首页> 外文期刊>European Journal of Pharmacology: An International Journal >Ouabain increases myofibrillar Ca(2+) sensitivity but does not influence the Ca(2+) release in human skinned fibres.
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Ouabain increases myofibrillar Ca(2+) sensitivity but does not influence the Ca(2+) release in human skinned fibres.

机译:哇巴因增加肌原纤维Ca(2+)的敏感性,但不影响人类皮肤纤维中Ca(2+)的释放。

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摘要

The present study investigated the impact of the Na(+) pump inhibitor ouabain (g-strophanthin) on Ca(2+) sensitivity and Ca(2+) release in human right auricular trabeculae (coronary bypass) and in skinned muscle fibres from left ventricular myocardium (cardiac transplantation, dilated cardiomyopathy). A time-dependent increase in force of contraction was observed in right auricular trabeculae in response to ouabain (100 nM) before the intracellular Ca(2+) transient (fura-2) increased (n=6). In triton X-skinned fibres (no sarcoplasmic reticulum) of human failing myocardium, ouabain (1-100 nM) concentration-dependently increased tension at a free extracellular Ca(2+) concentration of 1 microM and the Hill coefficient of the Ca(2+)-dependent tension development. Ouabain (1-100 nM) did not directly induce a Ca(2+) release out of the sarcoplasmic reticulum, nor did it alter the caffeine (10 mM) induced sarcoplasmic reticulum Ca(2+) release in saponin-skinned fibre preparations in which the sarcoplasmic reticulum had been Ca(2+)-loaded. In conclusion, ouabain increases myofibrillar Ca(2+) sensitivity possibly due to an increase in the cooperativity of the thick and thin myofilaments. This mechanism may additionally contribute to the positive inotropic effect of ouabain.
机译:本研究调查了Na(+)泵抑制剂哇巴因(g-stophanthin)对人右耳小梁(冠状动脉搭桥)和左皮肤皮肤肌纤维中Ca(2+)敏感性和Ca(2+)释放的影响。心室心肌(心脏移植,扩张型心肌病)。在细胞内Ca(2+)瞬变(fura-2)增加之前,观察到哇巴因(100 nM)对右耳小梁的收缩力随时间的增加(n = 6)。在人类衰竭的心肌的Triton X皮肤纤维(无肌浆网)中,哇巴因(1-100 nM)浓度依赖性地在自由的细胞外Ca(2+)浓度为1 microM和Ca(2)的Hill系数下增加张力。 +)依赖紧张的发展。瓦巴因(1-100 nM)不会直接诱导肌浆网释放Ca(2+),也不会改变咖啡因(10 mM)诱导皂苷皮纤维制剂中肌浆网Ca(2+)释放。肌浆网已被Ca(2+)加载。总之,哇巴因增加了肌原纤维Ca(2+)的敏感性,这可能是由于厚和薄肌丝的协同作用增加所致。该机制可能另外有助于哇巴因的正性肌力作用。

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