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前列环素稳定类似物贝拉普罗斯钠对离体豚鼠心肌的正性肌力和变时作用。

Positive inotropic and chronotropic effects of beraprost sodium, a stable analogue of prostacyclin, in isolated guinea pig myocardium.

作者信息

Ueno Y, Okazaki S, Isogaya M, Nishio S, Tanaka H, Kato Y, Shigenobu K

机构信息

Toray Industries, Inc., Basic Research Laboratories, Kanagawa, Japan.

出版信息

Gen Pharmacol. 1996 Jan;27(1):101-3. doi: 10.1016/0306-3623(95)00095-x.

Abstract
  1. Inotropic and chronotropic effects of beraprost sodium (beraprost), a chemically stable prostacyclin analogue, were examined in isolated myocardial preparations of guinea pigs. 2. In the left atria, 10(-9) - 10(-7) M beraprost had no significant effect on the contractile force, but 10(-6) and 10(-5) M produced a concentration-dependent positive inotropic response. This effect was antagonized by S-145, a potent and selective thromboxane A2 (TXA2) receptor antagonist, but not by propranolol. 3. Beraprost, from 10(-9) to 10(-5) M, had no significant inotropic effect in the right ventricular papillary muscles. 4. In the right atria, 10(-9) and 10(-8) M beraprost had no significant effect, but 10(-7) - 10(-5) M caused an increase in beating rate; this effect was not affected by S-145. 5. The present study demonstrates that beraprost has positive inotropic and chronotropic effects at high doses on isolated guinea pig atria. The inotropic effect may be mediated by the TXA2 receptor, but some mechanism other than the TXA2 receptor is responsible for the chronotropic effect.
摘要
  1. 对化学性质稳定的前列环素类似物贝拉前列素钠(beraprost)在豚鼠离体心肌制剂中的变力性和变时性作用进行了研究。2. 在左心房中,10^(-9) - 10^(-7) M的贝拉前列素对收缩力无显著影响,但10^(-6)和10^(-5) M产生浓度依赖性正性变力反应。这种作用被强效选择性血栓素A2(TXA2)受体拮抗剂S - 145拮抗,但不被普萘洛尔拮抗。3. 10^(-9)至10^(-5) M的贝拉前列素对右心室乳头肌无显著变力作用。4. 在右心房中,10^(-9)和10^(-8) M的贝拉前列素无显著作用,但10^(-7) - 10^(-5) M导致心率增加;这种作用不受S - 145影响。5. 本研究表明,贝拉前列素在高剂量时对离体豚鼠心房具有正性变力性和变时性作用。变力作用可能由TXA2受体介导,但变时作用是由TXA2受体以外的某些机制引起的。

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