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首页> 外文期刊>Japanese Journal of Pharmacology >Pinacidil Attenuates Positive Inotropic but Not Chronotropic Responses to Norepinephrine in Isolated Dog Atrial and Ventricular Preparations
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Pinacidil Attenuates Positive Inotropic but Not Chronotropic Responses to Norepinephrine in Isolated Dog Atrial and Ventricular Preparations

机译:吡那地尔减弱狗的心房和心室制剂中去甲肾上腺素对正性肌力反应的反应而不是对慢性反应的反应。

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References(35) Cited-By(1) We investigated whether pinacidil, a K+ATP channel opener like acetylcholine and adenosine, attenuated the positive chronotropic and inotropic responses to norepinephrine in isolated, blood-perfused dog atrial and ventricular preparations. Pinacidil (0.01-0.3 μmol) decreased atrial and ventricular contractile force to a much greater extent than sinus rate in a dose-related manner. Pinacidil dose-dependently attenuated increases in atrial and ventricular forces induced by norepinephrine but not increases in sinus rate. Pinacidil similarly attenuated the positive atrial and ventricular inotropic responses to Bay k 8644 and CaCl2. The pinacidil doses producing a fifty percent decrease (ED50) of the atrial and ventricular contractile force were not significantly different from the respective pinacidil doses producing a fifty percent inhibition (ID50) of the positive inotropic responses to norepinephrine, Bay k 8644 and CaCl2. Ouabain (5 and 15 nmol) did not affect the decreases in atrial and ventricular contractile force in response to pinacidil. These results suggest that the K+ATP-channel activator pinacidil, unlike acetylcholine or adenosine, functionally attenuates increases in ventricular and atrial contractile force in the responses to norepinephrine and other cardiotonics due to shortening of the action potential duration induced by K+ATP-channel activation in the dog heart.
机译:参考文献(35)被引用者(1)我们研究了吡那地尔是否是一种K + ATP通道开放剂,如乙酰胆碱和腺苷,在单独的,血液灌流的狗心房和心室制剂中是否减弱了对去甲肾上腺素的正变时性和变力反应。吡那地尔(0.01-0.3μmol)与剂量相关的窦性心律降低的心房和心室收缩力的程度要大得多。吡那地尔剂量依赖性地减弱了去甲肾上腺素引起的心房和心室力的增加,但窦窦率没有增加。吡那地尔同样减弱了对Bay k 8644和CaCl2的正性心房和心室正性肌力反应。产生心房和心室收缩力降低(ED50)50%的吡那地尔剂量与产生对去甲肾上腺素,Bay k 8644和CaCl2的正性肌力反应产生50%抑制(ID50)的相应吡那地尔剂量没有显着差异。瓦巴因(5和15 nmol)对吡那地尔的应答不影响心房和心室收缩力的降低。这些结果表明,与乙酰胆碱或腺苷不同,K + ATP通道激活剂吡那地尔在功能上减弱了对去甲肾上腺素和其他心脏运动反应的心室和心房收缩力的增加,这是由于K + ATP通道诱导的动作电位持续时间缩短了。激活狗的心脏。

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