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引用本文的文献

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本文引用的文献

1
The coupling of an enzymatic reaction to transmembrane flow of electric current in a synthetic "active transport" system.在一个合成的“主动运输”系统中,酶促反应与跨膜电流流动的耦合。
Biophys J. 1967 Nov;7(6):735-57. doi: 10.1016/S0006-3495(67)86620-7. Epub 2008 Dec 31.
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Work and heat in a muscle twitch.肌肉抽搐中的功与热。
Proc R Soc Lond B Biol Sci. 1949 Jun 23;136(883):220-8. doi: 10.1098/rspb.1949.0021.
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The heat of activation and the heat of shortening in a muscle twitch.肌肉收缩时的活化热与缩短热。
Proc R Soc Lond B Biol Sci. 1949 Jun 23;136(883):195-211. doi: 10.1098/rspb.1949.0019.
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The abrupt transition from rest to activity in muscle.肌肉从静止状态到活动状态的突然转变。
Proc R Soc Lond B Biol Sci. 1949 Oct;136(884):399-420. doi: 10.1098/rspb.1949.0033.
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Tropomyosin paracrystals formed by divalent cations.原肌球蛋白二价阳离子形成的副晶。
Science. 1966 May 6;152(3723):794-6. doi: 10.1126/science.152.3723.794.
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The relation between force and speed in muscular contraction.肌肉收缩中力与速度的关系。
J Physiol. 1939 Jun 14;96(1):45-64. doi: 10.1113/jphysiol.1939.sp003756.
7
Muscular force at different speeds of shortening.不同缩短速度下的肌肉力量。
J Physiol. 1935 Nov 22;85(3):277-97. doi: 10.1113/jphysiol.1935.sp003318.
8
A quantitative comparison between the energy liberated and the work performed by the isolated sartorius muscle of the frog.对青蛙离体缝匠肌释放的能量与所做的功进行定量比较。
J Physiol. 1923 Dec 28;58(2-3):175-203. doi: 10.1113/jphysiol.1923.sp002115.
9
Physical chemistry of contractile process in muscle. I. A physicochemical model of contractile mechanism.肌肉收缩过程的物理化学。I. 收缩机制的物理化学模型。
Am J Physiol. 1952 Mar;168(3):766-81. doi: 10.1152/ajplegacy.1952.168.3.766.
10
The heat production associated with the maintenance of a prolonged contraction and the extra heat produced during large shortening.与维持长时间收缩相关的产热以及在大幅度缩短过程中产生的额外热量。
J Physiol. 1951 Feb;112(3-4):438-45. doi: 10.1113/jphysiol.1951.sp004541.

自主能量转换。II. 肌肉收缩能量学的一种研究方法。

Autonomic energy conversion. II. An approach to the energetics of muscular contraction.

作者信息

Caplan S R

出版信息

Biophys J. 1968 Oct;8(10):1167-93. doi: 10.1016/S0006-3495(68)86547-6.

DOI:10.1016/S0006-3495(68)86547-6
PMID:5679394
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1367663/
Abstract

All discussions of muscle energetics concern themselves with the Hill force-velocity relation, which is also the general output relation of a class of self-regulated energy converters and as such contains only a single adjustable parameter -the degree of coupling. It is therefore important to see whether in principle muscle can be included in this class. One requirement is that the muscle should possess a working element characterized by a dissipation function of two terms: mechanical output and chemical input. This has been established by considering the initial steady phase of isotonic and isometric tetanic contraction to represent a stationary state of the fibrils (a considerable body of evidence supports this). Further requirements, which can be justified for the working element, are linearity and incomplete coupling. Thus the chemical input of the muscle may be expected to follow the inverse Hill equation (see Part I). The relatively large changes in activities of reactants which the equation demands could only be controlled by local operation of the regulator, and a scheme is outlined to show how such control may be achieved. Objections to this view recently raised by Wilkie and Woledge rest on at least two important assumptions, the validity of which is questioned: (a) that heat production by processes other than the immediate driving reaction is negligible, which disregards the regulatory mechanism (possibly this involves the calcium pump), and (b) that the affinity of the immediate driving reaction is determined by over-all concentrations. The division of heat production into "shortening heat" and "maintenance heat" or "activation heat" is found to be arbitrary.

摘要

所有关于肌肉能量学的讨论都围绕着希尔力-速度关系,它也是一类自我调节能量转换器的一般输出关系,因此只包含一个可调参数——耦合程度。所以,重要的是要看看原则上肌肉是否能归入这一类。一个要求是肌肉应具有一个工作元件,其特征在于由机械输出和化学输入这两项组成的耗散函数。通过将等张和等长强直收缩的初始稳定阶段视为肌原纤维的静止状态(大量证据支持这一点),这一点已经得到证实。对于该工作元件合理的进一步要求是线性和不完全耦合。因此,可以预期肌肉的化学输入遵循反希尔方程(见第一部分)。该方程所要求的反应物活性的相对较大变化只能通过调节器的局部作用来控制,并且概述了一个方案来说明如何实现这种控制。威尔基和沃利奇最近对这一观点提出的反对意见至少基于两个重要假设,其有效性受到质疑:(a)除直接驱动反应之外的过程产生的热量可忽略不计,这忽视了调节机制(可能涉及钙泵);(b)直接驱动反应的亲和力由总体浓度决定。将产热分为“缩短热”和“维持热”或“激活热”被发现是任意的。