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Aging-Associated Endothelial Dysfunction in Humans Is Reversed by L-Arginine
This study investigated the hypothesis that aging selectively impairs endothelium-dependent function, which may be reversible by administration of L-arginine. An impaired response to acetylcholine with aging has been demonstrated in humans. However, the mechanisms underlying this impaired response o...
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Published in: | Journal of the American College of Cardiology 1996-12, Vol.28 (7), p.1796-1804 |
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container_title | Journal of the American College of Cardiology |
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creator | Chauhan, Anoop More, Ranjit S. Mullins, Paul A. Taylor, Ged Petch, Michael C. Schofield, Peter M. |
description | This study investigated the hypothesis that aging selectively impairs endothelium-dependent function, which may be reversible by administration of L-arginine.
An impaired response to acetylcholine with aging has been demonstrated in humans. However, the mechanisms underlying this impaired response of the coronary microvasculature remain to be determined.
We infused the endothelium-independent vasodilators papaverine and glyceryl trinitrate (GTN) and the endothelium-dependent vasodilator acetylcholine (1,3,10 and 30 /g/min) into the left coronary artery of 34 patients (27 to 73 years old) with atypical chest pain, negative exercise test results, completely normal findings on coronary angiography and no coronary risk factors. Coronary blood flow was measured with an intracoronary Doppler catheter. The papaverine and acetylcholine infusions were repeated in 14 patients (27 to 73 years old) after an intracoronary infusion of L-arginine (160 μmol/min for 20 min).
There was a significant negative correlation between aging and the peak coronary blood flow response evoked by acetylcholine (r =-0.73, p < 0.0001). However, there was no correlation between aging and the peak coronary blood flow response to papaverine (r =-0.04, p = 0.82) and GTN (r = -0.24, p = 0.17). The peak coronary blood flow response evoked by acetylcholine correlated significantly with aging before L-arginine infusion (r =-0.87, p < 0.0001), but this negative correlation was lost after L-arginine infusion (r =-0.37, p = 0.19).
The results suggest that aging selectively impairs endothelium-dependent coronary microvascular function and that this impairment can be restored by administration of L-arginine, a precursor of nitric oxide. |
doi_str_mv | 10.1016/S0735-1097(96)00394-4 |
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An impaired response to acetylcholine with aging has been demonstrated in humans. However, the mechanisms underlying this impaired response of the coronary microvasculature remain to be determined.
We infused the endothelium-independent vasodilators papaverine and glyceryl trinitrate (GTN) and the endothelium-dependent vasodilator acetylcholine (1,3,10 and 30 /g/min) into the left coronary artery of 34 patients (27 to 73 years old) with atypical chest pain, negative exercise test results, completely normal findings on coronary angiography and no coronary risk factors. Coronary blood flow was measured with an intracoronary Doppler catheter. The papaverine and acetylcholine infusions were repeated in 14 patients (27 to 73 years old) after an intracoronary infusion of L-arginine (160 μmol/min for 20 min).
There was a significant negative correlation between aging and the peak coronary blood flow response evoked by acetylcholine (r =-0.73, p < 0.0001). However, there was no correlation between aging and the peak coronary blood flow response to papaverine (r =-0.04, p = 0.82) and GTN (r = -0.24, p = 0.17). The peak coronary blood flow response evoked by acetylcholine correlated significantly with aging before L-arginine infusion (r =-0.87, p < 0.0001), but this negative correlation was lost after L-arginine infusion (r =-0.37, p = 0.19).
The results suggest that aging selectively impairs endothelium-dependent coronary microvascular function and that this impairment can be restored by administration of L-arginine, a precursor of nitric oxide.</description><identifier>ISSN: 0735-1097</identifier><identifier>EISSN: 1558-3597</identifier><identifier>DOI: 10.1016/S0735-1097(96)00394-4</identifier><identifier>PMID: 8962569</identifier><identifier>CODEN: JACCDI</identifier><language>eng</language><publisher>New York, NY: Elsevier Inc</publisher><subject>Acetylcholine - pharmacology ; Adult ; Aged ; Aging - physiology ; Arginine - pharmacology ; Biological and medical sciences ; Blood coagulation ; Coronary Circulation - drug effects ; Coronary Vessels - drug effects ; Coronary Vessels - physiopathology ; Endothelium, Vascular - drug effects ; Endothelium, Vascular - physiopathology ; Female ; Humans ; Investigative techniques, diagnostic techniques (general aspects) ; Male ; Medical sciences ; Microcirculation - drug effects ; Microcirculation - physiology ; Middle Aged ; Nitroglycerin - pharmacology ; Papaverine - pharmacology ; Vasodilator Agents - pharmacology</subject><ispartof>Journal of the American College of Cardiology, 1996-12, Vol.28 (7), p.1796-1804</ispartof><rights>1996 American College of Cardiology</rights><rights>1997 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c490t-8ab628eb6898a37a1d445480e5ecf856ef9e98b12b8761c013e4cf4756e390b33</citedby><cites>FETCH-LOGICAL-c490t-8ab628eb6898a37a1d445480e5ecf856ef9e98b12b8761c013e4cf4756e390b33</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=2528708$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/8962569$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Chauhan, Anoop</creatorcontrib><creatorcontrib>More, Ranjit S.</creatorcontrib><creatorcontrib>Mullins, Paul A.</creatorcontrib><creatorcontrib>Taylor, Ged</creatorcontrib><creatorcontrib>Petch, Michael C.</creatorcontrib><creatorcontrib>Schofield, Peter M.</creatorcontrib><title>Aging-Associated Endothelial Dysfunction in Humans Is Reversed by L-Arginine</title><title>Journal of the American College of Cardiology</title><addtitle>J Am Coll Cardiol</addtitle><description>This study investigated the hypothesis that aging selectively impairs endothelium-dependent function, which may be reversible by administration of L-arginine.
An impaired response to acetylcholine with aging has been demonstrated in humans. However, the mechanisms underlying this impaired response of the coronary microvasculature remain to be determined.
We infused the endothelium-independent vasodilators papaverine and glyceryl trinitrate (GTN) and the endothelium-dependent vasodilator acetylcholine (1,3,10 and 30 /g/min) into the left coronary artery of 34 patients (27 to 73 years old) with atypical chest pain, negative exercise test results, completely normal findings on coronary angiography and no coronary risk factors. Coronary blood flow was measured with an intracoronary Doppler catheter. The papaverine and acetylcholine infusions were repeated in 14 patients (27 to 73 years old) after an intracoronary infusion of L-arginine (160 μmol/min for 20 min).
There was a significant negative correlation between aging and the peak coronary blood flow response evoked by acetylcholine (r =-0.73, p < 0.0001). However, there was no correlation between aging and the peak coronary blood flow response to papaverine (r =-0.04, p = 0.82) and GTN (r = -0.24, p = 0.17). The peak coronary blood flow response evoked by acetylcholine correlated significantly with aging before L-arginine infusion (r =-0.87, p < 0.0001), but this negative correlation was lost after L-arginine infusion (r =-0.37, p = 0.19).
The results suggest that aging selectively impairs endothelium-dependent coronary microvascular function and that this impairment can be restored by administration of L-arginine, a precursor of nitric oxide.</description><subject>Acetylcholine - pharmacology</subject><subject>Adult</subject><subject>Aged</subject><subject>Aging - physiology</subject><subject>Arginine - pharmacology</subject><subject>Biological and medical sciences</subject><subject>Blood coagulation</subject><subject>Coronary Circulation - drug effects</subject><subject>Coronary Vessels - drug effects</subject><subject>Coronary Vessels - physiopathology</subject><subject>Endothelium, Vascular - drug effects</subject><subject>Endothelium, Vascular - physiopathology</subject><subject>Female</subject><subject>Humans</subject><subject>Investigative techniques, diagnostic techniques (general aspects)</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Microcirculation - drug effects</subject><subject>Microcirculation - physiology</subject><subject>Middle Aged</subject><subject>Nitroglycerin - pharmacology</subject><subject>Papaverine - pharmacology</subject><subject>Vasodilator Agents - pharmacology</subject><issn>0735-1097</issn><issn>1558-3597</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1996</creationdate><recordtype>article</recordtype><recordid>eNqFkMtOwzAQRS0EgvL4hEpZIASLgJ3Yjr1CVSkPqRISj7XlOBMwSh3wJJX694S26pbVLO65M6NDyJjRa0aZvHmlRS5SRnVxqeUVpbnmKd8jIyaESnOhi30y2iFH5Bjxi1IqFdOH5FBpmQmpR2Q--fDhI50gts7bDqpkFqq2-4TG2ya5W2HdB9f5NiQ-JI_9wgZMnjB5gSVEHOhylczTSRyW-ACn5KC2DcLZdp6Q9_vZ2_QxnT8_PE0n89RxTbtU2VJmCkqptLJ5YVnFueCKggBXKyGh1qBVybJSFZI5ynLgrubFkOSalnl-Qi42e79j-9MDdmbh0UHT2ABtj6ZQMsuU1AMoNqCLLWKE2nxHv7BxZRg1fxbN2qL5U2S0NGuLhg-98fZAXy6g2rW22ob8fJtbdLapow3O4w7LRKYKqgbsdoPBIGPpIRp0HoKDykdwnala_88jv1GijWU</recordid><startdate>19961201</startdate><enddate>19961201</enddate><creator>Chauhan, Anoop</creator><creator>More, Ranjit S.</creator><creator>Mullins, Paul A.</creator><creator>Taylor, Ged</creator><creator>Petch, Michael C.</creator><creator>Schofield, Peter M.</creator><general>Elsevier Inc</general><general>Elsevier Science</general><scope>6I.</scope><scope>AAFTH</scope><scope>IQODW</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></search><sort><creationdate>19961201</creationdate><title>Aging-Associated Endothelial Dysfunction in Humans Is Reversed by L-Arginine</title><author>Chauhan, Anoop ; More, Ranjit S. ; Mullins, Paul A. ; Taylor, Ged ; Petch, Michael C. ; Schofield, Peter M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c490t-8ab628eb6898a37a1d445480e5ecf856ef9e98b12b8761c013e4cf4756e390b33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1996</creationdate><topic>Acetylcholine - pharmacology</topic><topic>Adult</topic><topic>Aged</topic><topic>Aging - physiology</topic><topic>Arginine - pharmacology</topic><topic>Biological and medical sciences</topic><topic>Blood coagulation</topic><topic>Coronary Circulation - drug effects</topic><topic>Coronary Vessels - drug effects</topic><topic>Coronary Vessels - physiopathology</topic><topic>Endothelium, Vascular - drug effects</topic><topic>Endothelium, Vascular - physiopathology</topic><topic>Female</topic><topic>Humans</topic><topic>Investigative techniques, diagnostic techniques (general aspects)</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Microcirculation - drug effects</topic><topic>Microcirculation - physiology</topic><topic>Middle Aged</topic><topic>Nitroglycerin - pharmacology</topic><topic>Papaverine - pharmacology</topic><topic>Vasodilator Agents - pharmacology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chauhan, Anoop</creatorcontrib><creatorcontrib>More, Ranjit S.</creatorcontrib><creatorcontrib>Mullins, Paul A.</creatorcontrib><creatorcontrib>Taylor, Ged</creatorcontrib><creatorcontrib>Petch, Michael C.</creatorcontrib><creatorcontrib>Schofield, Peter M.</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Pascal-Francis</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><jtitle>Journal of the American College of Cardiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chauhan, Anoop</au><au>More, Ranjit S.</au><au>Mullins, Paul A.</au><au>Taylor, Ged</au><au>Petch, Michael C.</au><au>Schofield, Peter M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Aging-Associated Endothelial Dysfunction in Humans Is Reversed by L-Arginine</atitle><jtitle>Journal of the American College of Cardiology</jtitle><addtitle>J Am Coll Cardiol</addtitle><date>1996-12-01</date><risdate>1996</risdate><volume>28</volume><issue>7</issue><spage>1796</spage><epage>1804</epage><pages>1796-1804</pages><issn>0735-1097</issn><eissn>1558-3597</eissn><coden>JACCDI</coden><abstract>This study investigated the hypothesis that aging selectively impairs endothelium-dependent function, which may be reversible by administration of L-arginine.
An impaired response to acetylcholine with aging has been demonstrated in humans. However, the mechanisms underlying this impaired response of the coronary microvasculature remain to be determined.
We infused the endothelium-independent vasodilators papaverine and glyceryl trinitrate (GTN) and the endothelium-dependent vasodilator acetylcholine (1,3,10 and 30 /g/min) into the left coronary artery of 34 patients (27 to 73 years old) with atypical chest pain, negative exercise test results, completely normal findings on coronary angiography and no coronary risk factors. Coronary blood flow was measured with an intracoronary Doppler catheter. The papaverine and acetylcholine infusions were repeated in 14 patients (27 to 73 years old) after an intracoronary infusion of L-arginine (160 μmol/min for 20 min).
There was a significant negative correlation between aging and the peak coronary blood flow response evoked by acetylcholine (r =-0.73, p < 0.0001). However, there was no correlation between aging and the peak coronary blood flow response to papaverine (r =-0.04, p = 0.82) and GTN (r = -0.24, p = 0.17). The peak coronary blood flow response evoked by acetylcholine correlated significantly with aging before L-arginine infusion (r =-0.87, p < 0.0001), but this negative correlation was lost after L-arginine infusion (r =-0.37, p = 0.19).
The results suggest that aging selectively impairs endothelium-dependent coronary microvascular function and that this impairment can be restored by administration of L-arginine, a precursor of nitric oxide.</abstract><cop>New York, NY</cop><pub>Elsevier Inc</pub><pmid>8962569</pmid><doi>10.1016/S0735-1097(96)00394-4</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Acetylcholine - pharmacology Adult Aged Aging - physiology Arginine - pharmacology Biological and medical sciences Blood coagulation Coronary Circulation - drug effects Coronary Vessels - drug effects Coronary Vessels - physiopathology Endothelium, Vascular - drug effects Endothelium, Vascular - physiopathology Female Humans Investigative techniques, diagnostic techniques (general aspects) Male Medical sciences Microcirculation - drug effects Microcirculation - physiology Middle Aged Nitroglycerin - pharmacology Papaverine - pharmacology Vasodilator Agents - pharmacology |
title | Aging-Associated Endothelial Dysfunction in Humans Is Reversed by L-Arginine |
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