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咖啡因和兰尼碱对冬眠花栗鼠心肌电机械偶联作用的比较:细胞内钙储备的作用

Comparison between effects of caffeine and ryanodine on electromechanical coupling in myocardium of hibernating chipmunks: role of internal Ca stores.

作者信息

Kondo N

机构信息

Mitsubishi-Kasei Institute of Life Sciences, Tokyo, Japan.

出版信息

Br J Pharmacol. 1988 Dec;95(4):1287-91. doi: 10.1111/j.1476-5381.1988.tb11766.x.

Abstract
  1. To clarify the cause of uncoupling of Ca influx through Ca channels and the contractility of the myocardium in hibernating chipmunks, the electromechanical effects of two different internal Ca store inhibitors, caffeine and ryanodine, and a cardiotonic agent, isoprenaline, were investigated in papillary muscles of hibernating animals. 2. Ryanodine (10(-6) M), an inhibitor of internal Ca release, abolished the contraction with a marked inhibition of the action potential plateau (APp). In such preparations, an increase in Ca influx induced by isoprenaline (5 x 10(-8) M) failed to augment the contraction, indicating uncoupling of Ca influx and contraction. 3. In ryanodine pretreated preparations, 10 mM caffeine produced an early phase of APp, but did not affect the contraction abolished by ryanodine, while a higher concentration of caffeine (25 mM) markedly increased the contraction with an augmentation of the electrical response. 4. In the absence of ryanodine, caffeine (5 mM) almost abolished the contraction with a greater inhibition of APp. In such preparations, isoprenaline greatly increased the contraction with an augmentation of the early phase of APp. 5. These effects were not significantly affected by additional application of ryanodine, but were inhibited by nifedipine, a Ca channel blocker. 6. These observations suggest that in cardiac muscles of hibernating animals, lack of the positive inotropic effect of isoprenaline may be attributed to a rapid and effective sequestration of increased cytoplasmic Ca through Ca influx by internal stores, probably by enhancement of their ability to take up Ca.
摘要
  1. 为阐明冬眠花栗鼠中通过钙通道的钙内流与心肌收缩性解偶联的原因,在冬眠动物的乳头肌中研究了两种不同的细胞内钙储存抑制剂咖啡因和ryanodine以及强心剂异丙肾上腺素的机电效应。2. Ryanodine(10⁻⁶ M),一种细胞内钙释放抑制剂,消除了收缩并显著抑制了动作电位平台期(APp)。在这类制剂中,异丙肾上腺素(5×10⁻⁸ M)诱导的钙内流增加未能增强收缩,表明钙内流与收缩解偶联。3. 在经ryanodine预处理的制剂中,10 mM咖啡因产生了APp的早期阶段,但不影响被ryanodine消除的收缩,而更高浓度的咖啡因(25 mM)显著增加了收缩并增强了电反应。4. 在没有ryanodine的情况下,咖啡因(5 mM)几乎消除了收缩并更大程度地抑制了APp。在这类制剂中,异丙肾上腺素极大地增加了收缩并增强了APp的早期阶段。5. 这些效应不受额外应用ryanodine的显著影响,但被钙通道阻滞剂硝苯地平抑制。6. 这些观察结果表明,在冬眠动物的心肌中,异丙肾上腺素缺乏正性肌力作用可能归因于细胞内储存通过钙内流对增加的细胞质钙的快速有效隔离,可能是通过增强它们摄取钙的能力。

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