Kelkar V V, Gupta R S, Jariwala N U, Joshi N J
Pharmacology. 1979;18(6):319-26. doi: 10.1159/000137272.
Antiacetylcholine activity some beta-adrenoceptor-blocking drugs was investigated using isolated guinea pig cremaster muscle and frog fectus abdominis muscle. On the cremaster muscle, the antagonism to acetylcholine was non competitive in K0 1313, (+/-)-INPEA and (--)-INPEA, competitive in (+)-INPEA and functional in practolol; All three INPEA isomers, practolol and propranolol behaved as noncompetitive antagonists of acetylcholine on frog rectus muscle. Caffeine-induced contractions of this muscle were partially inhibited by propranolol but not by the other drugs. It is suggested that the beta-adrenoceptor-blocking drugs produce their antiacetylcholine action by interaction with sites on the muscle which are different from the cholinceptor, and which vary between compounds and species.
利用豚鼠离体提睾肌和蛙胎腹直肌研究了某些β-肾上腺素受体阻断药的抗乙酰胆碱活性。在提睾肌上,K0 1313、(±)-INPEA和(-)-INPEA对乙酰胆碱的拮抗作用是非竞争性的,(+)-INPEA是竞争性的,而醋丁洛尔是功能性的;所有三种INPEA异构体、醋丁洛尔和普萘洛尔在蛙腹直肌上均表现为乙酰胆碱的非竞争性拮抗剂。普萘洛尔可部分抑制该肌肉由咖啡因诱导的收缩,但其他药物则无此作用。提示β-肾上腺素受体阻断药通过与肌肉上不同于胆碱受体的位点相互作用产生抗乙酰胆碱作用,且这些位点在不同化合物和不同物种之间存在差异。