Book W J, Abel M, Eisenkraft J B
Department of Anesthesiology, Mount Sinai Medical Center, New York, New York.
Drug Saf. 1994 May;10(5):331-49. doi: 10.2165/00002018-199410050-00001.
Muscle relaxants block neuromuscular transmission, acting at nicotinic acetylcholine receptors of the neuromuscular junction. Suxamethonium (succinylcholine) is a depolarising agent, whereas all other relaxants in clinical use are nondepolarising. The desired neuromuscular block results from the structural similarity of muscle relaxants to acetylcholine, enabling the interaction with receptors at the neuromuscular junction. Adverse effects of suxamethonium are generally related to its agonist mode of action. Autonomic cardiovascular effects may result. Other adverse effects include anaphylactic or anaphylactoid reactions, and histamine release. Various disease states may present specific considerations in the use of muscle relaxants. Although many complications of muscle relaxants (such as prolonged block or resistance) are easily treated, others may require immediate intervention and vigorous therapy. Careful selection of appropriate relaxants for particular patients will usually prevent the occurrence of complications.
肌肉松弛剂作用于神经肌肉接头的烟碱型乙酰胆碱受体,阻断神经肌肉传递。琥珀酰胆碱是一种去极化剂,而临床使用的所有其他松弛剂都是非去极化剂。理想的神经肌肉阻滞是由于肌肉松弛剂与乙酰胆碱在结构上相似,从而能够与神经肌肉接头处的受体相互作用。琥珀酰胆碱的不良反应通常与其激动剂作用模式有关。可能会产生自主心血管效应。其他不良反应包括过敏或类过敏反应以及组胺释放。在使用肌肉松弛剂时,各种疾病状态可能需要特殊考虑。尽管肌肉松弛剂的许多并发症(如阻滞延长或耐药)易于治疗,但其他一些并发症可能需要立即干预和积极治疗。为特定患者仔细选择合适的松弛剂通常可以预防并发症的发生。