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Cisatracurium

順-阿屈庫銨

Mechanism of action:

Cisatracurium 是一種非去極化型神經肌肉阻斷劑(non-depolarizing neuromuscular blocker),屬於芐基異喹啉鎓(benzylisoquinolinium)類分子。Cisatracurium 在運動終板(motor end-plate)的菸鹼型乙醯膽鹼受體(nicotinic acetylcholine receptor)上與乙醯膽鹼(acetylcholine)競爭結合位點,阻止該受體活化,進而阻止鈉離子通道開啟,導致無法產生終板電位(end-plate potential),肌肉因此無法去極化與收縮。

​Reference(s):

1. Szakmany T et al. (2015). Use of cisatracurium in critical care: a review of the literature. Minerva Anestesiol. 


2. Bryson HM et al. (1997). Cisatracurium besilate: A review of its pharmacology and clinical potential in anaesthetic practice. Drugs. 


3. Kisor DF et al. (1999). Clinical pharmacokinetics of cisatracurium besilate. Clin Pharmacokinet.

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