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内皮素-1促进猪冠状动脉再生内皮释放内皮衍生内过氧化物和血栓素A_2(英文)
引用本文:Seung-Jung PARK,John J LEE,Paul M VANHOUTTE. 内皮素-1促进猪冠状动脉再生内皮释放内皮衍生内过氧化物和血栓素A_2(英文)[J]. Acta pharmacologica Sinica, 1999, 0(10)
作者姓名:Seung-Jung PARK  John J LEE  Paul M VANHOUTTE
作者单位:Center for Experimental Therapeutics,Department of Medicine,Baylor College of Medicine,One Baylor Plaza,Houston TX 77030,USA,Center for Experimental Therapeutics,Department of Medicine,Baylor College of Medicine,One Baylor Plaza,Houston TX 77030,USA,Center for Experimental Therapeutics,Department of Medicine,Baylor College of Medicine,One Baylor Plaza,Houston TX 77030,USA
基金项目:Project supported in part by NIH grant HL 31547.
摘    要:AIM: To determine the role of endothelium-derivedcontracting factor (EDCF) in the response toendothelin-1 in arteries with regenerated endothelium.METHODS: Rings of porcine coronary arteries, withand without endothelium of previously deendothelializedleft anterior descending coronary arteries and native leftcircumflex coronary arteries, were suspended inconventional organ chambers for the measurement ofisometric force. RESULTS: In quiescent rings of thepreviously deendothelialized left anterior descending

关 键 词:冠状血管  内皮素-1  吲哚美辛  前列腺素内过氧化物合酶  一氧化氮  血栓素A_2  血管内皮

Endothelin-1 releases endothelium-deri ved endoperoxides and thromboxane A_2 in porcine coronary arteries with regenerated endothelium
Seung-Jung PARK,John J LEE,Paul M VANHOUTTE. Endothelin-1 releases endothelium-deri ved endoperoxides and thromboxane A_2 in porcine coronary arteries with regenerated endothelium[J]. Acta pharmacologica Sinica, 1999, 0(10)
Authors:Seung-Jung PARK  John J LEE  Paul M VANHOUTTE
Abstract:AIM: To determine the role of endothelium-derived contracting factor ( EDCF) in the response to endothelin-1 in arteries with regenerated endothelium. METHODS: Rings of porcine coronary arteries, with and without endothelium of previously deendothelialized left anterior descending coronary arteries and native left circumflex coronary arteries, were suspended in conventional organ chambers for the measurement of isometric force. RESULTS: In quiescent rings of the previously deendothelialized left anterior descending coronary artery treated with the NO-synthase inhibitor nitro-L-arginine, endothelin-1 caused contractions which were larger in rings with than that in those without endothelium. Under the same experimental conditions, in the left circumflex coronary artery, the contractions to endothelin-1 were augmented markedly by the removal of the endothelium. In rings with endothelium of the previously deendothelialized left anterior descending coronary artery, indometacin (inhibitor of cyclooxygenase) and ridogrel (thromboxane A2 receptor antagonist and inhibitor of thromboxanesynthase ) inhibited contractions to endothelin-1. Dazoxiben ( inhibitor of thromboxane synthase ) inhibited, to the same extent as indometacin and ridogel, the response to higher concentrations of endothelin-1. The endothelium-dependent component of the response to lower concentrations of endothelin-1 was inhibited by indometacin and ridogrel, but not by dazoxiben. In rings without endothelium of both previously deendothelialized left anterior descending and native left circumflex coronary arteries, indometacin and ridogrel did not affect the contractions to endothelin-1. CONCLUSION: These findings suggest that in regenerated endothelium, high concentrations of endothelin-1 stimulate the release of thromboxane A2. Endoperoxides generated by activation of endothelial cyclooxygenase may be the endothelium-derived contracting factor (s) released in regenerated endothelium by lower concentrations of the peptide.
Keywords:coronary vessels  endothelin-1  indomethacin  prostaglandin-endoperoxide synthase  nitric oxide  thromboxane A_2  vascular endothelium
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