Oxidative stress and ageing: is ageing a cysteine deficiency syndrome?
Reactive oxygen species (ROS) are constantly produced in biological tissues and play a role in various signalling pathways. Abnormally high ROS concentrations cause oxidative stress associated with tissue damage and dysregulation of physiological signals. There is growing evidence that oxidative str...
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Veröffentlicht in: | Philosophical transactions of the Royal Society of London. Series B. Biological sciences 2005-12, Vol.360 (1464), p.2355-2372 |
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description | Reactive oxygen species (ROS) are constantly produced in biological tissues and play a role in various signalling pathways. Abnormally high ROS concentrations cause oxidative stress associated with tissue damage and dysregulation of physiological signals. There is growing evidence that oxidative stress increases with age. It has also been shown that the life span of worms, flies and mice can be significantly increased by mutations which impede the insulin receptor signalling cascade. Molecular studies revealed that the insulin-independent basal activity of the insulin receptor is increased by ROS and downregulated by certain antioxidants. Complementary clinical studies confirmed that supplementation of the glutathione precursor cysteine decreases insulin responsiveness in the fasted state. In several clinical trials, cysteine supplementation improved skeletal muscle functions, decreased the body fat/lean body mass ratio, decreased plasma levels of the inflammatory cytokine tumour necrosis factor α (TNF-α), improved immune functions, and increased plasma albumin levels. As all these parameters degenerate with age, these findings suggest: (i) that loss of youth, health and quality of life may be partly explained by a deficit in cysteine and (ii) that the dietary consumption of cysteine is generally suboptimal and everybody is likely to have a cysteine deficiency sooner or later. |
doi_str_mv | 10.1098/rstb.2005.1770 |
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Abnormally high ROS concentrations cause oxidative stress associated with tissue damage and dysregulation of physiological signals. There is growing evidence that oxidative stress increases with age. It has also been shown that the life span of worms, flies and mice can be significantly increased by mutations which impede the insulin receptor signalling cascade. Molecular studies revealed that the insulin-independent basal activity of the insulin receptor is increased by ROS and downregulated by certain antioxidants. Complementary clinical studies confirmed that supplementation of the glutathione precursor cysteine decreases insulin responsiveness in the fasted state. In several clinical trials, cysteine supplementation improved skeletal muscle functions, decreased the body fat/lean body mass ratio, decreased plasma levels of the inflammatory cytokine tumour necrosis factor α (TNF-α), improved immune functions, and increased plasma albumin levels. As all these parameters degenerate with age, these findings suggest: (i) that loss of youth, health and quality of life may be partly explained by a deficit in cysteine and (ii) that the dietary consumption of cysteine is generally suboptimal and everybody is likely to have a cysteine deficiency sooner or later.</description><identifier>ISSN: 0962-8436</identifier><identifier>EISSN: 1471-2970</identifier><identifier>DOI: 10.1098/rstb.2005.1770</identifier><identifier>PMID: 16321806</identifier><language>eng</language><publisher>London: The Royal Society</publisher><subject>Aging - physiology ; Blood plasma ; Body Composition - drug effects ; Cysteine ; Cysteine - chemistry ; Cysteine - deficiency ; Cysteine - metabolism ; Cysteine - pharmacology ; cysteine in vivo ; Dietary Supplements ; Glutathione - blood ; Glutathione - metabolism ; Humans ; Hydrogen ; Immune Functions ; Immunity, Cellular - drug effects ; Inflammatory Cytokines ; Insulin ; Insulin Signalling ; Muscle Functions ; Muscle, Skeletal - drug effects ; Natural killer cells ; Oxidative stress ; Oxidative Stress - physiology ; Peroxides ; Protein Tyrosine Phosphatases - antagonists & inhibitors ; Protein Tyrosine Phosphatases - metabolism ; Reactive oxygen species ; Reactive Oxygen Species - metabolism ; Receptor, Insulin - antagonists & inhibitors ; Receptor, Insulin - metabolism ; Receptors ; Redox Status ; Serum Albumin ; Signal Transduction - physiology ; T lymphocytes ; Transcription factors ; Tumor Necrosis Factor-alpha - metabolism</subject><ispartof>Philosophical transactions of the Royal Society of London. Series B. Biological sciences, 2005-12, Vol.360 (1464), p.2355-2372</ispartof><rights>Copyright 2005 The Royal Society</rights><rights>2005 The Royal Society</rights><rights>2005 The Royal Society 2005</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c591t-41a63ab45bc6ca4599463897f366f395e3da118f419330fffb4d0c5989674573</citedby><cites>FETCH-LOGICAL-c591t-41a63ab45bc6ca4599463897f366f395e3da118f419330fffb4d0c5989674573</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/30041426$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/30041426$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>230,314,723,776,780,799,881,27901,27902,53766,53768,57992,58225</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16321806$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wulf Dröge</creatorcontrib><title>Oxidative stress and ageing: is ageing a cysteine deficiency syndrome?</title><title>Philosophical transactions of the Royal Society of London. Series B. Biological sciences</title><addtitle>Philos Trans R Soc Lond B Biol Sci</addtitle><description>Reactive oxygen species (ROS) are constantly produced in biological tissues and play a role in various signalling pathways. Abnormally high ROS concentrations cause oxidative stress associated with tissue damage and dysregulation of physiological signals. There is growing evidence that oxidative stress increases with age. It has also been shown that the life span of worms, flies and mice can be significantly increased by mutations which impede the insulin receptor signalling cascade. Molecular studies revealed that the insulin-independent basal activity of the insulin receptor is increased by ROS and downregulated by certain antioxidants. Complementary clinical studies confirmed that supplementation of the glutathione precursor cysteine decreases insulin responsiveness in the fasted state. In several clinical trials, cysteine supplementation improved skeletal muscle functions, decreased the body fat/lean body mass ratio, decreased plasma levels of the inflammatory cytokine tumour necrosis factor α (TNF-α), improved immune functions, and increased plasma albumin levels. As all these parameters degenerate with age, these findings suggest: (i) that loss of youth, health and quality of life may be partly explained by a deficit in cysteine and (ii) that the dietary consumption of cysteine is generally suboptimal and everybody is likely to have a cysteine deficiency sooner or later.</description><subject>Aging - physiology</subject><subject>Blood plasma</subject><subject>Body Composition - drug effects</subject><subject>Cysteine</subject><subject>Cysteine - chemistry</subject><subject>Cysteine - deficiency</subject><subject>Cysteine - metabolism</subject><subject>Cysteine - pharmacology</subject><subject>cysteine in vivo</subject><subject>Dietary Supplements</subject><subject>Glutathione - blood</subject><subject>Glutathione - metabolism</subject><subject>Humans</subject><subject>Hydrogen</subject><subject>Immune Functions</subject><subject>Immunity, Cellular - drug effects</subject><subject>Inflammatory Cytokines</subject><subject>Insulin</subject><subject>Insulin Signalling</subject><subject>Muscle Functions</subject><subject>Muscle, Skeletal - drug effects</subject><subject>Natural killer cells</subject><subject>Oxidative stress</subject><subject>Oxidative Stress - physiology</subject><subject>Peroxides</subject><subject>Protein Tyrosine Phosphatases - antagonists & inhibitors</subject><subject>Protein Tyrosine Phosphatases - metabolism</subject><subject>Reactive oxygen species</subject><subject>Reactive Oxygen Species - metabolism</subject><subject>Receptor, Insulin - antagonists & inhibitors</subject><subject>Receptor, Insulin - metabolism</subject><subject>Receptors</subject><subject>Redox Status</subject><subject>Serum Albumin</subject><subject>Signal Transduction - physiology</subject><subject>T lymphocytes</subject><subject>Transcription factors</subject><subject>Tumor Necrosis Factor-alpha - metabolism</subject><issn>0962-8436</issn><issn>1471-2970</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kU2P0zAQhi0EYsvClRsoJ24pdvzNAdhdKCCtWIEqrpab2K1LGhfbWTb_HodUhR7gZFvzzjOjxwA8RXCOoBQvQ0yreQUhnSPO4T0wQ4SjspIc3gczKFlVCoLZGXgU4xZCKCknD8EZYrhCArIZWNzcuUYnd2uKmIKJsdBdU-i1cd36VeHi4Vrooh5iyldTNMa62pmuHoo4dE3wO_PmMXhgdRvNk8N5DpaL98urj-X1zYdPVxfXZU0lSiVBmmG9InRVs1oTKiVhWEhuMWMWS2pwoxESliCJMbTWrkgDc6uQjBPK8Tl4PWH3_Wpnmtp0KehW7YPb6TAor506rXRuo9b-ViHKJBUiA14cAMH_6E1MaudibdpWd8b3UTEhKKR8DM6nYB18jMHY4xAE1WhejebVaF6N5nPD879X-xM_qM4BPAWCH7IinxWmQW19H7r8_Df22dS1jcmHIxVDSBCpRmo51V3-nbtjXYfvinHMqfomiLoU7xbo89el-pLzb6f8xq03P10w6mSd39Nr36XsT2GWdyKMqApTqmzfZtONzQj0X4Qf9hly0ox_AaFr0qw</recordid><startdate>20051229</startdate><enddate>20051229</enddate><creator>Wulf Dröge</creator><general>The Royal Society</general><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20051229</creationdate><title>Oxidative stress and ageing: is ageing a cysteine deficiency syndrome?</title><author>Wulf Dröge</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c591t-41a63ab45bc6ca4599463897f366f395e3da118f419330fffb4d0c5989674573</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Aging - physiology</topic><topic>Blood plasma</topic><topic>Body Composition - drug effects</topic><topic>Cysteine</topic><topic>Cysteine - chemistry</topic><topic>Cysteine - deficiency</topic><topic>Cysteine - metabolism</topic><topic>Cysteine - pharmacology</topic><topic>cysteine in vivo</topic><topic>Dietary Supplements</topic><topic>Glutathione - blood</topic><topic>Glutathione - metabolism</topic><topic>Humans</topic><topic>Hydrogen</topic><topic>Immune Functions</topic><topic>Immunity, Cellular - drug effects</topic><topic>Inflammatory Cytokines</topic><topic>Insulin</topic><topic>Insulin Signalling</topic><topic>Muscle Functions</topic><topic>Muscle, Skeletal - drug effects</topic><topic>Natural killer cells</topic><topic>Oxidative stress</topic><topic>Oxidative Stress - physiology</topic><topic>Peroxides</topic><topic>Protein Tyrosine Phosphatases - antagonists & inhibitors</topic><topic>Protein Tyrosine Phosphatases - metabolism</topic><topic>Reactive oxygen species</topic><topic>Reactive Oxygen Species - metabolism</topic><topic>Receptor, Insulin - antagonists & inhibitors</topic><topic>Receptor, Insulin - metabolism</topic><topic>Receptors</topic><topic>Redox Status</topic><topic>Serum Albumin</topic><topic>Signal Transduction - physiology</topic><topic>T lymphocytes</topic><topic>Transcription factors</topic><topic>Tumor Necrosis Factor-alpha - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wulf Dröge</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Philosophical transactions of the Royal Society of London. Series B. Biological sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wulf Dröge</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Oxidative stress and ageing: is ageing a cysteine deficiency syndrome?</atitle><jtitle>Philosophical transactions of the Royal Society of London. Series B. Biological sciences</jtitle><addtitle>Philos Trans R Soc Lond B Biol Sci</addtitle><date>2005-12-29</date><risdate>2005</risdate><volume>360</volume><issue>1464</issue><spage>2355</spage><epage>2372</epage><pages>2355-2372</pages><issn>0962-8436</issn><eissn>1471-2970</eissn><abstract>Reactive oxygen species (ROS) are constantly produced in biological tissues and play a role in various signalling pathways. Abnormally high ROS concentrations cause oxidative stress associated with tissue damage and dysregulation of physiological signals. There is growing evidence that oxidative stress increases with age. It has also been shown that the life span of worms, flies and mice can be significantly increased by mutations which impede the insulin receptor signalling cascade. Molecular studies revealed that the insulin-independent basal activity of the insulin receptor is increased by ROS and downregulated by certain antioxidants. Complementary clinical studies confirmed that supplementation of the glutathione precursor cysteine decreases insulin responsiveness in the fasted state. In several clinical trials, cysteine supplementation improved skeletal muscle functions, decreased the body fat/lean body mass ratio, decreased plasma levels of the inflammatory cytokine tumour necrosis factor α (TNF-α), improved immune functions, and increased plasma albumin levels. As all these parameters degenerate with age, these findings suggest: (i) that loss of youth, health and quality of life may be partly explained by a deficit in cysteine and (ii) that the dietary consumption of cysteine is generally suboptimal and everybody is likely to have a cysteine deficiency sooner or later.</abstract><cop>London</cop><pub>The Royal Society</pub><pmid>16321806</pmid><doi>10.1098/rstb.2005.1770</doi><tpages>18</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Aging - physiology Blood plasma Body Composition - drug effects Cysteine Cysteine - chemistry Cysteine - deficiency Cysteine - metabolism Cysteine - pharmacology cysteine in vivo Dietary Supplements Glutathione - blood Glutathione - metabolism Humans Hydrogen Immune Functions Immunity, Cellular - drug effects Inflammatory Cytokines Insulin Insulin Signalling Muscle Functions Muscle, Skeletal - drug effects Natural killer cells Oxidative stress Oxidative Stress - physiology Peroxides Protein Tyrosine Phosphatases - antagonists & inhibitors Protein Tyrosine Phosphatases - metabolism Reactive oxygen species Reactive Oxygen Species - metabolism Receptor, Insulin - antagonists & inhibitors Receptor, Insulin - metabolism Receptors Redox Status Serum Albumin Signal Transduction - physiology T lymphocytes Transcription factors Tumor Necrosis Factor-alpha - metabolism |
title | Oxidative stress and ageing: is ageing a cysteine deficiency syndrome? |
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