Understanding the coronary circulation through studies at the microvascular level
Studies of the coronary circulation have divided vascular resistances into three large components: large vessels, small resistance vessels, and veins. Studies of the epicardial microcirculation in the beating heart using stroboscopic illumination have suggested that resistance is more precisely cont...
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Veröffentlicht in: | Circulation (New York, N.Y.) N.Y.), 1990-07, Vol.82 (1), p.1-7 |
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creator | MARCUS, M. L CHILIAN, W. M KANATSUKA, H DELLSPERGER, K. C EASTHAM, C. L LAMPING, K. G |
description | Studies of the coronary circulation have divided vascular resistances into three large components: large vessels, small resistance vessels, and veins. Studies of the epicardial microcirculation in the beating heart using stroboscopic illumination have suggested that resistance is more precisely controlled in different segments of the circulation. Measurements of coronary pressure in different sized arteries and arterioles have indicated that under normal conditions, 45-50% of total coronary vascular resistance resides in vessels larger than 100 microns. This distribution of vascular resistance can be altered in a nonuniform manner by a variety of physiological (autoregulation, increases in myocardial oxygen consumption, sympathetic stimulation) and pharmacological stimuli (norepinephrine, papaverine, dipyridamole, serotonin, vasopressin, nitroglycerin, adenosine, and endothelin). Studies of exchange of macromolecules in the microcirculation using fluorescent-labeled dextrans have also identified the size of the small pore (35-50 A) in coronary microvessels that can be altered by myocardial ischemia. Studies of the coronary microcirculation have demonstrated that the control of vascular resistance is extremely complex, and mechanisms responsible for these heterogeneous responses need further examination. |
doi_str_mv | 10.1161/01.cir.82.1.1 |
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L ; CHILIAN, W. M ; KANATSUKA, H ; DELLSPERGER, K. C ; EASTHAM, C. L ; LAMPING, K. G</creator><creatorcontrib>MARCUS, M. L ; CHILIAN, W. M ; KANATSUKA, H ; DELLSPERGER, K. C ; EASTHAM, C. L ; LAMPING, K. G</creatorcontrib><description>Studies of the coronary circulation have divided vascular resistances into three large components: large vessels, small resistance vessels, and veins. Studies of the epicardial microcirculation in the beating heart using stroboscopic illumination have suggested that resistance is more precisely controlled in different segments of the circulation. Measurements of coronary pressure in different sized arteries and arterioles have indicated that under normal conditions, 45-50% of total coronary vascular resistance resides in vessels larger than 100 microns. This distribution of vascular resistance can be altered in a nonuniform manner by a variety of physiological (autoregulation, increases in myocardial oxygen consumption, sympathetic stimulation) and pharmacological stimuli (norepinephrine, papaverine, dipyridamole, serotonin, vasopressin, nitroglycerin, adenosine, and endothelin). Studies of exchange of macromolecules in the microcirculation using fluorescent-labeled dextrans have also identified the size of the small pore (35-50 A) in coronary microvessels that can be altered by myocardial ischemia. Studies of the coronary microcirculation have demonstrated that the control of vascular resistance is extremely complex, and mechanisms responsible for these heterogeneous responses need further examination.</description><identifier>ISSN: 0009-7322</identifier><identifier>EISSN: 1524-4539</identifier><identifier>DOI: 10.1161/01.cir.82.1.1</identifier><identifier>PMID: 2114232</identifier><identifier>CODEN: CIRCAZ</identifier><language>eng</language><publisher>Hagerstown, MD: Lippincott Williams & Wilkins</publisher><subject>Animals ; Biological and medical sciences ; Blood Pressure ; Cardiology. Vascular system ; Coronary Circulation - drug effects ; Coronary Vessels - physiology ; Homeostasis ; Humans ; Medical sciences ; Microcirculation ; Nervous System Physiological Phenomena ; Nifedipine - pharmacology ; Nitroglycerin - pharmacology ; Vascular Resistance ; Vasodilation - physiology</subject><ispartof>Circulation (New York, N.Y.), 1990-07, Vol.82 (1), p.1-7</ispartof><rights>1993 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c421t-38e2d83eea94dd41b17b3c5d3136a81619f31be5889df67d751ded7a9c012f393</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,3687,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=4613068$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/2114232$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>MARCUS, M. L</creatorcontrib><creatorcontrib>CHILIAN, W. M</creatorcontrib><creatorcontrib>KANATSUKA, H</creatorcontrib><creatorcontrib>DELLSPERGER, K. C</creatorcontrib><creatorcontrib>EASTHAM, C. L</creatorcontrib><creatorcontrib>LAMPING, K. G</creatorcontrib><title>Understanding the coronary circulation through studies at the microvascular level</title><title>Circulation (New York, N.Y.)</title><addtitle>Circulation</addtitle><description>Studies of the coronary circulation have divided vascular resistances into three large components: large vessels, small resistance vessels, and veins. Studies of the epicardial microcirculation in the beating heart using stroboscopic illumination have suggested that resistance is more precisely controlled in different segments of the circulation. Measurements of coronary pressure in different sized arteries and arterioles have indicated that under normal conditions, 45-50% of total coronary vascular resistance resides in vessels larger than 100 microns. This distribution of vascular resistance can be altered in a nonuniform manner by a variety of physiological (autoregulation, increases in myocardial oxygen consumption, sympathetic stimulation) and pharmacological stimuli (norepinephrine, papaverine, dipyridamole, serotonin, vasopressin, nitroglycerin, adenosine, and endothelin). Studies of exchange of macromolecules in the microcirculation using fluorescent-labeled dextrans have also identified the size of the small pore (35-50 A) in coronary microvessels that can be altered by myocardial ischemia. Studies of the coronary microcirculation have demonstrated that the control of vascular resistance is extremely complex, and mechanisms responsible for these heterogeneous responses need further examination.</description><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Blood Pressure</subject><subject>Cardiology. Vascular system</subject><subject>Coronary Circulation - drug effects</subject><subject>Coronary Vessels - physiology</subject><subject>Homeostasis</subject><subject>Humans</subject><subject>Medical sciences</subject><subject>Microcirculation</subject><subject>Nervous System Physiological Phenomena</subject><subject>Nifedipine - pharmacology</subject><subject>Nitroglycerin - pharmacology</subject><subject>Vascular Resistance</subject><subject>Vasodilation - physiology</subject><issn>0009-7322</issn><issn>1524-4539</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1990</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo9kN1LwzAUxYMoc04ffRT6IL615ib9SB5l-DEYiOKeQ5rcbpWunUk78L83c2VPl8P5cbjnEHILNAHI4ZFCYmqXCJZAAmdkChlL4zTj8pxMKaUyLjhjl-TK--8gc15kEzJhACnjbEo-Vq1F53vd2rpdR_0GI9O5rtXuNwqxZmh0X3dtMFw3rDeR7wdbo490_89ua-O6vfYHzkUN7rG5JheVbjzejHdGVi_PX_O3ePn-upg_LWOTMuhjLpBZwRG1TK1NoYSi5CazHHiuRSgmKw4lZkJIW-WFLTKwaAstDQVWccln5OGYu3Pdz4C-V9vaG2wa3WI3eFVIkUkmD2B8BMOr3jus1M7V21BQAVWHCRUFNV98KsEUKAj83Rg8lFu0J3rcLPj3ox9666ZyujW1P2FpDpzmgv8BmGl6NA</recordid><startdate>19900701</startdate><enddate>19900701</enddate><creator>MARCUS, M. 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G</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c421t-38e2d83eea94dd41b17b3c5d3136a81619f31be5889df67d751ded7a9c012f393</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1990</creationdate><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Blood Pressure</topic><topic>Cardiology. Vascular system</topic><topic>Coronary Circulation - drug effects</topic><topic>Coronary Vessels - physiology</topic><topic>Homeostasis</topic><topic>Humans</topic><topic>Medical sciences</topic><topic>Microcirculation</topic><topic>Nervous System Physiological Phenomena</topic><topic>Nifedipine - pharmacology</topic><topic>Nitroglycerin - pharmacology</topic><topic>Vascular Resistance</topic><topic>Vasodilation - physiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>MARCUS, M. L</creatorcontrib><creatorcontrib>CHILIAN, W. M</creatorcontrib><creatorcontrib>KANATSUKA, H</creatorcontrib><creatorcontrib>DELLSPERGER, K. C</creatorcontrib><creatorcontrib>EASTHAM, C. L</creatorcontrib><creatorcontrib>LAMPING, K. G</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>Circulation (New York, N.Y.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>MARCUS, M. L</au><au>CHILIAN, W. M</au><au>KANATSUKA, H</au><au>DELLSPERGER, K. C</au><au>EASTHAM, C. L</au><au>LAMPING, K. G</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Understanding the coronary circulation through studies at the microvascular level</atitle><jtitle>Circulation (New York, N.Y.)</jtitle><addtitle>Circulation</addtitle><date>1990-07-01</date><risdate>1990</risdate><volume>82</volume><issue>1</issue><spage>1</spage><epage>7</epage><pages>1-7</pages><issn>0009-7322</issn><eissn>1524-4539</eissn><coden>CIRCAZ</coden><abstract>Studies of the coronary circulation have divided vascular resistances into three large components: large vessels, small resistance vessels, and veins. Studies of the epicardial microcirculation in the beating heart using stroboscopic illumination have suggested that resistance is more precisely controlled in different segments of the circulation. Measurements of coronary pressure in different sized arteries and arterioles have indicated that under normal conditions, 45-50% of total coronary vascular resistance resides in vessels larger than 100 microns. This distribution of vascular resistance can be altered in a nonuniform manner by a variety of physiological (autoregulation, increases in myocardial oxygen consumption, sympathetic stimulation) and pharmacological stimuli (norepinephrine, papaverine, dipyridamole, serotonin, vasopressin, nitroglycerin, adenosine, and endothelin). Studies of exchange of macromolecules in the microcirculation using fluorescent-labeled dextrans have also identified the size of the small pore (35-50 A) in coronary microvessels that can be altered by myocardial ischemia. Studies of the coronary microcirculation have demonstrated that the control of vascular resistance is extremely complex, and mechanisms responsible for these heterogeneous responses need further examination.</abstract><cop>Hagerstown, MD</cop><pub>Lippincott Williams & Wilkins</pub><pmid>2114232</pmid><doi>10.1161/01.cir.82.1.1</doi><tpages>7</tpages></addata></record> |
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subjects | Animals Biological and medical sciences Blood Pressure Cardiology. Vascular system Coronary Circulation - drug effects Coronary Vessels - physiology Homeostasis Humans Medical sciences Microcirculation Nervous System Physiological Phenomena Nifedipine - pharmacology Nitroglycerin - pharmacology Vascular Resistance Vasodilation - physiology |
title | Understanding the coronary circulation through studies at the microvascular level |
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