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Characterization of endothelium-dependent vasodilation and vasoconstriction in coronary arteries from spontaneously hypertensive rats
Coronary artery disease often occurs in patients with hypertension. The present study was designed to evaluate coronary vascular function in isolated coronary arteries of spontaneously hypertensive rats (SHR) and Wistar-Kyoto (WKY) rats and to determine the effect of antihypertensive treatment on co...
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Published in: | American journal of hypertension 1996-05, Vol.9 (5), p.475-483 |
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description | Coronary artery disease often occurs in patients with hypertension. The present study was designed to evaluate coronary vascular function in isolated coronary arteries of spontaneously hypertensive rats (SHR) and Wistar-Kyoto (WKY) rats and to determine the effect of antihypertensive treatment on coronary vascular responsiveness. Male SHR and WKY rats (12 to 14 weeks old) were divided into control and hydralazine-treated (120 mg/L drinking water for 10 days) groups. After 10 days, arterial pressure and heart rate were recorded while rats were conscious and unrestrained. Left ventricular coronary arteries (200 to 300 μm diameter) were isolated and intraluminal diameter was continuously recorded while vessels were maintained at a constant intraluminal pressure of 40 mm Hg. Relaxation of coronary arteries to both acetylcholine and nitroprusside was slightly, but significantly, enhanced in vessels from SHR compared to WKY rats. The enhanced relaxation was a specific effect, since isoproterenol induced similar relaxation in coronary arteries from SHR and WKY rats. Contraction to phenylephrine, but not endothelin-1, was augmented in coronary arteries from SHR compared to WKY rats. Treatment with hydralazine significantly lowered arterial pressure in SHR and WKY rats, but did not alter the enhanced contraction to phenylephrine or the enhanced relaxation to acetylcholine and nitroprusside in coronary arteries from SHR. These results indicate that coronary arteries of 12 to 14 week-old SHR do not have impaired endothelium-dependent relaxation, but do exhibit enhanced α-adrenoreceptor-mediated contraction that is not reduced by lowering arterial pressure. |
doi_str_mv | 10.1016/0895-7061(95)00441-6 |
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The present study was designed to evaluate coronary vascular function in isolated coronary arteries of spontaneously hypertensive rats (SHR) and Wistar-Kyoto (WKY) rats and to determine the effect of antihypertensive treatment on coronary vascular responsiveness. Male SHR and WKY rats (12 to 14 weeks old) were divided into control and hydralazine-treated (120 mg/L drinking water for 10 days) groups. After 10 days, arterial pressure and heart rate were recorded while rats were conscious and unrestrained. Left ventricular coronary arteries (200 to 300 μm diameter) were isolated and intraluminal diameter was continuously recorded while vessels were maintained at a constant intraluminal pressure of 40 mm Hg. Relaxation of coronary arteries to both acetylcholine and nitroprusside was slightly, but significantly, enhanced in vessels from SHR compared to WKY rats. The enhanced relaxation was a specific effect, since isoproterenol induced similar relaxation in coronary arteries from SHR and WKY rats. Contraction to phenylephrine, but not endothelin-1, was augmented in coronary arteries from SHR compared to WKY rats. Treatment with hydralazine significantly lowered arterial pressure in SHR and WKY rats, but did not alter the enhanced contraction to phenylephrine or the enhanced relaxation to acetylcholine and nitroprusside in coronary arteries from SHR. These results indicate that coronary arteries of 12 to 14 week-old SHR do not have impaired endothelium-dependent relaxation, but do exhibit enhanced α-adrenoreceptor-mediated contraction that is not reduced by lowering arterial pressure.</description><identifier>ISSN: 0895-7061</identifier><identifier>EISSN: 1879-1905</identifier><identifier>EISSN: 1941-7225</identifier><identifier>DOI: 10.1016/0895-7061(95)00441-6</identifier><identifier>PMID: 8735179</identifier><language>eng</language><publisher>New York, NY: Elsevier Inc</publisher><subject>acetylcholine ; Adrenergic alpha-Agonists - pharmacology ; Animals ; Arterial hypertension. Arterial hypotension ; Biological and medical sciences ; Blood and lymphatic vessels ; Blood Pressure - drug effects ; Cardiology. Vascular system ; coronary arterioles ; Coronary Vessels - anatomy & histology ; Coronary Vessels - physiology ; endothelin-1 ; Endothelium, Vascular - physiology ; Experimental diseases ; Heart Rate - drug effects ; hydralazine ; Hydralazine - pharmacology ; Hypertension - genetics ; Hypertension - physiopathology ; In Vitro Techniques ; isoproterenol ; Isoproterenol - pharmacology ; Male ; Medical sciences ; Muscle, Smooth, Vascular - drug effects ; phenylephrine ; Phenylephrine - pharmacology ; Rats ; Rats, Inbred SHR ; Rats, Inbred WKY ; Receptors, Adrenergic, alpha - drug effects ; Receptors, Adrenergic, alpha - physiology ; Space life sciences ; Spontaneously hypertensive rats ; Vasoconstriction - drug effects ; Vasoconstriction - physiology ; Vasoconstrictor Agents - pharmacology ; Vasodilation - drug effects ; Vasodilation - physiology ; Vasodilator Agents - pharmacology ; Wistar-Kyoto rats</subject><ispartof>American journal of hypertension, 1996-05, Vol.9 (5), p.475-483</ispartof><rights>1996</rights><rights>1996 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c494t-64cd1dde7dc8fbed7c212b478ba4758ccb04ae73d07146601214ba28854e7633</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27922,27923</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=3087124$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/8735179$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Fuchs, Leslie C.</creatorcontrib><creatorcontrib>Nuno, Dan</creatorcontrib><creatorcontrib>Lamping, Kathryn G.</creatorcontrib><creatorcontrib>Kim Johnson, Alan</creatorcontrib><title>Characterization of endothelium-dependent vasodilation and vasoconstriction in coronary arteries from spontaneously hypertensive rats</title><title>American journal of hypertension</title><addtitle>AJH</addtitle><description>Coronary artery disease often occurs in patients with hypertension. The present study was designed to evaluate coronary vascular function in isolated coronary arteries of spontaneously hypertensive rats (SHR) and Wistar-Kyoto (WKY) rats and to determine the effect of antihypertensive treatment on coronary vascular responsiveness. Male SHR and WKY rats (12 to 14 weeks old) were divided into control and hydralazine-treated (120 mg/L drinking water for 10 days) groups. After 10 days, arterial pressure and heart rate were recorded while rats were conscious and unrestrained. Left ventricular coronary arteries (200 to 300 μm diameter) were isolated and intraluminal diameter was continuously recorded while vessels were maintained at a constant intraluminal pressure of 40 mm Hg. Relaxation of coronary arteries to both acetylcholine and nitroprusside was slightly, but significantly, enhanced in vessels from SHR compared to WKY rats. The enhanced relaxation was a specific effect, since isoproterenol induced similar relaxation in coronary arteries from SHR and WKY rats. Contraction to phenylephrine, but not endothelin-1, was augmented in coronary arteries from SHR compared to WKY rats. Treatment with hydralazine significantly lowered arterial pressure in SHR and WKY rats, but did not alter the enhanced contraction to phenylephrine or the enhanced relaxation to acetylcholine and nitroprusside in coronary arteries from SHR. These results indicate that coronary arteries of 12 to 14 week-old SHR do not have impaired endothelium-dependent relaxation, but do exhibit enhanced α-adrenoreceptor-mediated contraction that is not reduced by lowering arterial pressure.</description><subject>acetylcholine</subject><subject>Adrenergic alpha-Agonists - pharmacology</subject><subject>Animals</subject><subject>Arterial hypertension. Arterial hypotension</subject><subject>Biological and medical sciences</subject><subject>Blood and lymphatic vessels</subject><subject>Blood Pressure - drug effects</subject><subject>Cardiology. Vascular system</subject><subject>coronary arterioles</subject><subject>Coronary Vessels - anatomy & histology</subject><subject>Coronary Vessels - physiology</subject><subject>endothelin-1</subject><subject>Endothelium, Vascular - physiology</subject><subject>Experimental diseases</subject><subject>Heart Rate - drug effects</subject><subject>hydralazine</subject><subject>Hydralazine - pharmacology</subject><subject>Hypertension - genetics</subject><subject>Hypertension - physiopathology</subject><subject>In Vitro Techniques</subject><subject>isoproterenol</subject><subject>Isoproterenol - pharmacology</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Muscle, Smooth, Vascular - drug effects</subject><subject>phenylephrine</subject><subject>Phenylephrine - pharmacology</subject><subject>Rats</subject><subject>Rats, Inbred SHR</subject><subject>Rats, Inbred WKY</subject><subject>Receptors, Adrenergic, alpha - drug effects</subject><subject>Receptors, Adrenergic, alpha - physiology</subject><subject>Space life sciences</subject><subject>Spontaneously hypertensive rats</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>Wistar-Kyoto rats</subject><issn>0895-7061</issn><issn>1879-1905</issn><issn>1941-7225</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1996</creationdate><recordtype>article</recordtype><recordid>eNp9kM2O0zAUhSMEGsrAG4DIAiFYBOzEf9kgoQpm0FRiwSwQG8uxb1QPiZ2xnYqy571xm6rsWF35nu8e-ZyieI7RO4wwe49ESyuOGH7T0rcIEYIr9qBYYcHbCreIPixWZ-Rx8STGO5QpxvBFcSF4QzFvV8Wf9VYFpRME-1sl613p-xKc8WkLg53HysCUn-BSuVPRGzsslHLmuNDexRSsPi6tK7UP3qmwL1U4eEIs--DHMk7eJeXAz3HYl9v9BFl20e6gDCrFp8WjXg0Rnp3mZXH7-dPt-rrafL36sv64qTRpSaoY0QYbA9xo0XdguK5x3REuOkU4FVp3iCjgjUEc56AI15h0qhaCEuCsaS6L14vtFPz9DDHJ0UYNw7D8THJR14JSlEGygDr4GAP0cgp2zLEkRvJQvjw0Kw_NyjyP5UuWz16c_OduBHM-OrWd9VcnXUWthj4op208Yw0SHNckYy8XzKk0Bzjr6m6L25ZRkYlqIWxM8OsfEH5KxhtO5fX3H_Jmgym5EjfyW-Y_LDzkcncWgozagtNgbACdpPH2_8n-ApF1vsM</recordid><startdate>19960501</startdate><enddate>19960501</enddate><creator>Fuchs, Leslie C.</creator><creator>Nuno, Dan</creator><creator>Lamping, Kathryn G.</creator><creator>Kim Johnson, Alan</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>7X8</scope></search><sort><creationdate>19960501</creationdate><title>Characterization of endothelium-dependent vasodilation and vasoconstriction in coronary arteries from spontaneously hypertensive rats</title><author>Fuchs, Leslie C. ; Nuno, Dan ; Lamping, Kathryn G. ; Kim Johnson, Alan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c494t-64cd1dde7dc8fbed7c212b478ba4758ccb04ae73d07146601214ba28854e7633</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1996</creationdate><topic>acetylcholine</topic><topic>Adrenergic alpha-Agonists - pharmacology</topic><topic>Animals</topic><topic>Arterial hypertension. Arterial hypotension</topic><topic>Biological and medical sciences</topic><topic>Blood and lymphatic vessels</topic><topic>Blood Pressure - drug effects</topic><topic>Cardiology. Vascular system</topic><topic>coronary arterioles</topic><topic>Coronary Vessels - anatomy & histology</topic><topic>Coronary Vessels - physiology</topic><topic>endothelin-1</topic><topic>Endothelium, Vascular - physiology</topic><topic>Experimental diseases</topic><topic>Heart Rate - drug effects</topic><topic>hydralazine</topic><topic>Hydralazine - pharmacology</topic><topic>Hypertension - genetics</topic><topic>Hypertension - physiopathology</topic><topic>In Vitro Techniques</topic><topic>isoproterenol</topic><topic>Isoproterenol - pharmacology</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Muscle, Smooth, Vascular - drug effects</topic><topic>phenylephrine</topic><topic>Phenylephrine - pharmacology</topic><topic>Rats</topic><topic>Rats, Inbred SHR</topic><topic>Rats, Inbred WKY</topic><topic>Receptors, Adrenergic, alpha - drug effects</topic><topic>Receptors, Adrenergic, alpha - physiology</topic><topic>Space life sciences</topic><topic>Spontaneously hypertensive rats</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>Wistar-Kyoto rats</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Fuchs, Leslie C.</creatorcontrib><creatorcontrib>Nuno, Dan</creatorcontrib><creatorcontrib>Lamping, Kathryn G.</creatorcontrib><creatorcontrib>Kim Johnson, Alan</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>MEDLINE - Academic</collection><jtitle>American journal of hypertension</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Fuchs, Leslie C.</au><au>Nuno, Dan</au><au>Lamping, Kathryn G.</au><au>Kim Johnson, Alan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Characterization of endothelium-dependent vasodilation and vasoconstriction in coronary arteries from spontaneously hypertensive rats</atitle><jtitle>American journal of hypertension</jtitle><addtitle>AJH</addtitle><date>1996-05-01</date><risdate>1996</risdate><volume>9</volume><issue>5</issue><spage>475</spage><epage>483</epage><pages>475-483</pages><issn>0895-7061</issn><eissn>1879-1905</eissn><eissn>1941-7225</eissn><abstract>Coronary artery disease often occurs in patients with hypertension. The present study was designed to evaluate coronary vascular function in isolated coronary arteries of spontaneously hypertensive rats (SHR) and Wistar-Kyoto (WKY) rats and to determine the effect of antihypertensive treatment on coronary vascular responsiveness. Male SHR and WKY rats (12 to 14 weeks old) were divided into control and hydralazine-treated (120 mg/L drinking water for 10 days) groups. After 10 days, arterial pressure and heart rate were recorded while rats were conscious and unrestrained. Left ventricular coronary arteries (200 to 300 μm diameter) were isolated and intraluminal diameter was continuously recorded while vessels were maintained at a constant intraluminal pressure of 40 mm Hg. Relaxation of coronary arteries to both acetylcholine and nitroprusside was slightly, but significantly, enhanced in vessels from SHR compared to WKY rats. The enhanced relaxation was a specific effect, since isoproterenol induced similar relaxation in coronary arteries from SHR and WKY rats. Contraction to phenylephrine, but not endothelin-1, was augmented in coronary arteries from SHR compared to WKY rats. Treatment with hydralazine significantly lowered arterial pressure in SHR and WKY rats, but did not alter the enhanced contraction to phenylephrine or the enhanced relaxation to acetylcholine and nitroprusside in coronary arteries from SHR. These results indicate that coronary arteries of 12 to 14 week-old SHR do not have impaired endothelium-dependent relaxation, but do exhibit enhanced α-adrenoreceptor-mediated contraction that is not reduced by lowering arterial pressure.</abstract><cop>New York, NY</cop><pub>Elsevier Inc</pub><pmid>8735179</pmid><doi>10.1016/0895-7061(95)00441-6</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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subjects | acetylcholine Adrenergic alpha-Agonists - pharmacology Animals Arterial hypertension. Arterial hypotension Biological and medical sciences Blood and lymphatic vessels Blood Pressure - drug effects Cardiology. Vascular system coronary arterioles Coronary Vessels - anatomy & histology Coronary Vessels - physiology endothelin-1 Endothelium, Vascular - physiology Experimental diseases Heart Rate - drug effects hydralazine Hydralazine - pharmacology Hypertension - genetics Hypertension - physiopathology In Vitro Techniques isoproterenol Isoproterenol - pharmacology Male Medical sciences Muscle, Smooth, Vascular - drug effects phenylephrine Phenylephrine - pharmacology Rats Rats, Inbred SHR Rats, Inbred WKY Receptors, Adrenergic, alpha - drug effects Receptors, Adrenergic, alpha - physiology Space life sciences Spontaneously hypertensive rats Vasoconstriction - drug effects Vasoconstriction - physiology Vasoconstrictor Agents - pharmacology Vasodilation - drug effects Vasodilation - physiology Vasodilator Agents - pharmacology Wistar-Kyoto rats |
title | Characterization of endothelium-dependent vasodilation and vasoconstriction in coronary arteries from spontaneously hypertensive rats |
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