric data. Optimal diagnosis and treatment strategies for LC are: 1) screening and early detection of LC; 2) availability of experienced thoracic surgeons because of complexity of radical procedures; 3) aggressive en block surgery and adequate lymph node dissection for completeness; 4) precise prediction; 5) adjuvant chemoimmunoradiotherapy for LCP with unfavorable prognosis.
CDSCO and Phamacovigilance {Regulatory body in India}NEHA GUPTA
The Central Drugs Standard Control Organization (CDSCO) is India's national regulatory body for pharmaceuticals and medical devices. Operating under the Directorate General of Health Services, Ministry of Health & Family Welfare, Government of India, the CDSCO is responsible for approving new drugs, conducting clinical trials, setting standards for drugs, controlling the quality of imported drugs, and coordinating the activities of State Drug Control Organizations by providing expert advice.
Pharmacovigilance, on the other hand, is the science and activities related to the detection, assessment, understanding, and prevention of adverse effects or any other drug-related problems. The primary aim of pharmacovigilance is to ensure the safety and efficacy of medicines, thereby protecting public health.
In India, pharmacovigilance activities are monitored by the Pharmacovigilance Programme of India (PvPI), which works closely with CDSCO to collect, analyze, and act upon data regarding adverse drug reactions (ADRs). Together, they play a critical role in ensuring that the benefits of drugs outweigh their risks, maintaining high standards of patient safety, and promoting the rational use of medicines.
Explore natural remedies for syphilis treatment in Singapore. Discover alternative therapies, herbal remedies, and lifestyle changes that may complement conventional treatments. Learn about holistic approaches to managing syphilis symptoms and supporting overall health.
Ozempic: Preoperative Management of Patients on GLP-1 Receptor Agonists Saeid Safari
Preoperative Management of Patients on GLP-1 Receptor Agonists like Ozempic and Semiglutide
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NYSORA Guideline
2 Case Reports of Gastric Ultrasound
New Drug Discovery and Development .....NEHA GUPTA
The "New Drug Discovery and Development" process involves the identification, design, testing, and manufacturing of novel pharmaceutical compounds with the aim of introducing new and improved treatments for various medical conditions. This comprehensive endeavor encompasses various stages, including target identification, preclinical studies, clinical trials, regulatory approval, and post-market surveillance. It involves multidisciplinary collaboration among scientists, researchers, clinicians, regulatory experts, and pharmaceutical companies to bring innovative therapies to market and address unmet medical needs.
ARTIFICIAL INTELLIGENCE IN HEALTHCARE.pdfAnujkumaranit
Artificial intelligence (AI) refers to the simulation of human intelligence processes by machines, especially computer systems. It encompasses tasks such as learning, reasoning, problem-solving, perception, and language understanding. AI technologies are revolutionizing various fields, from healthcare to finance, by enabling machines to perform tasks that typically require human intelligence.
Title: Sense of Taste
Presenter: Dr. Faiza, Assistant Professor of Physiology
Qualifications:
MBBS (Best Graduate, AIMC Lahore)
FCPS Physiology
ICMT, CHPE, DHPE (STMU)
MPH (GC University, Faisalabad)
MBA (Virtual University of Pakistan)
Learning Objectives:
Describe the structure and function of taste buds.
Describe the relationship between the taste threshold and taste index of common substances.
Explain the chemical basis and signal transduction of taste perception for each type of primary taste sensation.
Recognize different abnormalities of taste perception and their causes.
Key Topics:
Significance of Taste Sensation:
Differentiation between pleasant and harmful food
Influence on behavior
Selection of food based on metabolic needs
Receptors of Taste:
Taste buds on the tongue
Influence of sense of smell, texture of food, and pain stimulation (e.g., by pepper)
Primary and Secondary Taste Sensations:
Primary taste sensations: Sweet, Sour, Salty, Bitter, Umami
Chemical basis and signal transduction mechanisms for each taste
Taste Threshold and Index:
Taste threshold values for Sweet (sucrose), Salty (NaCl), Sour (HCl), and Bitter (Quinine)
Taste index relationship: Inversely proportional to taste threshold
Taste Blindness:
Inability to taste certain substances, particularly thiourea compounds
Example: Phenylthiocarbamide
Structure and Function of Taste Buds:
Composition: Epithelial cells, Sustentacular/Supporting cells, Taste cells, Basal cells
Features: Taste pores, Taste hairs/microvilli, and Taste nerve fibers
Location of Taste Buds:
Found in papillae of the tongue (Fungiform, Circumvallate, Foliate)
Also present on the palate, tonsillar pillars, epiglottis, and proximal esophagus
Mechanism of Taste Stimulation:
Interaction of taste substances with receptors on microvilli
Signal transduction pathways for Umami, Sweet, Bitter, Sour, and Salty tastes
Taste Sensitivity and Adaptation:
Decrease in sensitivity with age
Rapid adaptation of taste sensation
Role of Saliva in Taste:
Dissolution of tastants to reach receptors
Washing away the stimulus
Taste Preferences and Aversions:
Mechanisms behind taste preference and aversion
Influence of receptors and neural pathways
Impact of Sensory Nerve Damage:
Degeneration of taste buds if the sensory nerve fiber is cut
Abnormalities of Taste Detection:
Conditions: Ageusia, Hypogeusia, Dysgeusia (parageusia)
Causes: Nerve damage, neurological disorders, infections, poor oral hygiene, adverse drug effects, deficiencies, aging, tobacco use, altered neurotransmitter levels
Neurotransmitters and Taste Threshold:
Effects of serotonin (5-HT) and norepinephrine (NE) on taste sensitivity
Supertasters:
25% of the population with heightened sensitivity to taste, especially bitterness
Increased number of fungiform papillae
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2. The leishmaniasis is endemic in 88 countries
on five continents—Africa, Asia, Europe, North
America and South America.
350 million people at risk.
12 million people are affected by
leishmaniasis
1.5-2 million new cases of leishmaniasis
estimated to occur annually.
500,000 new cases of VL which occur
annually
Geographical distribution
3. New world leishmaniasisOld world leishmaniasis
Leishmania braziliensis complexLeishmania donovani
Leishmania mexicana complexLeishmania infantum
Leishmania chagasiLeishmania tropica
Leishmania peruvianaLeishmania major
Leishmania aethiopica
Classification of Leishmania based on
Geographical Distribution
4. Three different diseases are caused by various species
of genus Leishmania. These are:
Visceral leishmaniasis: The species L. donovani
complex infecting internal organs (liver, spleen, and
bone marrow) of human is the causative parasite.
€Cutaneous leishmaniasis: The species L. tropica
complex, L. aethiopica, L. major and L. mexicana
complex are the causative parasite.
€Mucocutaneous leishmaniasis: It is caused by
the L. braziliensis complex .
5. The parasite exists in 2 forms:
Amastigote form: in humans and other mammals.
Promastigote form: in the sandfl y and in artificial
culture.
Morphology of Leishmania donovani. A. Amastigote, B. Promastigote
A B
polymorphomorphology
6. L. donovani completes its life cycle in 2 hosts.
Defi nitive host: Man, dog, and other mammals.
Vector: Female sandfl y (Phlebotomus species).
Infective form: Promastigote form present in
midgut of female sandfly.
Mode of transmission:
€Humans acquire by bite of an infected female
Sandfly(Phlebotomus and Lutzomyia).
. It can also be transmitted vertically from mother to
fetus, by blood transfusion, and accidental
inoculation in the laboratory.
Incubation period: Usually 2–6 months,
occasionally it may be as short as 10 days or as long as
2 years.
Life Cycle of Leishmania
8. Infection with Leishmania species can result in 3 main
types of disease depending on the species, geographic
region and host immune response.
Leishmania donovani produces visceral
leishmaniasis (kala-azar). Symptoms include fever
(often 2 fever spikes per day), enlargement of the
spleen and liver, weakness, and progressive
emaciation. The disease is often fatal without
treatment, but survivors often develop immunity.
Symptoms/Pathology
9. Leishmania tropica and L. mexicana produce
cutaneous leishmaniasis which is characterized by skin
lesions (oriental sore). Infected macrophages
containing amastigotes are found primarily at the site
of infection around the sores. The sores are
chracterized by an elevated rim encircling the
lesion. The sores generally heal by themselves within a
year, but secondary bacterial infections are possible in
open sores.
Symptoms/Pathology
10. Leishmania braziliensis produces mucocutaneous
leishmaniasis, characterized by lesions near mucosal
membranes. The intitial site if infection is a small red
papule that ulcerates in a few weeks. The lesions are
flat (no raised rim) and often oozing. Infections of the
ear, nose and mouth area lead to degeneration of the
cartilage and soft tissues, resulting in disfigurement.
Symptoms/Pathology
11. By demonstrations of LD bodies in peripheral blood,
bone marrow aspirate, splenic aspirate, and lymph
node aspirate; culture done in NNN medium; aldehyde
test; detection of specifi c antigen and antibody by IIF,
ELISA,
DAT and rapid rk 39 antibody detection test.
Blood picture: Anemia, thrombocytopenia, leuco penia
with relative lymphocytosis, and hypergammaglobulinemia
Sodium stibogluconate amphotericinB, and oral miltefosine.
Diagnosis:
Treatment:
12. Control of sandfly population by insecticides and
sanitation measures.
Personal protection by use of protective clothing and
use of insect repellants.
Elimination of mammalian reservoir.
Prophylaxis