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儿茶酚胺、组胺、电起搏以及缺氧刺激豚鼠离体灌流心脏时,冠状动脉血管舒张代谢产物的释放。

The release of a coronary vasodilator metabolite from the guinea-pig isolated perfused heart stimulated by catecholamines, histamine and electrical pacing and by exposure to anoxia.

作者信息

Broadley K J

出版信息

Br J Pharmacol. 1976 Sep;58(1):89-100. doi: 10.1111/j.1476-5381.1976.tb07696.x.

Abstract

1 A procedure involving two guinea-pig isolated hearts perfused in series is described for detecting in the recipient heart the release of a possible coronary vasodilator metabolite from the donor heart. 2 Adrenaline and isoprenaline stimulated the rate and force of contraction and produced a multiphasic coronary vascular response, the predominant phase of which was vasodilatation. When the beta-adrenoceptors of the recipient heart were blocked, stimulation of the donor heart by the catecholamines was associated with a coronary vasodilatation of the recipient heart. 3 Histamine stimulated rate and force of contraction and was predominantly coronary vasodilator. After blockade of histamine H1- and H2-receptors in the recipient heart, coronary vasodilatation followed increases in activity of the donor heart in response to histamine. 4 These vasodilator responses of the recipient heart were attributed to the release from the donor heart of a vasodilator metabolite by the increased activity. This is the proposed mechanism for the predominant coronary vasodilator response to catecholamines and histamine. 5 Periods of electrically-paced tachycardia and anoxia of the donor heart also led to the release of vasodilator activity. 6 The possible identity of the metabolite is discussed.

摘要
  1. 本文描述了一种涉及两个串联灌注的豚鼠离体心脏的实验方法,用于检测受体心脏中是否释放了来自供体心脏的一种可能的冠状血管舒张代谢物。2. 肾上腺素和异丙肾上腺素刺激了收缩速率和力量,并产生了多相性冠状血管反应,其中主要阶段是血管舒张。当受体心脏的β - 肾上腺素受体被阻断时,儿茶酚胺对供体心脏的刺激与受体心脏的冠状血管舒张相关。3. 组胺刺激了收缩速率和力量,且主要是冠状血管舒张剂。在受体心脏中组胺H1和H2受体被阻断后,供体心脏对组胺反应活性增加后,冠状血管舒张随之出现。4. 受体心脏的这些血管舒张反应归因于供体心脏因活性增加而释放出一种血管舒张代谢物。这是对儿茶酚胺和组胺主要冠状血管舒张反应的提出的机制。5. 供体心脏的电刺激心动过速期和缺氧期也导致了血管舒张活性的释放。6. 讨论了该代谢物可能的身份。

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