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新型强心剂TA-064(多巴胺)、异丙肾上腺素和哇巴因对豚鼠心室肌的正性肌力作用比较

Comparative positive inotropic effects of TA-064 (denopamine), a new cardiotonic agent, and isoproterenol and ouabain on guinea pig ventricular muscles.

作者信息

Sato T, Imanishi S, Arita M

机构信息

Department of Physiology, Medical College of Oita, Japan.

出版信息

J Cardiovasc Pharmacol. 1989 Oct;14(4):519-25. doi: 10.1097/00005344-198910000-00002.

Abstract

The effects of TA-064 (TA) on "fast" and "slow" response action potentials and contractile tensions were studied in isolated guinea pig papillary muscles, and the findings were compared with those of isoproterenol (ISP) and ouabain. The results are as follows: (a) TA produced a dose-dependent (10(-7)-10(-5) M) increase in developed tension, with no significant changes in the resting membrane potential (RMP), action potential duration (APD), and maximum rate of rise of action potential (Vmax). (b) The concentration required to increase the developed tension by threefold ("equivalent concentration") were 10(-6) M with both TA and ouabain, while that of ISP was 5 x 10(-8) M. (c) TA increased the maximum rate of rise, dP/dtmax, and the maximum rate of fall, dR/dtmax, of the developed tension to the same extent, unlike those of ISP and ouabain. (d) Positive inotropic effects of TA (10(-7)-10(-5) M) were not completely abolished by atenolol (3.8 x 10(-5) M), a specific beta 1 blocker, whereas those of ISP were completely abolished. (e) The increasing effects of "equivalent concentration" of TA (10(-6) M) on the Vmax of the slow response were less than those of ISP (5 x 10(-8) M). These results suggest that the positive inotropic effects of TA are mainly due to stimulation of beta 1 adrenoceptors, but that the mode of action of the drug differs in several respects from that of ISP or ouabain.

摘要

在离体豚鼠乳头肌中研究了TA - 064(TA)对“快”和“慢”反应动作电位及收缩张力的影响,并将结果与异丙肾上腺素(ISP)和哇巴因的结果进行了比较。结果如下:(a)TA使舒张期张力呈剂量依赖性增加(10⁻⁷ - 10⁻⁵ M),静息膜电位(RMP)、动作电位时程(APD)和动作电位最大上升速率(Vmax)无明显变化。(b)使舒张期张力增加三倍所需的浓度(“等效浓度”),TA和哇巴因均为10⁻⁶ M,而ISP为5×10⁻⁸ M。(c)与ISP和哇巴因不同,TA使舒张期张力的最大上升速率dP/dtmax和最大下降速率dR/dtmax增加的程度相同。(d)TA(10⁻⁷ - 10⁻⁵ M)的正性肌力作用未被特异性β₁受体阻滞剂阿替洛尔(3.8×10⁻⁵ M)完全消除,而异丙肾上腺素的正性肌力作用则被完全消除。(e)TA(10⁻⁶ M)“等效浓度”对慢反应Vmax的增加作用小于ISP(5×10⁻⁸ M)。这些结果表明,TA的正性肌力作用主要是由于刺激β₁肾上腺素能受体,但该药物的作用方式在几个方面与ISP或哇巴因不同。

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