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部分肌浆网钙耗竭对用20 mM乙二醇双四乙酸(EGTA)平衡的青蛙离体肌纤维中钙释放的影响。

Effects of partial sarcoplasmic reticulum calcium depletion on calcium release in frog cut muscle fibers equilibrated with 20 mM EGTA.

作者信息

Pape P C, Jong D S, Chandler W K

机构信息

Department of Cellular and Molecular Physiology, Yale University School of Medicine, New Haven, Connecticut 06510-8026, USA.

出版信息

J Gen Physiol. 1998 Sep;112(3):263-95. doi: 10.1085/jgp.112.3.263.

Abstract

Resting sarcoplasmic reticulum (SR) Ca content ([CaSR]R) was varied in cut fibers equilibrated with an internal solution that contained 20 mM EGTA and 0-1.76 mM Ca. SR Ca release and [CaSR]R were measured with the EGTA-phenol red method (. J. Gen. Physiol. 106:259-336). After an action potential, the fractional amount of Ca released from the SR increased from 0.17 to 0.50 when [CaSR]R was reduced from 1, 200 to 140 microM. This increase was associated with a prolongation of release (final time constant, from 1-2 to 10-15 ms) and of the action potential (by 1-2 ms). Similar changes in release were observed with brief stimulations to -20 mV in voltage-clamped fibers, in which charge movement (Qcm) could be measured. The peak values of Qcm and the fractional rate of SR Ca release, as well as their ON time courses, were little affected by reducing [CaSR]R from 1,200 to 140 microM. After repolarization, however, the OFF time courses of Qcm and the rate of SR Ca release were slowed by factors of 1.5-1.7 and 6.5, respectively. These and other results suggest that, after action potential stimulation of fibers in normal physiological condition, the increase in myoplasmic free [Ca] that accompanies SR Ca release exerts three negative feedback effects that tend to reduce additional release: (a) the action potential is shortened by current through Ca-activated potassium channels in the surface and/or tubular membranes; (b) the OFF kinetics of Qcm is accelerated; and (c) Ca inactivation of Ca release is increased. Some of these effects of Ca on an SR Ca channel or its voltage sensor appear to be regulated by the value of [Ca] within 22 nm of the mouth of the channel.

摘要

在与含有20 mM乙二醇双四乙酸(EGTA)和0 - 1.76 mM钙的内部溶液平衡的切断纤维中,静息肌浆网(SR)钙含量([CaSR]R)有所变化。采用EGTA - 酚红法(《普通生理学杂志》106:259 - 336)测量SR钙释放和[CaSR]R。动作电位后,当[CaSR]R从1200 μM降至140 μM时,从SR释放的钙的分数从0.17增加到0.50。这种增加与释放的延长(最终时间常数,从1 - 2毫秒延长至10 - 15毫秒)和动作电位的延长(延长1 - 2毫秒)相关。在电压钳制的纤维中,当短暂刺激至 - 20 mV时,也观察到了类似的释放变化,其中可以测量电荷移动(Qcm)。将[CaSR]R从1200 μM降至140 μM对Qcm的峰值、SR钙释放的分数速率及其开启时间进程影响很小。然而,复极化后,Qcm和SR钙释放速率的关闭时间进程分别减慢了1.5 - 1.7倍和6.5倍。这些以及其他结果表明,在正常生理条件下对纤维进行动作电位刺激后,伴随SR钙释放的肌浆游离[Ca]增加会产生三种负反馈效应,倾向于减少额外的释放:(a)通过表面和/或管状膜中的钙激活钾通道的电流使动作电位缩短;(b)Qcm的关闭动力学加速;(c)钙释放的钙失活增加。钙对SR钙通道或其电压传感器的这些影响中的一些似乎受通道口22纳米内[Ca]值的调节。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ccc4/2229420/f4b67a2a486c/JGP7694.r1.jpg

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