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1
Predicted delays in the activation of the contractile system.收缩系统激活的预测延迟。
Biophys J. 1968 May;8(5):608-25. doi: 10.1016/S0006-3495(68)86511-7.
2
A reconstruction of charge movement during the action potential in frog skeletal muscle.青蛙骨骼肌动作电位期间电荷移动的重建。
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Electrical properties of the transverse tubular system.横管系统的电特性。
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Capacitance of the surface and transverse tubular membrane of frog sartorius muscle fibers.青蛙缝匠肌纤维表面和横管膜的电容
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Linear electrical properties of the transverse tubules and surface membrane of skeletal muscle fibers.骨骼肌纤维横小管和表面膜的线性电特性。
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Reconstruction of the action potential of frog sartorius muscle.青蛙缝匠肌动作电位的重建。
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Electromechanical coupling in tubular muscle fibers. II. Resistance and capacitance of one transverse tubule.管状肌纤维中的机电耦合。II. 一条横小管的电阻和电容。
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[Fiber-type morphology and function of the triads in frog (Rana esculenta) skeletal muscle)].[青蛙(食用蛙)骨骼肌三联体的纤维类型形态与功能]
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Radial spread of contraction in frog muscle fibres.青蛙肌肉纤维收缩的径向扩展。
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Electromechanical coupling in tubular muscle fibers. I. The organization of tubular muscle fibers in the scorpion Leiurus quinquestriatus.管状肌纤维中的机电耦合。I. 蝎子五条纹肥尾蝎管状肌纤维的组织结构。
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本文引用的文献

1
The potassium and chloride conductance of frog muscle membrane.青蛙肌肉膜的钾离子和氯离子电导率。
J Physiol. 1962 Aug;163(1):61-103. doi: 10.1113/jphysiol.1962.sp006959.
2
An analysis of the end-plate potential recorded with an intracellular electrode.用细胞内电极记录的终板电位分析。
J Physiol. 1951 Nov 28;115(3):320-70. doi: 10.1113/jphysiol.1951.sp004675.
3
THE RELATION BETWEEN THE LATE AFTER-POTENTIAL AND THE SIZE OF THE TRANSVERSE TUBULAR SYSTEM OF FROG MUSCLE.蛙肌迟后电位与横管系统大小之间的关系。
J Gen Physiol. 1964 Nov;48(2):235-63. doi: 10.1085/jgp.48.2.235.
4
Is muscle contraction initiated by internal current flow?肌肉收缩是由内部电流流动引发的吗?
J Physiol. 1960 May;151(2):363-84. doi: 10.1113/jphysiol.1960.sp006444.
5
The effect of sudden changes in ionic concentrations on the membrane potential of single muscle fibres.离子浓度突然变化对单根肌纤维膜电位的影响。
J Physiol. 1960 Sep;153(2):370-85. doi: 10.1113/jphysiol.1960.sp006540.
6
The effect of nitrate and other anions on the mechanical response of single muscle fibres.硝酸盐及其他阴离子对单根肌纤维力学反应的影响。
J Physiol. 1960 Sep;153(2):404-12. doi: 10.1113/jphysiol.1960.sp006542.
7
Potassium contractures in single muscle fibres.单根肌纤维中的钾挛缩
J Physiol. 1960 Sep;153(2):386-403. doi: 10.1113/jphysiol.1960.sp006541.
8
Local activation of striated muscle fibres.横纹肌纤维的局部激活。
J Physiol. 1958 Dec 30;144(3):426-41. doi: 10.1113/jphysiol.1958.sp006111.
9
Muscle structure and theories of contraction.肌肉结构与收缩理论。
Prog Biophys Biophys Chem. 1957;7:255-318.
10
The ineffectiveness of the `window field' in the initiation of muscle contraction.“窗孔区”在引发肌肉收缩方面的无效性。
J Physiol. 1954 Aug 27;125(2):396-404. doi: 10.1113/jphysiol.1954.sp005167.

收缩系统激活的预测延迟。

Predicted delays in the activation of the contractile system.

作者信息

Falk G

出版信息

Biophys J. 1968 May;8(5):608-25. doi: 10.1016/S0006-3495(68)86511-7.

DOI:10.1016/S0006-3495(68)86511-7
PMID:5699799
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1367403/
Abstract

The capacitance C'(e), presumed to be located across the walls of the transverse tubules of twitch fibers, was identified in earlier impedance measurements by virtue of having a resistance in series with it. When the voltage V(m) across the surface membrane is made to vary, the voltage V(c) across C'(e) will be delayed with respect to V(m), the extent of the delay depending on the location of the series resistance. Model 1 assumes that the resistivity of the lumen of the tubules is negligible; model 2 assumes that the series resistance arises entirely in the tubular lumen; model 3 assumes that the resistivity of the tubular lumen is small, but not negligible and that the bulk of the resistance arises in a structure directly in series with C'(e) and having a similar geometric distribution. If V(m) varies sinusoidally, the relative value of V(c(max)) will fall with increasingly higher powers of the frequency at the center of the fiber if model 2 is applicable, whereas models 1 and 3 predict that V(c(max)) will fall at high frequency only in proportion to the frequency everywhere in the cross-section of the fiber. Equations have been derived for the voltage change V(c) in response to a step change of V(m) and during an action potential. On the assumption that contraction is initiated when V(c) reaches mechanical threshold, the delay between the activation of myofibrils on the axis of the fiber and at the surface would amount to 2.6 msec in model 2 and 0.25 msec in model 3 for frog fibers of about 100 mum diameter during a twitch.

摘要

电容C'(e)被认为位于单收缩纤维横管的管壁上,在早期的阻抗测量中,因其串联有一个电阻而被识别出来。当表面膜上的电压V(m)发生变化时,C'(e)两端的电压V(c)相对于V(m)会出现延迟,延迟程度取决于串联电阻的位置。模型1假设小管管腔的电阻率可忽略不计;模型2假设串联电阻完全来自于小管管腔;模型3假设小管管腔的电阻率较小但不可忽略,且大部分电阻来自于与C'(e)直接串联且具有相似几何分布的结构。如果V(m)呈正弦变化,若模型2适用,在纤维中心处,V(c(max))的相对值将随着频率的幂次增加而下降,而模型1和3预测V(c(max))仅在纤维横截面上的所有位置与频率成比例地在高频时下降。已经推导出了V(m)发生阶跃变化以及在动作电位期间电压变化V(c)的方程。假设当V(c)达到机械阈值时引发收缩,对于直径约为100μm的青蛙纤维,在单收缩过程中,模型2中纤维轴上和表面肌原纤维激活之间的延迟为2.6毫秒,模型3中为0.25毫秒。