1) The study evaluated changes in the expression of hypoxia-associated genes in mouse lung tissue at various time points after radiation exposure. A microarray analysis found that 44 genes related to metabolism, growth, apoptosis, inflammation, oxidative stress, and fibrosis were upregulated after radiation.
2) Treatment with the antioxidant AEOL10150 after radiation exposure attenuated the elevated expression of 31 of these hypoxia-associated genes. This suggests that expression of many hypoxia genes is regulated by early oxidative stress following radiation.
3) The hypoxia-associated genes identified provide insight into how hypoxic signaling may contribute to radiation-induced lung injury. The study also provides clues about how AEOL10150's antioxidant properties confer radi
Evaluation of salicin isolated from salix subserrata as a radioprotectorRam Sahu
1) The study investigated the radioprotective effects of salicin, a compound found in willow trees, against gamma radiation damage in rat spleen tissue.
2) Irradiation significantly increased lipid peroxidation in spleen tissue but salicin treatment reduced this effect.
3) Ultrastructural examination found no abnormalities in control or salicin groups but irradiation caused lesions and cell loss, which salicin provided some protection against.
4) Changes to protein and enzyme patterns from irradiation were detected electrophoretically and salicin treatment prevented some of these qualitative effects.
Ameliorative effect of salicin against gamma irradiation inducedRam Sahu
This document summarizes a study that investigated the radioprotective effects of salicin against gamma irradiation-induced changes in the brain tissue of male rats. The study found that salicin administration reduced lipid peroxidation and minimized changes to protein patterns caused by irradiation. Specifically, salicin showed the highest protective effect against irradiation in rats that received salicin treatment after irradiation. However, salicin was not able to fully prevent abnormalities to lipoprotein patterns or quantitative changes to protein bands caused by irradiation. Overall, the results suggest salicin has radioprotective abilities against gamma irradiation effects on various electrophoretic patterns in brain tissue.
Vitamin C, glutathione, and various enzymes have radioprotective effects against cellular damage caused by ionizing radiation. Vitamin C is an antioxidant that can scavenge reactive oxygen species produced by radiation and protect DNA and membranes. Glutathione is also a free radical scavenger that protects against radiation damage. Various enzymes also help scavenge free radicals produced by radiation. The presentation concludes that vitamin C, glutathione, and enzymes play an important role in mitigating the effects of ionizing radiation exposure.
This study investigates the hypothesis that age-related hearing loss (presbyacusis) is caused by reactive oxygen metabolites (ROM) damaging mitochondrial DNA (mtDNA). The study assigns 130 rats to treatment groups receiving antioxidants, calorie restriction, or placebo. It finds that calorie-restricted rats had the best hearing, fewest mtDNA deletions, and least hair cell loss. Antioxidant-treated rats also had improved hearing and fewer mtDNA deletions than placebo rats. The results support that interventions reducing ROM damage can protect against presbyacusis by reducing mtDNA damage.
1) Oxidative stress activates the transcription factor sterol regulatory element-binding protein 2 (SREBP2) in vascular endothelial cells. 2) SREBP2 increases expression of microRNA-92a (miR-92a), which targets genes involved in endothelial homeostasis like sirtuin 1, Krüppel-like factor 2, and Krüppel-like factor 4. 3) This leads to activation of the NLRP3 inflammasome and reduced nitric oxide bioavailability, exacerbating endothelial dysfunction during oxidative stress.
This document summarizes a study that evaluated the potential of an adeno-associated virus (AAV) vector delivering a peptide derived from the Nrf2 protein to target the Nrf2 signaling pathway in the retina. The Nrf2 peptide was fused to a cell-penetrating peptide sequence (Tat-peptide) and expressed from an AAV vector. In vitro, the TatNrf2mer peptide induced antioxidant gene expression, blocked IL-1β secretion, and protected cells from oxidative injury. In mouse models, TatNrf2mer expression partially protected photoreceptor function and decreased inflammatory cytokines and cells in models of retinal oxidative injury and uveitis. The results suggest this AAV-delivered TatNrf
Effect Of Ethanol In Oligodendrocytes, research miamiLydia Cortes
This study aimed to determine if ethanol's protective effects against oxidative stress in injured organisms is due to increasing cAMP signaling pathways. The researchers hypothesized that treating cells with ethanol after injury would increase cAMP, PKA, and CREB production, decreasing cell death. Their methods involved inducing spinal cord injuries in rats, culturing cells from the spinal cord and brain, treating cells with ethanol and hydrogen peroxide, and analyzing PKA and CREB levels and cell apoptosis. Their results showed that treating cells with 5% ethanol for 24 hours after oxidative stress increased PKA and CREB levels and reduced cell death. They concluded that combining a 5% ethanol treatment for 24 hours with a pharmacological agent could be a functional treatment to reduce paralysis
Reactive oxygen species along with reactive nitrogen species (rosrns) as the ...banafsheh61
Multiple Sclerosis is a condition of demyelination of the nerve cells in the brain and spinal cord. It is possible that multiple factors are involved in causing multiple sclerosis, including DNA defects in nuclear and mitochondrial genomes, viral infection, hypoxia, oxidative stress, lack of sunlight, and increased macrophages and lymphocytes in the brain. This meta-analysis has gone through many researches and reviews to find the similarities and differences in the cause of this disease. The role of mitochondrial metabolism, environmental temperature and distance from the equator has been discussed in this research, and the amounts of Reactive Oxygen Species (ROS) and Reactive Nitrogen Species (RNS) has been found to be the most possible cause of multiple sclerosis in men and women
Evaluation of salicin isolated from salix subserrata as a radioprotectorRam Sahu
1) The study investigated the radioprotective effects of salicin, a compound found in willow trees, against gamma radiation damage in rat spleen tissue.
2) Irradiation significantly increased lipid peroxidation in spleen tissue but salicin treatment reduced this effect.
3) Ultrastructural examination found no abnormalities in control or salicin groups but irradiation caused lesions and cell loss, which salicin provided some protection against.
4) Changes to protein and enzyme patterns from irradiation were detected electrophoretically and salicin treatment prevented some of these qualitative effects.
Ameliorative effect of salicin against gamma irradiation inducedRam Sahu
This document summarizes a study that investigated the radioprotective effects of salicin against gamma irradiation-induced changes in the brain tissue of male rats. The study found that salicin administration reduced lipid peroxidation and minimized changes to protein patterns caused by irradiation. Specifically, salicin showed the highest protective effect against irradiation in rats that received salicin treatment after irradiation. However, salicin was not able to fully prevent abnormalities to lipoprotein patterns or quantitative changes to protein bands caused by irradiation. Overall, the results suggest salicin has radioprotective abilities against gamma irradiation effects on various electrophoretic patterns in brain tissue.
Vitamin C, glutathione, and various enzymes have radioprotective effects against cellular damage caused by ionizing radiation. Vitamin C is an antioxidant that can scavenge reactive oxygen species produced by radiation and protect DNA and membranes. Glutathione is also a free radical scavenger that protects against radiation damage. Various enzymes also help scavenge free radicals produced by radiation. The presentation concludes that vitamin C, glutathione, and enzymes play an important role in mitigating the effects of ionizing radiation exposure.
This study investigates the hypothesis that age-related hearing loss (presbyacusis) is caused by reactive oxygen metabolites (ROM) damaging mitochondrial DNA (mtDNA). The study assigns 130 rats to treatment groups receiving antioxidants, calorie restriction, or placebo. It finds that calorie-restricted rats had the best hearing, fewest mtDNA deletions, and least hair cell loss. Antioxidant-treated rats also had improved hearing and fewer mtDNA deletions than placebo rats. The results support that interventions reducing ROM damage can protect against presbyacusis by reducing mtDNA damage.
1) Oxidative stress activates the transcription factor sterol regulatory element-binding protein 2 (SREBP2) in vascular endothelial cells. 2) SREBP2 increases expression of microRNA-92a (miR-92a), which targets genes involved in endothelial homeostasis like sirtuin 1, Krüppel-like factor 2, and Krüppel-like factor 4. 3) This leads to activation of the NLRP3 inflammasome and reduced nitric oxide bioavailability, exacerbating endothelial dysfunction during oxidative stress.
This document summarizes a study that evaluated the potential of an adeno-associated virus (AAV) vector delivering a peptide derived from the Nrf2 protein to target the Nrf2 signaling pathway in the retina. The Nrf2 peptide was fused to a cell-penetrating peptide sequence (Tat-peptide) and expressed from an AAV vector. In vitro, the TatNrf2mer peptide induced antioxidant gene expression, blocked IL-1β secretion, and protected cells from oxidative injury. In mouse models, TatNrf2mer expression partially protected photoreceptor function and decreased inflammatory cytokines and cells in models of retinal oxidative injury and uveitis. The results suggest this AAV-delivered TatNrf
Effect Of Ethanol In Oligodendrocytes, research miamiLydia Cortes
This study aimed to determine if ethanol's protective effects against oxidative stress in injured organisms is due to increasing cAMP signaling pathways. The researchers hypothesized that treating cells with ethanol after injury would increase cAMP, PKA, and CREB production, decreasing cell death. Their methods involved inducing spinal cord injuries in rats, culturing cells from the spinal cord and brain, treating cells with ethanol and hydrogen peroxide, and analyzing PKA and CREB levels and cell apoptosis. Their results showed that treating cells with 5% ethanol for 24 hours after oxidative stress increased PKA and CREB levels and reduced cell death. They concluded that combining a 5% ethanol treatment for 24 hours with a pharmacological agent could be a functional treatment to reduce paralysis
Reactive oxygen species along with reactive nitrogen species (rosrns) as the ...banafsheh61
Multiple Sclerosis is a condition of demyelination of the nerve cells in the brain and spinal cord. It is possible that multiple factors are involved in causing multiple sclerosis, including DNA defects in nuclear and mitochondrial genomes, viral infection, hypoxia, oxidative stress, lack of sunlight, and increased macrophages and lymphocytes in the brain. This meta-analysis has gone through many researches and reviews to find the similarities and differences in the cause of this disease. The role of mitochondrial metabolism, environmental temperature and distance from the equator has been discussed in this research, and the amounts of Reactive Oxygen Species (ROS) and Reactive Nitrogen Species (RNS) has been found to be the most possible cause of multiple sclerosis in men and women
1. Snake venom and radiation toxins cause similar pathology through necrosis, apoptosis, and disruption of homeostasis. Clinically, anti-venom and radiation antidotes can reverse many detrimental effects if administered quickly.
2. The toxins disrupt cell membranes and mitochondria, triggering inflammation and cell damage. Specific toxins are thought to play a key role in the inflammatory response.
3. Studies on phospholipase C and excitotoxicity aim to better understand the mechanisms of tissue damage and regeneration after radiation exposure.
The document discusses DNA repair mechanisms in human lymphocytes. It describes how oxidized purines in DNA are repaired through the base excision repair pathway involving the OGG1 glycosylase. This repair requires activation by the transcription factor NF-YA, which upregulates OGG1 expression when DNA is at risk of oxidation. The repair of oxidized bases by OGG1 in human lymphocytes is slow but can be activated by phytohemagglutinin. Disruption of this global repair of oxidized purines may be due to downregulation of OGG1. A second document discusses how green tea acts as an antioxidant to protect against oxidative stress and influence DNA damage and repair through activation of the Nrf2 transcription factor and upreg
This document is an undergraduate thesis that examines the effects of ethanol-induced oxidative stress on antioxidant enzyme expression levels in three tissues of the zebrafish Danio rerio. The student measured expression levels of the antioxidant enzymes CuZnSOD, MnSOD, and CAT in the brain, liver, and gonads of zebrafish after acute ethanol exposure. The results showed that different tissues exhibited distinct expression patterns, with the highest levels found in gonad tissue and no significant changes in brain tissue. The study provides insight into how antioxidant enzymes may protect against oxidative DNA damage caused by excess reactive oxygen species produced during ethanol metabolism.
This document summarizes the relationship between antioxidants, telomeres, aging, and disease. It discusses how free radicals cause oxidative damage that leads to cellular aging and death. Antioxidants can neutralize free radicals and protect telomeres, the protective caps at the end of chromosomes. Shortened telomeres are associated with aging and disease as cells can no longer divide. Compounds in Moringa oleifera like vitamins A, C, E, and selenium act as antioxidants that may protect telomeres from oxidative damage and slow cellular aging.
The document discusses the biosynthesis of enediyne antitumor antibiotics. It summarizes that enediynes are secondary metabolites produced by Actinomycetes that have potent anticancer and antibiotic properties. The biosynthesis of these compounds involves numerous unique structural features. The gene clusters for five enediynes have been cloned and sequenced to help understand their complex biosynthesis in nature. The review focuses on delineating the biosynthesis of enediynes, using the model compound C-1027.
The document describes a thesis submitted by TeQuion Brookins on March 26, 2012 about the influence of the protein cross-linker diethyl acetylenedicarboxylate (DAD) on degradation of proteins by the 20S core particle of the 26S proteasome. The thesis explores how DAD-mediated electrophilic modification can cross-link proteins like the peroxiredoxin Tsa1, inactivate them, and potentially inhibit their degradation by the proteasome. Experiments were conducted to detect increased accumulation of ubiquitin, known proteasomal substrates, and damaged proteins like Tsa1 when yeast cells were treated with DAD, which would indicate disturbance of the cellular protein degradation mechanism. P
Peer Review of Synergistic Effects of Pesticides and Metals in Parkinson'sAfonte4
The document summarizes research into how certain pesticides and metals can accelerate the formation of fibrils made of the protein alpha-synuclein, which are implicated in Parkinson's disease. The researchers found that some common pesticides like rotenone and DDT, as well as metals like aluminum, iron, and manganese, can induce a conformational change in alpha-synuclein that makes it more prone to aggregate into fibrils. They also observed a synergistic effect between certain pesticides and metals, where together the agents had a much greater accelerating effect on fibril formation than individually. The findings suggest environmental toxins that cause alpha-synuclein misfolding and aggregation may contribute
This study investigated the effects of low-frequency electromagnetic fields (EMFs) on alveolar bone in rats and whether melatonin (MLT) and Ganoderma lucidum (GL) provided protection. 56 rats were divided into groups exposed to EMFs, EMFs with MLT, EMFs with GL, or no exposure (control). Half were sacrificed after 26 days and half after 52 days. Histological and immunohistochemical analysis found that EMF exposure caused bone damage that was reduced by MLT and GL administration, suggesting they have protective effects against EMF harm.
Analisi di variazioni nucleotidiche in geni di gestione del ferro in pazienti...MerqurioEditore_redazione
This document summarizes the analysis of genetic variations in genes related to iron metabolism in patients with Parkinson's disease and other movement disorders. The researchers scanned several iron-related genes for mutations in patients with Parkinson's and neurodegeneration with brain iron accumulation. They identified several known and novel sequence variations in ceruloplasmin, iron regulatory protein 2, hemopexin, hepcidin, and hemojuvelin genes. However, none of the variations found were significantly associated with the movement disorders studied. The results suggest that iron metabolism genes may contribute to disease risk but specific variants in these genes do not have a major effect on susceptibility to Parkinson's and related disorders.
1) Rats treated with 3-nitropropionic acid (3-NP), a model of Huntington's disease, exhibited weight loss, gait abnormalities, and striatal lesions.
2) The study found a dose-dependent reduction in complex-I activity in the cerebral cortex of 3-NP treated rats, as measured spectrophotometrically and by blue native-polyacrylamide gel electrophoresis.
3) Succinate driven State 3 respiration was significantly inhibited both in vivo and in isolated mitochondria from the cortex of 3-NP treated rats, suggesting complex-I dysfunction in addition to inhibition of complex-II and succinate dehydrogenase activity contributes to cortico-striatal lesions in this model
Acute and chronic hyperammonemia modulate antioxidantrkkoiri
1) The study examines the effects of acute and chronic hyperammonemia on antioxidant enzyme levels and oxidative damage in the cerebral cortex and cerebellum of rats.
2) Acute hyperammonemia decreased antioxidant enzyme levels in both brain regions but increased lipid peroxidation only in the cerebellum.
3) Chronic hyperammonemia increased antioxidant enzyme levels in the cerebral cortex but decreased levels in the cerebellum, suggesting the cerebellum is more susceptible to oxidative stress during chronic hyperammonemia.
Poor cellular and cardiovascular health is becoming a worldwide epidemic. An unhealthy diet of processed, high-calorie, high-fat foods, pollution, smoking and sedentary lifestyles all contribute to poor cell and heart health. Scientists revealed The French Paradox, which states that even though the French drink, smoke and eat high-fat foods they have some of the lowest incidences of poor cardiovascular and cellular health. Scientists attribute this to the large amounts of red wine that the French consume, or more importantly, an extract found in red wine, resveratrol.
This document discusses phenolic Michael reaction acceptors that can act as both direct and indirect antioxidants. Specifically:
1) Phenolic Michael acceptors like chalcones and bis(benzylidene)acetone analogues can directly scavenge two types of radicals - the nitrogen-centered ABTS+ radical cation and the oxygen-centered galvinoxyl radical.
2) These same phenolic Michael acceptors can also indirectly increase antioxidant defenses by inducing phase 2 cytoprotective enzymes like glutathione, glutathione reductase, and thioredoxin reductase in human keratinocyte cells.
3) Therefore, phenolic Michael acceptors that are both direct
LY2886721 is a potent inhibitor of BACE1 that was studied in mice, dogs, and humans. It showed high selectivity against other proteases. In mice and dogs, it efficiently lowered amyloid beta levels in the brain and cerebrospinal fluid after oral administration. Similar amyloid beta lowering was seen in plasma and cerebrospinal fluid of healthy humans given single or multiple doses of LY2886721, supporting its potential as a disease-modifying therapy for Alzheimer's disease. Crystallography confirmed LY2886721 bound tightly to the active site of BACE1.
The document discusses antioxidants and their role in reducing oxidative stress and free radicals in the body. It provides information on various antioxidants like vitamins A, C, E, carotenoids such as astaxanthin and lutein. Astaxanthin is highlighted as a powerful antioxidant found in marine organisms that is more effective than vitamins C and E. It has anti-inflammatory properties and can protect cells from damage caused by reactive oxygen species. Studies show astaxanthin may help reduce the risk of diseases like cardiovascular disease and dementia by lowering oxidative stress.
This document describes a study that compared the antioxidative and anti-inflammatory effects of Taraxacum officinale (common dandelion) methanol extract (TOME) and water extract (TOWE) in lipopolysaccharide-stimulated RAW 264.7 cells. The extracts reduced nitric oxide production and restored depleted glutathione levels and antioxidant enzyme activities. Both extracts also inhibited lipopolysaccharide-induced inducible nitric oxide synthase gene expression and nuclear factor-κB activation. TOME showed more potent effects than TOWE, which was attributed to its higher phenol, luteolin, and chicoric acid content. The results suggest the extracts inhibit oxidative stress and inflammation by elevating antioxidant enzymes and suppressing
The document discusses phytonutrients and how they provide health benefits. It notes that modern farming practices have reduced the phytonutrient content of many fruits and vegetables. The document then describes a product called GYV that contains concentrated phytonutrients to compensate for these reductions. It discusses several phytonutrients in GYV, including quercetin, resveratrol, and coenzyme Q10, and summarizes relevant scientific research on their health benefits such as antioxidant, anti-inflammatory, and cardiovascular effects.
This study investigated the effects of lithium on the MEK-ERK signaling pathway in astrocytes and neurons. The key findings were:
1) In astrocytes, lithium decreased MEK and ERK phosphorylation in a time- and dose-dependent manner, inhibiting DNA synthesis and inducing cell cycle arrest.
2) In neurons, lithium enhanced MEK and ERK phosphorylation in a concentration-dependent way.
3) The opposing effects of lithium on the MEK-ERK pathway in astrocytes versus neurons suggest lithium may promote neural repair by inhibiting reactive gliosis while stimulating neurons.
This document discusses the multifunctional roles of antimicrobial polypeptides in innate immunity. While initially studied for their antibacterial properties, these polypeptides are now recognized to have diverse inflammatory and immunomodulatory functions. For example, the cathelicidin LL-37/hCAP-18 induces angiogenesis in addition to its antimicrobial activity. The discovery of additional functions raises new questions about using these polypeptides therapeutically given their potential effects on multiple biological pathways. Defining their precise roles in vivo remains an ongoing challenge due to the complex interplay of factors in natural infections.
Chordify Management Consultants provides IT staff augmentation and consulting services with a focus on big data analytics, visualization, mobile and cloud applications, and business intelligence application development and integration. They have over 3,000 consultants who help global Fortune 1000 companies and small/medium businesses implement IT solutions. Chordify prides itself on adopting a data-driven approach and measuring the effectiveness of its service delivery.
El equilibrio químico es un estado en el que no se observan cambios en el sistema. Los cambios de coloración muestran el progreso hacia el equilibrio químico cuando dos sustancias reaccionan. La temperatura y la presión afectan el equilibrio químico: un aumento de temperatura modifica el valor de la constante de equilibrio, mientras que un aumento de presión desplaza la reacción hacia donde haya menos moles gaseosas.
1. Snake venom and radiation toxins cause similar pathology through necrosis, apoptosis, and disruption of homeostasis. Clinically, anti-venom and radiation antidotes can reverse many detrimental effects if administered quickly.
2. The toxins disrupt cell membranes and mitochondria, triggering inflammation and cell damage. Specific toxins are thought to play a key role in the inflammatory response.
3. Studies on phospholipase C and excitotoxicity aim to better understand the mechanisms of tissue damage and regeneration after radiation exposure.
The document discusses DNA repair mechanisms in human lymphocytes. It describes how oxidized purines in DNA are repaired through the base excision repair pathway involving the OGG1 glycosylase. This repair requires activation by the transcription factor NF-YA, which upregulates OGG1 expression when DNA is at risk of oxidation. The repair of oxidized bases by OGG1 in human lymphocytes is slow but can be activated by phytohemagglutinin. Disruption of this global repair of oxidized purines may be due to downregulation of OGG1. A second document discusses how green tea acts as an antioxidant to protect against oxidative stress and influence DNA damage and repair through activation of the Nrf2 transcription factor and upreg
This document is an undergraduate thesis that examines the effects of ethanol-induced oxidative stress on antioxidant enzyme expression levels in three tissues of the zebrafish Danio rerio. The student measured expression levels of the antioxidant enzymes CuZnSOD, MnSOD, and CAT in the brain, liver, and gonads of zebrafish after acute ethanol exposure. The results showed that different tissues exhibited distinct expression patterns, with the highest levels found in gonad tissue and no significant changes in brain tissue. The study provides insight into how antioxidant enzymes may protect against oxidative DNA damage caused by excess reactive oxygen species produced during ethanol metabolism.
This document summarizes the relationship between antioxidants, telomeres, aging, and disease. It discusses how free radicals cause oxidative damage that leads to cellular aging and death. Antioxidants can neutralize free radicals and protect telomeres, the protective caps at the end of chromosomes. Shortened telomeres are associated with aging and disease as cells can no longer divide. Compounds in Moringa oleifera like vitamins A, C, E, and selenium act as antioxidants that may protect telomeres from oxidative damage and slow cellular aging.
The document discusses the biosynthesis of enediyne antitumor antibiotics. It summarizes that enediynes are secondary metabolites produced by Actinomycetes that have potent anticancer and antibiotic properties. The biosynthesis of these compounds involves numerous unique structural features. The gene clusters for five enediynes have been cloned and sequenced to help understand their complex biosynthesis in nature. The review focuses on delineating the biosynthesis of enediynes, using the model compound C-1027.
The document describes a thesis submitted by TeQuion Brookins on March 26, 2012 about the influence of the protein cross-linker diethyl acetylenedicarboxylate (DAD) on degradation of proteins by the 20S core particle of the 26S proteasome. The thesis explores how DAD-mediated electrophilic modification can cross-link proteins like the peroxiredoxin Tsa1, inactivate them, and potentially inhibit their degradation by the proteasome. Experiments were conducted to detect increased accumulation of ubiquitin, known proteasomal substrates, and damaged proteins like Tsa1 when yeast cells were treated with DAD, which would indicate disturbance of the cellular protein degradation mechanism. P
Peer Review of Synergistic Effects of Pesticides and Metals in Parkinson'sAfonte4
The document summarizes research into how certain pesticides and metals can accelerate the formation of fibrils made of the protein alpha-synuclein, which are implicated in Parkinson's disease. The researchers found that some common pesticides like rotenone and DDT, as well as metals like aluminum, iron, and manganese, can induce a conformational change in alpha-synuclein that makes it more prone to aggregate into fibrils. They also observed a synergistic effect between certain pesticides and metals, where together the agents had a much greater accelerating effect on fibril formation than individually. The findings suggest environmental toxins that cause alpha-synuclein misfolding and aggregation may contribute
This study investigated the effects of low-frequency electromagnetic fields (EMFs) on alveolar bone in rats and whether melatonin (MLT) and Ganoderma lucidum (GL) provided protection. 56 rats were divided into groups exposed to EMFs, EMFs with MLT, EMFs with GL, or no exposure (control). Half were sacrificed after 26 days and half after 52 days. Histological and immunohistochemical analysis found that EMF exposure caused bone damage that was reduced by MLT and GL administration, suggesting they have protective effects against EMF harm.
Analisi di variazioni nucleotidiche in geni di gestione del ferro in pazienti...MerqurioEditore_redazione
This document summarizes the analysis of genetic variations in genes related to iron metabolism in patients with Parkinson's disease and other movement disorders. The researchers scanned several iron-related genes for mutations in patients with Parkinson's and neurodegeneration with brain iron accumulation. They identified several known and novel sequence variations in ceruloplasmin, iron regulatory protein 2, hemopexin, hepcidin, and hemojuvelin genes. However, none of the variations found were significantly associated with the movement disorders studied. The results suggest that iron metabolism genes may contribute to disease risk but specific variants in these genes do not have a major effect on susceptibility to Parkinson's and related disorders.
1) Rats treated with 3-nitropropionic acid (3-NP), a model of Huntington's disease, exhibited weight loss, gait abnormalities, and striatal lesions.
2) The study found a dose-dependent reduction in complex-I activity in the cerebral cortex of 3-NP treated rats, as measured spectrophotometrically and by blue native-polyacrylamide gel electrophoresis.
3) Succinate driven State 3 respiration was significantly inhibited both in vivo and in isolated mitochondria from the cortex of 3-NP treated rats, suggesting complex-I dysfunction in addition to inhibition of complex-II and succinate dehydrogenase activity contributes to cortico-striatal lesions in this model
Acute and chronic hyperammonemia modulate antioxidantrkkoiri
1) The study examines the effects of acute and chronic hyperammonemia on antioxidant enzyme levels and oxidative damage in the cerebral cortex and cerebellum of rats.
2) Acute hyperammonemia decreased antioxidant enzyme levels in both brain regions but increased lipid peroxidation only in the cerebellum.
3) Chronic hyperammonemia increased antioxidant enzyme levels in the cerebral cortex but decreased levels in the cerebellum, suggesting the cerebellum is more susceptible to oxidative stress during chronic hyperammonemia.
Poor cellular and cardiovascular health is becoming a worldwide epidemic. An unhealthy diet of processed, high-calorie, high-fat foods, pollution, smoking and sedentary lifestyles all contribute to poor cell and heart health. Scientists revealed The French Paradox, which states that even though the French drink, smoke and eat high-fat foods they have some of the lowest incidences of poor cardiovascular and cellular health. Scientists attribute this to the large amounts of red wine that the French consume, or more importantly, an extract found in red wine, resveratrol.
This document discusses phenolic Michael reaction acceptors that can act as both direct and indirect antioxidants. Specifically:
1) Phenolic Michael acceptors like chalcones and bis(benzylidene)acetone analogues can directly scavenge two types of radicals - the nitrogen-centered ABTS+ radical cation and the oxygen-centered galvinoxyl radical.
2) These same phenolic Michael acceptors can also indirectly increase antioxidant defenses by inducing phase 2 cytoprotective enzymes like glutathione, glutathione reductase, and thioredoxin reductase in human keratinocyte cells.
3) Therefore, phenolic Michael acceptors that are both direct
LY2886721 is a potent inhibitor of BACE1 that was studied in mice, dogs, and humans. It showed high selectivity against other proteases. In mice and dogs, it efficiently lowered amyloid beta levels in the brain and cerebrospinal fluid after oral administration. Similar amyloid beta lowering was seen in plasma and cerebrospinal fluid of healthy humans given single or multiple doses of LY2886721, supporting its potential as a disease-modifying therapy for Alzheimer's disease. Crystallography confirmed LY2886721 bound tightly to the active site of BACE1.
The document discusses antioxidants and their role in reducing oxidative stress and free radicals in the body. It provides information on various antioxidants like vitamins A, C, E, carotenoids such as astaxanthin and lutein. Astaxanthin is highlighted as a powerful antioxidant found in marine organisms that is more effective than vitamins C and E. It has anti-inflammatory properties and can protect cells from damage caused by reactive oxygen species. Studies show astaxanthin may help reduce the risk of diseases like cardiovascular disease and dementia by lowering oxidative stress.
This document describes a study that compared the antioxidative and anti-inflammatory effects of Taraxacum officinale (common dandelion) methanol extract (TOME) and water extract (TOWE) in lipopolysaccharide-stimulated RAW 264.7 cells. The extracts reduced nitric oxide production and restored depleted glutathione levels and antioxidant enzyme activities. Both extracts also inhibited lipopolysaccharide-induced inducible nitric oxide synthase gene expression and nuclear factor-κB activation. TOME showed more potent effects than TOWE, which was attributed to its higher phenol, luteolin, and chicoric acid content. The results suggest the extracts inhibit oxidative stress and inflammation by elevating antioxidant enzymes and suppressing
The document discusses phytonutrients and how they provide health benefits. It notes that modern farming practices have reduced the phytonutrient content of many fruits and vegetables. The document then describes a product called GYV that contains concentrated phytonutrients to compensate for these reductions. It discusses several phytonutrients in GYV, including quercetin, resveratrol, and coenzyme Q10, and summarizes relevant scientific research on their health benefits such as antioxidant, anti-inflammatory, and cardiovascular effects.
This study investigated the effects of lithium on the MEK-ERK signaling pathway in astrocytes and neurons. The key findings were:
1) In astrocytes, lithium decreased MEK and ERK phosphorylation in a time- and dose-dependent manner, inhibiting DNA synthesis and inducing cell cycle arrest.
2) In neurons, lithium enhanced MEK and ERK phosphorylation in a concentration-dependent way.
3) The opposing effects of lithium on the MEK-ERK pathway in astrocytes versus neurons suggest lithium may promote neural repair by inhibiting reactive gliosis while stimulating neurons.
This document discusses the multifunctional roles of antimicrobial polypeptides in innate immunity. While initially studied for their antibacterial properties, these polypeptides are now recognized to have diverse inflammatory and immunomodulatory functions. For example, the cathelicidin LL-37/hCAP-18 induces angiogenesis in addition to its antimicrobial activity. The discovery of additional functions raises new questions about using these polypeptides therapeutically given their potential effects on multiple biological pathways. Defining their precise roles in vivo remains an ongoing challenge due to the complex interplay of factors in natural infections.
Chordify Management Consultants provides IT staff augmentation and consulting services with a focus on big data analytics, visualization, mobile and cloud applications, and business intelligence application development and integration. They have over 3,000 consultants who help global Fortune 1000 companies and small/medium businesses implement IT solutions. Chordify prides itself on adopting a data-driven approach and measuring the effectiveness of its service delivery.
El equilibrio químico es un estado en el que no se observan cambios en el sistema. Los cambios de coloración muestran el progreso hacia el equilibrio químico cuando dos sustancias reaccionan. La temperatura y la presión afectan el equilibrio químico: un aumento de temperatura modifica el valor de la constante de equilibrio, mientras que un aumento de presión desplaza la reacción hacia donde haya menos moles gaseosas.
1) Holly is kidnapped from her home and taken to an abandoned warehouse, where she is bound and beaten.
2) Holly's friends receive demands and threats from her kidnapper to complete tasks over 48 hours to earn clues to find her.
3) As the friends struggle with their tasks, one friend discovers a clue that Holly is in the Screaming Woods, leading her there to search for Holly while being watched by the kidnapper.
Debemos tener en cuenta que la informática en la actualidad forma parte esencial de la cotidianidad de las personas, porque con cada uno de los programas que nos ofrece, nos esta permitiendo una comunicación mucho mas avanzada que en los tiempos de nuestros antepasados, ya que nos es mas fácil comunicarnos con otros sin necesidad de trasladarnos y a tan solo segúnpor mas grande que fuese la distancia, la informática es un instrumento que se ha vuelto indispensable en la sociedad moderna, ya que gracias a esta se pueden realizar desde actividades simples como una tarea escolar; hasta actividades complejas en grandes compañías
Milad e rasool aur asateen e ummat by allama maualan rahat ali khan qadriMuhammad Tariq
Milad E Rasool Aur Asateen E Ummat By Allama Maualan Rahat Ali Khan Qadri,Milad, Meelad, Melad, mowalid, Meelad un Nabi, Milad e nabi, Birthday,molood, میلاد ، مولد، میلا د النبی، ،عید میلاد النبی،,Eid Milad un Nab
O documento resume o currículo de Eric Gallardo, um profissional de TI brasileiro com quase 20 anos de experiência em projetos para internet e gestão corporativa utilizando diversas linguagens e metodologias como .NET, Java, Scrum e ITIL. O treinamento aborda conceitos e frameworks como ASP.NET, MVC, WebForms, Entity Framework e AJAX/jQuery além de ferramentas como Visual Studio e plugins.
Here Are Some New Trends On TV Everywhere ConsumptionAdobe
TV Everywhere consumption via connected devices like Apple TV and Roku are at an all time high, according to Adobe Digital Index's Q3 Digital Video Report.
El documento compara las características de la escuela tradicional y la escuela nueva, destacando que la escuela tradicional se centra en el profesor y los libros de texto, mientras que la escuela nueva se basa en los intereses y necesidades de los alumnos de forma más constructivista. También presenta información sobre el pedagogo Ovide Decroly y su método basado en los "centros de interés", donde los temas de estudio se centran en los intereses de los alumnos para dar respuesta a sus necesidades.
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1. Original Contribution
Temporal expression of hypoxia-regulated genes is associated with early
changes in redox status in irradiated lung
Isabel L. Jackson a,1
, Xiuwu Zhang b,1
, Caroline Hadley b
, Zahid N. Rabbani b
,
Yu Zhang b
, Sam Marks b
, Zeljko Vujaskovic a,b,n
a
Department of Pathology, Duke University Medical Center, Durham, NC 27710, USA
b
Department of Radiation Oncology, Duke University Medical Center, Durham, NC 27710, USA
a r t i c l e i n f o
Article history:
Received 4 August 2011
Received in revised form
9 April 2012
Accepted 10 April 2012
Available online 25 April 2012
Keywords:
Radiation-induced lung injury
Oxidative stress
Hypoxia-inducible factor
Inflammation
Free radicals
a b s t r a c t
The development of normal lung tissue toxicity after radiation exposure results from multiple changes
in cell signaling and communication initiated at the time of the ionizing event. The onset of gross
pulmonary injury is preceded by tissue hypoxia and chronic oxidative stress. We have previously
shown that development of debilitating lung injury can be mitigated or prevented by administration of
AEOL10150, a potent catalytic antioxidant, 24 h after radiation. This suggests that hypoxia-mediated
signaling pathways may play a role in late radiation injury, but the exact mechanism remains unclear.
The purpose of this study was to evaluate changes in the temporal expression of hypoxia-associated
genes in irradiated mouse lung and determine whether AEOL10150 alters expression of these genes. A
focused oligo array was used to establish a hypoxia-associated gene expression signature for lung tissue
from sham-irradiated or irradiated mice treated with or without AEOL10150. Results were further
verified by RT-PCR. Forty-four genes associated with metabolism, cell growth, apoptosis, inflammation,
oxidative stress, and extracellular matrix synthesis were upregulated after radiation. Elevated expres-
sion of 31 of these genes was attenuated in animals treated with AEOL10150, suggesting that
expression of a number of hypoxia-associated genes is regulated by early development of oxidative
stress after radiation. Genes identified herein could provide insight into the role of hypoxic signaling in
radiation lung injury, suggesting novel therapeutic targets, as well as clues to the mechanism by which
AEOL10150 confers pulmonary radioprotection.
& 2012 Elsevier Inc. All rights reserved.
Introduction
The risk of radiation-induced normal tissue toxicity limits the
therapeutic dose of radiation that can be used in treating human
cancers. This limitation is a significant barrier to achieving
successful tumor control in all tumor types, but it is particularly
confounding in treating tumors of the thoracic region because of
the extreme radiosensitivity of the lungs. Although the mechan-
isms underlying radiation-induced normal tissue injury have
been partially elucidated, the way in which radiation affects
specific inter- and intracellular signaling pathways and inflam-
matory mediators is not completely understood.
It is well known that the initial ionizing event not only directly
damages DNA, causing apoptosis or mitotic catastrophe, but also
affects cellular macromolecules, and lipid membranes. The initial
cellular damage begins a series of reactions that ultimately result in
chronic oxidative stress, tissue hypoxia, inflammation, and fibropro-
liferation. If left unresolved, these conditions may result in tissue
damage, diminished quality of life, and complete organ failure.
The development of chronic oxidative stress within irradiated
tissue begins during the initial exposure and is perpetuated by
molecules activated within minutes or hours postirradiation [1].
Transforming growth factor-b (TGF-b1), a proinflammatory and
profibrogenic cytokine, is a prominent effector in the response of
tissue to radiation. Within seconds of radiation exposure, TGF-b1 is
activated by cleavage of the active protein from its latency-associated
complex by hydroxyl radical [2]. Once activated, TGF-b1 can induce
synthesis of NADPH oxidase, an oxidant-generating enzyme [3,4].
The increase in active NADPH oxidase causes chronic reactive oxygen
and nitrogen species (ROS and RNS, respectively) overproduction,
creating an imbalance in free radical production and the antioxidant
capabilities of the cell. This self-perpetuating increase in production
of radical species in the cell causes continuous activation of proa-
poptotic, hypoxia-mediated, proinflammatory, and profibrogenic
pathways long after the initial radiation exposure.
Continuous activity of these pathways contributes signifi-
cantly to vascular dysfunction and tissue hypoxia [1,5]. As areas
Contents lists available at SciVerse ScienceDirect
journal homepage: www.elsevier.com/locate/freeradbiomed
Free Radical Biology and Medicine
0891-5849/$ - see front matter & 2012 Elsevier Inc. All rights reserved.
http://dx.doi.org/10.1016/j.freeradbiomed.2012.04.014
n
Corresponding author. Fax: þ1 919 681 2651.
E-mail address: vujas@radonc.duke.edu (Z. Vujaskovic).
1
These authors contributed equally to this work.
Free Radical Biology and Medicine 53 (2012) 337–346
2. of hypoxia develop, inflammatory cells, most notably macro-
phages, are recruited to the site of injury where they undergo
the respiratory burst, further increasing tissue levels of ROS/
RNS [6]. These high levels of ROS/RNS are responsible for activa-
tion of molecules involved in radiation-induced normal tissue
injury, including TGF-b1, nuclear factor kB, and hypoxia-inducible
factor 1a (HIF-1a) [7,8]. The cyclic nature of these events creates
a self-perpetuating pathologic environment characterized by
chronic oxidative stress, tissue hypoxia, and continual activation
of redox-regulated signaling molecules and pathways involved in
inflammation and fibroproliferation.
In our previous studies, we have shown that the potent
catalytic antioxidant AEOL10150 [9] can mitigate or prevent
radiation-induced lung injury in a rodent model when given
before or after radiation exposure [10,11]. In these studies,
treatment with AEOL10150 significantly reduced oxidative
damage to DNA (8-OHdG), TGF-b1-mediated fibrosis, and expres-
sion of HIF-1a and its downstream products carbonic anhydrase
IX (CA IX) and VEGF [11].
In this study we hypothesized that the development of radia-
tion-induced lung injury is facilitated by genes upregulated by
hypoxia and that expression of these genes is affected by redox-
mediated signaling. To investigate this hypothesis, we used a
hypoxia signaling pathway-specific oligo DNA microarray to
examine hypoxia-associated gene expression in C57BL/6 J mouse
lungs 1 day, 3 day, 1 week, 3 weeks, 6 weeks, and 6 months after a
single dose of 15 Gy to the whole thorax. Next, we evaluated
whether the potent catalytic antioxidant AEOL10150 could influ-
ence expression of select hypoxia-associated genes when admi-
nistered for 4 weeks after radiation exposure.
The transcriptome profile for hypoxia-associated genes identi-
fied in this study provides valuable insight into the sequence
of events associated with development of normal tissue injury
after radiation exposure. We hypothesize that the protective
effect of AEOL10150, shown in our previous studies [10,12], is
due to its effects on redox-regulated cell signaling, which may
include, but is not limited to, hypoxia-induced gene expression.
Additional evaluation of hypoxia-associated genes not affected by
AEOL10150 may lead to a better understanding of the pathologi-
cal mechanisms underlying the development of injury and may
identify new targets for therapeutic intervention.
Materials and methods
Animal irradiation
Female C57BL/6 J mice (8–10 weeks) received a single 15-Gy
dose of X-ray irradiation (Therapax 320; Pantak, East Haven, CT,
USA) at a dose rate of 67 cGy/min using a beam energy of 320 kV
(75 SSD, Filter ¼ 2 mm Al, HVLE2 mm Cu). Radiation was delivered
to the whole thorax through adjustable apertures (1.25–1.5 cm)
with 8 mm lead shielding the rest of the body. Sham-irradiated
animals were subjected to the same scenario, but the radiation
source was not turned on. All mice were anesthetized before
irradiation with an intraperitoneal (ip) injection of a ketamine
(100 mg/kg)/xylazine (10 mg/kg) mixture. Radiation dosimetry was
performed using a calibrated ionization chamber and single-use
MOSFET radiation detectors placed in tissue-equivalent material or
within the chest cavity of non-study-related C57BL/6 J mice [13,14].
The variation in dose rate across the field profile was less than 6%.
Animals were euthanized and tissue was harvested at predeter-
mined time points of 1 day, 3 day, 1 week, 3 weeks, 6 weeks, and
6 months. At the time of euthanasia (4250 mg/kg sodium pento-
barbital, ip), lungs were snap-frozen in liquid nitrogen and stored at
À80 1C (n¼7/group). All studies were performed and approved by
the Institutional Animal Care and Use Committee at Duke University
Medical Center.
AEOL10150 regimen
To determine whether AEOL10150 affects the transcriptome
profile of hypoxia-associated genes, a separate cohort of animals
was randomized into the following groups: (a) sham irradiation,
(b) AEOL10150 alone, (c) 15 Gy whole-thorax irradiation (WTI),
and (d) 15 Gy WTIþAEOL10150. Each group contained six ani-
mals. AEOL10150 was supplied by Aeolus Pharmaceuticals (San
Diego, CA, USA). Animals receiving AEOL10150 were given a
loading dose of 40 mg/kg/day by subcutaneous injection 2 h after
radiation. This was followed by a maintenance dose of 20 mg/kg
every other day for 4 weeks. Animals were euthanized six weeks
post-irradiation and lung tissue harvested for analysis of hypoxia-
associated gene expression.
Histopathology and immunohistochemistry
To visualize histopathologic damage in sham-irradiated and
irradiated tissue at each of the predetermined time points, hema-
toxylin and eosin (H&E) staining was carried out as previously
described [15]. Immunostaining for carbonic anhydrase was per-
formed as previously described by Gauter-Fleckenstein et al. [16].
Briefly, 5-mm-thick paraffin-embedded tissue sections were
deparaffinized and rehydrated using xylene and graded alcohol
(100–80%) concentrations. Hydrogen peroxide (10%) was used to
block endogenous peroxidase activity and antigen retrieval per-
formed with citrate buffer (Biogenex, San Ramon, CA, USA). Slides
were incubated at 4 1C overnight with a rabbit polyclonal antibody
to carbonic anhydrase IX (1:200; Abcam, Cambridge, MA, USA)
followed by washing in phosphate-buffered saline and incubation
for 1 h at room temperature with a donkey anti-rabbit secondary
antibody (1:200; Jackson ImmunoResearch, West Grove, PA, USA).
Slides were counterstained with Harris hematoxylin and visualized
under light microscopy using a 40 Â objective.
Pimonidazole
Pimonidazole hydrochloride (70 mg/kg ip; Chemicon Interna-
tional, Temecula, CA, USA) was injected 3 h before euthanasia and
immunostaining performed as previously described [17].
RNA isolation
Snap-frozen whole-lung tissue was homogenized in 5 ml
TRIzol reagent (Invitrogen, Carlsbad, CA, USA) with the PowerGen
125 homogenizer (Fisher Scientific, Pittsburgh, PA, USA). The total
RNA was isolated using TRIzol reagent following the manufac-
turer’s instructions (Invitrogen). The RNA was repeatedly purified
until the A260:A280 was greater than 2.0 and A260:A230 was greater
than 1.7.
Probe preparation
cDNA synthesis, cRNA synthesis, and cRNA labeling were
performed using the TrueLabeling-AMP 2.0 kit (SA Bioscience,
Frederick, MD, USA) according to the manufacturer’s manual.
Briefly, 10 mg of pooled total RNA was used for the cDNA
synthesis. The RNA pool was produced by mixing equal amounts
of total RNA from each sample in the same group. The cDNA was
then subjected to cRNA synthesis and labeling with biotinylated-
UTP overnight at 37 1C. After purification with the SA Bioscience
ArrayGrade cRNA cleanup kit (SA Bioscience), 15 mg of biotin-
labeled cRNA was used for hybridization.
I.L. Jackson et al. / Free Radical Biology and Medicine 53 (2012) 337–346338
3. Hybridization
A mouse hypoxia signaling pathway-specific Oligo GEArray
DNA microarray (SA Bioscience, Cat. No. OMM-032) was used to
determine temporal changes in the expression of 113 genes after
thoracic irradiation. Before hybridization, array membranes were
prewetted with 5 ml of deionized water for 5 min and then
prehybridized with 2 ml of prewarmed GEAhyb hybridization
solution (SA Bioscience, Cat. No. H-01) for 4 h at 60 1C. The array
membrane was hybridized with 15 mg of purified biotin-labeled
cRNA probes overnight at 60 1C with continuous agitation. The
membranes were then washed with Wash Solution 1 (2 Â SSC, 1%
SDS) for 20 min at 60 1C followed by Wash Solution 2 (0.1 Â SSC,
0.5% SDS) for 15 min at 60 1C with continuous agitation.
Chemiluminescence detection and data analysis
The signal was visualized using the Chemiluminescent Detec-
tion kit (SA Bioscience, Cat No. D-01). Briefly, after being blocked,
the membranes were bound with alkaline phosphatase-conju-
gated streptavidin. After being washed, the membranes were
incubated with chemiluminescence substrate for 5 min and
exposed to X-ray film. Gene spots with signal intensity higher
than the blank on the same membrane were considered detect-
able. The densitometry of GAPDH in the radiation group was
normalized to that in the control group. Densitometry for each
gene spot was then normalized to the adjusted GAPDH. For the
time-point experiment, the average increased densitometry from
two repeated experiments was graded in five expression degrees,
of which 1 represents a weak increase and 5 represents the
highest increase. If the gene spot was undetectable in both the
control and the irradiated mice at same time point, it was
designated as 0. For the AEOL10150 regimen, the densitometry
of each gene in four groups was directly compared. The percen-
tage of reversal by AEOL10150 was calculated.
RT-PCR
Total RNA isolation was performed as described above. Reverse
transcription was performed by incubating 3 mg of pooled total
RNA, 2.5 mM random primer, and 200 units of Superscript III
reverse transcriptase (Invitrogen), for a total reaction volume of
20 ml, for 10 min at 25 1C followed by 60 min at 50 1C. PCR
amplification was carried out using Platinum Taq DNA polymer-
ase (Invitrogen) and two pairs of primers in one reaction, one
amplifying the target gene fragment and another amplifying a
1-kb GAPDH fragment to serve as an internal control. PCR
products were visualized on 1.5% agarose gel containing 0.5 mg/
ml ethidium bromide. The ratio of PCR product of the target gene
to GAPDH better reflected the RNA level in the samples. Primer
sequences and the sizes of PCR products are listed in Table 1.
Western blotting
Snap-frozen left lungs were prepared for Western blot analysis
by immersing the lung in homogenization buffer containing pro-
tease and phosphatase inhibitors (Roche Applied Sciences, Indiana-
polis, IN, USA) and sonicating the samples to disrupt the cell
membranes. Samples were centrifuged to remove undigested tissue.
The supernatants were diluted 1:1 in Laemmli sample buffer (95%
Laemmli sample buffer, 5% b-mercaptoethanol) (Bio-Rad, Berkeley,
CA, USA). The prepared samples were then boiled and centrifuged
before loading (10 ml per well) onto 10% SDS–PAGE gels. After
electrophoresis, the proteins were transferred onto polyvinylidene
difluoride membranes and probed with a specific antibody to
HIF-1a (Novus Biologicals, Littleton, CO, USA), HIF-2a (Abcam,
Cambridge, MA, USA), or HIF-3a (Novus Biologicals) diluted in 5%
nonfat milk in TBSþ0.1% Tween 20. After secondary antibody
incubation (Cell Signaling, Beverly, MA, USA), signals were visualized
using the SuperSignal West Pico Chemiluminescent Substrate
(Thermo Scientific, Rockford, IL, USA). Films were scanned using
an HP ScanJet 3110. Band intensity was quantified using ImageJ
software (NIH, Bethesda, MD, USA). Measured intensities were
normalized using a-tubulin expression and then averaged within
groups. Comparisons between irradiated and nonirradiated controls
at each time point were made using a Student t test.
Results
Temporal changes in tissue oxygenation
Positive staining for carbonic anhydrase IX, an endogenous
marker of hypoxia, and the exogenous hypoxia marker pimonida-
zole was evident 3 day after radiation and was strongly increased at
1 week (Fig. 1). The development of tissue hypoxia occurred before
the overt onset of histopathologic damage (H&E stain, Fig. 1). By
6 months, architectural distortion and tissue fibrosis could be seen.
Changes in HIF-1a, 2a, 2b, and 3a mRNA expression after radiation
Differences in expression of HIF-1a, 2a, 2b, and 3a were
examined by comparing RT-PCR of pooled total RNA from the
lungs of the control and irradiated mice sacrificed at each time
point (n¼7). HIF-1a mRNA expression was constant across all of
the time points examined, whereas expression of HIF-2a was
upregulated in irradiated mice at multiple time points. HIF-2b
expression was upregulated in irradiated animals beginning
1 week after radiation, whereas expression of HIF-3a was not
upregulated until 6 months postradiation (Fig. 2).
HIF-1a, 2a, 2b, and 3a protein expression
Western blot analysis suggests a dynamic role for HIF-1a, 2a,
and 3a. Assessment of protein expression showed that HIF-1a
protein expression is elevated in irradiated animals 24 h after
Table 1
RT-PCR primers and product sizes
Gene symbol Primer sequence Fragment size (bp)
Adm-F 50
–AGCTGGTTTCCATCACCCTG-30
502
Adm-R 50
–CCTGGGAGGACTCCACAGTC-30
Angpt14-F 50
–GTGAGGACACAGCCTACAGC-30
333
Angpt14-R 50
–AGGCTGCTGTAGCCTCCATG-30
CTGF-F 50
–CTGCCTACCGACTGGAAGAC-30
495
CTGF-R 50
–ACATCTTCCTGTAGTACAGG-30
Eno-1a-F 50
–GCCAGAGAGATCTTTGACTC-30
443
Eno-1a-R 50
–CCGTTGATCACATTGAAAGC-30
Gna11-F 50
–CAGAGCGCAGGAAGTGGATC-30
427
Gna11-R 50
–ACTCCTTCAGGTTCAGCTGC-30
HIF-1a-F 50
–CTCAGTTTGAACTAACTGGAC-30
680
HIF-1a-R 50
–GTCGTGCTGAATAATACCAC-30
HIF-2a-F 50
–CGTGGTGACCCAAGACGGTGA-30
630
HIF-2a-R 50
–AGCATCCGGTACTGGCCAGA-30
HIF-2b-F 50
–CAGAACATATCCCAGATCTC-30
439
HIF-2b-R 50
–GGTCAGCAAAGTCCTCGATG-30
Ppara-F 50
–TGAAGCCATCTTCACGATGC-30
446
Ppara-R 50
–ATCTCTTGCAACAGTGGGTG-30
Rora-F 50
–TCATTACGTGTGAAGGCTGC-30
495
Rora-R 50
–CCAGATGCTGGTGTGTAGTC-30
Sord-F 50
–GAACAAGGTCCTTGTGTGTG-30
427
Sord-R 50
–GTCTTCGATGCAAGCATGGA-30
GAPDH-F 50
–GGTGAAGGTCGGTGTGAACG-30
990
GAPDH-R 50
–TGGAGGCCATGTAGGCCATG-30
I.L. Jackson et al. / Free Radical Biology and Medicine 53 (2012) 337–346 339
4. radiation, but does not differ significantly at any other time point
until 6 months postirradiation, when HIF-1a expression is
reduced relative to untreated controls (Fig. 3a). HIF-2a expression
was elevated 24 h postirradiation and again 6 months after
radiation. Differential expression was also observed at the 1-week
time point, but was not different between irradiated and control
H&E CA IX Pimonidazole
Control
1 Day
3 Days
1 Week
3 Weeks
6 Weeks
6 Months
Bars represent 100 µm
Fig. 1. The temporal progression of tissue hypoxia in lung after radiation. Tissue hypoxia is first noticeable around 3 day (CA IX, pimonidazole) postradiation and
progressively increases throughout the follow-up period (6 months). At 6 weeks, the first histopathologic lesions are seen (H&E). These are generally focal in nature and are
characterized by thickening of the alveoli wall and increased inflammatory cell infiltrate. By 6 months, tissue damage has considerably worsened and a greater number of
focal lesions are observed. Brown indicates positive staining. Scale bars, 100 mm.
I.L. Jackson et al. / Free Radical Biology and Medicine 53 (2012) 337–346340
5. animals at any intervening time points (Fig. 3b). No significant
differential expression of HIF-3a protein was observed at any
point after radiation (Fig. 3c).
Genes with elevated postradiation expression at all time points
Oligo array assay revealed that beginning 1 day after radiation,
messenger RNA expression of Adm, Agpat2, Ard1, CTGF, Eno1,
HIF-2a, Gna11, Prkaa1, Sdh1, and Tuba3 was elevated in irra-
diated animals relative to control. This increase continued
throughout the 6-month follow-up period (Table 2). One week
after radiation increased expression of Agtpbp1, Angptl4, HIF-2b,
Nmyc1, Ppara, and Th was observed. Expression remained ele-
vated at all later time points (Fig. 4).
Genes exhibiting a biphasic increase after radiation
As shown in Table 2, mRNA expression of Cygb and Dapk3 is
briefly increased at two time points, the first beginning 1 day after
radiation and lasting no more than a few days and the second
beginning 6 weeks after radiation and continuing to the 6-month
time point. Dctn2, Gap43, Man2b1, Rora, and Rps7 mRNA expres-
sion was elevated for periods of differing duration 3 day after
radiation and again 6 weeks postradiation.
Genes expressed during the development of symptomatic injury
Six weeks after radiation, an increase in mRNA expression of
Car12, Cdc42, Eef1a1, Htatip, IL-1b, Lep, Lipe, Mmp14, Plod3, and
TGF-b1 was observed in all irradiated animals. Expression of Dr1,
Fabp4, Fnbp3, and Slc2a1 was elevated only at 6 months post-
radiation (Table 2).
AEOL10150 normalizes hypoxia-associated gene expression 6 weeks
after radiation
To further investigate changes in the hypoxia-associated
transcriptome, we analyzed the expression of the same 113
genes, 6 weeks after radiation and treatment with AEOL10150,
using a hypoxia signaling pathway-specific oligo DNA micro-
array. Thirty of the 31 genes observed to be upregulated in
mice six weeks after radiation alone showed no detectable
increase in expression after treatment with AEOL10150
(Table 3). The only hypoxia gene that remained upregulated
even when AEOL10150 was administered after radiation was
HIF-1α
GAPDH
1 d 3 d 1 wk 3 wk 6 wk 6 m
C R C R C R C R C R C RM
HIF-2α
GAPDH
1 d 3 d 1 wk 3 wk 6 wk 6 m
C R C R C R C R C R C RM
HIF-3α
GAPDH
1 d 3 d 1 wk 3 wk 6 wk 6 m
C R C R C R C R C R C RM
HIF-2
GAPDH
1 d 3 d 1 wk 3 wk 6 wk 6 m
C R C R C R C R C R C RM
Fig. 2. Temporal expression of HIF mRNA. The amplified PCR fragments were
visualized on 1.5% agarose gel containing 0.5 mg/ml ethidium bromide. The
GAPDH and HIF genes were amplified in the same reaction. The top band shows
a 1-kb GAPDH fragment and the bottom band shows the HIF gene fragment. C,
control; R, radiation.
Fig. 3. Western blot analysis illustrates the dynamic changes in stabilization of
(a) HIF-1a and (b) HIF-2a proteins over time after irradiation, whereas (c) HIF-3a
remains constant. Western blot bands were visualized and normalized based on
a-tubulin expression. The relative intensities were measured and averaged within
groups and irradiated animals were compared to time-matched controls.
(a) n
po0.01. (b) n
po0.05.
I.L. Jackson et al. / Free Radical Biology and Medicine 53 (2012) 337–346 341
7. study, we aimed to identify genes induced by tissue hypoxia
between the time of irradiation and development of lung injury.
We furthermore sought to determine whether the introduction of
a potent antioxidant, AEOL10150, during the first 4 weeks post-
irradiation could mitigate the expression of those genes 6 weeks
into the course of disease development. This study found dynamic
changes in hypoxia-inducible gene expression in lung tissue
during the 6 months between the time of thoracic irradiation
and the development of pulmonary injury. Furthermore, we
found that hypoxia-inducible gene expression could be modu-
lated by changes in the cellular redox environment resulting in
normalization of 30 of 31 genes upregulated six weeks after
radiation. These findings are consistent with previous studies by
other groups, who have suggested oxidative stress is a potent
inducer of hypoxia-associated genes [19].
It is believed that the first signs of tissue hypoxia can occur
within days after thoracic irradiation because of endothelial cell
swelling leading to capillary occlusion [20]. One of the most
prominent gene families regulated by hypoxia are the hypoxia-
inducible factors (HIFs). HIF proteins are transcriptional com-
plexes composed of a and b subunits that can activate a wide
number of downstream genes involved in cellular response
to stress. The a subunit of the HIF complex is the main hypo-
xia sensor. Under normoxic conditions, the a subunit is rapidly
degraded by the proteasome [21]. However, under hypoxic con-
ditions or oxidative/nitroxidative stress, the a subunit is stabi-
lized and associates with its binding partner, HIF-1b, to form
an activated transcriptional complex [21,22]. Three a subunit
isoforms have recently been identified in mammalian tissues,
HIF-1a, HIF-2a, and HIF-3a, all of which were evaluated in
this study.
HIF-1a and HIF-2a are closely homologous and recognize
hypoxia-responsive elements in the promoter regions of a vast
array of genes, including many of those found to be upregulated
in this study [23–26]. One of the most interesting findings in this
study was the contrast in mRNA expression between HIF-1a and
HIF-2a after radiation. Although no increase in HIF-1a mRNA was
observed in irradiated lung tissue at any of the time points
evaluated, HIF-2a mRNA was strongly increased as early as 24 h
postradiation. However, an increase in protein stabilization of
both HIF-1a and HIF-2a subunits was observed. The stabilization
of the a subunits of both HIF proteins was coupled with a mild
increase in tissue hypoxia measured by CA IX and pimonidazole
staining. These data provide evidence that hypoxia develops in
irradiated mouse lung within the first few days after exposure.
Recent studies using HIF-1a or HIF-2a knockout mice revealed
different characteristics and functions of the two isoforms [27,28].
Unlike HIF-2a knockout mice, which develop multiple-organ
deficiency and biochemical abnormalities [29], HIF-1a knockout
mice mainly show abnormal vascular development and embryo-
nic lethality [30]. Furthermore, distinct transcriptional targets for
HIF-1a and HIF-2a have also been proposed [31]. Thus, the
regulation of HIF exhibits a complex pattern in irradiated lung.
Further clarification of the mechanisms and consequences of HIF
activation in lung postradiation is warranted.
One of the primary mechanisms by which the a subunit of HIF
is stabilized under both normoxic and hypoxic conditions is
through S-nitrosylation of a cysteine residue (Cys533) in the
oxygen-dependent domain [32]. It is thought that oxidative stress
is a more potent stabilizer of HIF than the prolyl hydroxylase
pathway [33]. Chronic oxidative stress is an important feature of
radiation-induced lung injury and can be exacerbated by tissue
hypoxia [1]. Thus, it is not surprising that many of the genes
induced after radiation in this study were those coding for
oxidoreductases such as cytoglobin (Cygb), sorbitol dehydrogen-
ase (Sdh1), procollagen-lysine, 2-oxoglutarate 5-dioxygenase 3
(Plod3), and tyrosine hydrolase (Th). Treatment with AEOL10150
resulted in reduced expression of both Sdh1 and Th (Table 3).
Increased expression of oxidoreductases is consistent with the
known increase in oxidative/nitroxidative stress in the lung after
radiation exposure and attenuation of this increase in oxidative
stress with antioxidant therapy has been shown to mitigate lung
injury [1,11,16,34,35].
The induction of the gene encoding cytoglobin at 1 to 3 day
and again at 6 weeks to 6 months was particularly interesting.
Cytoglobin is an oxygen-binding globin predominantly expressed
in activated fibroblasts under hypoxic conditions [36]. The pri-
mary role of cytoglobin is to maintain the redox status of the cell
during periods of oxidative stress by scavenging hydrogen per-
oxide, nitric oxide, and peroxynitrite [37–39]. Several recent
studies have evaluated cytoglobin as a therapeutic target in
fibrotic disease [38–41]. Xu et al. [39] found that viral-mediated
overexpression of cytoglobin in primary hepatic stellate cells
prevented H2O2-mediated fibroblast differentiation, TGF-b1
expression, and collagen synthesis. Thus, cytoglobin may prove
to be a potential therapeutic target in the lung and warrants
further exploration.
Our prior studies have shown a continuous and persistent
increase in cell death between 24 h and 6 months postradiat-
ion [52]. In this study, increased expression of the gene encoding
Table 3
The increased ratios of gene expression and reversal by AEOL10150
Gene
symbol
Description Increased fold
with radiation
% reversal
with AEOL
Add1a Adducin 1 (a) 10.1 0
Adm Adrenomedulin 11.6 84.1
Agpat2 1-Acylglycerol-3-phosphate
O-acyltransferase 2
10.8 85.2
Agtpbp1 RIKEN cDNA A230056J06 gene 8.6 94.2
Angptl4 Angiopoietin-like 4 8.8 499
Ard1 N-acetyltransferase ARD1
homolog
9 91
Hif-2b Aryl hydrocarbon receptor
nuclear translocator 2
5.7 499
Car12 Carbonic anhydrase 12 1.3 499
Cdc42 Cell division cycle 42 homolog 1.6 499
CTGF Connective tissue growth factor 1.7 499
Dapk3 Death-associated kinase 3 1.6 499
Dctn2 Dynactin 2 2.9 499
Eef1a1 Eukaryotic translation elongation
factor 1 a1
1.2 499
Eno1 Enolase 1, a nonneuron 11.2 76.3
Hif-2a Endothelial PAS domain
protein 1
11.4 80.8
Gna11 Guanine nucleotide binding
protein, a11
8.1 95.2
IL1b Interleukin-1b 1.7 499
Man2a1 Mannosidase 2, aB1 2.8 499
Mmp14 Matrix metalloproteinase 14 1.5 499
Nmyc1 Neuroblastoma myc-related
oncogene 1
1.3 499
Ppara Peroxisome proliferator-
activated receptor a
7.1 499
Ppp2cb Protein phosphatase 2a, catalytic
subunit, b isoform
1.7 499
Prka1 Protein kinase, AMP-activated,
a1 catalytic subunit
3.7 499
Rora RAR-related orphan receptor a 5.1 96.3
Rps7 Ribosomal protein S7 1.9 499
Sdh1 Sorbitol dehydrogenase 1 5.9 95.7
Snrp70 U1 small nuclear
ribonucleoprotein polypeptide A
1.5 499
Sumo2 SMT3 suppressor of mif two
3 homolog 2
1.7 499
TGF-b1 Transforming growth factor, b1 1.4 499
Th Tyrosine hydroxylase 1.6 499
Tuba3 Tubulin, a3 5.5 89.4
I.L. Jackson et al. / Free Radical Biology and Medicine 53 (2012) 337–346 343
8. death-associated protein kinase (Dapk), a protein involved in
programmed cell death, autophagy, and inflammation [43], was
observed 1 and 3 day postradiation and again at 6 weeks and
6 months. Death-inducing signals, such as TGF-b, IFN-g, and Myc,
as well as DNA-damaging agents, can influence Dapk gene
expression and increase Dapk-mediated apoptosis and autophagy
of nutrient-starved cells [43]. Dapk expression was reduced by
more than 99% in animals treated with AEOL10150 after radia-
tion. This observation is consistent with our previous studies,
which demonstrated a significant decrease in cell death 6 weeks
postradiation in animals treated with AEOL10150 [42].
Other interesting genes upregulated after radiation were those
encoding dynactin subunit 2 (Dctn2) and growth-associated
protein-43 (Gap43), both of which are involved in tissue regen-
eration and cell proliferation/differentiation, and genes involved
in cell cycle progression (CdC42) and DNA damage repair (Dr1).
AEOL10150 mitigated expression of both Dctn2 and Cdc42, genes
primarily involved in cytoskeletal reorganization and biogenesis,
by more than 99%.
It is well known that hypoxia can stimulate both resident lung
cells and inflammatory cells, such as macrophages, to secret
proinflammatory cytokines, chemokines, and growth factors
[6,44,45]. Interleukin-1b (IL-1b), a cytokine produced by activated
macrophages, is an important mediator of cell proliferation,
differentiation, and apoptosis as part of the inflammatory
response [46–48]. The gene encoding IL-1b and those encoding
fatty acid-binding protein 4 (Fabp4) and leptin, both of which are
involved in the inflammatory response, were all upregulated at
6 weeks after radiation. TGF-b1 and matrix metalloproteinase-14
(Mmp14), which are involved in collagen deposition and fibro-
genesis, were also upregulated in this time frame. These later
changes are indicative of initiation of late injury disease pro-
cesses. Expression of peroxisome proliferator-activated receptor-
a (Ppara), which plays a role in the anti-inflammatory response
by negatively regulating macrophage foamy cell differentiation
[49], is upregulated at all time points after radiation. Increased
Ppara expression is probably a compensatory response to the
increase in foamy macrophages observed in C57BL/6J mice after
radiation [50]. Expression of IL-1b, TGF-b1, and Ppara was
reduced in irradiated lungs of mice treated with AEOL10150,
suggesting a reduction in overall pulmonary inflammation, which
is consistent with the reduced lung weights and decreased macro-
phage infiltrate seen in rodents treated with AEOL10150 [11].
In conclusion, upregulation of hypoxia-associated genes begins
after radiation and continues at least throughout the first
6 months postexposure. These genes participate in a variety of
physiological and pathological functions, including hypoxia
response, inflammation, oxidative stress, transcriptional regula-
tion, signal transduction, cell metabolism, proliferation and dif-
ferentiation, and apoptosis. Radiation-induced overexpression of
31 hypoxia-related genes was suppressed 6 weeks after radiation
following 4 weeks of postradiation administration of AEOL10150,
a potent catalytic antioxidant. It has been previously demon-
strated that AEOL10150 can attenuate development of late radia-
tion-induced pulmonary injury in rats after a single dose [10] or
fractionated radiation [12]. A relationship between early signaling
changes and late injury would support the initiation of therapeu-
tic interventions in the first few weeks postexposure to protect
Fig. 5. Expression of genes after AEOL10150 treatment. The amplified PCR fragments were visualized on 1.5% agarose gel containing 0.5 mg/ml ethidium bromide. The
GAPDH and target genes were amplified in the same reaction. The top band shows a 1-kb GAPDH fragment and the bottom band shows the targeted gene fragment.
I.L. Jackson et al. / Free Radical Biology and Medicine 53 (2012) 337–346344
9. the lungs from developing acute and chronic lung damage. This
may not be the only therapeutic option, however, as the biphasic
wave of gene expression observed in this study and in previous
studies [51] suggests that there may be a larger window of
opportunity for intervening in the progression of disease pro-
cesses. More important to this study, however, was that the
observed reversal of radiation-induced gene expression after
treatment with AEOL10150 suggests that these genes may be
involved in the cellular response to oxidative stress or the
generation of ROS/RNS. Identifying the roles of these genes in
pulmonary radiation injury could provide insight into the role of
hypoxia-associated genes in radiation lung injury, widen the
temporal window for therapeutic interventions, and introduce
novel therapeutic targets.
Acknowledgments
We thank Ross McGurk and Greta Toncheva for performing
radiation dosimetry, validation, and quality assurance. This study
was supported by National Institutes of Health Grant U19-
AI067798-06 and by AEOLUS Pharmaceuticals. Isabel L. Jackson
is a consultant for AEOLUS Pharmaceuticals, Inc.
References
[1] Fleckenstein, K.; Zgonjanin, L.; Chen, L.; Rabbani, Z.; Jackson, I. L.; Thrasher, B.,
et al. Temporal onset of hypoxia and oxidative stress after pulmonary
irradiation. Int. J. Radiat. Oncol. Biol. Phys. 68:196–204; 2007.
[2] Barcellos-Hoff, M. H.; Dix, T. A. Redox-mediated activation of latent trans-
forming growth factor-b1. Mol. Endocrinol. (Baltimore) 10:1077–1083; 1996.
[3] Cucoranu, I.; Clempus, R.; Dikalova, A.; Phelan, P. J.; Ariyan, S.; Dikalov, S.,
et al. NAD(P)H oxidase 4 mediates transforming growth factor-b1-induced
differentiation of cardiac fibroblasts into myofibroblasts. Circ. Res. 97:
900–907; 2005.
[4] Sturrock, A.; Cahill, B.; Norman, K.; Huecksteadt, T. P.; Hill, K.; Sanders, K.,
et al. Transforming growth factor-b1 induces Nox4 NAD(P)H oxidase and
reactive oxygen species-dependent proliferation in human pulmonary artery
smooth muscle cells. Am. J. Physiol. 290:L661–L673; 2006.
[5] Ward, W. F.; Solliday, N. H.; Molteni, A.; Port, C. D. Radiation injury in rat
lung. II. Angiotensin-converting enzyme activity. Radiat. Res. 96:294–300;
1983.
[6] Bosco, M. C.; Puppo, M.; Blengio, F.; Fraone, T.; Cappello, P.; Giovarelli, M.,
et al. Monocytes and dendritic cells in a hypoxic environment: spotlights on
chemotaxis and migration. Immunobiology 213:733–749; 2008.
[7] Mikkelsen, R. B.; Wardman, P. Biological chemistry of reactive oxygen and
nitrogen and radiation-induced signal transduction mechanisms. Oncogene
22:5734–5754; 2003.
[8] Yakovlev, V. A.; Rabender, C. S.; Sankala, H.; Gauter-Fleckenstein, B.; Fleck-
enstein, K.; Batinic-Haberle, I., et al. Proteomic analysis of radiation-induced
changes in rat lung: modulation by the superoxide dismutase mimetic MnTE-
2-PyP(5þ). Int. J. Radiat. Oncol. Biol. Phys 78:547–554; 2010.
[9] Batinic-Haberle, I.; Spasojevic, I.; Tse, H. M.; Tovmasyan, A.; Rajic St Z.; Clair,
D. K., et al. Design of Mn porphyrins for treating oxidative stress injuries and
their redox-based regulation of cellular transcriptional activities. Amino Acids
42:95–113; 2010.
[10] Rabbani, Z. N.; Batinic-Haberle, I.; Anscher, M. S.; Huang, J.; Day, B. J.;
Alexander, E., et al. Long-term administration of a small molecular weight
catalytic metalloporphyrin antioxidant, AEOL 10150, protects lungs from
radiation-induced injury. Int. J. Radiat. Oncol. Biol. Phys 67:573–580; 2007.
[11] Rabbani, Z. N.; Mi, J.; Zhang, Y.; Delong, M.; Jackson, I. L.; Fleckenstein, K.,
et al. Hypoxia inducible factor 1a signaling in fractionated radiation-induced
lung injury: role of oxidative stress and tissue hypoxia. Radiat. Res. 173:
165–174; 2010.
[12] Rabbani, Z. N.; Salahuddin, F. K.; Yarmolenko, P.; Batinic-Haberle, I.; Thrasher,
B. A.; Gauter-Fleckenstein, B., et al. Low molecular weight catalytic
metalloporphyrin antioxidant AEOL 10150 protects lungs from fractionated
radiation. Free Radic. Res. 41:1273–1282; 2007.
[13] Briere, T. M.; Lii, J.; Prado, K.; Gillin, M. T.; Beddar, A. S. Single-use MOSFET
radiation dosimeters for the quality assurance of megavoltage photon beams.
Phys. Med. Biol. 51:1139–1144; 2006.
[14] Beddar, A. S.; Salehpour, M.; Briere, T. M.; Hamidian, H.; Gillin, M. T.
Preliminary evaluation of implantable MOSFET radiation dosimeters. Phys.
Med. Biol. 50:141–149; 2005.
[15] Jackson, I. L.; Vujaskovic, Z.; Down, J. D. A further comparison of pathologies
after thoracic irradiation among different mouse strains: finding the best
preclinical model for evaluating therapies directed against radiation-induced
lung damage. Radiat. Res. 175:510–518; 2011.
[16] Gauter-Fleckenstein, B.; Fleckenstein, K.; Owzar, K.; Jiang, C.; Reboucas, J. S.;
Batinic-Haberle, I., et al. Early and late administration of MnTE-2-PyP5þ in
mitigation and treatment of radiation-induced lung damage. Free Radic. Biol.
Med. 48:1034–1043; 2010.
[17] Vujaskovic, Z.; Anscher, M. S.; Feng, Q. F.; Rabbani, Z. N.; Amin, K.; Samulski,
T. S., et al. Radiation-induced hypoxia may perpetuate late normal tissue
injury. Int. J. Radiat. Oncol. Biol. Phys. 50:851–855; 2001.
[18] Jackson, I. L.; Chen, L.; Batinic-Haberle, I.; Vujaskovic, Z. Superoxide dis-
mutase mimetic reduces hypoxia-induced O2
nÀ
, TGF-b, and VEGF production
by macrophages. Free Radic. Res. 41:8–14; 2007.
[19] Dewhirst, M. W.; Cao, Y.; Moeller, B. Cycling hypoxia and free radicals
regulate angiogenesis and radiotherapy response. Nat. Rev. 8:425–437;
2008.
[20] Maisin, J. R. The influence of radiation on blood vessels and circulation.
Chap. 3. Ultrastructure of the vessel wall. Curr. Top. Radiat. Res. Q. 10:29–57;
1974.
[21] Huang, L. E.; Gu, J.; Schau, M.; Bunn, H. F. Regulation of hypoxia-inducible
factor 1a is mediated by an O2-dependent degradation domain via the
ubiquitin–proteasome pathway. Proc. Natl. Acad. Sci. USA 95:7987–7992;
1998.
[22] Li, F.; Sonveaux, P.; Rabbani, Z. N.; Liu, S.; Yan, B.; Huang, Q., et al. Regulation
of HIF-1a stability through S-nitrosylation. Mol. Cell 26:63–74; 2007.
[23] Mole, D. R.; Blancher, C.; Copley, R. R.; Pollard, P. J.; Gleadle, J. M.; Ragoussis,
J., et al. Genome-wide association of hypoxia-inducible factor (HIF)-1a and
HIF-2a DNA binding with expression profiling of hypoxia-inducible tran-
scripts. J. Biol. Chem 284:16767–16775; 2009.
[24] Pugh, C. W.; Ratcliffe, P. J. Regulation of angiogenesis by hypoxia: role of the
HIF system. Nat. Med 9:677–684; 2003.
[25] Pugh, C. W.; Ratcliffe, P. J. The von Hippel-Lindau tumor suppressor, hypoxia-
inducible factor-1 (HIF-1) degradation, and cancer pathogenesis. Semin.
Cancer Biol. 13:83–89; 2003.
[26] Tian, H.; McKnight, S. L.; Russell, D. W. Endothelial PAS domain protein 1
(EPAS1), a transcription factor selectively expressed in endothelial cells.
Genes Dev. 11:72–82; 1997.
[27] Rosenberger, C.; Mandriota, S.; Jurgensen, J. S.; Wiesener, M. S.; Horstrup, J.
H.; Frei, U., et al. Expression of hypoxia-inducible factor-1a and -2a in
hypoxic and ischemic rat kidneys. J. Am. Soc. Nephrol 13:1721–1732; 2002.
[28] Holmquist-Mengelbier, L.; Fredlund, E.; Lofstedt, T.; Noguera, R.; Navarro, S.;
Nilsson, H., et al. Recruitment of HIF-1a and HIF-2a to common target genes
is differentially regulated in neuroblastoma: HIF-2a promotes an aggressive
phenotype. Cancer Cell 10:413–423; 2006.
[29] Scortegagna, M.; Ding, K.; Oktay, Y.; Gaur, A.; Thurmond, F.; Yan, L. J., et al.
Multiple organ pathology, metabolic abnormalities and impaired home-
ostasis of reactive oxygen species in Epas1À/À mice. Nat. Genet. 35:
331–340; 2003.
[30] Ryan, H. E.; Lo, J.; Johnson, R. S. HIF-1a is required for solid tumor formation
and embryonic vascularization. EMBO J. 17:3005–3015; 1998.
[31] Raval, R. R.; Lau, K. W.; Tran, M. G.; Sowter, H. M.; Mandriota, S. J.; Li, J. L.,
et al. Contrasting properties of hypoxia-inducible factor 1 (HIF-1) and HIF-2
in von Hippel-Lindau-associated renal cell carcinoma. Mol. Cell. Biol 25:
5675–5686; 2005.
[32] Li, F.; Sonveaux, P.; Rabbani, Z. N.; Liu, S.; Yan, B.; Huang, Q., et al. Regulation
of HIF-1a stability through S-nitrosylation. Mol. Cell 26:63–74; 2007.
[33] Dewhirst, M. W. Relationships between cycling hypoxia, HIF-1, angiogenesis
and oxidative stress. Radiat. Res. 172:653–665; 2009.
[34] Epperly, M. W.; Sikora, C. A.; DeFilippi, S. J.; Gretton, J. E.; Bar-Sagi, D.;
Archer, H., et al. Pulmonary irradiation-induced expression of VCAM-I and
ICAM-I is decreased by manganese superoxide dismutase-plasmid/liposome
(MnSOD-PL) gene therapy. Biol. Blood Marrow Transplant 8:175–187; 2002.
[35] Moulder, J. E.; Cohen, E. P. Future strategies for mitigation and treatment of
chronic radiation-induced normal tissue injury. Semin. Radiat. Oncol.
17:141–148; 2007.
[36] Schmidt, M.; Gerlach, F.; Avivi, A.; Laufs, T.; Wystub, S.; Simpson, J. C., et al.
Cytoglobin is a respiratory protein in connective tissue and neurons, which is
up-regulated by hypoxia. J. Biol. Chem. 279:8063–8069; 2004.
[37] Burmester, T.; Gerlach, F.; Hankeln, T. Regulation and role of neuroglobin and
cytoglobin under hypoxia. Adv. Exp. Med. Biol. 618:169–180; 2007.
[38] Lv, Y.; Wang, Q.; Diao, Y.; Xu, R. Cytoglobin: a novel potential gene medicine
for fibrosis and cancer therapy. Curr. Gene Ther. 8:287–294; 2008.
[39] Xu, R.; Harrison, P. M.; Chen, M.; Li, L.; Tsui, T. Y.; Fung, P. C., et al. Cytoglobin
overexpression protects against damage-induced fibrosis. Mol. Ther. 13:
1093–1100; 2006.
[40] Nakatani, K.; Okuyama, H.; Shimahara, Y.; Saeki, S.; Kim, D. H.; Nakajima, Y.,
et al. Cytoglobin/STAP, its unique localization in splanchnic fibroblast-like
cells and function in organ fibrogenesis. Lab. Invest 84:91–101; 2004.
[41] Mimura, I.; Nangaku, M.; Nishi, H.; Inagi, R.; Tanaka, T.; Cytoglobin, Fujita T. a
novel globin, plays an antifibrotic role in the kidney. Am. J. Physiol. Renal
Physiol 299:F1120–1133; 2010.
[42] Zhang, Y.; Zhang, X.; Rabbani, Z. N.; Jackson, I. L.; Vujaskovic, Z. Oxidative
stress mediates lung injury by inducing apoptosis. Int. J. Radiat. Oncol. Biol.
Phys. 83:740–748; 2012.
[43] Lin, Y.; Hupp, T. R.; Stevens, C. Death-associated protein kinase (DAPK) and
signal transduction: additional roles beyond cell death. FEBS J. 277:48–57;
2010.
[44] Drakopanagiotakis, F.; Xifteri, A.; Polychronopoulos, V.; Bouros, D. Apoptosis
in lung injury and fibrosis. Eur. Respir. J. 32:1631–1638; 2008.
I.L. Jackson et al. / Free Radical Biology and Medicine 53 (2012) 337–346 345
10. [45] Lewis, J. S.; Lee, J. A.; Underwood, J. C.; Harris, A. L.; Lewis, C. E. Macrophage
responses to hypoxia: relevance to disease mechanisms. J. Leukocyte Biol.
66:889–900; 1999.
[46] Hempel, S. L.; Monick, M. M.; Hunninghake, G. W. Effect of hypoxia on release
of IL-1 and TNF by human alveolar macrophages. Am. J. Respir. Cell Mol. Biol
14:170–176; 1996.
[47] Carmi, Y.; Voronov, E.; Dotan, S.; Lahat, N.; Rahat, M. A.; Fogel, M., et al. The
role of macrophage-derived IL-1 in induction and maintenance of angiogen-
esis. J. Immunol 183:4705–4714; 2009.
[48] McCourtie, A. S.; Farivar, A. S.; Woolley, S. M.; Merry, H. E.; Wolf, P. S.;
Mackinnon-Patterson, B., et al. Alveolar macrophage secretory products
affect type 2 pneumocytes undergoing hypoxia–reoxygenation. Ann. Thorac.
Surg 86:1774–1779; 2008.
[49] Devchand, P. R.; Keller, H.; Peters, J. M.; Vazquez, M.; Gonzalez, F. J.; Wahli,
W. The PPARa-leukotriene B4 pathway to inflammation control. Nature
384:39–43; 1996.
[50] Chiang, C. S.; Liu, W. C.; Jung, S. M.; Chen, F. H.; Wu, C. R.; McBride, W. H.,
et al. Compartmental responses after thoracic irradiation of mice: strain
differences. Int. J. Radiat. Oncol. Biol. Phys. 62:862–871; 2005.
[51] Rubin, P.; Johnston, C. J.; Williams, J. P.; McDonald, S.; Finkelstein, J. N. A
perpetual cascade of cytokines postirradiation leads to pulmonary fibrosis.
Int. J. Radiat. Oncol. Biol. Phys. 33:99–109; 1995.
[52] Jackson, I. L., Zhang, X., Hadley, C., Zhang, Y., Rabbani, Z., Xu, P., Vujaskovic, Z.
Hypo-CpG methylation controls PTEN expression and cell apoptosis in
irradiated lung. 14th International Congress of Radiation Research; August
28-September 1, 2011; Warsaw, Poland.
I.L. Jackson et al. / Free Radical Biology and Medicine 53 (2012) 337–346346