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恶性高热:触发的药理学。

Malignant hyperthermia: pharmacology of triggering.

机构信息

Section of Translational Anaesthetic and Surgical Sciences, Leeds Institute of Molecular Medicine, University of Leeds, UK.

出版信息

Br J Anaesth. 2011 Jul;107(1):48-56. doi: 10.1093/bja/aer132. Epub 2011 May 30.

DOI:10.1093/bja/aer132
PMID:21624965
Abstract

Over the past 50 yr, many drugs have been implicated as triggers of malignant hyperthermia (MH), a potentially fatal pharmacogenetic disorder of skeletal muscle calcium regulation. This review discusses the potent inhalation agents as the principal triggers and evidence that the modern agents, desflurane, sevoflurane, and isoflurane, can cause florid MH reactions in the same way as halothane but also are associated with reactions whose onset is delayed for several hours into anaesthesia. There is evidence that the triggering of MH by drugs is dose-dependent but the minimum dose that will trigger the condition is unknown. This has implications for the preparation of anaesthetic machines when used for known or suspected MH patients. While succinylcholine enhances the response of potent inhalation anaesthetics, its role as an inherent trigger of the condition is controversial. Non-depolarizing neuromuscular blocking drugs appear to protect against the development of MH and this may be by blocking excitation-coupled calcium entry-a recently described route of skeletal muscle calcium entry that may also explain the mechanism of the effect of succinylcholine in MH. Another mechanism for extracellular calcium influx, store-operated calcium entry, is activated in MH muscle and may explain how a triggered reaction is sustained. Finally, reports of drugs that have been implicated as additional triggers of MH over the past 10 yr are discussed.

摘要

在过去的 50 年中,许多药物已被认为是恶性高热(MH)的触发因素,MH 是一种潜在致命的骨骼肌钙调节遗传疾病。本文讨论了强效吸入性麻醉剂作为主要触发因素的证据,以及现代麻醉剂地氟烷、七氟烷和异氟烷也可能以与氟烷相同的方式引起明显的 MH 反应,但也与几个小时后麻醉开始时出现的反应有关。有证据表明,药物引发 MH 是剂量依赖性的,但引发该病症的最小剂量尚不清楚。这对已知或疑似 MH 患者使用麻醉机的准备工作具有重要意义。虽然琥珀酰胆碱增强了强效吸入性麻醉剂的反应,但它作为该病症的固有触发因素的作用存在争议。非去极化神经肌肉阻滞剂似乎可以预防 MH 的发生,这可能是通过阻断兴奋偶联钙内流来实现的——这是一种最近描述的骨骼肌钙内流途径,也可以解释琥珀酰胆碱在 MH 中的作用机制。另一种细胞外钙内流的机制,即储存操纵钙内流,在 MH 肌肉中被激活,可能解释了触发反应是如何持续的。最后,还讨论了过去 10 年来被认为是 MH 其他触发因素的药物。

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