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前列腺素E2和环磷酸腺苷在心脏活动增强所致冠状动脉扩张中的作用

Prostaglandin E2 and cyclic AMP in the coronary vasodilatation due to cardiac hyperactivity.

作者信息

Sen A K, Sunahara F A, Talesnik J

出版信息

Can J Physiol Pharmacol. 1976 Apr;54(2):128-39. doi: 10.1139/y76-021.

Abstract

In the isolated perfused rat heart, the dose-related cardiostimulation produced by norepinephrine (NE) or calcium chloride (Ca2+) was followed by a corresponding increase in coronary flow (CF) and in the cardiac level of adenosine 3',5'-cyclic phosphate (cAMP). Prolonged prostaglandin E2 (pge2) infusion did not change the basic force of contraction, CF, or cAMP level but when NE or Ca2+ were administered, only the responses of the CF and the cAMP were diminished. A phosphodiesterase inhibitor, diazoxide (Dx), caused insignificant increase in the basal cAMP, without affecting the force of contraction or CF. With NE or Ca2+, during Dx both the changes in CF and cAMP were augmented compared to the nontreated hearts. The inhibitory effects of NE or Ca2+ remained unchanged. Propranolol abolished the NE but not the Ca2+ effects. It is suggested that PGE2 modulates the cardiac cAMP level and that the latter plays an important role in the adaptive regulation of the CF. It is also postulated that changes in cAMP levels may be brought about by the hyperactivity per se produced by a variety of cardiostimulating agents.

摘要

在离体灌注大鼠心脏中,去甲肾上腺素(NE)或氯化钙(Ca2+)产生的剂量相关的心脏刺激之后,冠状动脉血流量(CF)和心脏3',5'-环磷酸腺苷(cAMP)水平相应增加。长时间输注前列腺素E2(pge2)不会改变基本收缩力、CF或cAMP水平,但当给予NE或Ca2+时,只有CF和cAMP的反应减弱。磷酸二酯酶抑制剂二氮嗪(Dx)使基础cAMP略有增加,而不影响收缩力或CF。使用NE或Ca2+时,与未治疗的心脏相比,在Dx期间CF和cAMP的变化均增强。NE或Ca2+的抑制作用保持不变。普萘洛尔消除了NE的作用,但没有消除Ca2+的作用。提示PGE2调节心脏cAMP水平,且后者在CF的适应性调节中起重要作用。还推测cAMP水平的变化可能由多种心脏刺激剂本身的过度活性引起。

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