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普萘洛尔和美托洛尔对未麻醉的遗传性高血压大鼠和正常血压大鼠的β1 - β2阻断活性。

Beta 1 - beta 2 blocking activity of propranolol and metoprolol in the unanaesthetized genetically hypertensive and normotensive rat.

作者信息

Luca C, Marchini F, Usardi M M

出版信息

Pharmacol Res Commun. 1984 Apr;16(4):359-68. doi: 10.1016/s0031-6989(84)80004-1.

Abstract

The beta-antagonistic activity of propranolol and metoprolol has been evaluated, in terms of inhibition of isoproterenol effects, "in vitro" (isolated right atria and tracheae) and "in vivo" in unanaesthetized normotensive and spontaneously hypertensive rats (SHR). Metoprolol resulted 13 - 6.4 - 14 times more cardioselective than propranolol in the three aforementioned experimental models, respectively. SHR, because of its decreased baroceptor sensitivity to trigger the tachycardic reflex, proves a good model for the evaluation of beta 1 antagonistic activity of "cardioselective" beta- blockers, which could be underevaluated in the normotensive rat. Moreover, the agonistic activity of isoproterenol has been compared in normo and hypertensive rats in order to ascertain whether the different number of beta 1 receptors in the two strains could influence the biological response to their stimulation and/or or blockade.

摘要

已通过在“体外”(离体右心房和气管)以及在未麻醉的正常血压和自发性高血压大鼠(SHR)体内抑制异丙肾上腺素的作用,对普萘洛尔和美托洛尔的β受体拮抗活性进行了评估。在上述三种实验模型中,美托洛尔的心脏选择性分别比普萘洛尔高13 - 6.4 - 14倍。由于SHR的压力感受器触发心动过速反射的敏感性降低,它被证明是评估“心脏选择性”β受体阻滞剂β1拮抗活性的良好模型,而在正常血压大鼠中这种活性可能被低估。此外,还比较了正常大鼠和高血压大鼠中异丙肾上腺素的激动活性,以确定两种品系中不同数量的β1受体是否会影响对其刺激和/或阻断的生物学反应。

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