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咖啡因对青蛙骨骼肌纤维超微结构损伤的作用。钙诱导肌浆网释放钙参与其中的证据。

The action of caffeine in promoting ultrastructural damage in frog skeletal muscle fibres. Evidence for the involvement of the calcium-induced release of calcium from the sarcoplasmic reticulum.

作者信息

Duncan C J, Smith J L

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 1978 Nov;305(2):159-66. doi: 10.1007/BF00508287.

Abstract
  1. Caffeine at concentrations above 5 mM was shown to cause rapidly extensive ultrastructural damage to the myofibrils of frog skeletal muscle. 2. The effect was promoted at lower temperatures, whereas the myofibrils were protected by prior exposure to procaine. 3. It is argued that caffeine causes a Ca2+-induced release of Ca2+ (the CROC) from the S.R. and that the consequent rise in [Ca2+]i promotes the ultrastructural damage observed. 4. Myofibril digradation is also produced by treatment of the muscle with the divalent cation ionophore A23187; this effect is not protected by either procaine or Dantrolene sodium. 5. It is suggested that A23187 causes the release of Ca2+ from the S.R. by a mechanism that differs from both excitation and the CROC; the resultant rise in [Ca2+]i again causes myofibril degradation. 6. The ways in which a marked rise in [Ca2+]i could cause muscle damage and the possible relevance of these findings to the sequence of events in the development of myopathies of human skeletal muscle are discussed.
摘要
  1. 浓度高于5 mM的咖啡因被证明会迅速对青蛙骨骼肌的肌原纤维造成广泛的超微结构损伤。2. 在较低温度下这种效应会增强,而预先用普鲁卡因处理可保护肌原纤维。3. 有人认为咖啡因会导致钙离子从肌浆网中引发钙离子释放(CROC),并且随之而来的细胞内钙离子浓度升高会促使观察到的超微结构损伤。4. 用二价阳离子载体A23187处理肌肉也会产生肌原纤维降解;这种效应不受普鲁卡因或丹曲林钠的保护。5. 有人提出A23187通过一种不同于兴奋和CROC的机制使钙离子从肌浆网中释放;由此导致的细胞内钙离子浓度升高再次引起肌原纤维降解。6. 讨论了细胞内钙离子浓度显著升高导致肌肉损伤的方式以及这些发现与人类骨骼肌肌病发展过程中事件序列的可能相关性。

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