Influence of Decompression Sickness on Vasomotion of Isolated Rat Vessels
Abstract Abstract Several studies have demonstrated that endothelial function is impaired following a dive even without decompression sickness. During this study we determined the effect of decompression sickness on endothelium-dependent and independent vasoreactivity. For this purpose twenty-seven...
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Veröffentlicht in: | International journal of sports medicine 2014-06, Vol.35 (7), p.551-558 |
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creator | Mazur, A. Lambrechts, K. Buzzacott, P. Wang, Q. Belhomme, M. Theron, M. Mansourati, J. Guerrero, F. |
description | Abstract
Abstract
Several studies have demonstrated that endothelial function is impaired following a dive even without decompression sickness. During this study we determined the effect of decompression sickness on endothelium-dependent and independent vasoreactivity. For this purpose twenty-seven male Sprague-Dawley rats were submitted to a simulated dive up to 1 000 kPa absolute pressure and divided into 3 groups: safe diving without decompression sickness or dives provoking mild or severe sickness. A fourth control group remained at atmospheric pressure. Endothelium-dependent and independent vasomotion was assessed ex vivo by measuring isometric tension in rings of abdominal aorta and mesenteric arteries. Dose-response curves were obtained with phenylephrine, acetylcholine and sodium nitroprusside. Acetylcholine-induced relaxation was measured in the presence of L-NAME, indometacin or both of them at once.Contraction was significantly decreased after each protocol compared with the control rats. Additionally, the response in animals from the severe group was significantly different from that of the safe and mild groups. Dose response curves for acetylcholine alone and in the presence of inhibitors remained unchanged. We did not observe differences in endothelium-dependent vasodilation after diving or in the presence of decompression sickness. Contractile response to phenylephrine was progressively impaired with increased decompression stress. These results may indicate smooth muscle injury. |
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Abstract
Several studies have demonstrated that endothelial function is impaired following a dive even without decompression sickness. During this study we determined the effect of decompression sickness on endothelium-dependent and independent vasoreactivity. For this purpose twenty-seven male Sprague-Dawley rats were submitted to a simulated dive up to 1 000 kPa absolute pressure and divided into 3 groups: safe diving without decompression sickness or dives provoking mild or severe sickness. A fourth control group remained at atmospheric pressure. Endothelium-dependent and independent vasomotion was assessed ex vivo by measuring isometric tension in rings of abdominal aorta and mesenteric arteries. Dose-response curves were obtained with phenylephrine, acetylcholine and sodium nitroprusside. Acetylcholine-induced relaxation was measured in the presence of L-NAME, indometacin or both of them at once.Contraction was significantly decreased after each protocol compared with the control rats. Additionally, the response in animals from the severe group was significantly different from that of the safe and mild groups. Dose response curves for acetylcholine alone and in the presence of inhibitors remained unchanged. We did not observe differences in endothelium-dependent vasodilation after diving or in the presence of decompression sickness. Contractile response to phenylephrine was progressively impaired with increased decompression stress. These results may indicate smooth muscle injury.</description><identifier>ISSN: 0172-4622</identifier><identifier>EISSN: 1439-3964</identifier><identifier>DOI: 10.1055/s-0033-1358472</identifier><identifier>PMID: 24258471</identifier><identifier>CODEN: IJSMDA</identifier><language>eng</language><publisher>Stuttgart · New York: Georg Thieme Verlag KG</publisher><subject>Acetylcholine - pharmacology ; Animals ; Biological and medical sciences ; Catecholamines - blood ; Decompression Sickness - physiopathology ; Disease Models, Animal ; Diving - adverse effects ; Dose-Response Relationship, Drug ; Endothelium, Vascular - physiology ; Enzyme Inhibitors - pharmacology ; Fundamental and applied biological sciences. Psychology ; Human health and pathology ; Human physiology applied to population studies and life conditions. Human ecophysiology ; Hydrocortisone - blood ; Indomethacin - pharmacology ; Life Sciences ; Male ; Medical sciences ; NG-Nitroarginine Methyl Ester - pharmacology ; Nitroprusside - pharmacology ; Phenylephrine - pharmacology ; Physiology & Biochemistry ; Rats, Sprague-Dawley ; Tissues and Organs ; Vasoconstriction - drug effects ; Vasoconstriction - physiology ; Vasoconstrictor Agents - pharmacology ; Vasodilation - drug effects ; Vasodilation - physiology ; Vasodilator Agents - pharmacology ; Vertebrates: body movement. Posture. Locomotion. Flight. Swimming. Physical exercise. Rest. Sports</subject><ispartof>International journal of sports medicine, 2014-06, Vol.35 (7), p.551-558</ispartof><rights>2015 INIST-CNRS</rights><rights>Georg Thieme Verlag KG Stuttgart · New York.</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c463t-11ae2a284ad81bbd09183732ea2366411f0b67e1acf4d61b4d1f77e2b284edbc3</citedby><orcidid>0000-0002-3338-5205 ; 0000-0002-9654-0268 ; 0000-0002-0283-3503</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.thieme-connect.de/products/ejournals/pdf/10.1055/s-0033-1358472.pdf$$EPDF$$P50$$Gthieme$$H</linktopdf><linktohtml>$$Uhttps://www.thieme-connect.de/products/ejournals/html/10.1055/s-0033-1358472$$EHTML$$P50$$Gthieme$$H</linktohtml><link.rule.ids>230,314,780,784,885,3017,3018,27924,27925,54559,54560</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=28506157$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24258471$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://hal.univ-brest.fr/hal-00912957$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Mazur, A.</creatorcontrib><creatorcontrib>Lambrechts, K.</creatorcontrib><creatorcontrib>Buzzacott, P.</creatorcontrib><creatorcontrib>Wang, Q.</creatorcontrib><creatorcontrib>Belhomme, M.</creatorcontrib><creatorcontrib>Theron, M.</creatorcontrib><creatorcontrib>Mansourati, J.</creatorcontrib><creatorcontrib>Guerrero, F.</creatorcontrib><title>Influence of Decompression Sickness on Vasomotion of Isolated Rat Vessels</title><title>International journal of sports medicine</title><addtitle>Int J Sports Med</addtitle><description>Abstract
Abstract
Several studies have demonstrated that endothelial function is impaired following a dive even without decompression sickness. During this study we determined the effect of decompression sickness on endothelium-dependent and independent vasoreactivity. For this purpose twenty-seven male Sprague-Dawley rats were submitted to a simulated dive up to 1 000 kPa absolute pressure and divided into 3 groups: safe diving without decompression sickness or dives provoking mild or severe sickness. A fourth control group remained at atmospheric pressure. Endothelium-dependent and independent vasomotion was assessed ex vivo by measuring isometric tension in rings of abdominal aorta and mesenteric arteries. Dose-response curves were obtained with phenylephrine, acetylcholine and sodium nitroprusside. Acetylcholine-induced relaxation was measured in the presence of L-NAME, indometacin or both of them at once.Contraction was significantly decreased after each protocol compared with the control rats. Additionally, the response in animals from the severe group was significantly different from that of the safe and mild groups. Dose response curves for acetylcholine alone and in the presence of inhibitors remained unchanged. We did not observe differences in endothelium-dependent vasodilation after diving or in the presence of decompression sickness. Contractile response to phenylephrine was progressively impaired with increased decompression stress. These results may indicate smooth muscle injury.</description><subject>Acetylcholine - pharmacology</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Catecholamines - blood</subject><subject>Decompression Sickness - physiopathology</subject><subject>Disease Models, Animal</subject><subject>Diving - adverse effects</subject><subject>Dose-Response Relationship, Drug</subject><subject>Endothelium, Vascular - physiology</subject><subject>Enzyme Inhibitors - pharmacology</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Human health and pathology</subject><subject>Human physiology applied to population studies and life conditions. Human ecophysiology</subject><subject>Hydrocortisone - blood</subject><subject>Indomethacin - pharmacology</subject><subject>Life Sciences</subject><subject>Male</subject><subject>Medical sciences</subject><subject>NG-Nitroarginine Methyl Ester - pharmacology</subject><subject>Nitroprusside - pharmacology</subject><subject>Phenylephrine - pharmacology</subject><subject>Physiology & Biochemistry</subject><subject>Rats, Sprague-Dawley</subject><subject>Tissues and Organs</subject><subject>Vasoconstriction - drug effects</subject><subject>Vasoconstriction - physiology</subject><subject>Vasoconstrictor Agents - pharmacology</subject><subject>Vasodilation - drug effects</subject><subject>Vasodilation - physiology</subject><subject>Vasodilator Agents - pharmacology</subject><subject>Vertebrates: body movement. Posture. Locomotion. Flight. Swimming. Physical exercise. Rest. Sports</subject><issn>0172-4622</issn><issn>1439-3964</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqF0U1P3DAQBmCrKipbyrXHKpdK7SHU48_kiKAtK62ERAtXy3EmIjSJt5kEiX-Po13ghDh5NHpmbPll7DPwE-Ba_6CccylzkLpQVrxjK1CyzGVp1Hu24mBFrowQh-wj0R3noEqQH9ihUGLxsGLr9dB0Mw4Bs9hk5xhivx2RqI1D9qcN_4ZUZ6m-8RT7OC3t5NYUOz9hnV35KbtJBDv6xA4a3xEe788jdv3r59-zi3xz-Xt9drrJgzJyygE8Ci8K5esCqqrmJRTSSoFeSGMUQMMrYxF8aFRtoFI1NNaiqNII1lWQR-z7bu-t79x2bHs_PrjoW3dxunFLj6eVotT2HpL9trPbMf6fkSbXtxSw6_yAcSYHRmoujdXqbaql1aUwhUn0ZEfDGIlGbJ6fAdwtqThySypun0oa-LLfPVc91s_8KYYEvu6Bp-C7ZvRDaOnFFZob0Da5fOem2xZ7dHdxHof02a9d_AifWqBz</recordid><startdate>20140601</startdate><enddate>20140601</enddate><creator>Mazur, A.</creator><creator>Lambrechts, K.</creator><creator>Buzzacott, P.</creator><creator>Wang, Q.</creator><creator>Belhomme, M.</creator><creator>Theron, M.</creator><creator>Mansourati, J.</creator><creator>Guerrero, F.</creator><general>Georg Thieme Verlag KG</general><general>Thieme</general><general>Thieme Publishing</general><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><scope>7TS</scope><scope>1XC</scope><orcidid>https://orcid.org/0000-0002-3338-5205</orcidid><orcidid>https://orcid.org/0000-0002-9654-0268</orcidid><orcidid>https://orcid.org/0000-0002-0283-3503</orcidid></search><sort><creationdate>20140601</creationdate><title>Influence of Decompression Sickness on Vasomotion of Isolated Rat Vessels</title><author>Mazur, A. ; Lambrechts, K. ; Buzzacott, P. ; Wang, Q. ; Belhomme, M. ; Theron, M. ; Mansourati, J. ; Guerrero, F.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c463t-11ae2a284ad81bbd09183732ea2366411f0b67e1acf4d61b4d1f77e2b284edbc3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Acetylcholine - pharmacology</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Catecholamines - blood</topic><topic>Decompression Sickness - physiopathology</topic><topic>Disease Models, Animal</topic><topic>Diving - adverse effects</topic><topic>Dose-Response Relationship, Drug</topic><topic>Endothelium, Vascular - physiology</topic><topic>Enzyme Inhibitors - pharmacology</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Human health and pathology</topic><topic>Human physiology applied to population studies and life conditions. Human ecophysiology</topic><topic>Hydrocortisone - blood</topic><topic>Indomethacin - pharmacology</topic><topic>Life Sciences</topic><topic>Male</topic><topic>Medical sciences</topic><topic>NG-Nitroarginine Methyl Ester - pharmacology</topic><topic>Nitroprusside - pharmacology</topic><topic>Phenylephrine - pharmacology</topic><topic>Physiology & Biochemistry</topic><topic>Rats, Sprague-Dawley</topic><topic>Tissues and Organs</topic><topic>Vasoconstriction - drug effects</topic><topic>Vasoconstriction - physiology</topic><topic>Vasoconstrictor Agents - pharmacology</topic><topic>Vasodilation - drug effects</topic><topic>Vasodilation - physiology</topic><topic>Vasodilator Agents - pharmacology</topic><topic>Vertebrates: body movement. Posture. Locomotion. Flight. Swimming. Physical exercise. Rest. Sports</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mazur, A.</creatorcontrib><creatorcontrib>Lambrechts, K.</creatorcontrib><creatorcontrib>Buzzacott, P.</creatorcontrib><creatorcontrib>Wang, Q.</creatorcontrib><creatorcontrib>Belhomme, M.</creatorcontrib><creatorcontrib>Theron, M.</creatorcontrib><creatorcontrib>Mansourati, J.</creatorcontrib><creatorcontrib>Guerrero, F.</creatorcontrib><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><collection>Physical Education Index</collection><collection>Hyper Article en Ligne (HAL)</collection><jtitle>International journal of sports medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mazur, A.</au><au>Lambrechts, K.</au><au>Buzzacott, P.</au><au>Wang, Q.</au><au>Belhomme, M.</au><au>Theron, M.</au><au>Mansourati, J.</au><au>Guerrero, F.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Influence of Decompression Sickness on Vasomotion of Isolated Rat Vessels</atitle><jtitle>International journal of sports medicine</jtitle><addtitle>Int J Sports Med</addtitle><date>2014-06-01</date><risdate>2014</risdate><volume>35</volume><issue>7</issue><spage>551</spage><epage>558</epage><pages>551-558</pages><issn>0172-4622</issn><eissn>1439-3964</eissn><coden>IJSMDA</coden><abstract>Abstract
Abstract
Several studies have demonstrated that endothelial function is impaired following a dive even without decompression sickness. During this study we determined the effect of decompression sickness on endothelium-dependent and independent vasoreactivity. For this purpose twenty-seven male Sprague-Dawley rats were submitted to a simulated dive up to 1 000 kPa absolute pressure and divided into 3 groups: safe diving without decompression sickness or dives provoking mild or severe sickness. A fourth control group remained at atmospheric pressure. Endothelium-dependent and independent vasomotion was assessed ex vivo by measuring isometric tension in rings of abdominal aorta and mesenteric arteries. Dose-response curves were obtained with phenylephrine, acetylcholine and sodium nitroprusside. Acetylcholine-induced relaxation was measured in the presence of L-NAME, indometacin or both of them at once.Contraction was significantly decreased after each protocol compared with the control rats. Additionally, the response in animals from the severe group was significantly different from that of the safe and mild groups. Dose response curves for acetylcholine alone and in the presence of inhibitors remained unchanged. We did not observe differences in endothelium-dependent vasodilation after diving or in the presence of decompression sickness. Contractile response to phenylephrine was progressively impaired with increased decompression stress. These results may indicate smooth muscle injury.</abstract><cop>Stuttgart · New York</cop><pub>Georg Thieme Verlag KG</pub><pmid>24258471</pmid><doi>10.1055/s-0033-1358472</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0002-3338-5205</orcidid><orcidid>https://orcid.org/0000-0002-9654-0268</orcidid><orcidid>https://orcid.org/0000-0002-0283-3503</orcidid></addata></record> |
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subjects | Acetylcholine - pharmacology Animals Biological and medical sciences Catecholamines - blood Decompression Sickness - physiopathology Disease Models, Animal Diving - adverse effects Dose-Response Relationship, Drug Endothelium, Vascular - physiology Enzyme Inhibitors - pharmacology Fundamental and applied biological sciences. Psychology Human health and pathology Human physiology applied to population studies and life conditions. Human ecophysiology Hydrocortisone - blood Indomethacin - pharmacology Life Sciences Male Medical sciences NG-Nitroarginine Methyl Ester - pharmacology Nitroprusside - pharmacology Phenylephrine - pharmacology Physiology & Biochemistry Rats, Sprague-Dawley Tissues and Organs Vasoconstriction - drug effects Vasoconstriction - physiology Vasoconstrictor Agents - pharmacology Vasodilation - drug effects Vasodilation - physiology Vasodilator Agents - pharmacology Vertebrates: body movement. Posture. Locomotion. Flight. Swimming. Physical exercise. Rest. Sports |
title | Influence of Decompression Sickness on Vasomotion of Isolated Rat Vessels |
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