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格列本脲对青蛙骨骼肌的作用:疲劳期间钾离子ATP通道激活的证据。

The effect of glibenclamide on frog skeletal muscle: evidence for K+ATP channel activation during fatigue.

作者信息

Light P E, Comtois A S, Renaud J M

机构信息

University of Ottawa, Department of Physiology, Ontario, Canada.

出版信息

J Physiol. 1994 Mar 15;475(3):495-507. doi: 10.1113/jphysiol.1994.sp020088.

DOI:10.1113/jphysiol.1994.sp020088
PMID:8006831
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1160400/
Abstract
  1. The purpose of this study was to determine whether ATP-sensitive K+ (K+ATP) channels are activated and contribute to the decrease in force during fatigue development in the sartorius muscle of the frog, Rana pipiens. Tetanic force (elicited by field stimulation), action potential and membrane conductance (using conventional microelectrodes), were measured in the presence and absence of glibenclamide, a K+ATP channel antagonist. Experiments were performed in bicarbonate-buffered solutions at pH 7.2. 2. In unfatigued muscle 100 mumol l-1 glibenclamide had no effect on the resting potential, the overshoot, the half-depolarization time or the maximum rate of depolarization of action potentials, while the mean half-repolarization time increased by 19 +/- 4% (+/- S.E.M.) and the maximum rate of repolarization decreased by 17 +/- 5%. 3. Fatigue was elicited using 100 ms tetanic contractions every 1 s for 3 min. In the absence of glibenclamide the mean half-repolarization time increased from 0.57 +/- 0.05 to 0.89 +/- 0.05 ms during fatigue. The mean half-repolarization times after fatigue, when muscle fibres were exposed to 100 mumol l-1 glibenclamide either 60 min prior to fatigue or 60 s before the end of fatigue, were 1.16 +/- 0.08 and 1.17 +/- 0.07 ms respectively. Application of 100 mumol l-1 glibenclamide after 5 min of recovery did not increase the half-repolarization time, but decreased the rate of recovery compared to control values. 4. In unfatigued muscles, 100 mumol l-1 glibenclamide did not affect the tetanic contraction. In the absence of glibenclamide, the mean tetanic force after fatigue was 11.0 +/- 0.9% of prefatigue values. Application of 100 mumol l-1 glibenclamide 60 min before fatigue increased the rate of fatigue development as the mean tetanic force was 4.8 +/- 0.8% after 3 min of stimulation. The addition of 100 mumol l-1 glibenclamide 60 s before the end of fatigue had no effect on tetanic force during this time compared to control. 5. In the absence of glibenclamide, muscles recovered 90.1 +/- 1.6% of their tetanic force after 100 min. Addition of 100 mumol l-1 glibenclamide 60 min prior to fatigue significantly reduced the capacity of muscles to recover their tetanic force: after 100 min of recovery tetanic force was only 47.3 +/- 9.4% of the pre-fatigue value.(ABSTRACT TRUNCATED AT 400 WORDS)
摘要
  1. 本研究的目的是确定在牛蛙(Rana pipiens)的缝匠肌疲劳发展过程中,ATP敏感性钾离子(K⁺ATP)通道是否被激活并导致肌肉力量下降。在存在和不存在格列本脲(一种K⁺ATP通道拮抗剂)的情况下,测量强直收缩力(通过场刺激诱发)、动作电位和膜电导(使用传统微电极)。实验在pH 7.2的碳酸氢盐缓冲溶液中进行。2. 在未疲劳的肌肉中,100 μmol l⁻¹ 格列本脲对静息电位、超射、半去极化时间或动作电位的最大去极化速率没有影响,而平均半复极化时间增加了19±4%(±标准误),最大复极化速率降低了17±5%。3. 每隔1秒进行100毫秒的强直收缩,持续3分钟以诱发疲劳。在不存在格列本脲的情况下,疲劳过程中平均半复极化时间从0.57±0.05毫秒增加到0.89±0.05毫秒。当肌肉纤维在疲劳前60分钟或疲劳结束前60秒暴露于100 μmol l⁻¹ 格列本脲时,疲劳后的平均半复极化时间分别为1.16±0.08毫秒和1.17±0.07毫秒。恢复5分钟后应用100 μmol l⁻¹ 格列本脲并没有增加半复极化时间,但与对照值相比降低了恢复速率。4. 在未疲劳的肌肉中,100 μmol l⁻¹ 格列本脲不影响强直收缩。在不存在格列本脲的情况下,疲劳后的平均强直收缩力为疲劳前值的11.0±0.9%。在疲劳前60分钟应用100 μmol l⁻¹ 格列本脲增加了疲劳发展速率,因为刺激3分钟后的平均强直收缩力为4.8±0.8%。与对照相比,在疲劳结束前60秒添加100 μmol l⁻¹ 格列本脲在此期间对强直收缩力没有影响。5. 在不存在格列本脲的情况下,肌肉在100分钟后恢复了其强直收缩力的90.1±1.6%。在疲劳前60分钟添加100 μmol l⁻¹ 格列本脲显著降低了肌肉恢复其强直收缩力的能力:恢复100分钟后,强直收缩力仅为疲劳前值的47.3±9.4%。(摘要截断于400字)

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