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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
Main Authors: Fuchs, Leslie C., Nuno, Dan, Lamping, Kathryn G., Kim Johnson, Alan
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Nuno, Dan
Lamping, Kathryn G.
Kim Johnson, Alan
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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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 &amp; 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 &amp; 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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identifier ISSN: 0895-7061
ispartof American journal of hypertension, 1996-05, Vol.9 (5), p.475-483
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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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