Schaeffer P, Baissat J, Dureng G, Lamar J C, Stoclet J C
Eur J Pharmacol. 1986 Apr 9;123(1):155-9. doi: 10.1016/0014-2999(86)90699-0.
The effects of bepridil and its quaternary ammonium derivative (BN+) were compared, showing that: (i) both drugs inhibited K+-induced contractions with similar time courses and potencies, (ii) bepridil blocked the tonic but not the phasic component of contractions elicited by noradrenaline, whereas BN+ had no effect on noradrenaline-elicited contractions. These results, and the relative insensitivity of skinned taenia caeci to bepridil, suggest that this drug and BN+ do not act directly on contractile proteins but affect K+- and noradrenaline-induced calcium channel activities differentially.
比较了苄普地尔及其季铵衍生物(BN+)的作用,结果表明:(i)两种药物抑制钾离子诱导的收缩,其时间进程和效力相似;(ii)苄普地尔阻断去甲肾上腺素引起的收缩的强直成分,但不阻断其相性成分,而BN+对去甲肾上腺素引起的收缩无作用。这些结果,以及皮肤化的盲肠绦虫对苄普地尔相对不敏感,表明该药物和BN+并非直接作用于收缩蛋白,而是对钾离子和去甲肾上腺素诱导的钙通道活性有不同影响。