Duty S, Allen D G
Department of Physiology, University of Sydney, NSW, Australia.
Exp Physiol. 1995 Jul;80(4):529-41. doi: 10.1113/expphysiol.1995.sp003865.
In this study the effects of ATP-sensitive K+ channel modulators were studied in intact single fibres dissected from mouse skeletal muscle. Indo-1 was used to measure [Ca2+]i simultaneously with force during normal and fatiguing stimulation. In control fibres, opening of ATP-sensitive K+ channels with BRL 38227 produced a small reduction in tetanic force and [Ca2+]i. In contrast, glibenclamide, a selective blocker of the ATP-sensitive K+ channel, slightly increased tetanic force and [Ca2+]i in these fibres and also increased Ca2+ sensitivity. Glibenclamide produced a more marked increase in tetanic force and [Ca2+]i during the later stages of fatiguing stimulation, although this effect was observed in only 50% of fibres examined. We conclude from this study that glibenclamide produces a partial reversal of the later stages of fatigue in a subpopulation of muscle fibres. Opening of ATP-sensitive K+ channels may therefore contribute to the decline in tetanic force and [Ca2+]i characteristic of skeletal muscle fatigue.
在本研究中,对从小鼠骨骼肌分离出的完整单根纤维进行了ATP敏感性钾通道调节剂作用的研究。使用Indo-1在正常刺激和疲劳刺激过程中同时测量[Ca2+]i和肌力。在对照纤维中,用BRL 38227开放ATP敏感性钾通道会使强直肌力和[Ca2+]i略有降低。相比之下,ATP敏感性钾通道的选择性阻滞剂格列本脲会使这些纤维的强直肌力和[Ca2+]i略有增加,并且还增加了Ca2+敏感性。在疲劳刺激的后期,格列本脲使强直肌力和[Ca2+]i有更明显的增加,尽管仅在50%的检测纤维中观察到这种效应。我们从这项研究得出结论,格列本脲在一部分肌纤维中可使疲劳后期出现部分逆转。因此,ATP敏感性钾通道的开放可能导致骨骼肌疲劳特征性的强直肌力和[Ca2+]i下降。