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青蛙骨骼肌去极化与呼吸增加之间的步骤。

The steps between depolarization and the increase in the respiration of frog skeletal muscle.

作者信息

van der Kloot W

出版信息

J Physiol. 1969 Oct;204(3):551-69. doi: 10.1113/jphysiol.1969.sp008931.

Abstract
  1. For many years it has been known that when muscles are depolarized by raising K(+) there is an increase in respiration, even at levels of depolarization below the threshold for a detectable contracture.2. K(+)-stimulated respiration occurs in muscles in which protein synthesis is blocked with puromycin. Stimulation does not depend upon activation of phosphorylase kinase. In muscle poisoned with IIA and kept in N(2), depolarizations below the threshold for contracture cause a fall in creatine phosphate. Apparently an ATPase is activated by depolarization; the resulting ADP is probably the trigger for the increase in oxygen uptake.3. When the T-tubules are destroyed by the glycerol-osmotic shock method depolarization does not produce an increase in respiration.4. Caffeine is known to stimulate respiration at concentrations below the threshold for producing a contracture. Muscles that have been made refractory to stimulation by potassium are still stimulated by caffeine: the action of caffeine is not antagonized by an increase in extracellular Mg(2+). Caffeine must act on a later step in excitation-contraction coupling.5. K(+)-stimulated respiration ultimately depends on the presence of Ca(2+) in the Ringer. However, the Ca(2+) can be replaced by Ni(2+). It is known that Ni(2+) does not activate actomyosin. Ni(2+) is not sequestered by isolated fragments of the sarcoplasmic reticulum. It seems that the Ni(2+) or Ca(2+) in the extracellular solution is required for a superficial step in excitation-contraction coupling.6. Respiration is also often stimulated when muscles are placed in an isotonic sucrose solution, even though the fibres are hyperpolarized. A trace amount of Ca(2+) in the sucrose solution is probably necessary for the response.7. An interaction between Ca(2+) and a superficial membrane receptor appears to be an essential, early step in excitation-contraction coupling.
摘要
  1. 多年来人们已经知道,当通过提高细胞外钾离子浓度使肌肉去极化时,即使在去极化程度低于可检测到挛缩阈值的情况下,呼吸作用也会增强。

  2. 钾离子刺激的呼吸作用发生在用嘌呤霉素阻断蛋白质合成的肌肉中。刺激并不依赖于磷酸化酶激酶的激活。在用IIA中毒并置于氮气中的肌肉中,低于挛缩阈值的去极化会导致磷酸肌酸含量下降。显然,一种ATP酶被去极化激活;由此产生的ADP可能是氧气摄取增加的触发因素。

  3. 当通过甘油渗透休克法破坏T小管时,去极化不会导致呼吸作用增强。

  4. 已知咖啡因在低于产生挛缩阈值的浓度下会刺激呼吸作用。对钾离子刺激产生不应性的肌肉仍会被咖啡因刺激:咖啡因的作用不会因细胞外镁离子浓度增加而受到拮抗。咖啡因必定作用于兴奋-收缩偶联的后期步骤。

  5. 钾离子刺激的呼吸作用最终依赖于任氏液中钙离子的存在。然而,钙离子可以被镍离子替代。已知镍离子不会激活肌动球蛋白。镍离子不会被肌浆网的分离片段所螯合。似乎细胞外溶液中的镍离子或钙离子是兴奋-收缩偶联表面步骤所必需的。

  6. 当肌肉置于等渗蔗糖溶液中时,呼吸作用也常常会受到刺激,尽管肌纤维是超极化的。蔗糖溶液中微量的钙离子可能是产生这种反应所必需的。

  7. 钙离子与表面膜受体之间的相互作用似乎是兴奋-收缩偶联中一个必不可少的早期步骤。

相似文献

5
Restoration of potassium-stimulated respiration of glycerol-treated muscle.
Eur J Pharmacol. 1975 Feb;30(2):288-97. doi: 10.1016/0014-2999(75)90112-0.

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