犬冠状动脉循环狭窄功能状态的药理学评价。

V Kékesi, A Juhász-Nagy
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引用次数: 0

摘要

分析戊巴比妥钠麻醉下开胸犬冠状动脉大支的机械收缩与相关小阻力血管的自我调节能力的相互作用。用电磁流量计测量冠状动脉血流量(CBF)。逐步机械收缩逐渐消除腺苷诱导的冠状动脉血管舒张,而静息时平均CBF水平保持不变。此时,维拉帕米(0.2 mg/kg静脉注射),一种具有强大阻断腺苷作用的血管扩张剂,最终降低了CBF并增加了冠状动脉阻力。将这些药物直接注射到建立在颈动脉和左冠状动脉之间的搭桥中也获得了类似的结果。结果表明:(i)腺苷影响完成代偿性自动调节的相同冠状动脉段(ii);对于严重狭窄,维拉帕米通过抑制“内在”腺苷效应间接增强冠状动脉阻力(iii);冠脉狭窄的功能状态可以通过这些药理学试验来评估。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pharmacologic assessment of the functional state in stenosed coronary circulation of the dog.

In open chest dogs under sodium pentobarbital anaesthesia the interaction of mechanical constriction on a large coronary branch and autoregulatory capacity of the relevant small resistance vessels was analyzed. Coronary blood flow (CBF) was measured with an electromagnetic flowmeter. Step-by-step mechanical constriction gradually abolished adenosine-induced coronary vasodilation, whereas the resting level of mean CBF remained unaltered. At this point verapamil (0.2 mg/kg i.v.), a vasodilator with a strong potency of blocking adenosine action, eventually decreased CBF and increased coronary resistance. Similar results were obtained with these drugs injected directly into a bypass established between the carotid and left common coronary arteries. The results suggest that (i) adenosine affects the same coronary segments which accomplish compensatory autoregulation (ii); with critical stenosis verapamil augments indirectly coronary resistance by inhibiting an "intrinsic" adenosine effect (iii); the functional state of stenosed coronaries can be assessed with the aid of these pharmacologic tests.

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