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球囊剥脱术后局部内膜增厚的小型猪冠状动脉痉挛的发病机制

Pathogenesis of coronary artery spasm in miniature swine with regional intimal thickening after balloon denudation.

作者信息

Yamamoto Y, Tomoike H, Egashira K, Kobayashi T, Kawasaki T, Nakamura M

出版信息

Circ Res. 1987 Jan;60(1):113-21. doi: 10.1161/01.res.60.1.113.

Abstract

Pathogenesis of coronary artery spasm induced by histamine in miniature pigs was studied angiographically in in vivo and in vitro conditions. Endothelial balloon denudation was performed and the animals were fed laboratory chow for 3 months, after which coronary artery spasm was repeatedly provoked by histamine given intracoronarily. Regional hypercontraction of the coronary artery was documented by selective coronary arteriography, and the resulting myocardial ischemia was confirmed by ECG-ST changes. To evaluate coronary artery spasm without the influence of blood constituents and neural control and to quantitate the pharmacophysiological characteristics of histamine-induced coronary constriction in the coronary spasm, the same heart was isolated and perfused with Krebs-Henseleit solution under a constant perfusion pressure of 90 mm Hg. Histamine (10(-5) M) reduced the diameter of the coronary artery of the isolated heart by 29 +/- 4 and 67 +/- 3% (p less than 0.001) in nondenuded and denuded areas, respectively. These figures were similar to data obtained angiographically in vivo after the administration of histamine 10 micrograms/kg. The constriction of the denuded areas in response to histamine was topologically the same in vivo and in vitro. The degree of focal constriction induced by histamine, defined as a percent of stenoses from the mean diameter of the areas of proximal and distal to the spastic site, was similar in in vivo (10 micrograms/kg i.c.) and in vitro (10(-5) M) conditions. KCl (40 mM) reduced both the denuded and nondenuded coronary artery diameter by 67 +/- 3% and 68 +/- 3% (NS), respectively. The dose-response relation of the coronary diameter to histamine was not influenced by pretreatment with the nerve transmitter blockers guanethidine (3 X 10(-6) M), atropine (10(-6) M), and tetrodotoxin (3 X 10(-7) M). Phenylephrine (10(-5) M) did not potentiate constriction of the denuded areas.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

在体内和体外条件下,通过血管造影术研究了组胺诱导的小型猪冠状动脉痉挛的发病机制。进行内皮球囊剥脱术,动物喂食实验室饲料3个月,之后通过冠状动脉内给予组胺反复诱发冠状动脉痉挛。选择性冠状动脉造影记录冠状动脉局部过度收缩,心电图ST段改变证实由此导致的心肌缺血。为了评估不受血液成分和神经控制影响的冠状动脉痉挛,并定量组胺诱导的冠状动脉痉挛中冠状动脉收缩的药物生理特征,分离同一心脏并在90 mmHg的恒定灌注压力下用克雷布斯 - 亨塞尔特溶液灌注。组胺(10(-5) M)使离体心脏非剥脱区和剥脱区的冠状动脉直径分别减少29±4%和67±3%(p<0.001)。这些数据与体内给予10微克/千克组胺后血管造影获得的数据相似。体内和体外对组胺反应的剥脱区收缩在拓扑结构上相同。组胺诱导的局灶性收缩程度,定义为痉挛部位近端和远端区域平均直径的狭窄百分比,在体内(10微克/千克冠状动脉内注射)和体外(10(-5) M)条件下相似。氯化钾(40 mM)使剥脱区和非剥脱区冠状动脉直径分别减少了67±3%和68±3%(无显著差异)。冠状动脉直径与组胺的剂量反应关系不受神经递质阻滞剂胍乙啶(3×10(-6) M)、阿托品(10(-6) M)和河豚毒素(3×10(-7) M)预处理的影响。去氧肾上腺素(10(-5) M)不会增强剥脱区的收缩。(摘要截断于250字)

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