Bond M, Kitazawa T, Somlyo A P, Somlyo A V
J Physiol. 1984 Oct;355:677-95. doi: 10.1113/jphysiol.1984.sp015445.
The amplitude of interrupted contractions evoked by noradrenaline or caffeine in Ca2+-free, high-K+ solutions containing EGTA or La3+ was determined in small (40-60 micron thick) bundles of guinea-pig portal anterior mesenteric vein. Interrupted contractions were produced by removing the stimulating agent as soon as the amplitude of the tension record reached its peak. The distribution of intracellular Ca2+ was determined, with electron probe X-ray microanalysis, in cryosections of preparations frozen in the relaxed state and at the peak of noradrenaline-induced contractions. Interrupted contractions of maximal or near-maximal amplitudes could be evoked every 2 min for up to 15 min in the virtual absence of extracellular Ca2+. If noradrenaline was allowed to remain in the solution throughout the period of spontaneous relaxation, a subsequent contraction could no longer be evoked in the absence of extracellular Ca2+. Interrupted contractions, similar to those evoked by noradrenaline, could also be stimulated by caffeine. The amplitude of reproducible interrupted contractions in Ca2+-free, high-K+ solution was graded with noradrenaline concentration. The ability of these smooth muscles to contract repeatedly and maximally in Ca2+-free solutions indicates the recycling of Ca2+ released from an intracellular store. The occurrence of these contractions in high-K+ (depolarizing) solutions supports the conclusion (Devine, Somlyo & Somlyo, 1972) that the release of intracellular Ca2+ is one of the mechanisms of pharmacomechanical coupling. The number of subplasmalemmal regions in which high Ca concentrations (greater than 10 mmol/kg dry wt.) were detected, with approximately 75 nm diameter electron probes, was reduced in muscles frozen at the peak of contraction, from 4.7/cell periphery in the relaxed to 1.4/cell periphery in the contracted preparations. In freeze-substituted smooth muscles, in which the membranes of the junctional sarcoplasmic reticulum could be visualized, the regions containing high Ca were identified as part of the sarcoplasmic reticulum (s.r.), indicating that the s.r. is the store from which noradrenaline and caffeine release Ca2+.
在豚鼠门静脉前肠系膜静脉的小束(40 - 60微米厚)中,测定了在含EGTA或La3 +的无钙、高钾溶液中,去甲肾上腺素或咖啡因诱发的间断收缩的幅度。当张力记录的幅度达到峰值时,立即去除刺激剂,从而产生间断收缩。通过电子探针X射线微分析,在处于松弛状态和去甲肾上腺素诱导收缩峰值时冷冻的制剂的冰冻切片中,测定细胞内Ca2 +的分布。在几乎没有细胞外Ca2 +的情况下,每2分钟可诱发一次最大或接近最大幅度的间断收缩,持续长达15分钟。如果在自发松弛期间让去甲肾上腺素一直留在溶液中,那么在没有细胞外Ca2 +的情况下,随后就无法再诱发收缩。与去甲肾上腺素诱发的类似,咖啡因也能刺激间断收缩。在无钙、高钾溶液中,可重复的间断收缩幅度随去甲肾上腺素浓度而分级。这些平滑肌在无钙溶液中反复最大程度收缩的能力表明,从细胞内储存库释放的Ca2 +发生了再循环。这些收缩在高钾(去极化)溶液中的出现支持了这样的结论(Devine、Somlyo和Somlyo,1972年),即细胞内Ca2 +的释放是药物 - 机械偶联的机制之一。用直径约75纳米的电子探针检测到高钙浓度(大于10 mmol/kg干重)的质膜下区域数量,在收缩峰值时冷冻的肌肉中减少,从松弛状态下的4.7/细胞周边减少到收缩制剂中的1.4/细胞周边。在冷冻替代的平滑肌中,可以看到连接肌浆网的膜,含有高钙的区域被确定为肌浆网(s.r.)的一部分,这表明s.r.是去甲肾上腺素和咖啡因释放Ca2 +的储存库。