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The creatine phosphoryltransfer reaction in iodoacetate-poisoned muscle.碘乙酸中毒肌肉中的肌酸磷酸转移反应。
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Cellular mechanisms of muscle fatigue.肌肉疲劳的细胞机制。
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3
ATP formation and ATP hydrolysis during fatiguing, intermittent stimulation of different types of single muscle fibres from Xenopus laevis.在对非洲爪蟾不同类型单肌纤维进行疲劳性间歇性刺激过程中的ATP形成与ATP水解
J Muscle Res Cell Motil. 1993 Dec;14(6):608-18. doi: 10.1007/BF00141558.
4
Changes of the force-velocity relation, isometric tension and relaxation rate during fatigue in intact, single fibres of Xenopus skeletal muscle.非洲爪蟾骨骼肌完整单纤维疲劳过程中力-速度关系、等长张力和舒张速率的变化
J Muscle Res Cell Motil. 1994 Jun;15(3):287-98. doi: 10.1007/BF00123481.
5
Fatigue and metabolism of frog muscle fibers during stimulation and in response to caffeine.青蛙肌肉纤维在刺激过程中以及对咖啡因反应时的疲劳与代谢
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A simple analysis of the "phosphocreatine shuttle".“磷酸肌酸穿梭”的简单分析
Am J Physiol. 1984 May;246(5 Pt 1):C365-77. doi: 10.1152/ajpcell.1984.246.5.C365.
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The effects of ADP and phosphate on the contraction of muscle fibers.二磷酸腺苷(ADP)和磷酸盐对肌纤维收缩的影响。
Biophys J. 1985 Nov;48(5):789-98. doi: 10.1016/S0006-3495(85)83837-6.
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Effects on shortening velocity of rabbit skeletal muscle due to variations in the level of thin-filament activation.细肌丝激活水平变化对兔骨骼肌缩短速度的影响。
J Physiol. 1986 Aug;377:487-505. doi: 10.1113/jphysiol.1986.sp016199.
9
Force and membrane potential during and after fatiguing, intermittent tetanic stimulation of single Xenopus muscle fibres.在对非洲爪蟾单根肌纤维进行疲劳性间歇性强直刺激期间及之后的力和膜电位。
Acta Physiol Scand. 1986 Nov;128(3):369-78. doi: 10.1111/j.1748-1716.1986.tb07990.x.
10
Force and membrane potential during and after fatiguing, continuous high-frequency stimulation of single Xenopus muscle fibres.在对非洲爪蟾单根肌纤维进行疲劳性连续高频刺激期间及之后的力和膜电位。
Acta Physiol Scand. 1986 Nov;128(3):359-68. doi: 10.1111/j.1748-1716.1986.tb07989.x.

在非洲爪蟾骨骼肌完整纤维中观察到,在没有磷酸肌酸的情况下最大缩短速度降低。

Reduced maximum shortening velocity in the absence of phosphocreatine observed in intact fibres of Xenopus skeletal muscle.

作者信息

Westerblad H, Lännergren J

机构信息

Department of Physiology and Pharmacology, Karolinska Institutet, Stockholm, Sweden.

出版信息

J Physiol. 1995 Jan 15;482 ( Pt 2)(Pt 2):383-90. doi: 10.1113/jphysiol.1995.sp020525.

DOI:10.1113/jphysiol.1995.sp020525
PMID:7714829
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1157736/
Abstract
  1. ADP inhibits the maximum shortening velocity (V0) in skeletal muscle. [ADP] may increase considerably during contractions and reduce V0 in the absence of energy buffering by phosphocreatine (PCr). We have tested this hypothesis by comparing V0 in long and short tetani produced in situations where PCr buffering is absent. 2. Single, intact muscle fibres were dissected from toe muscles of Xenopus and stimulated by current pulses at 20 degrees C. The test sequence consisted of a 400 ms tetanus, followed after 3 s by a 1400 ms tetanus and after an additional 4 s by a 400 ms tetanus. V0 was measured with slack tests at 200 and 1200 ms, respectively. 3. The PCr system was inactivated in three ways: (i) fatiguing fibres with repeated short tetani; (ii) inhibition of the creatine kinase (CK) reaction with dinitrofluorobenzene; and (iii) inhibition of energy metabolism with iodoacetic acid and cyanide. 4. Under control conditions V0 was similar in all three test tetani. With inactive PCr buffering V0 was about 30% lower in the long tetanus. This slowing recovered fully in the second short tetanus in fatigue and with CK inhibition. 5. Calculations suggest that [ADP] can reach very high levels (about 3 mM) during prolonged contractions in the absence of PCr buffering.
摘要
  1. 二磷酸腺苷(ADP)抑制骨骼肌的最大缩短速度(V0)。在收缩过程中,[ADP]可能会大幅增加,并且在没有磷酸肌酸(PCr)进行能量缓冲的情况下会降低V0。我们通过比较在没有PCr缓冲的情况下产生的长强直收缩和短强直收缩中的V0来检验这一假设。2. 从非洲爪蟾的趾肌中分离出单根完整的肌纤维,并在20℃下用电流脉冲进行刺激。测试序列包括一个400毫秒的强直收缩,3秒后是一个1400毫秒的强直收缩,再过4秒后是一个400毫秒的强直收缩。分别在200毫秒和1200毫秒时用松弛测试来测量V0。3. 通过三种方式使PCr系统失活:(i)用重复的短强直收缩使纤维疲劳;(ii)用二硝基氟苯抑制肌酸激酶(CK)反应;(iii)用碘乙酸和氰化物抑制能量代谢。4. 在对照条件下,所有三次测试强直收缩中的V0相似。在PCr缓冲失活的情况下,长强直收缩中的V0降低了约30%。在疲劳和CK抑制的情况下,第二次短强直收缩中这种减慢完全恢复。5. 计算表明,在没有PCr缓冲的情况下,长时间收缩过程中[ADP]可达到非常高的水平(约3 mM)。