Effect of ethanol consumption on blood pressure and rat mesenteric arterial bed, aorta and carotid responsiveness
This study investigates whether chronic ethanol consumption increases blood pressure and alters vascular reactivity in different tissues. Changes in reactivity to phenylephrine and acetylcholine were investigated in the aorta, carotid artery and mesenteric arterial bed (MAB) isolated from rats pretr...
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Veröffentlicht in: | Journal of pharmacy and pharmacology 2007-07, Vol.59 (7), p.985-993 |
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creator | Tirapelli, Carlos R. Leone, Andreia F. C. Coelho, Eduardo B. Resstel, Leonardo B. M. Corrêa, Fernando M. A. Lanchote, Vera L. Uyemura, Sergio A. Padovan, Cláudia M. de Oliveira, Ana M. |
description | This study investigates whether chronic ethanol consumption increases blood pressure and alters vascular reactivity in different tissues. Changes in reactivity to phenylephrine and acetylcholine were investigated in the aorta, carotid artery and mesenteric arterial bed (MAB) isolated from rats pretreated with ethanol for 2 or 6 weeks. Mild hypertension was observed in chronically ethanol‐treated rats, which was due to rises in both systolic and diastolic pressures. Chronic ethanol consumption increased the contractile response to phenylephrine of endothelium‐intact and denuded rat aortic rings from rats pretreated with ethanol for 2 or 6 weeks. Conversely, no differences were found in acetylcholine‐induced relaxation. Neither phenylephrine‐induced contraction nor acetylcholine‐induced relaxation were altered in the rat carotid. Six weeks' ethanol consumption enhanced the contractile response to phenylephrine of endothelium‐intact, but not denuded rat MAB. On the other hand, 2 weeks' ethanol consumption did not affect phenylephrine‐induced increase in perfusion pressure. Moreover, acetylcholine‐induced endothelium‐dependent relaxation in the MAB was reduced after treatment with ethanol for 6 weeks but not after 2 weeks. In conclusion, ethanol affects both blood pressure and vessel reactivity, but the effect on vascular reactivity may take longer to become apparent in MAB than in the aorta, and was not evident in the carotid. Moreover, we provide evidence that the effect of ethanol depends on the agonist and blood vessel studied. |
doi_str_mv | 10.1211/jpp.59.7.0011 |
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C. ; Coelho, Eduardo B. ; Resstel, Leonardo B. M. ; Corrêa, Fernando M. A. ; Lanchote, Vera L. ; Uyemura, Sergio A. ; Padovan, Cláudia M. ; de Oliveira, Ana M.</creator><creatorcontrib>Tirapelli, Carlos R. ; Leone, Andreia F. C. ; Coelho, Eduardo B. ; Resstel, Leonardo B. M. ; Corrêa, Fernando M. A. ; Lanchote, Vera L. ; Uyemura, Sergio A. ; Padovan, Cláudia M. ; de Oliveira, Ana M.</creatorcontrib><description>This study investigates whether chronic ethanol consumption increases blood pressure and alters vascular reactivity in different tissues. Changes in reactivity to phenylephrine and acetylcholine were investigated in the aorta, carotid artery and mesenteric arterial bed (MAB) isolated from rats pretreated with ethanol for 2 or 6 weeks. Mild hypertension was observed in chronically ethanol‐treated rats, which was due to rises in both systolic and diastolic pressures. Chronic ethanol consumption increased the contractile response to phenylephrine of endothelium‐intact and denuded rat aortic rings from rats pretreated with ethanol for 2 or 6 weeks. Conversely, no differences were found in acetylcholine‐induced relaxation. Neither phenylephrine‐induced contraction nor acetylcholine‐induced relaxation were altered in the rat carotid. Six weeks' ethanol consumption enhanced the contractile response to phenylephrine of endothelium‐intact, but not denuded rat MAB. On the other hand, 2 weeks' ethanol consumption did not affect phenylephrine‐induced increase in perfusion pressure. Moreover, acetylcholine‐induced endothelium‐dependent relaxation in the MAB was reduced after treatment with ethanol for 6 weeks but not after 2 weeks. In conclusion, ethanol affects both blood pressure and vessel reactivity, but the effect on vascular reactivity may take longer to become apparent in MAB than in the aorta, and was not evident in the carotid. Moreover, we provide evidence that the effect of ethanol depends on the agonist and blood vessel studied.</description><identifier>ISSN: 0022-3573</identifier><identifier>EISSN: 2042-7158</identifier><identifier>DOI: 10.1211/jpp.59.7.0011</identifier><identifier>PMID: 17637194</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Acetylcholine - pharmacology ; Analysis of Variance ; Animals ; Aorta, Thoracic - drug effects ; Aorta, Thoracic - physiology ; Blood Glucose - metabolism ; Blood Pressure - drug effects ; Carotid Arteries - drug effects ; Carotid Arteries - physiology ; Central Nervous System Depressants - blood ; Central Nervous System Depressants - pharmacokinetics ; Central Nervous System Depressants - pharmacology ; Endothelium, Vascular - physiology ; Ethanol - blood ; Ethanol - pharmacokinetics ; Ethanol - pharmacology ; Heart Rate - drug effects ; In Vitro Techniques ; Male ; Mesenteric Arteries - drug effects ; Mesenteric Arteries - physiology ; Muscle Contraction - drug effects ; Phenylephrine - pharmacology ; Rats ; Rats, Wistar ; Vasoconstrictor Agents - pharmacology ; Vasodilator Agents - pharmacology</subject><ispartof>Journal of pharmacy and pharmacology, 2007-07, Vol.59 (7), p.985-993</ispartof><rights>2007 Royal Pharmaceutical Society of Great Britain</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4128-529d4d1a66448fddc54a2165dd974eb649016649c053e31c4097f8f1b2c3d3c33</citedby><cites>FETCH-LOGICAL-c4128-529d4d1a66448fddc54a2165dd974eb649016649c053e31c4097f8f1b2c3d3c33</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1211%2Fjpp.59.7.0011$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1211%2Fjpp.59.7.0011$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>315,782,786,1419,27931,27932,45581,45582</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17637194$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Tirapelli, Carlos R.</creatorcontrib><creatorcontrib>Leone, Andreia F. C.</creatorcontrib><creatorcontrib>Coelho, Eduardo B.</creatorcontrib><creatorcontrib>Resstel, Leonardo B. M.</creatorcontrib><creatorcontrib>Corrêa, Fernando M. A.</creatorcontrib><creatorcontrib>Lanchote, Vera L.</creatorcontrib><creatorcontrib>Uyemura, Sergio A.</creatorcontrib><creatorcontrib>Padovan, Cláudia M.</creatorcontrib><creatorcontrib>de Oliveira, Ana M.</creatorcontrib><title>Effect of ethanol consumption on blood pressure and rat mesenteric arterial bed, aorta and carotid responsiveness</title><title>Journal of pharmacy and pharmacology</title><addtitle>J Pharm Pharmacol</addtitle><description>This study investigates whether chronic ethanol consumption increases blood pressure and alters vascular reactivity in different tissues. Changes in reactivity to phenylephrine and acetylcholine were investigated in the aorta, carotid artery and mesenteric arterial bed (MAB) isolated from rats pretreated with ethanol for 2 or 6 weeks. Mild hypertension was observed in chronically ethanol‐treated rats, which was due to rises in both systolic and diastolic pressures. Chronic ethanol consumption increased the contractile response to phenylephrine of endothelium‐intact and denuded rat aortic rings from rats pretreated with ethanol for 2 or 6 weeks. Conversely, no differences were found in acetylcholine‐induced relaxation. Neither phenylephrine‐induced contraction nor acetylcholine‐induced relaxation were altered in the rat carotid. Six weeks' ethanol consumption enhanced the contractile response to phenylephrine of endothelium‐intact, but not denuded rat MAB. On the other hand, 2 weeks' ethanol consumption did not affect phenylephrine‐induced increase in perfusion pressure. Moreover, acetylcholine‐induced endothelium‐dependent relaxation in the MAB was reduced after treatment with ethanol for 6 weeks but not after 2 weeks. In conclusion, ethanol affects both blood pressure and vessel reactivity, but the effect on vascular reactivity may take longer to become apparent in MAB than in the aorta, and was not evident in the carotid. Moreover, we provide evidence that the effect of ethanol depends on the agonist and blood vessel studied.</description><subject>Acetylcholine - pharmacology</subject><subject>Analysis of Variance</subject><subject>Animals</subject><subject>Aorta, Thoracic - drug effects</subject><subject>Aorta, Thoracic - physiology</subject><subject>Blood Glucose - metabolism</subject><subject>Blood Pressure - drug effects</subject><subject>Carotid Arteries - drug effects</subject><subject>Carotid Arteries - physiology</subject><subject>Central Nervous System Depressants - blood</subject><subject>Central Nervous System Depressants - pharmacokinetics</subject><subject>Central Nervous System Depressants - pharmacology</subject><subject>Endothelium, Vascular - physiology</subject><subject>Ethanol - blood</subject><subject>Ethanol - pharmacokinetics</subject><subject>Ethanol - pharmacology</subject><subject>Heart Rate - drug effects</subject><subject>In Vitro Techniques</subject><subject>Male</subject><subject>Mesenteric Arteries - drug effects</subject><subject>Mesenteric Arteries - physiology</subject><subject>Muscle Contraction - drug effects</subject><subject>Phenylephrine - pharmacology</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>Vasoconstrictor Agents - pharmacology</subject><subject>Vasodilator Agents - pharmacology</subject><issn>0022-3573</issn><issn>2042-7158</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kEFv1DAQRi1ERZfCkSvyiVOz9cR2nBxhVbatqlIhEEfLsSciJYlT26H03-NlV-0NzUhzmDdPo4-Qd8DWUAKc3c3zWjZrtWYM4AVZlUyUhQJZvyQrxsqy4FLxY_I6xjvGmKqq6hU5BlVxBY1YkfvzrkObqO8opp9m8gO1forLOKfeTzR3O3jv6BwwxiUgNZOjwSQ6YsQpYegtNWE3zUBbdKfU-JDMP8ya4FOfcYxzdva_ccqSN-SoM0PEt4d5Qr5_Pv-2uSiuv2wvNx-vCyugrAtZNk44MFUlRN05Z6UwJVTSuUYJbCvRMMi7xjLJkYMVrFFd3UFbWu645fyEfNh75-DvF4xJj320OAxmQr9ErViuGmQGiz1og48xYKfn0I8mPGpgepexzhlr2Wildxln_v1BvLQjumf6EGoG-B546Ad8_L9NX91e3AJX9fMbfUz45-nKhF-6UlxJ_eNmq9n2k_oKmyst-F_W5Zfd</recordid><startdate>200707</startdate><enddate>200707</enddate><creator>Tirapelli, Carlos R.</creator><creator>Leone, Andreia F. C.</creator><creator>Coelho, Eduardo B.</creator><creator>Resstel, Leonardo B. M.</creator><creator>Corrêa, Fernando M. A.</creator><creator>Lanchote, Vera L.</creator><creator>Uyemura, Sergio A.</creator><creator>Padovan, Cláudia M.</creator><creator>de Oliveira, Ana M.</creator><general>Blackwell Publishing Ltd</general><scope>BSCLL</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>200707</creationdate><title>Effect of ethanol consumption on blood pressure and rat mesenteric arterial bed, aorta and carotid responsiveness</title><author>Tirapelli, Carlos R. ; Leone, Andreia F. C. ; Coelho, Eduardo B. ; Resstel, Leonardo B. M. ; Corrêa, Fernando M. A. ; Lanchote, Vera L. ; Uyemura, Sergio A. ; Padovan, Cláudia M. ; de Oliveira, Ana M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4128-529d4d1a66448fddc54a2165dd974eb649016649c053e31c4097f8f1b2c3d3c33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Acetylcholine - pharmacology</topic><topic>Analysis of Variance</topic><topic>Animals</topic><topic>Aorta, Thoracic - drug effects</topic><topic>Aorta, Thoracic - physiology</topic><topic>Blood Glucose - metabolism</topic><topic>Blood Pressure - drug effects</topic><topic>Carotid Arteries - drug effects</topic><topic>Carotid Arteries - physiology</topic><topic>Central Nervous System Depressants - blood</topic><topic>Central Nervous System Depressants - pharmacokinetics</topic><topic>Central Nervous System Depressants - pharmacology</topic><topic>Endothelium, Vascular - physiology</topic><topic>Ethanol - blood</topic><topic>Ethanol - pharmacokinetics</topic><topic>Ethanol - pharmacology</topic><topic>Heart Rate - drug effects</topic><topic>In Vitro Techniques</topic><topic>Male</topic><topic>Mesenteric Arteries - drug effects</topic><topic>Mesenteric Arteries - physiology</topic><topic>Muscle Contraction - drug effects</topic><topic>Phenylephrine - pharmacology</topic><topic>Rats</topic><topic>Rats, Wistar</topic><topic>Vasoconstrictor Agents - pharmacology</topic><topic>Vasodilator Agents - pharmacology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tirapelli, Carlos R.</creatorcontrib><creatorcontrib>Leone, Andreia F. C.</creatorcontrib><creatorcontrib>Coelho, Eduardo B.</creatorcontrib><creatorcontrib>Resstel, Leonardo B. M.</creatorcontrib><creatorcontrib>Corrêa, Fernando M. A.</creatorcontrib><creatorcontrib>Lanchote, Vera L.</creatorcontrib><creatorcontrib>Uyemura, Sergio A.</creatorcontrib><creatorcontrib>Padovan, Cláudia M.</creatorcontrib><creatorcontrib>de Oliveira, Ana M.</creatorcontrib><collection>Istex</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 pharmacy and pharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tirapelli, Carlos R.</au><au>Leone, Andreia F. C.</au><au>Coelho, Eduardo B.</au><au>Resstel, Leonardo B. M.</au><au>Corrêa, Fernando M. A.</au><au>Lanchote, Vera L.</au><au>Uyemura, Sergio A.</au><au>Padovan, Cláudia M.</au><au>de Oliveira, Ana M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effect of ethanol consumption on blood pressure and rat mesenteric arterial bed, aorta and carotid responsiveness</atitle><jtitle>Journal of pharmacy and pharmacology</jtitle><addtitle>J Pharm Pharmacol</addtitle><date>2007-07</date><risdate>2007</risdate><volume>59</volume><issue>7</issue><spage>985</spage><epage>993</epage><pages>985-993</pages><issn>0022-3573</issn><eissn>2042-7158</eissn><abstract>This study investigates whether chronic ethanol consumption increases blood pressure and alters vascular reactivity in different tissues. Changes in reactivity to phenylephrine and acetylcholine were investigated in the aorta, carotid artery and mesenteric arterial bed (MAB) isolated from rats pretreated with ethanol for 2 or 6 weeks. Mild hypertension was observed in chronically ethanol‐treated rats, which was due to rises in both systolic and diastolic pressures. Chronic ethanol consumption increased the contractile response to phenylephrine of endothelium‐intact and denuded rat aortic rings from rats pretreated with ethanol for 2 or 6 weeks. Conversely, no differences were found in acetylcholine‐induced relaxation. Neither phenylephrine‐induced contraction nor acetylcholine‐induced relaxation were altered in the rat carotid. Six weeks' ethanol consumption enhanced the contractile response to phenylephrine of endothelium‐intact, but not denuded rat MAB. On the other hand, 2 weeks' ethanol consumption did not affect phenylephrine‐induced increase in perfusion pressure. Moreover, acetylcholine‐induced endothelium‐dependent relaxation in the MAB was reduced after treatment with ethanol for 6 weeks but not after 2 weeks. In conclusion, ethanol affects both blood pressure and vessel reactivity, but the effect on vascular reactivity may take longer to become apparent in MAB than in the aorta, and was not evident in the carotid. Moreover, we provide evidence that the effect of ethanol depends on the agonist and blood vessel studied.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>17637194</pmid><doi>10.1211/jpp.59.7.0011</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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source | MEDLINE; Access via Wiley Online Library; Oxford University Press Journals All Titles (1996-Current) |
subjects | Acetylcholine - pharmacology Analysis of Variance Animals Aorta, Thoracic - drug effects Aorta, Thoracic - physiology Blood Glucose - metabolism Blood Pressure - drug effects Carotid Arteries - drug effects Carotid Arteries - physiology Central Nervous System Depressants - blood Central Nervous System Depressants - pharmacokinetics Central Nervous System Depressants - pharmacology Endothelium, Vascular - physiology Ethanol - blood Ethanol - pharmacokinetics Ethanol - pharmacology Heart Rate - drug effects In Vitro Techniques Male Mesenteric Arteries - drug effects Mesenteric Arteries - physiology Muscle Contraction - drug effects Phenylephrine - pharmacology Rats Rats, Wistar Vasoconstrictor Agents - pharmacology Vasodilator Agents - pharmacology |
title | Effect of ethanol consumption on blood pressure and rat mesenteric arterial bed, aorta and carotid responsiveness |
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