Wada A, Arita M, Takara H, Sumikawa K, Uezono Y, Izumi F
Department of Pharmacology, University of Occupational and Environmental Health, School of Medicine, Kitakyushu, Japan.
Naunyn Schmiedebergs Arch Pharmacol. 1989 Dec;340(6):605-9. doi: 10.1007/BF00717734.
In cultured bovine adrenal medullary cells, vecuronium, pancuronium and D-tubocurarine reduced carbachol-induced 45Ca2+ influx and catecholamine secretion by inhibiting 22Na+ influx via nicotinic receptor-ion channel complex with IC50 values of 0.43, 7.6 and 3.9 mumol/l, respectively. IC50 values of pancuronium and D-tubocurarine observed in adrenal medulla were one order of magnitude higher than the plasma concentrations of these muscle relaxants reported to produce 50% neuromuscular blockade, while IC50 of vecuronium was quite close between adrenal medulla and skeletal muscle.
在培养的牛肾上腺髓质细胞中,维库溴铵、泮库溴铵和筒箭毒碱通过抑制经由烟碱受体 - 离子通道复合物的22Na+内流,降低了卡巴胆碱诱导的45Ca2+内流和儿茶酚胺分泌,其半数抑制浓度(IC50)值分别为0.43、7.6和3.9 μmol/L。在肾上腺髓质中观察到的泮库溴铵和筒箭毒碱的IC50值比据报道产生50%神经肌肉阻滞的这些肌肉松弛剂的血浆浓度高一个数量级,而维库溴铵在肾上腺髓质和骨骼肌中的IC50相当接近。