Yamamoto Y, Suzuki A, Hotta K
Jpn J Physiol. 1977;27(1):95-109. doi: 10.2170/jjphysiol.27.95.
The effect of D2O and dantrolene-Na (DAN) on the electrical and mechanical responses of single muscle fiber (mouse EDL and frog semitendinosus), Ca2+ uptake and release of sarcoplasmic reticulum (SR) and contractile proteins was investigated to elucidate the coupling mechanism between depolarization and contraction. Both agents inhibited tension development induced by depolarization and caffeine, especially the initial phase of contraction (more pronounced in fast muscle) without affecting excitation of membrane and contractile machinery. The effect of DAN can be antagonized by increasing Ca2+ concentration and lowering the temperature of the medium. Ca2+ uptake and release abilities of isolated SR were not altered significantly in DAN, but were reduced considerably in D2O. These results suggest than there is a Ca2+-mediated trigger mechanism for the rapid release of activator Ca2+ from internal storage (SR). DAN and D2O interfere predominantly the action of the site(s) of this mechanism, probably on the T-tubules. In addition, D2O decelerates Ca2+ release from SR per se.
研究了重水(D2O)和丹曲林钠(DAN)对单根肌纤维(小鼠趾长伸肌和青蛙半腱肌)的电反应和机械反应、肌浆网(SR)的钙摄取和释放以及收缩蛋白的影响,以阐明去极化与收缩之间的偶联机制。这两种药物均抑制去极化和咖啡因诱导的张力发展,尤其是收缩的初始阶段(在快肌中更明显),而不影响膜和收缩机制的兴奋。DAN的作用可通过增加钙离子浓度和降低培养基温度来拮抗。在DAN中,分离的肌浆网的钙摄取和释放能力没有显著改变,但在D2O中则显著降低。这些结果表明,存在一种由钙介导的触发机制,用于从内部储存(肌浆网)快速释放激活钙。DAN和D2O主要干扰该机制位点的作用,可能作用于横管。此外,D2O本身会减缓肌浆网的钙释放。