Altered microvascular responses to C5a in rat striated muscle during two-kidney, one clip renovascular hypertension

OBJECTIVETo determine how two-kidney, one clip (2-K,1 C) renovascular hypertension alters microvascular responses in rat striated muscle to complement C5a, one of the most important inflammatory mediators. METHODS2-K,1C hypertension was induced in male Sprague-Dawley rats. Under anesthesia with pent...

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Veröffentlicht in:Journal of hypertension 1995-02, Vol.13 (2), p.227-234
Hauptverfasser: Yang, Sai, Luo, Hong Y, Wilson, Mark A, Wead, William B, Harri, Patrick D
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container_end_page 234
container_issue 2
container_start_page 227
container_title Journal of hypertension
container_volume 13
creator Yang, Sai
Luo, Hong Y
Wilson, Mark A
Wead, William B
Harri, Patrick D
description OBJECTIVETo determine how two-kidney, one clip (2-K,1 C) renovascular hypertension alters microvascular responses in rat striated muscle to complement C5a, one of the most important inflammatory mediators. METHODS2-K,1C hypertension was induced in male Sprague-Dawley rats. Under anesthesia with pentobarbital (50 mg/kg, intraperitoneally) the cremaster muscle microcirculatory preparation with intact neurovascular connections was studied in vivo by closed-circuit videomicroscopy. Recombinant human C5a was applied topically in the tissue bath at concentrations of 10 or 10 and 10mol/l, consecutively. Changes in the microvessel diameters in small arterioles, large arterioles and venules were measured. RESULTSIn normotensive rats complement C5a induces a significant dilation in small arterioles at low bath concentrations (10 or 10mol/l), but the dilation is attenuated at a higher concentration (10mol/1). In contrast, in 2-K,1C hypertensive rats C5a constricts small arterioles at a low concentration (10 or 10mol/1) but the dilates them at a higher concentration (10 mol/l). Large arterioles and venules have minimal responses to C5a in either normotensive or 2-K, 1C hypertensive rats. CONCLUSION2-K, 1C hypertension dramatically alters C5a-induced microvascular responses in small arterioles. The alteration might be attributable to the enhanced vasoconstrictor mechanisms and impaired vasodilator mechanisms during 2-K, 1C renovascular hypertension.
doi_str_mv 10.1097/00004872-199502000-00010
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METHODS2-K,1C hypertension was induced in male Sprague-Dawley rats. Under anesthesia with pentobarbital (50 mg/kg, intraperitoneally) the cremaster muscle microcirculatory preparation with intact neurovascular connections was studied in vivo by closed-circuit videomicroscopy. Recombinant human C5a was applied topically in the tissue bath at concentrations of 10 or 10 and 10mol/l, consecutively. Changes in the microvessel diameters in small arterioles, large arterioles and venules were measured. RESULTSIn normotensive rats complement C5a induces a significant dilation in small arterioles at low bath concentrations (10 or 10mol/l), but the dilation is attenuated at a higher concentration (10mol/1). In contrast, in 2-K,1C hypertensive rats C5a constricts small arterioles at a low concentration (10 or 10mol/1) but the dilates them at a higher concentration (10 mol/l). Large arterioles and venules have minimal responses to C5a in either normotensive or 2-K, 1C hypertensive rats. CONCLUSION2-K, 1C hypertension dramatically alters C5a-induced microvascular responses in small arterioles. The alteration might be attributable to the enhanced vasoconstrictor mechanisms and impaired vasodilator mechanisms during 2-K, 1C renovascular hypertension.</description><identifier>ISSN: 0263-6352</identifier><identifier>EISSN: 1473-5598</identifier><identifier>DOI: 10.1097/00004872-199502000-00010</identifier><identifier>PMID: 7615953</identifier><identifier>CODEN: JOHYD3</identifier><language>eng</language><publisher>Hagerstown, MD: Lippincott-Raven Publishers</publisher><subject>Animals ; Arterial hypertension. Arterial hypotension ; Biological and medical sciences ; Blood and lymphatic vessels ; Cardiology. Vascular system ; Clinical manifestations. Epidemiology. Investigative techniques. Etiology ; Complement C5a - pharmacology ; Hypertension, Renovascular - physiopathology ; Male ; Medical sciences ; Microcirculation - drug effects ; Microscopy, Video ; Muscle, Skeletal - blood supply ; Muscle, Skeletal - drug effects ; Rats ; Rats, Sprague-Dawley</subject><ispartof>Journal of hypertension, 1995-02, Vol.13 (2), p.227-234</ispartof><rights>Lippincott-Raven Publishers.</rights><rights>1995 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=3503665$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/7615953$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Yang, Sai</creatorcontrib><creatorcontrib>Luo, Hong Y</creatorcontrib><creatorcontrib>Wilson, Mark A</creatorcontrib><creatorcontrib>Wead, William B</creatorcontrib><creatorcontrib>Harri, Patrick D</creatorcontrib><title>Altered microvascular responses to C5a in rat striated muscle during two-kidney, one clip renovascular hypertension</title><title>Journal of hypertension</title><addtitle>J Hypertens</addtitle><description>OBJECTIVETo determine how two-kidney, one clip (2-K,1 C) renovascular hypertension alters microvascular responses in rat striated muscle to complement C5a, one of the most important inflammatory mediators. METHODS2-K,1C hypertension was induced in male Sprague-Dawley rats. Under anesthesia with pentobarbital (50 mg/kg, intraperitoneally) the cremaster muscle microcirculatory preparation with intact neurovascular connections was studied in vivo by closed-circuit videomicroscopy. Recombinant human C5a was applied topically in the tissue bath at concentrations of 10 or 10 and 10mol/l, consecutively. Changes in the microvessel diameters in small arterioles, large arterioles and venules were measured. RESULTSIn normotensive rats complement C5a induces a significant dilation in small arterioles at low bath concentrations (10 or 10mol/l), but the dilation is attenuated at a higher concentration (10mol/1). In contrast, in 2-K,1C hypertensive rats C5a constricts small arterioles at a low concentration (10 or 10mol/1) but the dilates them at a higher concentration (10 mol/l). Large arterioles and venules have minimal responses to C5a in either normotensive or 2-K, 1C hypertensive rats. CONCLUSION2-K, 1C hypertension dramatically alters C5a-induced microvascular responses in small arterioles. The alteration might be attributable to the enhanced vasoconstrictor mechanisms and impaired vasodilator mechanisms during 2-K, 1C renovascular hypertension.</description><subject>Animals</subject><subject>Arterial hypertension. Arterial hypotension</subject><subject>Biological and medical sciences</subject><subject>Blood and lymphatic vessels</subject><subject>Cardiology. Vascular system</subject><subject>Clinical manifestations. Epidemiology. Investigative techniques. Etiology</subject><subject>Complement C5a - pharmacology</subject><subject>Hypertension, Renovascular - physiopathology</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Microcirculation - drug effects</subject><subject>Microscopy, Video</subject><subject>Muscle, Skeletal - blood supply</subject><subject>Muscle, Skeletal - drug effects</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><issn>0263-6352</issn><issn>1473-5598</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1995</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kU2PFCEQhonRrOOuP8GEg_FkKx9N0xw3E7-STbzsnglDVzu4DLRUt5P598s443iShJBKPbyQpwihnH3gzOiPrK6216LhxigmatXUzdkzsuKtlo1Spn9OVkx0sumkEi_JK8SfFemNllfkSndcGSVXBG_jDAUGugu-5N8O_RJdoQVwygkB6ZzpWjkaEi1upjiX4OYjvqCPQIelhPSDzvvcPIYhweE9zQmoj2GqGelf4PYwQZkhYcjphrwYXUR4fT6vycPnT_frr83d9y_f1rd3jRdtyxozGse85EYJAxutaiU7pZ32YgTeDxutmWvNyL3zUDWMgnvDBB-04D3oUV6Td6fcqeRfC-BsdwE9xOgS5AWt1i2rkbqC_QmsChALjHYqYefKwXJmj77tX9_24tv-8V2vvjm_sWx2MFwungXX_ttzv5pwcSwu-YAXTKr6gU5VrD1h-3ycBz7GZQ_FbsHFeWv_N235BC20mO4</recordid><startdate>199502</startdate><enddate>199502</enddate><creator>Yang, Sai</creator><creator>Luo, Hong Y</creator><creator>Wilson, Mark A</creator><creator>Wead, William B</creator><creator>Harri, Patrick D</creator><general>Lippincott-Raven Publishers</general><general>Lippincott Williams &amp; Wilkins</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></search><sort><creationdate>199502</creationdate><title>Altered microvascular responses to C5a in rat striated muscle during two-kidney, one clip renovascular hypertension</title><author>Yang, Sai ; Luo, Hong Y ; Wilson, Mark A ; Wead, William B ; Harri, Patrick D</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2440-9f9a0c319529eb759a03657a7c2fe18db770a49f1cace995f21c9021d7218e7f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1995</creationdate><topic>Animals</topic><topic>Arterial hypertension. Arterial hypotension</topic><topic>Biological and medical sciences</topic><topic>Blood and lymphatic vessels</topic><topic>Cardiology. Vascular system</topic><topic>Clinical manifestations. Epidemiology. Investigative techniques. Etiology</topic><topic>Complement C5a - pharmacology</topic><topic>Hypertension, Renovascular - physiopathology</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Microcirculation - drug effects</topic><topic>Microscopy, Video</topic><topic>Muscle, Skeletal - blood supply</topic><topic>Muscle, Skeletal - drug effects</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yang, Sai</creatorcontrib><creatorcontrib>Luo, Hong Y</creatorcontrib><creatorcontrib>Wilson, Mark A</creatorcontrib><creatorcontrib>Wead, William B</creatorcontrib><creatorcontrib>Harri, Patrick D</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><jtitle>Journal of hypertension</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yang, Sai</au><au>Luo, Hong Y</au><au>Wilson, Mark A</au><au>Wead, William B</au><au>Harri, Patrick D</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Altered microvascular responses to C5a in rat striated muscle during two-kidney, one clip renovascular hypertension</atitle><jtitle>Journal of hypertension</jtitle><addtitle>J Hypertens</addtitle><date>1995-02</date><risdate>1995</risdate><volume>13</volume><issue>2</issue><spage>227</spage><epage>234</epage><pages>227-234</pages><issn>0263-6352</issn><eissn>1473-5598</eissn><coden>JOHYD3</coden><abstract>OBJECTIVETo determine how two-kidney, one clip (2-K,1 C) renovascular hypertension alters microvascular responses in rat striated muscle to complement C5a, one of the most important inflammatory mediators. METHODS2-K,1C hypertension was induced in male Sprague-Dawley rats. Under anesthesia with pentobarbital (50 mg/kg, intraperitoneally) the cremaster muscle microcirculatory preparation with intact neurovascular connections was studied in vivo by closed-circuit videomicroscopy. Recombinant human C5a was applied topically in the tissue bath at concentrations of 10 or 10 and 10mol/l, consecutively. Changes in the microvessel diameters in small arterioles, large arterioles and venules were measured. RESULTSIn normotensive rats complement C5a induces a significant dilation in small arterioles at low bath concentrations (10 or 10mol/l), but the dilation is attenuated at a higher concentration (10mol/1). In contrast, in 2-K,1C hypertensive rats C5a constricts small arterioles at a low concentration (10 or 10mol/1) but the dilates them at a higher concentration (10 mol/l). Large arterioles and venules have minimal responses to C5a in either normotensive or 2-K, 1C hypertensive rats. CONCLUSION2-K, 1C hypertension dramatically alters C5a-induced microvascular responses in small arterioles. The alteration might be attributable to the enhanced vasoconstrictor mechanisms and impaired vasodilator mechanisms during 2-K, 1C renovascular hypertension.</abstract><cop>Hagerstown, MD</cop><pub>Lippincott-Raven Publishers</pub><pmid>7615953</pmid><doi>10.1097/00004872-199502000-00010</doi><tpages>8</tpages></addata></record>
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subjects Animals
Arterial hypertension. Arterial hypotension
Biological and medical sciences
Blood and lymphatic vessels
Cardiology. Vascular system
Clinical manifestations. Epidemiology. Investigative techniques. Etiology
Complement C5a - pharmacology
Hypertension, Renovascular - physiopathology
Male
Medical sciences
Microcirculation - drug effects
Microscopy, Video
Muscle, Skeletal - blood supply
Muscle, Skeletal - drug effects
Rats
Rats, Sprague-Dawley
title Altered microvascular responses to C5a in rat striated muscle during two-kidney, one clip renovascular hypertension
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