Adnet P J, Krivosic-Horber R M, Adamantidis M M, Reyford H, Cordonnier C, Haudecoeur G
Department of Anesthesia, Faculty of Medicine, Lille, France.
Anesthesiology. 1991 Sep;75(3):413-9. doi: 10.1097/00000542-199109000-00006.
The purpose of this investigation was to determine if alteration in the function of the dihydropyridine receptor may in turn modify halothane-induced contractures in muscle bundles from patients susceptible to malignant hyperthermia (MH). The effects of Ca(2+)-free Krebs Ringer (KR) solution, 5 microM verapamil, 5 microM nifedipine, and 10 microM of the Ca2+ agonist BAY K 8644 on halothane-induced contracture were therefore investigated. The halothane-induced contracture was prevented in the absence of extracellular Ca2+ and significantly reduced in the presence of verapamil or nifedipine. BAY K 8644 significantly enhanced the 0.5-, 1.0-, and 1.5-vol % halothane-induced contracture in MH-susceptible muscle bundles. When BAY K 8644 was dissolved in Ca(2+)-free KR solution, no contracture was observed in MH-susceptible muscle bundles. These results on cut MH-susceptible human muscle bundles support the hypothesis that halothane-induced contracture in MH can be modified by the binding of Ca2+ agonists or antagonists to the dihydropyridine receptor. The role of Ca2+ entry phenomena remains unclear, but the results suggest that extracellular Ca2+ is required to reprime or to bind to some sites of the dihydropyridine receptors.
本研究的目的是确定二氢吡啶受体功能的改变是否会反过来改变恶性高热(MH)易感患者肌肉束中氟烷诱导的挛缩。因此,研究了无钙的克雷布斯林格(KR)溶液、5微摩尔维拉帕米、5微摩尔硝苯地平以及10微摩尔钙离子激动剂BAY K 8644对氟烷诱导挛缩的影响。在无细胞外钙离子的情况下,氟烷诱导的挛缩得到预防,而在维拉帕米或硝苯地平存在时则显著减轻。BAY K 8644显著增强了MH易感肌肉束中0.5%、1.0%和1.5%体积分数氟烷诱导的挛缩。当BAY K 8644溶解在无钙的KR溶液中时,在MH易感肌肉束中未观察到挛缩。这些关于切断的MH易感人肌肉束的结果支持这样一种假说,即MH中氟烷诱导的挛缩可通过钙离子激动剂或拮抗剂与二氢吡啶受体的结合而改变。钙离子内流现象的作用仍不清楚,但结果表明细胞外钙离子是重新启动或结合到二氢吡啶受体某些位点所必需的。