Cardiac effects of clinically available Kampo medicine assessed with canine isolated, blood-perfused heart preparations.

A. Sugiyama, A. Takahara, Y. Satoh, M. Yoneyama, Y. Saegusa, K. Hashimoto
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引用次数: 9

Abstract

Cardiac effects of 10 kinds of clinically available Kampo medicines were investigated: Kakkon-to (TJ-1), Dai-saiko-to (TJ-8), Boi-ogi-to (TJ-20), Chorei-to (TJ-40), Rokumi-gan (TJ-87), Tsu-do-san (TJ-105), Gosha-jinki-gan (TJ-107), San'o-shashin-to (TJ-113), Sairei-to (TJ-114) and Inchin-gorei-san (TJ-117). Chronotropic and inotropic effects were studied using canine isolated, blood-perfused heart preparations, while subcellular mechanisms were analyzed by measuring the drug-induced changes of the adenylate cyclase activity in the canine ventricular membrane preparation. Intracoronary injections of TJ-1, TJ-20, TJ-105 and TJ-113 increased the sinoatrial rate and developed tension of papillary muscle in a dose-related manner, which was significantly attenuated by the pretreatment of the preparations with beta-blocker propranolol. Meanwhile, the other extracts hardly affected these parameters. TJ-1, TJ-20 and TJ-113 increased the adenylate cyclase activity in a dose-related manner, but their potency was significantly less compared with that by an equivalent concentration of isoproterenol. Moreover, TJ-105 did not increase the adenylate cyclase activity. These results suggest that the positive chronotropic and inotropic effects of TJ-1, TJ-20, TJ- 105 and TJ-113 may be exerted through the direct stimulation of the beta-adrenoceptor and/or the norepinephrine release from the postganglionic nerve terminals in the heart.
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临床可用的汉布药对心脏的影响评估与犬分离,血液灌注心脏制剂。
研究了10种临床使用的汉布药:Kakkon-to (TJ-1)、daisaiko -to (TJ-8)、Boi-ogi-to (TJ-20)、Chorei-to (TJ-40)、Rokumi-gan (TJ-87)、tsudo - San (TJ-105)、goha -jinki-gan (TJ-107)、San'o-shashin-to (TJ-113)、saiei -to (TJ-114)和injin -gorei- San (TJ-117)的心脏作用。研究了犬离体血灌注心脏制剂的变时和变肌力作用,并通过测量犬心室膜制剂中腺苷酸环化酶活性的药物诱导变化分析了亚细胞机制。冠状动脉内注射TJ-1、TJ-20、TJ-105和TJ-113使窦房率升高,乳头肌张力呈剂量相关,经β受体阻滞剂心得安预处理后明显减弱。而其他提取物对这些参数几乎没有影响。TJ-1、TJ-20和TJ-113均能增加腺苷酸环化酶的活性,但与同等浓度的异丙肾上腺素相比,TJ-1、TJ-20和TJ-113的效力显著降低。此外,TJ-105没有增加腺苷酸环化酶的活性。这些结果提示,TJ-1、TJ-20、TJ- 105和TJ-113的正性变时性和正性肌力作用可能是通过直接刺激β -肾上腺素受体和/或从心脏神经节后神经末梢释放去甲肾上腺素来发挥的。
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