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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。
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2
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。
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THE EFFECT OF LOAD ON THE HEAT OF SHORTENING OF MUSCLE.负荷对肌肉缩短热的影响。
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Sinusoidal analysis: a high resolution method for correlating biochemical reactions with physiological processes in activated skeletal muscles of rabbit, frog and crayfish.正弦分析:一种将生化反应与兔、蛙和小龙虾活化骨骼肌的生理过程相关联的高分辨率方法。
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Control of sarcomere length in skinned muscle fibres of Rana temporaria during mechanical transients.机械瞬态期间林蛙皮肤肌肉纤维中肌节长度的控制
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8
Initiation of active contraction by photogeneration of adenosine-5'-triphosphate in rabbit psoas muscle fibres.通过在兔腰大肌纤维中光生成三磷酸腺苷引发主动收缩
J Physiol. 1984 Sep;354:605-24. doi: 10.1113/jphysiol.1984.sp015395.
9
Relaxation of rabbit psoas muscle fibres from rigor by photochemical generation of adenosine-5'-triphosphate.通过光化学产生三磷酸腺苷-5'-磷酸使处于强直收缩状态的兔腰大肌纤维松弛。
J Physiol. 1984 Sep;354:577-604. doi: 10.1113/jphysiol.1984.sp015394.
10
Dissociation of the actin.subfragment 1 complex by adenyl-5'-yl imidodiphosphate, ADP, and PPi.肌动蛋白亚片段1复合物被腺苷-5'-亚氨二磷酸、ADP和焦磷酸解离。
J Biol Chem. 1980 Jan 25;255(2):543-8.

通过在兔腰大肌纤维中光解笼锁ATP研究MgADP存在时的横桥动力学。

Cross-bridge kinetics in the presence of MgADP investigated by photolysis of caged ATP in rabbit psoas muscle fibres.

作者信息

Dantzig J A, Hibberd M G, Trentham D R, Goldman Y E

机构信息

Department of Physiology, University of Pennsylvania, Philadelphia 19104.

出版信息

J Physiol. 1991 Jan;432:639-80. doi: 10.1113/jphysiol.1991.sp018405.

DOI:10.1113/jphysiol.1991.sp018405
PMID:1886072
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1181346/
Abstract
  1. The interaction between MgADP and rigor cross-bridges in glycerol-extracted single fibres from rabbit psoas muscle has been investigated using laser pulse photolysis of caged ATP (P3-1(2-nitrophenyl)ethyladenosine 5'-triphosphate) in the presence of MgADP and following small length changes applied to the rigor fibre. 2. Addition of 465 microM-MgADP to a rigor fibre caused rigor tension to decrease by 15.3 +/- 0.7% (S.E.M., n = 24 trials in thirteen fibres). The half-saturation value for this tension reduction was 18 +/- 4 microM (n = 23, thirteen fibres). 3. Relaxation from rigor by photolysis of caged ATP in the absence of Ca2+ was markedly slowed by inclusion of 20 microM-2 mM-MgADP in the photolysis medium. 4. Four phases of tension relaxation occurred with MgADP in the medium: at, a quick partial relaxation (in pre-stretch fibres); bt, a slowing of relaxation or a rise in tension for 50-100 ms; ct, a sudden acceleration of relaxation; and dt, a final, nearly exponential relaxation. 5. Experiments at varied MgATP and MgADP concentrations suggested that phase at is due to MgATP binding to nucleotide-free cross-bridges. 6. Phase bt was abbreviated by including 1-20 mM-orthophosphate (Pi) in the photolysis medium, or by applying quick stretches before photolysis or during phase bt. These results suggest that phases bt and ct are complex processes involving ADP dissociation, cross-bridge reattachment and co-operative detachment involving filament sliding and the Ca(2+)-regulatory system. 7. Stretching relaxed muscle fibres to 3.2-3.4 microns striation spacing followed by ATP removal and release of the rigor fibre until tension fell below the relaxed level allowed investigation of the strain dependence of relaxation in the regions of negative cross-bridge strain. In the presence of 50 microM-2 mM-MgADP and either 10 mM-Pi or 20 mM-2,3-butanedione monoxime, relaxation following photolysis of caged ATP was 6- to 8-fold faster for negatively strained cross-bridges than for positively strained ones. This marked strain dependence of cross-bridge detachment is predicted from the model of A. F. Huxley (1957). 8. In the presence of Ca2+, activation of contraction following photolysis of caged ATP was slowed by inclusion of 20-500 microM-MgADP in the medium. An initial decrease in tension related to cross-bridge detachment by MgATP was markedly suppressed in the presence of MgADP. 9. Ten millimolar Pi partly suppressed active tension generation in the presence of MgADP.(ABSTRACT TRUNCATED AT 400 WORDS)
摘要
  1. 利用笼状ATP(P3-1(2-硝基苯基)乙基腺苷5'-三磷酸)的激光脉冲光解,在存在MgADP且对强直纤维施加微小长度变化的情况下,研究了MgADP与兔腰大肌甘油提取单纤维中强直横桥之间的相互作用。2. 向强直纤维中添加465微摩尔/升的MgADP,导致强直张力降低15.3±0.7%(标准误,13根纤维进行了24次试验)。这种张力降低的半饱和值为18±4微摩尔/升(n = 23,13根纤维)。3. 在光解介质中加入20微摩尔/升至2毫摩尔/升的MgADP,在无Ca2+时通过笼状ATP光解使强直松弛明显减慢。4. 介质中有MgADP时,张力松弛出现四个阶段:at,快速部分松弛(预拉伸纤维中);bt,松弛减慢或张力升高50 - 100毫秒;ct,松弛突然加速;dt,最终近乎指数式的松弛。5. 不同MgATP和MgADP浓度下的实验表明,at阶段是由于MgATP与无核苷酸横桥结合。6. 在光解介质中加入1至20毫摩尔/升的正磷酸盐(Pi),或在光解前或bt阶段施加快速拉伸,可缩短bt阶段。这些结果表明,bt和ct阶段是复杂过程,涉及ADP解离、横桥重新附着以及涉及细丝滑动和Ca(2+)调节系统的协同解离。7. 将松弛的肌肉纤维拉伸至3.2 - 3.4微米条纹间距,然后去除ATP并释放强直纤维,直到张力降至松弛水平以下,从而可以研究负横桥应变区域中松弛的应变依赖性。在存在50微摩尔/升至2毫摩尔/升的MgADP以及10毫摩尔/升的Pi或20毫摩尔/升的2,3 - 丁二酮单肟的情况下,笼状ATP光解后的松弛,负应变横桥比正应变横桥快6至8倍。这种横桥解离对应变的明显依赖性是根据A. F. 赫胥黎(1957年)的模型预测的。8. 在有Ca2+存在时,介质中加入20至500微摩尔/升的MgADP会减慢笼状ATP光解后的收缩激活。在有MgADP存在时,与MgATP导致的横桥解离相关的初始张力降低明显受到抑制。9. 10毫摩尔/升的Pi在有MgADP存在时部分抑制了主动张力的产生。