Bonnet V, Badaoui A, Huchet-Cadiou C, Léoty C
Laboratoire de Physiologie Générale, URA CNRS 1340, Faculté des Sciences et des Techniques, Nantes, France.
Eur J Pharmacol. 1994 Oct 13;264(1):69-76. doi: 10.1016/0014-2999(94)90637-8.
In frog atrial fibres, cyclopiazonic acid as well as thapsigargin, which are inhibitors of sarcoplasmic reticulum Ca(2+)-ATPase, induced a significant increase in the twitch amplitude without detectable changes in its kinetics. The measurements performed on chemically skinned fibres show that cyclopiazonic acid has no effect on the properties of contractile proteins. In the presence of a T-type Ca2+ channel blocker or L-type Ca2+ channel blocker, cyclopiazonic acid still induced a potentiation of the twitch while no effect was found in the presence of a Na(+)-Ca2+ exchange blocker. The effect of cyclopiazonic acid was not related to any modification in myofibrillar Ca2+ sensitivity or in Ca2+ influx through Ca2+ channels. It is proposed that the inhibition of the sarcoplasmic reticulum Ca(2+)-ATPase resulted in a potentiation of the effect of the Ca2+ influx and that the major role of the sarcoplasmic reticulum was to limit the intracellular Ca2+ concentration.
在蛙心房纤维中,环匹阿尼酸以及毒胡萝卜素(肌浆网Ca(2+)-ATP酶抑制剂)可使单收缩幅度显著增加,但其动力学未出现可检测到的变化。对化学去膜纤维进行的测量表明,环匹阿尼酸对收缩蛋白的特性无影响。在存在T型Ca2+通道阻滞剂或L型Ca2+通道阻滞剂的情况下,环匹阿尼酸仍可使单收缩增强,而在存在Na(+)-Ca2+交换阻滞剂时则未发现影响。环匹阿尼酸的作用与肌原纤维Ca2+敏感性或通过Ca2+通道的Ca2+内流的任何改变无关。有人提出,肌浆网Ca(2+)-ATP酶的抑制导致Ca2+内流作用增强,且肌浆网的主要作用是限制细胞内Ca2+浓度。