Lewis S E, Anderson P, Goldspink D F
Biochem J. 1982 Apr 15;204(1):257-64. doi: 10.1042/bj2040257.
Several experimental procedures were used to increase the intracellular concentration of Ca2+ and determine its effects on protein turnover in isolated extensor digitorum longus and soleus muscle. These methods included the use of ionophore A23187, caffeine, dibucaine, thymol and procaine, all agents known to induce the release of calcium by acting either on the sarcolemma and/or on the sarcoplasmic reticulum. Another approach involved varying the external concentration of Ca2+ in the media in which the muscles were incubated. The changes in muscle Ca2+ concentrations after exposure to the various calcium-releasing agents were in keeping with accepted modes of action of these agents on muscle membranes. The findings suggest that increasing the sarcoplasmic concentration of Ca2+ inhibits protein synthesis and enhances protein breakdown. These catabolic effects of Ca2+ are compared with the changes induced in muscle protein turnover after exposure to insulin or cyclic nucleotides, and in myopathic muscle and situations of work overload. Attention is also drawn to some of the difficulties involved in definitively implicating Ca2+ as a factor involved in the normal regulation of protein turnover.
采用了几种实验方法来提高细胞内Ca2+浓度,并确定其对离体趾长伸肌和比目鱼肌蛋白质周转的影响。这些方法包括使用离子载体A23187、咖啡因、丁卡因、百里酚和普鲁卡因,所有这些试剂都已知通过作用于肌膜和/或肌浆网来诱导钙的释放。另一种方法是改变孵育肌肉的培养基中Ca2+的外部浓度。暴露于各种钙释放剂后肌肉Ca2+浓度的变化与这些试剂对肌肉膜的公认作用模式一致。研究结果表明,增加肌浆中Ca2+浓度会抑制蛋白质合成并增强蛋白质分解。将Ca2+的这些分解代谢作用与暴露于胰岛素或环核苷酸后、在肌病性肌肉和工作负荷过重情况下肌肉蛋白质周转所诱导的变化进行了比较。还提请注意在明确将Ca2+视为参与蛋白质周转正常调节的一个因素方面所涉及的一些困难。