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Niacin protects the isolated heart from ischemia-reperfusion injury
Nicotinic acid (niacin) has been shown to decrease myocyte injury. Because interventions that lower the cytosolic NADH/NAD(+) ratio inprove glycolysis and limit infarct size, we hypothesized that 1) niacin, as a precursor of NAD(+), would lower the NADH/NAD(+) ratio, increase glycolysis, and limit i...
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Published in: | American journal of physiology. Heart and circulatory physiology 2000-08, Vol.48 (2), p.H764-H771 |
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container_end_page | H771 |
container_issue | 2 |
container_start_page | H764 |
container_title | American journal of physiology. Heart and circulatory physiology |
container_volume | 48 |
creator | TRUEBLOOD, N. A RAMASAMY, R LI FENG WANG SCHAEFER, S |
description | Nicotinic acid (niacin) has been shown to decrease myocyte injury. Because interventions that lower the cytosolic NADH/NAD(+) ratio inprove glycolysis and limit infarct size, we hypothesized that 1) niacin, as a precursor of NAD(+), would lower the NADH/NAD(+) ratio, increase glycolysis, and limit ischemic injury and 2) these cardioprotective benefits of niacin would be limited in conditions that block lactate removal. |
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A ; RAMASAMY, R ; LI FENG WANG ; SCHAEFER, S</creator><creatorcontrib>TRUEBLOOD, N. A ; RAMASAMY, R ; LI FENG WANG ; SCHAEFER, S</creatorcontrib><description>Nicotinic acid (niacin) has been shown to decrease myocyte injury. Because interventions that lower the cytosolic NADH/NAD(+) ratio inprove glycolysis and limit infarct size, we hypothesized that 1) niacin, as a precursor of NAD(+), would lower the NADH/NAD(+) ratio, increase glycolysis, and limit ischemic injury and 2) these cardioprotective benefits of niacin would be limited in conditions that block lactate removal.</description><identifier>ISSN: 0363-6135</identifier><identifier>EISSN: 1522-1539</identifier><identifier>CODEN: AJPPDI</identifier><language>eng</language><publisher>Bethesda, MD: American Physiological Society</publisher><subject>Biochemistry ; Biological and medical sciences ; Cardiovascular system ; Heart ; Injuries ; Medical sciences ; Miscellaneous ; Pharmacology. Drug treatments</subject><ispartof>American journal of physiology. Heart and circulatory physiology, 2000-08, Vol.48 (2), p.H764-H771</ispartof><rights>2000 INIST-CNRS</rights><rights>Copyright American Physiological Society Aug 2000</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=1477415$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>TRUEBLOOD, N. A</creatorcontrib><creatorcontrib>RAMASAMY, R</creatorcontrib><creatorcontrib>LI FENG WANG</creatorcontrib><creatorcontrib>SCHAEFER, S</creatorcontrib><title>Niacin protects the isolated heart from ischemia-reperfusion injury</title><title>American journal of physiology. Heart and circulatory physiology</title><description>Nicotinic acid (niacin) has been shown to decrease myocyte injury. Because interventions that lower the cytosolic NADH/NAD(+) ratio inprove glycolysis and limit infarct size, we hypothesized that 1) niacin, as a precursor of NAD(+), would lower the NADH/NAD(+) ratio, increase glycolysis, and limit ischemic injury and 2) these cardioprotective benefits of niacin would be limited in conditions that block lactate removal.</description><subject>Biochemistry</subject><subject>Biological and medical sciences</subject><subject>Cardiovascular system</subject><subject>Heart</subject><subject>Injuries</subject><subject>Medical sciences</subject><subject>Miscellaneous</subject><subject>Pharmacology. 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A</creator><creator>RAMASAMY, R</creator><creator>LI FENG WANG</creator><creator>SCHAEFER, S</creator><general>American Physiological Society</general><scope>IQODW</scope><scope>7QP</scope><scope>7QR</scope><scope>7TS</scope><scope>7U7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>P64</scope></search><sort><creationdate>20000801</creationdate><title>Niacin protects the isolated heart from ischemia-reperfusion injury</title><author>TRUEBLOOD, N. A ; RAMASAMY, R ; LI FENG WANG ; SCHAEFER, S</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p563-2a33008241925d74e11c0e8647393f53424ff3d66b587d3e2c25fc35747b63bb3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2000</creationdate><topic>Biochemistry</topic><topic>Biological and medical sciences</topic><topic>Cardiovascular system</topic><topic>Heart</topic><topic>Injuries</topic><topic>Medical sciences</topic><topic>Miscellaneous</topic><topic>Pharmacology. Drug treatments</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>TRUEBLOOD, N. A</creatorcontrib><creatorcontrib>RAMASAMY, R</creatorcontrib><creatorcontrib>LI FENG WANG</creatorcontrib><creatorcontrib>SCHAEFER, S</creatorcontrib><collection>Pascal-Francis</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Physical Education Index</collection><collection>Toxicology Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><jtitle>American journal of physiology. Heart and circulatory physiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>TRUEBLOOD, N. A</au><au>RAMASAMY, R</au><au>LI FENG WANG</au><au>SCHAEFER, S</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Niacin protects the isolated heart from ischemia-reperfusion injury</atitle><jtitle>American journal of physiology. Heart and circulatory physiology</jtitle><date>2000-08-01</date><risdate>2000</risdate><volume>48</volume><issue>2</issue><spage>H764</spage><epage>H771</epage><pages>H764-H771</pages><issn>0363-6135</issn><eissn>1522-1539</eissn><coden>AJPPDI</coden><abstract>Nicotinic acid (niacin) has been shown to decrease myocyte injury. Because interventions that lower the cytosolic NADH/NAD(+) ratio inprove glycolysis and limit infarct size, we hypothesized that 1) niacin, as a precursor of NAD(+), would lower the NADH/NAD(+) ratio, increase glycolysis, and limit ischemic injury and 2) these cardioprotective benefits of niacin would be limited in conditions that block lactate removal.</abstract><cop>Bethesda, MD</cop><pub>American Physiological Society</pub></addata></record> |
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identifier | ISSN: 0363-6135 |
ispartof | American journal of physiology. Heart and circulatory physiology, 2000-08, Vol.48 (2), p.H764-H771 |
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language | eng |
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source | American Physiological Society Free |
subjects | Biochemistry Biological and medical sciences Cardiovascular system Heart Injuries Medical sciences Miscellaneous Pharmacology. Drug treatments |
title | Niacin protects the isolated heart from ischemia-reperfusion injury |
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