The NAD + -Dependent Family of Sirtuins in Cerebral Ischemia and Preconditioning
Sirtuins are an evolutionarily conserved family of NAD -dependent lysine deacylases and ADP ribosylases. Their requirement for NAD as a cosubstrate allows them to act as metabolic sensors that couple changes in the energy status of the cell to changes in cellular physiological processes. NAD levels...
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Veröffentlicht in: | Antioxidants & redox signaling 2018-03, Vol.28 (8), p.691-710 |
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creator | Khoury, Nathalie Koronowski, Kevin B Young, Juan I Perez-Pinzon, Miguel A |
description | Sirtuins are an evolutionarily conserved family of NAD
-dependent lysine deacylases and ADP ribosylases. Their requirement for NAD
as a cosubstrate allows them to act as metabolic sensors that couple changes in the energy status of the cell to changes in cellular physiological processes. NAD
levels are affected by several NAD
-producing and NAD
-consuming pathways as well as by cellular respiration. Thus their intracellular levels are highly dynamic and are misregulated in a spectrum of metabolic disorders including cerebral ischemia. This, in turn, compromises several NAD
-dependent processes that may ultimately lead to cell death. Recent Advances: A number of efforts have been made to replenish NAD
in cerebral ischemic injuries as well as to understand the functions of one its important mediators, the sirtuin family of proteins through the use of pharmacological modulators or genetic manipulation approaches either before or after the insult. Critical Issues and Future Directions: The results of these studies have regarded the sirtuins as promising therapeutic targets for cerebral ischemia. Yet, additional efforts are needed to understand the role of some of the less characterized members and to address the sex-specific effects observed with some members. Sirtuins also exhibit cell-type-specific expression in the brain as well as distinct subcellular and regional localizations. As such, they are involved in diverse and sometimes opposing cellular processes that can either promote neuroprotection or further contribute to the injury; which also stresses the need for the development and use of sirtuin-specific pharmacological modulators. Antioxid. Redox Signal. 28, 691-710. |
doi_str_mv | 10.1089/ars.2017.7258 |
format | Article |
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-dependent lysine deacylases and ADP ribosylases. Their requirement for NAD
as a cosubstrate allows them to act as metabolic sensors that couple changes in the energy status of the cell to changes in cellular physiological processes. NAD
levels are affected by several NAD
-producing and NAD
-consuming pathways as well as by cellular respiration. Thus their intracellular levels are highly dynamic and are misregulated in a spectrum of metabolic disorders including cerebral ischemia. This, in turn, compromises several NAD
-dependent processes that may ultimately lead to cell death. Recent Advances: A number of efforts have been made to replenish NAD
in cerebral ischemic injuries as well as to understand the functions of one its important mediators, the sirtuin family of proteins through the use of pharmacological modulators or genetic manipulation approaches either before or after the insult. Critical Issues and Future Directions: The results of these studies have regarded the sirtuins as promising therapeutic targets for cerebral ischemia. Yet, additional efforts are needed to understand the role of some of the less characterized members and to address the sex-specific effects observed with some members. Sirtuins also exhibit cell-type-specific expression in the brain as well as distinct subcellular and regional localizations. As such, they are involved in diverse and sometimes opposing cellular processes that can either promote neuroprotection or further contribute to the injury; which also stresses the need for the development and use of sirtuin-specific pharmacological modulators. Antioxid. Redox Signal. 28, 691-710.</description><identifier>ISSN: 1523-0864</identifier><identifier>EISSN: 1557-7716</identifier><identifier>DOI: 10.1089/ars.2017.7258</identifier><identifier>PMID: 28683567</identifier><language>eng</language><publisher>United States: Mary Ann Liebert, Inc</publisher><subject>Adenosine diphosphate ; Brain ; Brain - metabolism ; Brain - pathology ; Brain injury ; Brain Ischemia - genetics ; Brain Ischemia - metabolism ; Brain Ischemia - pathology ; Cell death ; Energy balance ; Forum Review ; Humans ; Intracellular levels ; Ischemia ; Lysine ; Metabolic disorders ; Metabolism ; Modulators ; NAD ; NAD - metabolism ; Neuromodulation ; Neuroprotection ; Oxidation-Reduction ; Pharmacology ; Preconditioning ; Proteins ; Sirtuins ; Sirtuins - genetics</subject><ispartof>Antioxidants & redox signaling, 2018-03, Vol.28 (8), p.691-710</ispartof><rights>(©) Copyright 2018, Mary Ann Liebert, Inc.</rights><rights>Copyright 2018, Mary Ann Liebert, Inc. 2018</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c415t-d9f19e4ece5b89938dbda3655384236212fb6e438e668859c5a5352381b971493</citedby><cites>FETCH-LOGICAL-c415t-d9f19e4ece5b89938dbda3655384236212fb6e438e668859c5a5352381b971493</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28683567$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Khoury, Nathalie</creatorcontrib><creatorcontrib>Koronowski, Kevin B</creatorcontrib><creatorcontrib>Young, Juan I</creatorcontrib><creatorcontrib>Perez-Pinzon, Miguel A</creatorcontrib><title>The NAD + -Dependent Family of Sirtuins in Cerebral Ischemia and Preconditioning</title><title>Antioxidants & redox signaling</title><addtitle>Antioxid Redox Signal</addtitle><description>Sirtuins are an evolutionarily conserved family of NAD
-dependent lysine deacylases and ADP ribosylases. Their requirement for NAD
as a cosubstrate allows them to act as metabolic sensors that couple changes in the energy status of the cell to changes in cellular physiological processes. NAD
levels are affected by several NAD
-producing and NAD
-consuming pathways as well as by cellular respiration. Thus their intracellular levels are highly dynamic and are misregulated in a spectrum of metabolic disorders including cerebral ischemia. This, in turn, compromises several NAD
-dependent processes that may ultimately lead to cell death. Recent Advances: A number of efforts have been made to replenish NAD
in cerebral ischemic injuries as well as to understand the functions of one its important mediators, the sirtuin family of proteins through the use of pharmacological modulators or genetic manipulation approaches either before or after the insult. Critical Issues and Future Directions: The results of these studies have regarded the sirtuins as promising therapeutic targets for cerebral ischemia. Yet, additional efforts are needed to understand the role of some of the less characterized members and to address the sex-specific effects observed with some members. Sirtuins also exhibit cell-type-specific expression in the brain as well as distinct subcellular and regional localizations. As such, they are involved in diverse and sometimes opposing cellular processes that can either promote neuroprotection or further contribute to the injury; which also stresses the need for the development and use of sirtuin-specific pharmacological modulators. Antioxid. Redox Signal. 28, 691-710.</description><subject>Adenosine diphosphate</subject><subject>Brain</subject><subject>Brain - metabolism</subject><subject>Brain - pathology</subject><subject>Brain injury</subject><subject>Brain Ischemia - genetics</subject><subject>Brain Ischemia - metabolism</subject><subject>Brain Ischemia - pathology</subject><subject>Cell death</subject><subject>Energy balance</subject><subject>Forum Review</subject><subject>Humans</subject><subject>Intracellular levels</subject><subject>Ischemia</subject><subject>Lysine</subject><subject>Metabolic disorders</subject><subject>Metabolism</subject><subject>Modulators</subject><subject>NAD</subject><subject>NAD - metabolism</subject><subject>Neuromodulation</subject><subject>Neuroprotection</subject><subject>Oxidation-Reduction</subject><subject>Pharmacology</subject><subject>Preconditioning</subject><subject>Proteins</subject><subject>Sirtuins</subject><subject>Sirtuins - genetics</subject><issn>1523-0864</issn><issn>1557-7716</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdkU1LHTEYhYO0VKtdui2BboQy13xMvjaCXGsriAq165CZeccbmUmuyYzgvzeDVmpXCeThcE4ehA4pWVGizbFLecUIVSvFhN5Be1QIVSlF5YflznhFtKx30eec7wkhjFLyCe0yLTUXUu2hm9sN4KvTM_wdV2ewhdBBmPC5G_3whGOPf_s0zT5k7ANeQ4ImuQFf5HYDo3fYhQ7fJGhj6PzkY_Dh7gB97N2Q4cvruY_-nP-4Xf-qLq9_XqxPL6u2pmKqOtNTAzW0IBptDNdd0zkuheC6ZlwyyvpGQs01SKm1MK1wgpc5mjZG0drwfXTykrudmxG6ttQu1ew2-dGlJxudt-9fgt_Yu_hohWZ1bVQJOHoNSPFhhjzZ0ecWhsEFiHO21FBViii6oN_-Q-_jnEKZZ1n5U8GlMaxQ1QvVpphzgv6tDCV2cWWLK7u4sourwn_9d8Eb_VcOfwaicI3Z</recordid><startdate>20180310</startdate><enddate>20180310</enddate><creator>Khoury, Nathalie</creator><creator>Koronowski, Kevin B</creator><creator>Young, Juan I</creator><creator>Perez-Pinzon, Miguel A</creator><general>Mary Ann Liebert, Inc</general><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>7QL</scope><scope>7QP</scope><scope>7T5</scope><scope>7TK</scope><scope>7TM</scope><scope>7TO</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20180310</creationdate><title>The NAD + -Dependent Family of Sirtuins in Cerebral Ischemia and Preconditioning</title><author>Khoury, Nathalie ; Koronowski, Kevin B ; Young, Juan I ; Perez-Pinzon, Miguel A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c415t-d9f19e4ece5b89938dbda3655384236212fb6e438e668859c5a5352381b971493</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Adenosine diphosphate</topic><topic>Brain</topic><topic>Brain - metabolism</topic><topic>Brain - pathology</topic><topic>Brain injury</topic><topic>Brain Ischemia - genetics</topic><topic>Brain Ischemia - metabolism</topic><topic>Brain Ischemia - pathology</topic><topic>Cell death</topic><topic>Energy balance</topic><topic>Forum Review</topic><topic>Humans</topic><topic>Intracellular levels</topic><topic>Ischemia</topic><topic>Lysine</topic><topic>Metabolic disorders</topic><topic>Metabolism</topic><topic>Modulators</topic><topic>NAD</topic><topic>NAD - metabolism</topic><topic>Neuromodulation</topic><topic>Neuroprotection</topic><topic>Oxidation-Reduction</topic><topic>Pharmacology</topic><topic>Preconditioning</topic><topic>Proteins</topic><topic>Sirtuins</topic><topic>Sirtuins - genetics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Khoury, Nathalie</creatorcontrib><creatorcontrib>Koronowski, Kevin B</creatorcontrib><creatorcontrib>Young, Juan I</creatorcontrib><creatorcontrib>Perez-Pinzon, Miguel A</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Immunology Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Antioxidants & redox signaling</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Khoury, Nathalie</au><au>Koronowski, Kevin B</au><au>Young, Juan I</au><au>Perez-Pinzon, Miguel A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The NAD + -Dependent Family of Sirtuins in Cerebral Ischemia and Preconditioning</atitle><jtitle>Antioxidants & redox signaling</jtitle><addtitle>Antioxid Redox Signal</addtitle><date>2018-03-10</date><risdate>2018</risdate><volume>28</volume><issue>8</issue><spage>691</spage><epage>710</epage><pages>691-710</pages><issn>1523-0864</issn><eissn>1557-7716</eissn><abstract>Sirtuins are an evolutionarily conserved family of NAD
-dependent lysine deacylases and ADP ribosylases. Their requirement for NAD
as a cosubstrate allows them to act as metabolic sensors that couple changes in the energy status of the cell to changes in cellular physiological processes. NAD
levels are affected by several NAD
-producing and NAD
-consuming pathways as well as by cellular respiration. Thus their intracellular levels are highly dynamic and are misregulated in a spectrum of metabolic disorders including cerebral ischemia. This, in turn, compromises several NAD
-dependent processes that may ultimately lead to cell death. Recent Advances: A number of efforts have been made to replenish NAD
in cerebral ischemic injuries as well as to understand the functions of one its important mediators, the sirtuin family of proteins through the use of pharmacological modulators or genetic manipulation approaches either before or after the insult. Critical Issues and Future Directions: The results of these studies have regarded the sirtuins as promising therapeutic targets for cerebral ischemia. Yet, additional efforts are needed to understand the role of some of the less characterized members and to address the sex-specific effects observed with some members. Sirtuins also exhibit cell-type-specific expression in the brain as well as distinct subcellular and regional localizations. As such, they are involved in diverse and sometimes opposing cellular processes that can either promote neuroprotection or further contribute to the injury; which also stresses the need for the development and use of sirtuin-specific pharmacological modulators. Antioxid. Redox Signal. 28, 691-710.</abstract><cop>United States</cop><pub>Mary Ann Liebert, Inc</pub><pmid>28683567</pmid><doi>10.1089/ars.2017.7258</doi><tpages>20</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adenosine diphosphate Brain Brain - metabolism Brain - pathology Brain injury Brain Ischemia - genetics Brain Ischemia - metabolism Brain Ischemia - pathology Cell death Energy balance Forum Review Humans Intracellular levels Ischemia Lysine Metabolic disorders Metabolism Modulators NAD NAD - metabolism Neuromodulation Neuroprotection Oxidation-Reduction Pharmacology Preconditioning Proteins Sirtuins Sirtuins - genetics |
title | The NAD + -Dependent Family of Sirtuins in Cerebral Ischemia and Preconditioning |
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