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Influence of nitric oxide on neurogenic contraction and relaxation of the human gastroepiploic artery
The objective of this study was to characterize the neurogenic contraction and relaxation of the human gastroepiploic artery and to determine whether the responses are mediated by nitric oxide (NO) from neural or endothelial origin. Rings of human gastroepiploic artery were obtained from 18 patients...
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Published in: | American journal of hypertension 2003-01, Vol.16 (1), p.28-32 |
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creator | Medina, Pascual Segarra, Gloria Peiro, Marta Flor, Blas Martínez-León, Juan B Vila, José M Lluch, Salvador |
description | The objective of this study was to characterize the neurogenic contraction and relaxation of the human gastroepiploic artery and to determine whether the responses are mediated by nitric oxide (NO) from neural or endothelial origin.
Rings of human gastroepiploic artery were obtained from 18 patients (12 men, 6 women) undergoing gastrectomy. The rings were suspended in organ baths for isometric recording of tension. We studied the contractile and relaxant responses to electrical field stimulation.
In arteries under resting conditions, electrical field stimulation (2 to 8 Hz) caused frequency-dependent contractions that were of greater magnitude in arteries denuded of endothelium and blocked by tetrodotoxin (10−6 mol/L). The inhibitor of NO synthesis NG-monomethyl-l-arginine (L-NMMA, 10−4 mol/L) increased contractile responses only in arteries with endothelium. In preparations contracted with norepinephrine in the presence of guanethidine (10−6 mol/L) and atropine (10−6 mol/L), electrical stimulation induced frequency-dependent relaxations. This neurogenic relaxation was prevented by L-NMMA (10−4 mol/L) and tetrodotoxin (10−6 mol/L), but was unaffected by removal of the endothelium.
The results provide functional evidence that NO is released by autonomic nerves of the human gastroepiploic artery. We hypothesize that the release of NO from both endothelial and neurogenic origin may modulate resistance of the human gastroepiploic artery. Dysfunction in any of these sources of NO should be considered in some form of vasospasm. |
doi_str_mv | 10.1016/S0895-7061(02)03156-4 |
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Rings of human gastroepiploic artery were obtained from 18 patients (12 men, 6 women) undergoing gastrectomy. The rings were suspended in organ baths for isometric recording of tension. We studied the contractile and relaxant responses to electrical field stimulation.
In arteries under resting conditions, electrical field stimulation (2 to 8 Hz) caused frequency-dependent contractions that were of greater magnitude in arteries denuded of endothelium and blocked by tetrodotoxin (10−6 mol/L). The inhibitor of NO synthesis NG-monomethyl-l-arginine (L-NMMA, 10−4 mol/L) increased contractile responses only in arteries with endothelium. In preparations contracted with norepinephrine in the presence of guanethidine (10−6 mol/L) and atropine (10−6 mol/L), electrical stimulation induced frequency-dependent relaxations. This neurogenic relaxation was prevented by L-NMMA (10−4 mol/L) and tetrodotoxin (10−6 mol/L), but was unaffected by removal of the endothelium.
The results provide functional evidence that NO is released by autonomic nerves of the human gastroepiploic artery. We hypothesize that the release of NO from both endothelial and neurogenic origin may modulate resistance of the human gastroepiploic artery. Dysfunction in any of these sources of NO should be considered in some form of vasospasm.</description><identifier>ISSN: 0895-7061</identifier><identifier>EISSN: 1879-1905</identifier><identifier>EISSN: 1941-7225</identifier><identifier>DOI: 10.1016/S0895-7061(02)03156-4</identifier><identifier>PMID: 12517679</identifier><identifier>CODEN: AJHYE6</identifier><language>eng</language><publisher>New York, NY: Elsevier Inc</publisher><subject>Aged ; Aged, 80 and over ; Anesthetics, Local - pharmacology ; Arginine - pharmacology ; Autonomic Nervous System - physiology ; Biological and medical sciences ; Blood vessels and receptors ; Endothelial factors ; Endothelium, Vascular - metabolism ; Enzyme Inhibitors - pharmacology ; Female ; Fundamental and applied biological sciences. Psychology ; Gastroepiploic Artery - innervation ; Gastroepiploic Artery - physiology ; human gastroepiploic artery ; Humans ; In Vitro Techniques ; Male ; Middle Aged ; neurotransmission ; nitric oxide ; Nitric Oxide - metabolism ; Nitric Oxide Synthase - antagonists & inhibitors ; omega-N-Methylarginine - pharmacology ; Tetrodotoxin - pharmacology ; Vasoconstriction - drug effects ; Vasoconstriction - physiology ; Vasodilation - drug effects ; Vasodilation - physiology ; Vertebrates: cardiovascular system</subject><ispartof>American journal of hypertension, 2003-01, Vol.16 (1), p.28-32</ispartof><rights>2003 American Journal of Hypertension, Ltd.</rights><rights>2003 INIST-CNRS</rights><rights>Copyright Nature Publishing Group Jan 2003</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c593t-9f0f8aa8fdde48b3be47c420046bb7c5b77dc6277eba0fdb6a15c22cc86687693</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,4024,27923,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=14463120$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12517679$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Medina, Pascual</creatorcontrib><creatorcontrib>Segarra, Gloria</creatorcontrib><creatorcontrib>Peiro, Marta</creatorcontrib><creatorcontrib>Flor, Blas</creatorcontrib><creatorcontrib>Martínez-León, Juan B</creatorcontrib><creatorcontrib>Vila, José M</creatorcontrib><creatorcontrib>Lluch, Salvador</creatorcontrib><title>Influence of nitric oxide on neurogenic contraction and relaxation of the human gastroepiploic artery</title><title>American journal of hypertension</title><addtitle>AJH</addtitle><description>The objective of this study was to characterize the neurogenic contraction and relaxation of the human gastroepiploic artery and to determine whether the responses are mediated by nitric oxide (NO) from neural or endothelial origin.
Rings of human gastroepiploic artery were obtained from 18 patients (12 men, 6 women) undergoing gastrectomy. The rings were suspended in organ baths for isometric recording of tension. We studied the contractile and relaxant responses to electrical field stimulation.
In arteries under resting conditions, electrical field stimulation (2 to 8 Hz) caused frequency-dependent contractions that were of greater magnitude in arteries denuded of endothelium and blocked by tetrodotoxin (10−6 mol/L). The inhibitor of NO synthesis NG-monomethyl-l-arginine (L-NMMA, 10−4 mol/L) increased contractile responses only in arteries with endothelium. In preparations contracted with norepinephrine in the presence of guanethidine (10−6 mol/L) and atropine (10−6 mol/L), electrical stimulation induced frequency-dependent relaxations. This neurogenic relaxation was prevented by L-NMMA (10−4 mol/L) and tetrodotoxin (10−6 mol/L), but was unaffected by removal of the endothelium.
The results provide functional evidence that NO is released by autonomic nerves of the human gastroepiploic artery. We hypothesize that the release of NO from both endothelial and neurogenic origin may modulate resistance of the human gastroepiploic artery. Dysfunction in any of these sources of NO should be considered in some form of vasospasm.</description><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Anesthetics, Local - pharmacology</subject><subject>Arginine - pharmacology</subject><subject>Autonomic Nervous System - physiology</subject><subject>Biological and medical sciences</subject><subject>Blood vessels and receptors</subject><subject>Endothelial factors</subject><subject>Endothelium, Vascular - metabolism</subject><subject>Enzyme Inhibitors - pharmacology</subject><subject>Female</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Gastroepiploic Artery - innervation</subject><subject>Gastroepiploic Artery - physiology</subject><subject>human gastroepiploic artery</subject><subject>Humans</subject><subject>In Vitro Techniques</subject><subject>Male</subject><subject>Middle Aged</subject><subject>neurotransmission</subject><subject>nitric oxide</subject><subject>Nitric Oxide - metabolism</subject><subject>Nitric Oxide Synthase - antagonists & inhibitors</subject><subject>omega-N-Methylarginine - pharmacology</subject><subject>Tetrodotoxin - pharmacology</subject><subject>Vasoconstriction - drug effects</subject><subject>Vasoconstriction - physiology</subject><subject>Vasodilation - drug effects</subject><subject>Vasodilation - physiology</subject><subject>Vertebrates: cardiovascular system</subject><issn>0895-7061</issn><issn>1879-1905</issn><issn>1941-7225</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><recordid>eNqFkUFv1DAQhS0EotvCTwBFQkjtIcV2Yjs5VahAW1Gphy6i4mI59qTrJWsvtoO2_x5nd9U9crJm_L03nmeE3hF8TjDhn-5x07JSYE5OMT3DFWG8rF-gGWlEW5IWs5do9owcoeMYlxjjmnPyGh0Ryojgop0huHH9MILTUPi-cDYFqwu_sSbXrnAwBv8ILve0dykonWxuK2eKAIPaqG2ZhWkBxWJcKVc8qpiCh7VdDz7LVEgQnt6gV70aIrzdnyfox7ev88vr8vbu6uby822pWVulsu1x3yjV9MZA3XRVB7XQNZ2e3XVCs04IozkVAjqFe9NxRZimVOuG80bwtjpBH3a-6-D_jBCTXPoxuDxSEkw5a3ErcKbYjtLBxxigl-tgVyo8ZUhO4cptuHJKTmIqt-HKOuve793HbgXmoNqnmYGPe0BFrYY-KKdtPHB1zStC8cHIqTQGeAbUcpGXrVgGyh1gY4LN4T78llxUgsnrh19y_jD_fl99-Sknw4sdDzncvxaCjNpOn2psAJ2k8fY_u_0DvF-xlQ</recordid><startdate>200301</startdate><enddate>200301</enddate><creator>Medina, Pascual</creator><creator>Segarra, Gloria</creator><creator>Peiro, Marta</creator><creator>Flor, Blas</creator><creator>Martínez-León, Juan B</creator><creator>Vila, José M</creator><creator>Lluch, Salvador</creator><general>Elsevier Inc</general><general>Oxford University Press</general><general>Elsevier Science</general><scope>BSCLL</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>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope></search><sort><creationdate>200301</creationdate><title>Influence of nitric oxide on neurogenic contraction and relaxation of the human gastroepiploic artery</title><author>Medina, Pascual ; Segarra, Gloria ; Peiro, Marta ; Flor, Blas ; Martínez-León, Juan B ; Vila, José M ; Lluch, Salvador</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c593t-9f0f8aa8fdde48b3be47c420046bb7c5b77dc6277eba0fdb6a15c22cc86687693</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Anesthetics, Local - pharmacology</topic><topic>Arginine - pharmacology</topic><topic>Autonomic Nervous System - physiology</topic><topic>Biological and medical sciences</topic><topic>Blood vessels and receptors</topic><topic>Endothelial factors</topic><topic>Endothelium, Vascular - metabolism</topic><topic>Enzyme Inhibitors - pharmacology</topic><topic>Female</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Gastroepiploic Artery - innervation</topic><topic>Gastroepiploic Artery - physiology</topic><topic>human gastroepiploic artery</topic><topic>Humans</topic><topic>In Vitro Techniques</topic><topic>Male</topic><topic>Middle Aged</topic><topic>neurotransmission</topic><topic>nitric oxide</topic><topic>Nitric Oxide - metabolism</topic><topic>Nitric Oxide Synthase - antagonists & inhibitors</topic><topic>omega-N-Methylarginine - pharmacology</topic><topic>Tetrodotoxin - pharmacology</topic><topic>Vasoconstriction - drug effects</topic><topic>Vasoconstriction - physiology</topic><topic>Vasodilation - drug effects</topic><topic>Vasodilation - physiology</topic><topic>Vertebrates: cardiovascular system</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Medina, Pascual</creatorcontrib><creatorcontrib>Segarra, Gloria</creatorcontrib><creatorcontrib>Peiro, Marta</creatorcontrib><creatorcontrib>Flor, Blas</creatorcontrib><creatorcontrib>Martínez-León, Juan B</creatorcontrib><creatorcontrib>Vila, José M</creatorcontrib><creatorcontrib>Lluch, Salvador</creatorcontrib><collection>Istex</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>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><jtitle>American journal of hypertension</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Medina, Pascual</au><au>Segarra, Gloria</au><au>Peiro, Marta</au><au>Flor, Blas</au><au>Martínez-León, Juan B</au><au>Vila, José M</au><au>Lluch, Salvador</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Influence of nitric oxide on neurogenic contraction and relaxation of the human gastroepiploic artery</atitle><jtitle>American journal of hypertension</jtitle><addtitle>AJH</addtitle><date>2003-01</date><risdate>2003</risdate><volume>16</volume><issue>1</issue><spage>28</spage><epage>32</epage><pages>28-32</pages><issn>0895-7061</issn><eissn>1879-1905</eissn><eissn>1941-7225</eissn><coden>AJHYE6</coden><abstract>The objective of this study was to characterize the neurogenic contraction and relaxation of the human gastroepiploic artery and to determine whether the responses are mediated by nitric oxide (NO) from neural or endothelial origin.
Rings of human gastroepiploic artery were obtained from 18 patients (12 men, 6 women) undergoing gastrectomy. The rings were suspended in organ baths for isometric recording of tension. We studied the contractile and relaxant responses to electrical field stimulation.
In arteries under resting conditions, electrical field stimulation (2 to 8 Hz) caused frequency-dependent contractions that were of greater magnitude in arteries denuded of endothelium and blocked by tetrodotoxin (10−6 mol/L). The inhibitor of NO synthesis NG-monomethyl-l-arginine (L-NMMA, 10−4 mol/L) increased contractile responses only in arteries with endothelium. In preparations contracted with norepinephrine in the presence of guanethidine (10−6 mol/L) and atropine (10−6 mol/L), electrical stimulation induced frequency-dependent relaxations. This neurogenic relaxation was prevented by L-NMMA (10−4 mol/L) and tetrodotoxin (10−6 mol/L), but was unaffected by removal of the endothelium.
The results provide functional evidence that NO is released by autonomic nerves of the human gastroepiploic artery. We hypothesize that the release of NO from both endothelial and neurogenic origin may modulate resistance of the human gastroepiploic artery. Dysfunction in any of these sources of NO should be considered in some form of vasospasm.</abstract><cop>New York, NY</cop><pub>Elsevier Inc</pub><pmid>12517679</pmid><doi>10.1016/S0895-7061(02)03156-4</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
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source | Oxford Journals Online |
subjects | Aged Aged, 80 and over Anesthetics, Local - pharmacology Arginine - pharmacology Autonomic Nervous System - physiology Biological and medical sciences Blood vessels and receptors Endothelial factors Endothelium, Vascular - metabolism Enzyme Inhibitors - pharmacology Female Fundamental and applied biological sciences. Psychology Gastroepiploic Artery - innervation Gastroepiploic Artery - physiology human gastroepiploic artery Humans In Vitro Techniques Male Middle Aged neurotransmission nitric oxide Nitric Oxide - metabolism Nitric Oxide Synthase - antagonists & inhibitors omega-N-Methylarginine - pharmacology Tetrodotoxin - pharmacology Vasoconstriction - drug effects Vasoconstriction - physiology Vasodilation - drug effects Vasodilation - physiology Vertebrates: cardiovascular system |
title | Influence of nitric oxide on neurogenic contraction and relaxation of the human gastroepiploic artery |
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