Hashimoto S, Shibata O, Tsuda A, Iwanaga S, Makita T, Sumikawa K
Department of Anesthesiology, Nagasaki University School of Medicine, Japan.
Res Commun Mol Pathol Pharmacol. 1998 Jun;100(3):255-63.
Interaction of the steroidal muscle relaxants, pancuronium, vecuronium and rocuronium with airway muscarinic receptors of rat trachea was investigated in vitro concerning the contractile and phosphatidylinositol (PI) responses. Pancuronium and vecuronium attenuated, while rocuronium did not affect carbachol (CCh)-induced contraction and CCh-induced IP1 accumulation. Pancuronium could inhibit completely CCh-induced contraction at a dose of 30 microM, while it could not inhibit completely CCh-induced IP1 accumulation at the same dose. These drugs attenuated KCl-induced contraction. These results suggest that pancuronium and vecuronium would attenuate airway smooth muscle contraction through the inhibition of muscarinic receptor-mediated PI response, and that the inhibition of voltage-operated Ca++ channel might be involved, in part, in the attenuation by pancuronium of the contraction.
在体外研究了甾体类肌肉松弛剂泮库溴铵、维库溴铵和罗库溴铵与大鼠气管气道毒蕈碱受体的相互作用,涉及收缩反应和磷脂酰肌醇(PI)反应。泮库溴铵和维库溴铵可减弱收缩反应,而罗库溴铵不影响卡巴胆碱(CCh)诱导的收缩和CCh诱导的IP1积累。泮库溴铵在30 microM剂量时可完全抑制CCh诱导的收缩,但在相同剂量下不能完全抑制CCh诱导的IP1积累。这些药物可减弱氯化钾诱导的收缩。这些结果表明,泮库溴铵和维库溴铵可能通过抑制毒蕈碱受体介导的PI反应来减弱气道平滑肌收缩,并且泮库溴铵对收缩的减弱作用可能部分涉及对电压门控Ca++通道的抑制。