Isomaa B, Ahlroth T
Acta Pharmacol Toxicol (Copenh). 1979 Nov;45(5):387-93. doi: 10.1111/j.1600-0773.1979.tb02406.x.
The effects of surface-active alkyltrimethylammonium salts (C10--C20) on the contractile activity of isolated rat jejunum and on the gastrointestinal motility in anaesthetized rats were studied. The surfactants caused a dose-dependent depression of spontaneous contractions and of acetyl-beta-methylcholine and BaCl2 induced contractions of isolated rat jejunum. The depressant activity of the surface-active alkyltrimethylammonium salts on smooth muscle contraction increased with an increase in the length of the alkyl chain to maximum activity at C16. It is suggested that the depressant activity of the surface-active alkyltrimethylammonium salts on smooth muscle contraction is due to a non-specific interaction of the surfactants with the cellmembrane of the muscle cells. No effect on gastric and intestinal motility in vivo was observed following intragastric or intraintestinal administrations of surface-active alkyltrimethylammonium salts. This lack of effect upon intraintestinal or intragastric administration probably depends on an inability of the surfactants to reach the site of action when administered from the mucosal side.
研究了表面活性烷基三甲基铵盐(C10 - C20)对离体大鼠空肠收缩活性以及对麻醉大鼠胃肠运动的影响。这些表面活性剂引起离体大鼠空肠自发收缩以及乙酰-β-甲基胆碱和BaCl2诱导的收缩呈剂量依赖性抑制。表面活性烷基三甲基铵盐对平滑肌收缩的抑制活性随着烷基链长度的增加而增强,在C16时达到最大活性。提示表面活性烷基三甲基铵盐对平滑肌收缩的抑制活性是由于表面活性剂与肌肉细胞的细胞膜发生非特异性相互作用所致。经胃内或肠内给予表面活性烷基三甲基铵盐后,未观察到对体内胃肠运动有影响。经肠内或胃内给药无此作用可能是因为从黏膜侧给药时表面活性剂无法到达作用部位。