Specificity of Vascular Reactivity and Remodeling After Repeated Endothelial Injury in a Swine Model

We investigated the difference in vascular responses and remodeling between coronary and iliac arteries after repeated endothelial denudation. Endothelial denudation of the left anterior descending coronary artery (LAD) and the right common iliac artery (RIA) was repeated 4 times twice a month using...

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Veröffentlicht in:International Heart Journal 2006, Vol.47(2), pp.297-310
Hauptverfasser: Ohwada, Takayuki, Saito, Tomiyoshi, Saitoh, Shu-ichi, Osugi, Taku, Ohtake, Atsushi, Maehara, Kazuhira, Ishibashi, Toshiyuki, Maruyama, Yukio
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container_end_page 310
container_issue 2
container_start_page 297
container_title International Heart Journal
container_volume 47
creator Ohwada, Takayuki
Saito, Tomiyoshi
Saitoh, Shu-ichi
Osugi, Taku
Ohtake, Atsushi
Maehara, Kazuhira
Ishibashi, Toshiyuki
Maruyama, Yukio
description We investigated the difference in vascular responses and remodeling between coronary and iliac arteries after repeated endothelial denudation. Endothelial denudation of the left anterior descending coronary artery (LAD) and the right common iliac artery (RIA) was repeated 4 times twice a month using a Fogarty catheter in 21 pigs. Vascular responses to vasoactive drugs were evaluated as % luminal diameter changes on contrast angiography 2 weeks after the last denudation. Corresponding nondenuded sites, ie, the left circumflex coronary artery (LCX) and the left common iliac artery (LIA), were used as references. Acetylcholine (1 μg/kg) did not constrict the LCX (0 ± 1%) and the LAD (1 ± 1%, P < 0.05), whereas it constricted the RIA (20 ± 6%) but not the LIA (−3 ± 3%, P < 0.01). Alternatively, serotonin (10 μg/kg) constricted the LAD strikingly (88 ± 5%, P < 0.01 versus LCX and RIA), as well as the RIA (35 ± 10%, P < 0.05 versus LIA). Vasodilator responses to substance P and isosorbide dinitrate were not different after injury in both arteries. The intima-to-media ratio and adventitia-to-media ratio of the relevant site in cross section of tissue sample from LAD were greater than those from LCX, and were more prominent than those from RIA. The results show that vascular tone regulation after the endothelial injury and vascular remodeling might be altered in a vessel-specific manner.
doi_str_mv 10.1536/ihj.47.297
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Endothelial denudation of the left anterior descending coronary artery (LAD) and the right common iliac artery (RIA) was repeated 4 times twice a month using a Fogarty catheter in 21 pigs. Vascular responses to vasoactive drugs were evaluated as % luminal diameter changes on contrast angiography 2 weeks after the last denudation. Corresponding nondenuded sites, ie, the left circumflex coronary artery (LCX) and the left common iliac artery (LIA), were used as references. Acetylcholine (1 μg/kg) did not constrict the LCX (0 ± 1%) and the LAD (1 ± 1%, P &lt; 0.05), whereas it constricted the RIA (20 ± 6%) but not the LIA (−3 ± 3%, P &lt; 0.01). Alternatively, serotonin (10 μg/kg) constricted the LAD strikingly (88 ± 5%, P &lt; 0.01 versus LCX and RIA), as well as the RIA (35 ± 10%, P &lt; 0.05 versus LIA). Vasodilator responses to substance P and isosorbide dinitrate were not different after injury in both arteries. The intima-to-media ratio and adventitia-to-media ratio of the relevant site in cross section of tissue sample from LAD were greater than those from LCX, and were more prominent than those from RIA. 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Heart J.</addtitle><description>We investigated the difference in vascular responses and remodeling between coronary and iliac arteries after repeated endothelial denudation. Endothelial denudation of the left anterior descending coronary artery (LAD) and the right common iliac artery (RIA) was repeated 4 times twice a month using a Fogarty catheter in 21 pigs. Vascular responses to vasoactive drugs were evaluated as % luminal diameter changes on contrast angiography 2 weeks after the last denudation. Corresponding nondenuded sites, ie, the left circumflex coronary artery (LCX) and the left common iliac artery (LIA), were used as references. Acetylcholine (1 μg/kg) did not constrict the LCX (0 ± 1%) and the LAD (1 ± 1%, P &lt; 0.05), whereas it constricted the RIA (20 ± 6%) but not the LIA (−3 ± 3%, P &lt; 0.01). Alternatively, serotonin (10 μg/kg) constricted the LAD strikingly (88 ± 5%, P &lt; 0.01 versus LCX and RIA), as well as the RIA (35 ± 10%, P &lt; 0.05 versus LIA). Vasodilator responses to substance P and isosorbide dinitrate were not different after injury in both arteries. The intima-to-media ratio and adventitia-to-media ratio of the relevant site in cross section of tissue sample from LAD were greater than those from LCX, and were more prominent than those from RIA. 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Saito, Tomiyoshi ; Saitoh, Shu-ichi ; Osugi, Taku ; Ohtake, Atsushi ; Maehara, Kazuhira ; Ishibashi, Toshiyuki ; Maruyama, Yukio</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c488t-8ddcfc94931011897c45083450a50d55bed51ccfc218fcaa59883227b06ac0d23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Acetylcholine - pharmacology</topic><topic>Animals</topic><topic>Coronary Angiography</topic><topic>Coronary Vessels - pathology</topic><topic>Coronary Vessels - physiopathology</topic><topic>Endothelial injury</topic><topic>Endothelium, Vascular - pathology</topic><topic>Heart Rate - drug effects</topic><topic>Hyperplasia - etiology</topic><topic>Iliac Artery - diagnostic imaging</topic><topic>Iliac Artery - pathology</topic><topic>Iliac Artery - physiopathology</topic><topic>Isosorbide Dinitrate - pharmacology</topic><topic>Male</topic><topic>Muscle, Smooth, Vascular - drug effects</topic><topic>Serotonin - pharmacology</topic><topic>Substance P - pharmacology</topic><topic>Swine</topic><topic>Vascular remodeling</topic><topic>Vascular response</topic><topic>Vasoconstriction - drug effects</topic><topic>Vasoconstrictor Agents - pharmacology</topic><topic>Vasodilation - drug effects</topic><topic>Vasodilator Agents - pharmacology</topic><topic>Vasomotor System - drug effects</topic><topic>Vessel specificity</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ohwada, Takayuki</creatorcontrib><creatorcontrib>Saito, Tomiyoshi</creatorcontrib><creatorcontrib>Saitoh, Shu-ichi</creatorcontrib><creatorcontrib>Osugi, Taku</creatorcontrib><creatorcontrib>Ohtake, Atsushi</creatorcontrib><creatorcontrib>Maehara, Kazuhira</creatorcontrib><creatorcontrib>Ishibashi, Toshiyuki</creatorcontrib><creatorcontrib>Maruyama, Yukio</creatorcontrib><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>International Heart Journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ohwada, Takayuki</au><au>Saito, Tomiyoshi</au><au>Saitoh, Shu-ichi</au><au>Osugi, Taku</au><au>Ohtake, Atsushi</au><au>Maehara, Kazuhira</au><au>Ishibashi, Toshiyuki</au><au>Maruyama, Yukio</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Specificity of Vascular Reactivity and Remodeling After Repeated Endothelial Injury in a Swine Model</atitle><jtitle>International Heart Journal</jtitle><addtitle>Int. 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Acetylcholine (1 μg/kg) did not constrict the LCX (0 ± 1%) and the LAD (1 ± 1%, P &lt; 0.05), whereas it constricted the RIA (20 ± 6%) but not the LIA (−3 ± 3%, P &lt; 0.01). Alternatively, serotonin (10 μg/kg) constricted the LAD strikingly (88 ± 5%, P &lt; 0.01 versus LCX and RIA), as well as the RIA (35 ± 10%, P &lt; 0.05 versus LIA). Vasodilator responses to substance P and isosorbide dinitrate were not different after injury in both arteries. The intima-to-media ratio and adventitia-to-media ratio of the relevant site in cross section of tissue sample from LAD were greater than those from LCX, and were more prominent than those from RIA. The results show that vascular tone regulation after the endothelial injury and vascular remodeling might be altered in a vessel-specific manner.</abstract><cop>Japan</cop><pub>International Heart Journal Association</pub><pmid>16607056</pmid><doi>10.1536/ihj.47.297</doi><tpages>14</tpages><oa>free_for_read</oa></addata></record>
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source MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; J-STAGE (Japan Science & Technology Information Aggregator, Electronic) Freely Available Titles - Japanese
subjects Acetylcholine - pharmacology
Animals
Coronary Angiography
Coronary Vessels - pathology
Coronary Vessels - physiopathology
Endothelial injury
Endothelium, Vascular - pathology
Heart Rate - drug effects
Hyperplasia - etiology
Iliac Artery - diagnostic imaging
Iliac Artery - pathology
Iliac Artery - physiopathology
Isosorbide Dinitrate - pharmacology
Male
Muscle, Smooth, Vascular - drug effects
Serotonin - pharmacology
Substance P - pharmacology
Swine
Vascular remodeling
Vascular response
Vasoconstriction - drug effects
Vasoconstrictor Agents - pharmacology
Vasodilation - drug effects
Vasodilator Agents - pharmacology
Vasomotor System - drug effects
Vessel specificity
title Specificity of Vascular Reactivity and Remodeling After Repeated Endothelial Injury in a Swine Model
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