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青蛙骨骼肌纤维中的超慢收缩失活

Ultraslow contractile inactivation in frog skeletal muscle fibers.

作者信息

Caputo C, Bolaños P

机构信息

Centro de Biofisica y Bioquímica, Instituto Venezolano de Investagiciones Científicas (IVIC), Caracas.

出版信息

J Gen Physiol. 1990 Jul;96(1):47-56. doi: 10.1085/jgp.96.1.47.

Abstract

After a contracture response, skeletal muscle fibers enter into a state of contractile refractoriness or inactivation. Contractile inactivation starts soon after membrane depolarization, and causes spontaneous relaxation from the contracture response. Here we demonstrate that contractile inactivation continues to develop for tens of seconds if the membrane remains in a depolarized state. We have studied this phenomenon using short (1.5 mm) frog muscle fibers dissected from the Lumbricalis brevis muscles of the frog, with a two-microelectrode voltage-clamp technique. After a contracture caused by membrane depolarization to 0 mV, from a holding potential of -100 mV, a second contracture can be developed only if the membrane is repolarized beyond a determined potential value for a certain period of time. We have used a repriming protocol of 1 or 2 s at -100 mV. After this repriming period a fiber, if depolarized again to 0 mV, may develop a second contracture, whose magnitude and time course will depend on the duration of the period during which the fiber was maintained at 0 mV before the repriming process. With this procedure it is possible to demonstrate that the inactivation process builds up with a very slow time course, with a half time of approximately 35 s and completion in greater than 100 s. After prolonged depolarizations (greater than 100 s), the repriming time course is slower and the inactivation curve (obtained by plotting the extent of repriming against the repriming membrane potential) is shifted toward more negative potentials by greater than 30 mV when compared with similar curves obtained after shorter depolarizing periods (10-30 s). These results indicate that important changes occur in the physical state of the molecular moiety that is responsible for the inactivation phenomenon. The shift of the inactivation curve can be partially reversed by a low concentration (50 microM) of lanthanum ions. In the presence of 0.5 mM caffeine, larger responses can be obtained even after prolonged depolarization periods, indicating that the fibers maintain their capacity to liberate calcium.

摘要

在挛缩反应之后,骨骼肌纤维进入收缩不应期或失活状态。收缩失活在膜去极化后不久开始,并导致从挛缩反应中自发松弛。在此我们证明,如果膜保持在去极化状态,收缩失活会持续发展数十秒。我们使用从青蛙的短蚓状肌中分离出的短(1.5毫米)青蛙肌肉纤维,采用双微电极电压钳技术研究了这一现象。在将膜从 -100 mV 的钳制电位去极化至 0 mV 引起挛缩后,只有当膜复极化超过一个确定的电位值并持续一定时间后,才能引发第二次挛缩。我们采用了在 -100 mV 下 1 或 2 秒的再激发方案。在此再激发期后,如果纤维再次去极化至 0 mV,可能会引发第二次挛缩,其幅度和时间进程将取决于在再激发过程之前纤维保持在 0 mV 的时间段。通过这个过程可以证明,失活过程以非常缓慢的时间进程建立,半衰期约为 35 秒,且在超过 100 秒时完成。在长时间去极化(大于 100 秒)后,再激发时间进程更慢,并且与较短去极化期(10 - 30 秒)后获得的类似曲线相比,失活曲线(通过绘制再激发程度与再激发膜电位的关系得到)向更负的电位偏移超过 30 mV。这些结果表明,负责失活现象的分子部分的物理状态发生了重要变化。失活曲线的偏移可以被低浓度(50 microM)的镧离子部分逆转。在存在 0.5 mM 咖啡因的情况下,即使在长时间去极化期后也能获得更大的反应,表明纤维保持了释放钙的能力。

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