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本文引用的文献

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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。
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2
The force exerted by active striated muscle during and after change of length.主动横纹肌在长度改变期间及之后所施加的力。
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THE MAXIMUM SARCOMERE LENGTH FOR CONTRACTION OF ISOLATED MYOFIBRILS.分离肌原纤维收缩的最大肌节长度。
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The maximum length for contraction in vertebrate straiated muscle.脊椎动物横纹肌收缩的最大长度。
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Enhancement of mechanical performance in frog muscle fibres after quick increases in load.负荷快速增加后青蛙肌纤维机械性能的增强。
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The effects of muscle length on intracellular calcium transients in mammalian cardiac muscle.肌肉长度对哺乳动物心肌细胞内钙瞬变的影响。
J Physiol. 1982 Jun;327:79-94. doi: 10.1113/jphysiol.1982.sp014221.
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Residual force enhancement after stretch of contracting frog single muscle fibers.收缩状态下的青蛙单根肌纤维被拉伸后的残余力增强
J Gen Physiol. 1982 Nov;80(5):769-84. doi: 10.1085/jgp.80.5.769.
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Skeletal muscle: length-dependent effects of potentiating agents.骨骼肌:增强剂的长度依赖性效应。
Science. 1981 Oct 2;214(4516):79-82. doi: 10.1126/science.6974399.
9
Depression of mechanical performance by active shortening during twitch and tetanus of vertebrate muscle fibres.脊椎动物肌纤维单收缩和强直收缩期间主动缩短导致的力学性能降低。
Acta Physiol Scand. 1980 May;109(1):15-26. doi: 10.1111/j.1748-1716.1980.tb06559.x.
10
31P NMR studies of resting muscle in normal human subjects.正常人类受试者静息肌肉的31P核磁共振研究。
Adv Exp Med Biol. 1984;170:333-47. doi: 10.1007/978-1-4684-4703-3_28.

主动预缩短对单根青蛙肌纤维等长和等张收缩性能的影响。

Effect of active pre-shortening on isometric and isotonic performance of single frog muscle fibres.

作者信息

Granzier H L, Pollack G H

机构信息

Division of Bioengineering, University of Washington, Seattle 98195.

出版信息

J Physiol. 1989 Aug;415:299-327. doi: 10.1113/jphysiol.1989.sp017723.

DOI:10.1113/jphysiol.1989.sp017723
PMID:2640463
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1189178/
Abstract
  1. We studied the effects of shortening history on isometric force and isotonic velocity in single intact frog fibres. Fibres were isometrically tetanized. When force reached a plateau, shortening was imposed, after which the fibre was held isometric again. Isometric force after shortening could then be compared with controls in which no shortening had taken place. 2. Sarcomere length was measured simultaneously with two independent methods: a laser-diffraction method and a segment-length method that detects the distance between two markers attached to the surface of the fibre, about 800 microns apart. 3. The fibre was mounted between two servomotors. One was used to impose the load clamp while the other cancelled the translation that occurred during this load clamp. Thus, translation of the segment under investigation could be minimized. 4. Initial experiments were performed at the fibre level. We found that active preshortening reduced isometric force considerably, thereby confirming earlier work of others. Force reductions as large as 70% were observed. 5. Under conditions in which there were large effects of shortening at the fibre level, we measured sarcomere length changes in the central region of the fibre. These sarcomeres shortened much less than the fibre's average. In fact, when the load was high, these sarcomeres lengthened while the fibre as a whole shortened. Thus, while the fibre-length signal implied that sarcomeres might have shortened to some intermediate length, in reality some sarcomeres were much longer, others much shorter. 6. Experiments performed at the sarcomere level revealed that isometric force was unaffected by previous sarcomere shortening provided the shortening occurred against either a low load or over a short distance. However, if the work done during shortening was high, force after previous shortening was less than if sarcomeres had remained at the final length throughout contraction. The correlation between the force deficit and the work done during shortening was statistically significant (P = 0.0001). 7. Interrupting the tetanus for 0.5-3.0 s did not reverse the effects of shortening on isometric force; at least 5-10 min of rest were required before force recovered completely. 8. Sarcomeres accelerated during the period of shortening under constant load, indicating that the sarcomeres became progressively stronger. However, the acceleration was less than that predicted from the force-velocity relation applicable at each of the sarcomere lengths transversed during shortening. 9. Velocity of shortening appeared to be much more sensitive to previous shortening than isometric force. 10. Results obtained with the diffraction method were the same as those obtained with the segment method.(ABSTRACT TRUNCATED AT 400 WORDS)
摘要
  1. 我们研究了缩短历史对单个完整青蛙纤维等长力和等张速度的影响。纤维进行等长强直收缩。当力达到平台期时,施加缩短,之后纤维再次保持等长。然后可以将缩短后的等长力与未发生缩短的对照进行比较。2. 采用两种独立方法同时测量肌节长度:激光衍射法和检测附着在纤维表面、相距约800微米的两个标记之间距离的节段长度法。3. 将纤维安装在两个伺服电机之间。一个用于施加负荷钳制,另一个抵消在此负荷钳制期间发生的平移。因此,可以将所研究节段的平移降至最低。4. 最初的实验在纤维水平进行。我们发现主动预缩短会显著降低等长力,从而证实了其他人早期的工作。观察到力的降低高达70%。5. 在纤维水平存在缩短的显著影响的条件下,我们测量了纤维中部区域的肌节长度变化。这些肌节的缩短远小于纤维的平均缩短。实际上,当负荷较高时,这些肌节会延长而纤维整体缩短。因此,虽然纤维长度信号表明肌节可能已经缩短到某个中间长度,但实际上一些肌节更长,另一些更短。6. 在肌节水平进行的实验表明,只要缩短是在低负荷或短距离下进行,等长力不受先前肌节缩短的影响。然而,如果缩短过程中所做的功较高,先前缩短后的力小于肌节在整个收缩过程中一直保持在最终长度时的力。力的不足与缩短过程中所做功之间的相关性具有统计学意义(P = 0.0001)。7. 将强直收缩中断0.5 - 3.0秒并不能逆转缩短对等长力的影响;至少需要5 - 10分钟的休息,力才能完全恢复。8. 在恒定负荷下缩短期间,肌节加速,表明肌节变得越来越有力。然而,加速度小于根据缩短过程中所经过的每个肌节长度适用的力 - 速度关系所预测的加速度。9. 缩短速度似乎比等长力对先前的缩短更敏感。10. 用衍射法获得的结果与用节段法获得的结果相同。(摘要截取自400字)