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绵羊浦肯野纤维中的细胞内钠以及藜芦碱和强心苷的正性肌力作用。

Intracellular sodium and the positive inotropic effect of veratridine and cardiac glycoside in sheep Purkinje fibers.

作者信息

Brill D M, Wasserstrom J A

出版信息

Circ Res. 1986 Jan;58(1):109-19. doi: 10.1161/01.res.58.1.109.

Abstract

Veratridine is a sodium channel toxin that exerts a powerful positive inotropic effect and prolongs the action potential duration in the heart. To determine the basis of the inotropic action of veratridine and to examine the effects of dissimilar methods of raising intracellular sodium activity on contractility, we measured twitch tension and intracellular sodium activity using sodium-sensitive microelectrodes in stimulated sheep Purkinje fibers exposed to veratridine and in voltage-clamped fibers exposed to veratridine and cardiac glycoside. In stimulated fibers, veratridine (0.1-1 microM) produced coincident increases in intracellular sodium activity, action potential duration, and tension. In voltage-clamped fibers, veratridine (1-2 microM) and acetylstrophanthidin (0.1 microM) raised intracellular sodium activity and tension to a comparable degree. Tetrodotoxin (10 microM) abolished the mechanical, electrophysiological, and ionic changes produced by veratridine. The relationship between intracellular sodium activity and tension in voltage-clamped fibers (n = 6) was indistinguishable for veratridine and acetylstrophanthidin and could be fitted either with a linear function with slopes of 122.8% and 124.2%, respectively, or with a power function with slopes of 4.60 and 4.54, respectively, where the slope represents the exponential power of intracellular sodium activity to which tension is proportional. These results indicate that the positive inotropic action of veratridine is entirely accounted for by accumulation of intracellular sodium, which increases intracellular calcium available for contraction by sodium-calcium exchange. This study is the first direct demonstration that veratridine or any other sodium channel toxin affects intracellular sodium activity and suggests that the inotropic potency of veratridine and cardiac glycoside rely on the same mechanism, namely, elevation of intracellular sodium.

摘要

藜芦定是一种钠通道毒素,可产生强大的正性肌力作用,并延长心脏动作电位时程。为了确定藜芦定正性肌力作用的基础,并研究提高细胞内钠活性的不同方法对收缩性的影响,我们使用钠敏感微电极,在暴露于藜芦定的受刺激绵羊浦肯野纤维以及暴露于藜芦定和强心苷的电压钳制纤维中,测量了收缩张力和细胞内钠活性。在受刺激的纤维中,藜芦定(0.1 - 1微摩尔)使细胞内钠活性、动作电位时程和张力同时增加。在电压钳制的纤维中,藜芦定(1 - 2微摩尔)和乙酰洋地黄毒苷(0.1微摩尔)使细胞内钠活性和张力升高到相似程度。河豚毒素(10微摩尔)消除了藜芦定引起的机械、电生理和离子变化。对于藜芦定和乙酰洋地黄毒苷,电压钳制纤维(n = 6)中细胞内钠活性与张力之间的关系无法区分,并且可以分别用斜率为122.8%和124.2%的线性函数或斜率分别为4.60和4.54的幂函数拟合,其中斜率表示张力与之成比例的细胞内钠活性的指数幂。这些结果表明,藜芦定的正性肌力作用完全由细胞内钠的积累所解释,细胞内钠通过钠 - 钙交换增加了可用于收缩的细胞内钙。本研究首次直接证明藜芦定或任何其他钠通道毒素会影响细胞内钠活性,并表明藜芦定和强心苷的正性肌力作用依赖于相同的机制,即细胞内钠升高。

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