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Cell stem cell, ISSN 1934-5909, 2012, Volume 11, Issue 3, pp. 401 - 414
.... This protective effect of rapamycin is mediated by the increase in expression... 
MAMMALIAN TARGET | CANCER PATIENTS | RAPAMYCIN | HEAD | AGING PHENOTYPES | MANGANESE SUPEROXIDE-DISMUTASE | STRESS-RESPONSE | TUMOR | NECK | SKIN | CELL & TISSUE ENGINEERING | CELL BIOLOGY | Cell Death - radiation effects | TOR Serine-Threonine Kinases - metabolism | Keratinocytes - radiation effects | Carcinoma, Squamous Cell - pathology | Epithelial Cells - drug effects | Humans | Cellular Senescence - drug effects | Cell Compartmentation - radiation effects | Mucositis - prevention & control | Mouth Mucosa - drug effects | TOR Serine-Threonine Kinases - antagonists & inhibitors | Mouth Mucosa - radiation effects | Mucositis - pathology | Stem Cells - enzymology | Mucositis - enzymology | Cellular Senescence - radiation effects | Cytoprotection - drug effects | Clone Cells | Oxidative Stress - radiation effects | Cell Death - drug effects | Head and Neck Neoplasms - enzymology | Mouth Mucosa - pathology | Keratinocytes - enzymology | Superoxide Dismutase - metabolism | Radiation, Ionizing | Carcinoma, Squamous Cell - enzymology | Epithelial Cells - radiation effects | Cells, Cultured | Stem Cells - radiation effects | Epithelial Cells - pathology | Radiation Injuries - enzymology | Sirolimus - pharmacology | Head and Neck Neoplasms - pathology | Keratinocytes - pathology | Animals | Keratinocytes - drug effects | Radiation Injuries - prevention & control | Epithelial Cells - enzymology | Cell Compartmentation - drug effects | Stem Cells - drug effects | Stem Cells - pathology | Radiation Injuries - pathology | Cell Proliferation - drug effects | Mice | Oxidative Stress - drug effects | Cytoprotection - radiation effects | Cell Proliferation - radiation effects
Journal Article
PloS one, ISSN 1932-6203, 11/2012, Volume 7, Issue 11, p. e50778
.... Moreover, the effect on mitochondrial function upon lycopene exposure was assessed. Methods and Findings... 
ISCHEMIA-REPERFUSION INJURY | INFARCT SIZE | OXYGEN | INDUCED ACTIVATION | PATHWAY | MULTIDISCIPLINARY SCIENCES | DISEASE | CAROTENOIDS | ANEMIC RATS | AMERICAN-HEART-ASSOCIATION | CELL-DEATH | Animals, Newborn | Cell Survival - drug effects | Cell Hypoxia - drug effects | Mitochondrial Membrane Transport Proteins - chemistry | Mitochondrial Membrane Transport Proteins - metabolism | Myocytes, Cardiac - cytology | Apoptosis - drug effects | Mice, Inbred C57BL | Protein Conformation - drug effects | Mitochondria - metabolism | Mitochondria - drug effects | Carotenoids - pharmacology | Lycopene | Oxygen - metabolism | Animals | Myocytes, Cardiac - drug effects | Signal Transduction - drug effects | Cytoprotection - drug effects | Myocytes, Cardiac - metabolism | Mice | Oxidative Stress - drug effects | Cytochrome c | Infants (Newborn) | Antioxidants | Analysis | Heart cells | Permeability | Apoptosis | Cytochrome | Neonates | Reactive oxygen species | Heart attacks | Mitochondrial permeability transition pore | Membrane permeability | Cardiovascular disease | Activation | Caspase-3 | Neurotoxicity | Mitochondria | Reperfusion | Carotenoids | Ischemia | Rodents | Penicillin | Occupational health | Membrane potential | Pretreatment | Cardiology | Cardiovascular system | Oxygen | Caspase | Cardiomyocytes | Pharmacology | Malondialdehyde | Hypotheses | Hospitals | Hypoxia | MPTP | Laboratory animals | Cytoplasm
Journal Article
Biomaterials, ISSN 0142-9612, 2016, Volume 84, pp. 25 - 41
Abstract Curcumin (Cur) has been demonstrated to have wide pharmacological window including anti-oxidant and anti-inflammatory properties. However,... 
Advanced Basic Science | Dentistry | Photodegradation | Phototoxicity | Curcumin | Apoptosis/necrosis | Photoprotection | Nanoformulation | ACTIVATION | MATERIALS SCIENCE, BIOMATERIALS | MECHANISM | INDUCED APOPTOSIS | ENGINEERING, BIOMEDICAL | DNA-DAMAGE | MITOCHONDRIA | KERATINOCYTES | DEATH | BCL-2 | SUNLIGHT | BAX | DNA Breaks - drug effects | NIH 3T3 Cells | Reactive Oxygen Species - metabolism | Nanoparticles - chemistry | Apoptosis - drug effects | Apoptosis - radiation effects | Keratinocytes - radiation effects | Membrane Potential, Mitochondrial - radiation effects | Humans | Extracellular Signal-Regulated MAP Kinases - metabolism | Membrane Potential, Mitochondrial - drug effects | RNA, Messenger - metabolism | DNA Breaks - radiation effects | Photosensitizing Agents - pharmacology | Ultraviolet Rays | Protective Agents - pharmacology | Cytoprotection - drug effects | Oxidative Stress - radiation effects | Signal Transduction - radiation effects | Proto-Oncogene Proteins c-akt - metabolism | Keratinocytes - enzymology | Keratinocytes - ultrastructure | Cell Membrane - drug effects | Cell Membrane - radiation effects | Cell Line | Cell Survival - drug effects | Lactic Acid - chemistry | RNA, Messenger - genetics | Curcumin - pharmacology | Absorption, Radiation | Cell Survival - radiation effects | Animals | Cell Cycle Checkpoints - radiation effects | Keratinocytes - drug effects | Signal Transduction - drug effects | Cell Cycle Checkpoints - drug effects | Polyglycolic Acid - chemistry | Drug Liberation | Mice | Molecular Docking Simulation | Oxidative Stress - drug effects | Cytoprotection - radiation effects | Nanoparticles | Genetic research | Analysis | Index Medicus | Biotechnology | Phosphorylation | Cascades | Sunlight | Exposure | Biological | Apoptosis
Journal Article
Gastroenterology (New York, N.Y. 1943), ISSN 0016-5085, 2014, Volume 146, Issue 7, pp. 1763 - 1774
Background & Aims The NACHT, LRR, and pyrin domain–containing protein 3 (NLRP3) inflammasome induces inflammation in response to organ injury, but little is... 
Gastroenterology and Hepatology | Innate Immune Response | Immune Regulation | Pancreas | Mouse Model | ACTIVATION | NLRP3 INFLAMMASOME | GPR81 | AGONISTS | GENE | TLR9 | MICE | HEPATOTOXICITY | GASTROENTEROLOGY & HEPATOLOGY | EXPRESSION | SEVERITY | Liver - pathology | Inflammasomes - metabolism | Receptors, G-Protein-Coupled - metabolism | NLR Family, Pyrin Domain-Containing 3 Protein | Humans | Male | NF-kappa B - metabolism | Monocytes - immunology | Lipopolysaccharides | Liver - immunology | Liver - drug effects | RNA Interference | Interleukin-1beta - metabolism | Toll-Like Receptors - drug effects | Anti-Inflammatory Agents - administration & dosage | Toll-Like Receptors - metabolism | Cytoprotection | Disease Models, Animal | Galactosamine | Chemical and Drug Induced Liver Injury - prevention & control | Anti-Inflammatory Agents - pharmacology | Down-Regulation | Liver - metabolism | Injections, Intraperitoneal | Pancreas - pathology | Pancreas - metabolism | Pancreas - immunology | Toll-Like Receptor 4 - metabolism | Chemical and Drug Induced Liver Injury - immunology | Monocytes - drug effects | Macrophages - metabolism | Signal Transduction - drug effects | Chemical and Drug Induced Liver Injury - metabolism | Sodium Lactate - pharmacology | beta-Arrestins | Mice | Receptors, G-Protein-Coupled - genetics | RNA, Small Interfering - metabolism | Monocytes - metabolism | Pancreatitis - prevention & control | Arrestins - metabolism | Dose-Response Relationship, Drug | Pancreatitis - genetics | Transfection | Inflammasomes - drug effects | Sodium Lactate - administration & dosage | Pancreatitis - immunology | Chemical and Drug Induced Liver Injury - pathology | Chemical and Drug Induced Liver Injury - etiology | Macrophages - immunology | Cell Line | Immunity, Innate - drug effects | Toll-Like Receptor 4 - drug effects | Mice, Inbred C57BL | Pancreas - drug effects | Chemical and Drug Induced Liver Injury - genetics | Pancreatitis - chemically induced | Animals | Carrier Proteins - metabolism | beta-Arrestin 2 | Inflammasomes - immunology | Macrophages - drug effects | Pancreatitis - pathology | Pancreatitis - metabolism | Ceruletide | Lactates | Gastrointestinal diseases | Inflammation
Journal Article
Autophagy, ISSN 1554-8627, 05/2012, Volume 8, Issue 5, pp. 812 - 825
.... Furthermore, our results revealed that curcumin causes some novel cellular mechanisms that promote autophagy as a protective effect... 
autophagy | endothelial cell | FOXO1 | oxidative stress | curcumin | Binding | Proteins | Landes | Calcium | Bioscience | Biology | Cell | Cycle | Cancer | Organogenesis | Oxidative stress | Endothelial cell | Curcumin | Autophagy | TOR Serine-Threonine Kinases - metabolism | Apoptosis - drug effects | Humans | Phosphatidylinositol 3-Kinases - metabolism | Protein Transport - drug effects | Autophagy - drug effects | Gene Knockdown Techniques | Proto-Oncogene Proteins c-bcl-2 - metabolism | Cell Nucleus - metabolism | Forkhead Transcription Factors - metabolism | Protective Agents - pharmacology | Protein Binding - drug effects | Cytoprotection - drug effects | Membrane Proteins - metabolism | Proto-Oncogene Proteins c-akt - metabolism | Beclin-1 | Hydrogen Peroxide - toxicity | rab GTP-Binding Proteins - metabolism | Cell Survival - drug effects | Human Umbilical Vein Endothelial Cells - drug effects | Curcumin - pharmacology | Down-Regulation - drug effects | Ubiquitin-Activating Enzymes - metabolism | Apoptosis Regulatory Proteins - metabolism | Up-Regulation - drug effects | Acetylation - drug effects | Autophagy-Related Protein 7 | Human Umbilical Vein Endothelial Cells - enzymology | Signal Transduction - drug effects | Models, Biological | Human Umbilical Vein Endothelial Cells - pathology | Forkhead Box Protein O1 | Oxidative Stress - drug effects | Cell Nucleus - drug effects | CELL BIOLOGY
Journal Article
Journal
Cell stem cell, ISSN 1934-5909, 2016, Volume 19, Issue 1, pp. 23 - 37
Journal Article
PloS one, ISSN 1932-6203, 2012, Volume 7, Issue 4, p. e34200
Nimesulide, an anti-inflammatory and analgesic drug, is reported to cause severe hepatotoxicity... 
DRUG | IN-VITRO | LIVER | BIOLOGY | MICE | EXPRESSION | DAMAGE | PERMEABILITY TRANSITION | PROTECTS | Transcription, Genetic - drug effects | Caspase 9 - metabolism | Electron Transport - drug effects | Antioxidants - metabolism | Caspase 3 - metabolism | Oxidants - metabolism | Male | Biological Products - pharmacology | Membrane Potential, Mitochondrial - drug effects | Terpenes - pharmacology | Proteolysis - drug effects | Liver - drug effects | Cytoprotection - drug effects | Cell Death - drug effects | Homeostasis - drug effects | Permeability - drug effects | Rats | Mitochondria - metabolism | Apoptosis Regulatory Proteins - secretion | Mitochondria - drug effects | Mitochondria - pathology | Nucleotides - metabolism | Rats, Sprague-Dawley | Animals | Mitochondria - secretion | Lipid Metabolism - drug effects | Sulfonamides - toxicity | Liver - cytology | DNA Damage | Oxidative Stress - drug effects | Cytochrome c | Antioxidants | Oxidative stress | Enzymes | RNA | DNA damage | Superoxide | Permeability | Bilirubin | Terpenes | Histochemistry | Apoptosis | Cytochrome | DNA-formamidopyrimidine glycosylase | Downstream effects | Biochemistry | Males | Damage prevention | Caspase-3 | Proteins | Hepatitis | Toxicology | Mitochondria | Histopathology | Camphene | Biocompatibility | Copper | Hepatotoxicity | Drug dosages | Deoxyribonucleic acid--DNA | Free radicals | Liver diseases | Macromolecules | Apoptosis-inducing factor | Gene expression | Molecular modelling | Caspase-9 | Biomarkers | Clinical medicine | Laboratories | Toxicity | Membrane permeability | Homeostasis | Biology | Arthritis | DNA glycosylase | Depolarization | Oxidation resistance | Rodents | Pretreatment | Nonsteroidal anti-inflammatory drugs | Caspase | Inflammation | Zinc | Medicine | NAD | Endonuclease | Manganese | Deoxyribonucleic acid | DNA
Journal Article
PloS one, ISSN 1932-6203, 08/2016, Volume 11, Issue 8, pp. e0159998 - e0159998
...) scavenger or alleviate the acute toxic metal overload in vivo. In this study, we investigated the inhibitory effect of Tiron on matrix metalloproteinase (MMP... 
IRRADIATION | OXIDATIVE STRESS | HUMAN SKIN | MULTIDISCIPLINARY SCIENCES | GENE-EXPRESSION | MECHANISMS | SODIUM 4,5-DIHYDROXYBENZENE-1,3-DISULFONATE | INDUCTION | C-JUN | NF-KAPPA-B | PROTEIN-KINASES | Promoter Regions, Genetic - radiation effects | Binding Sites - radiation effects | Humans | Transcriptional Activation - drug effects | Skin Aging - radiation effects | 1,2-Dihydroxybenzene-3,5-Disulfonic Acid Disodium Salt - pharmacology | Promoter Regions, Genetic - drug effects | Transcription Factor AP-1 - metabolism | Dermis - drug effects | Cytoprotection - drug effects | Signal Transduction - radiation effects | Dermis - cytology | Matrix Metalloproteinase 1 - genetics | Fibroblasts - metabolism | MAP Kinase Signaling System - radiation effects | Dermis - metabolism | Skin Aging - drug effects | Transcriptional Activation - radiation effects | Cells, Cultured | Dermis - radiation effects | Matrix Metalloproteinase 3 - metabolism | Antioxidants - pharmacology | Ultraviolet Rays - adverse effects | MAP Kinase Signaling System - drug effects | Fibroblasts - radiation effects | Signal Transduction - drug effects | Fibroblasts - drug effects | Transcription Factor AP-1 - radiation effects | Cytoprotection - genetics | Matrix Metalloproteinase 1 - metabolism | Cytoprotection - radiation effects | Matrix Metalloproteinase 3 - genetics | Genetic aspects | Skin | Genetic transcription | RNA | Analysis | Enzyme-linked immunosorbent assay | Oxidative stress | Reactive oxygen species | Transcription factors | Senescence | Oncology | Activation | Matrix metalloproteinase | Kinases | Proteins | Antioxidants | Signal transduction | Consent | Transcription activation | Fibroblasts | Aging | Biocompatibility | Metalloproteinase | Interstitial collagenase | Stromelysin 1 | Oxygen | Wound healing | U.V. radiation | Activator protein 1 | MAP kinase | Gene expression | Medicine | Signaling | Collagen | In vivo methods and tests | Mutation | Binding sites | Apoptosis | Index Medicus
Journal Article
Circulation (New York, N.Y.), ISSN 0009-7322, 12/2002, Volume 106, Issue 23, pp. 2973 - 2979
Background-Erythropoietin (EPO) is a critical regulator for the proliferation of immature erythroid precursors, but its role as a potential cytoprotectant in... 
Cytochrome c | Proteins, mitochondrial | Proteins, proto-oncogene | Cysteine endopeptidases | Apoptosis | CARDIAC & CARDIOVASCULAR SYSTEMS | IN-VIVO EVIDENCE | INJURY | apoptosis | PROGRAMMED CELL-DEATH | proteins, proto-oncogene | cysteine endopeptidases | ENDOTHELIAL-CELLS | NEURONS | PERIPHERAL VASCULAR DISEASE | cytochrome c | HEMATOLOGY | proteins, mitochondrial | BRAIN | ERYTHROID PROGENITORS | Endothelium, Vascular - cytology | Erythropoietin - pharmacology | Mitochondria - enzymology | Cell Hypoxia - physiology | Microcirculation - metabolism | Intracellular Membranes - physiology | Apoptosis - drug effects | Endothelium, Vascular - drug effects | Cytoprotection - physiology | Cysteine Endopeptidases - drug effects | Microcirculation - drug effects | Brain - blood supply | Cysteine Endopeptidases - metabolism | Cytoprotection - drug effects | Cell Membrane - metabolism | Proto-Oncogene Proteins | DNA Fragmentation - drug effects | Mitochondria - chemistry | Cell Membrane - drug effects | Protein-Serine-Threonine Kinases - metabolism | Membrane Potentials - drug effects | Cell Survival - drug effects | Phosphatidylserines - metabolism | Cells, Cultured | Enzyme Inhibitors - pharmacology | Rats | Mitochondria - drug effects | Enzyme Activation - drug effects | Rats, Sprague-Dawley | Antibodies - pharmacology | Proto-Oncogene Proteins c-akt | Microcirculation - cytology | Animals | Signal Transduction - drug effects | Endothelium, Vascular - metabolism | Erythropoietin - antagonists & inhibitors | Intracellular Membranes - drug effects
Journal Article
The Journal of pharmacology and experimental therapeutics, ISSN 0022-3565, 07/2012, Volume 342, Issue 1, pp. 81 - 90
...) is a natural phytoalexin that exhibits multiple therapeutic potentials, including antioxidative and anti-inflammatory effects in animals. Paraquat (PQ... 
TRANSCRIPTION FACTOR NRF2 | CARCINOGENESIS | PROTECTION | PHENOLIC ANTIOXIDANTS | INDUCED LUNG INJURY | RATS | PHARMACOLOGY & PHARMACY | EXPRESSION | PULMONARY-FIBROSIS | MICE LACKING | MOLECULAR-MECHANISMS | Tumor Necrosis Factor-alpha - metabolism | NF-E2-Related Factor 2 - antagonists & inhibitors | Epithelial Cells - metabolism | Reactive Oxygen Species - metabolism | Apoptosis - drug effects | Antioxidants - metabolism | Epithelial Cells - drug effects | Humans | Transforming Growth Factor beta1 - metabolism | Tumor Necrosis Factor-alpha - genetics | Apoptosis - genetics | Stilbenes - pharmacology | Paraquat - antagonists & inhibitors | Myofibroblasts - metabolism | Inflammation - metabolism | Cell Death - genetics | Mitochondria - genetics | Inflammation - drug therapy | Cytoprotection - drug effects | NF-E2-Related Factor 2 - genetics | Response Elements - genetics | Cell Death - drug effects | Paraquat - pharmacology | Interleukin-6 - metabolism | Fibroblasts - metabolism | Interleukin-6 - genetics | Cells, Cultured | Oxidative Stress - genetics | Mitochondria - metabolism | Signal Transduction - genetics | Transforming Growth Factor beta1 - genetics | Mitochondria - drug effects | Myofibroblasts - drug effects | Mice, Knockout | Response Elements - drug effects | Animals | Signal Transduction - drug effects | Fibroblasts - drug effects | NF-E2-Related Factor 2 - metabolism | Cytoprotection - genetics | Mice | Oxidative Stress - drug effects | Index Medicus
Journal Article
PloS one, ISSN 1932-6203, 2011, Volume 6, Issue 3, p. e17328
Repairing trauma to the central nervous system by replacement of glial support cells is an increasingly attractive therapeutic strategy. We have focused on the... 
GLIAL-RESTRICTED PRECURSORS | GAP-JUNCTIONS | GLUTAMATE TRANSPORTERS | OLIGODENDROCYTE PROGENITORS | MULTIDISCIPLINARY SCIENCES | EMBRYONIC STEM-CELLS | LOCOMOTOR RECOVERY | AXONAL REGENERATION | REACTIVE ASTROCYTES | CENTRAL-NERVOUS-SYSTEM | ADULT-RAT-BRAIN | Neurons - pathology | Recovery of Function - drug effects | Humans | Motor Activity - drug effects | Stem Cells - cytology | Glial Fibrillary Acidic Protein - metabolism | Neuroglia - drug effects | Neuroglia - cytology | Cytoprotection - drug effects | Recovery of Function - physiology | Female | Astrocytes - transplantation | Neurons - drug effects | Spinal Cord Injuries - therapy | Bone Morphogenetic Proteins - pharmacology | Ciliary Neurotrophic Factor - pharmacology | Astrocytes - cytology | Astrocytes - drug effects | Cell Survival - drug effects | Rats | Rats, Sprague-Dawley | Cell Shape - drug effects | Cell Movement - drug effects | Animals | Cell Differentiation - drug effects | Stem Cells - drug effects | Spinal Cord Injuries - physiopathology | Graft Survival - drug effects | Ciliary neurotrophic factor | Bone morphogenetic proteins | Spinal cord injuries | Spinal cord | Transcription factors | Transplants & implants | Central nervous system | Conservation | Recovery of function | Homeostasis | Nervous system | Transplantation | Neurosurgery | Spinal cord injury | Recovery | Proteins | Pain | Rodents | Injuries | Cell survival | Neurons | Astrocytes | Fetuses | Maintenance | Laminates | Gene expression | Survival | Trauma | Feet | Medicine | Regeneration | Adenoviruses | Morphology | Stem cells | Differentiation | Apoptosis | Osteoprogenitor cells | Axonogenesis | Therapeutic applications | Embryos | Glial stem cells | Neuronal-glial interactions | Foot | Neural stem cells
Journal Article