Hormesis, cellular stress response and vitagenes as critical determinants in aging and longevity (1050 views)
Molecular Aspects Of Medicine (ISSN: 1872-9452, 0098-2997), 2011 Sep; 32(4-6): 279-304.
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Paper type: Journal Article, Research Support, Non-U. S. Gov'T, Review,
Impact factor: 9.97, 5-year impact factor: 10.272
Url: http://www.scopus.com/inward/record.url?eid=2-s2.0-81855201861&partnerID=40&md5=4e55567d426f64af47e0d23cda940c35
Keywords: Caloric Restriction, Cellular Stress Response, Hormesis, Redox Status, Vitagenes, Acylcarnitine, Anserine, Carnosine, Heat Shock Protein 32, Heme Oxygenase, Homocarnosine, Immunoglobulin Enhancer Binding Protein, Polyphenol Derivative, Protein Bcl 2, Reactive Oxygen Metabolite, Sirtuin, Thioredoxin, Transcription Factor Nrf2, Acetylation, Aging, Alzheimer Disease, Article, Cell Stress, Cell Survival, Chronic Fatigue Syndrome, Deacetylation, Degenerative Disease, Depression, Diabetic Neuropathy, Drug Mechanism, Environmental Factor, Genetic Manipulation, Homeostasis, Human, Human Immunodeficiency Virus Infection, Lifespan, Longevity, Mitochondrion, Morbidity, Multiple Sclerosis, Neurologic Disease, Neuroprotection, Nonhuman, Nutrient, Oxidative Stress, Regulatory Mechanism, Signal Transduction, Animals, Oxidation-Reduction,
Affiliations:
*** IBB - CNR ***
Department of Chemistry, University of Catania, Viale Andrea Doria, 95100 Catania, Italy. calabres@unict.it
Department of Clinical and Experimental Medicine and Pharmacology, School of Medicine, University of Messina, via C. Valeria (Gazzi), 98125 Messina, Italy
Environmental Health Sciences Division, School of Public Health, University of Massachusetts, Amherst, MA, United States
Interuniversity Consortium INBB, Catania, Italy
Institute of Occupational Medicine, School of Medicine, Catholic University of the Sacred Heart, Rome, Italy
IRCCS Centro Neurolesi bonino-pulejo, Via Palermo C.Da Casazza, 98100 Messina, Italy
References:
Not available.
Molecular Aspects Of Medicine (ISSN: 1872-9452, 0098-2997), 2011 Sep; 32(4-6): 279-304.
Export to BibTeX Export to EndNote
Paper type: Journal Article, Research Support, Non-U. S. Gov'T, Review,
Impact factor: 9.97, 5-year impact factor: 10.272
Url: http://www.scopus.com/inward/record.url?eid=2-s2.0-81855201861&partnerID=40&md5=4e55567d426f64af47e0d23cda940c35
Keywords: Caloric Restriction, Cellular Stress Response, Hormesis, Redox Status, Vitagenes, Acylcarnitine, Anserine, Carnosine, Heat Shock Protein 32, Heme Oxygenase, Homocarnosine, Immunoglobulin Enhancer Binding Protein, Polyphenol Derivative, Protein Bcl 2, Reactive Oxygen Metabolite, Sirtuin, Thioredoxin, Transcription Factor Nrf2, Acetylation, Aging, Alzheimer Disease, Article, Cell Stress, Cell Survival, Chronic Fatigue Syndrome, Deacetylation, Degenerative Disease, Depression, Diabetic Neuropathy, Drug Mechanism, Environmental Factor, Genetic Manipulation, Homeostasis, Human, Human Immunodeficiency Virus Infection, Lifespan, Longevity, Mitochondrion, Morbidity, Multiple Sclerosis, Neurologic Disease, Neuroprotection, Nonhuman, Nutrient, Oxidative Stress, Regulatory Mechanism, Signal Transduction, Animals, Oxidation-Reduction,
Affiliations:
*** IBB - CNR ***
Department of Chemistry, University of Catania, Viale Andrea Doria, 95100 Catania, Italy. calabres@unict.it
Department of Clinical and Experimental Medicine and Pharmacology, School of Medicine, University of Messina, via C. Valeria (Gazzi), 98125 Messina, Italy
Environmental Health Sciences Division, School of Public Health, University of Massachusetts, Amherst, MA, United States
Interuniversity Consortium INBB, Catania, Italy
Institute of Occupational Medicine, School of Medicine, Catholic University of the Sacred Heart, Rome, Italy
IRCCS Centro Neurolesi bonino-pulejo, Via Palermo C.Da Casazza, 98100 Messina, Italy
References:
Not available.
Hormesis, cellular stress response and vitagenes as critical determinants in aging and longevity
Understanding mechanisms of aging and determinants of life span will help to reduce age-related morbidity and facilitate healthy aging. Average lifespan has increased over the last centuries, as a consequence of medical and environmental factors, but maximal life span remains unchanged. Extension of maximal life span is currently possible in animal models with measures such as genetic manipulations and caloric restriction (CR). CR appears to prolong life by reducing reactive oxygen species (ROS)-mediated oxidative damage. But ROS formation, which is positively implicated in cellular stress response mechanisms, is a highly regulated process controlled by a complex network of intracellular signaling pathways. By sensing the intracellular nutrient and energy status, the functional state of mitochondria, and the concentration of ROS produced in mitochondria, the longevity network regulates life span across species by co-ordinating information flow along its convergent, divergent and multiply branched signaling pathways, including vitagenes which are genes involved in preserving cellular homeostasis during stressful conditions. Vitagenes encode for heat shock proteins (Hsp) Hsp32, Hsp70, the thioredoxin and the sirtuin protein systems. Dietary antioxidants, such as carnosine, carnitines or polyphenols, have recently been demonstrated to be neuroprotective through the activation of hormetic pathways, including vitagenes. The hormetic dose-response, challenges long-standing beliefs about the nature of the dose-response in a lowdose zone, having the potential to affect significantly the design of pre-clinical studies and clinical trials as well as strategies for optimal patient dosing in the treatment of numerous diseases. Given the broad cytoprotective properties of the heat shock response there is now strong interest in discovering and developing pharmacological agents capable of inducing stress responses. In this review we discuss the most current and up to date understanding of the possible signaling mechanisms by which caloric restriction, as well hormetic caloric restriction-mimetics compounds by activating vitagenes can enhance defensive systems involved in bioenergetic and stress resistance homeostasis with consequent impact on longevity processes. Copyright 2011 Elsevier Ltd. All rights reserved.
Understanding mechanisms of aging and determinants of life span will help to reduce age-related morbidity and facilitate healthy aging. Average lifespan has increased over the last centuries, as a consequence of medical and environmental factors, but maximal life span remains unchanged. Extension of maximal life span is currently possible in animal models with measures such as genetic manipulations and caloric restriction (CR). CR appears to prolong life by reducing reactive oxygen species (ROS)-mediated oxidative damage. But ROS formation, which is positively implicated in cellular stress response mechanisms, is a highly regulated process controlled by a complex network of intracellular signaling pathways. By sensing the intracellular nutrient and energy status, the functional state of mitochondria, and the concentration of ROS produced in mitochondria, the longevity network regulates life span across species by co-ordinating information flow along its convergent, divergent and multiply branched signaling pathways, including vitagenes which are genes involved in preserving cellular homeostasis during stressful conditions. Vitagenes encode for heat shock proteins (Hsp) Hsp32, Hsp70, the thioredoxin and the sirtuin protein systems. Dietary antioxidants, such as carnosine, carnitines or polyphenols, have recently been demonstrated to be neuroprotective through the activation of hormetic pathways, including vitagenes. The hormetic dose-response, challenges long-standing beliefs about the nature of the dose-response in a lowdose zone, having the potential to affect significantly the design of pre-clinical studies and clinical trials as well as strategies for optimal patient dosing in the treatment of numerous diseases. Given the broad cytoprotective properties of the heat shock response there is now strong interest in discovering and developing pharmacological agents capable of inducing stress responses. In this review we discuss the most current and up to date understanding of the possible signaling mechanisms by which caloric restriction, as well hormetic caloric restriction-mimetics compounds by activating vitagenes can enhance defensive systems involved in bioenergetic and stress resistance homeostasis with consequent impact on longevity processes. Copyright 2011 Elsevier Ltd. All rights reserved.
Hormesis, cellular stress response and vitagenes as critical determinants in aging and longevity
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Hormesis, cellular stress response and vitagenes as critical determinants in aging and longevity
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* RedOx status, proteasome and APEH: Insights into anticancer mechanisms of t10, c12-conjugated linoleic acid isomer on A375 melanoma cells (748 views)
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Impact Factor: 2.26
View Export to BibTeX Export to EndNote
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Impact Factor: 2.187
View Export to BibTeX Export to EndNote
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Impact Factor: 0.913
View Export to BibTeX Export to EndNote
8 Records (7 excluding Abstracts).
Total impact factor: 30.397 (26.863 excluding Abstracts).
Total 5 year impact factor: 28.838 (24.823 excluding Abstracts).
Total impact factor: 30.397 (26.863 excluding Abstracts).
Total 5 year impact factor: 28.838 (24.823 excluding Abstracts).
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