Kakimoto S, Saito H, Matsuki N
Department of Chemical Pharmacology, Faculty of Pharmaceutical Science, The University of Tokyo, Bunkyo-ku, Japan.
Biol Pharm Bull. 1997 May;20(5):486-9. doi: 10.1248/bpb.20.486.
The ability of three cardiac glycosides, ouabain, digitonin and digitoxin, to induce emesis and their mechanism(s) of action were investigated in Suncus murinus. The intraperitoneal injection of ouabain but not digitonin nor digitoxin caused vomiting in a dose-dependent manner. However, the administration of ouabain into the cerebroventricle did not cause emesis. Ouabain-induced emesis was partly prevented by surgical abdominal vagotomy. Pretreatment with tropisetron, a selective 5-HT3 (5-hydroxytriptamine) receptor antagonist, did not affect the emetic response evoked by ouabain. These results suggest that ouabain exerts emetic effects via peripheral mechanism(s), but 5-HT3 receptors are not involved in the pathway.
在小家鼠中研究了三种强心苷(哇巴因、洋地黄皂苷和地高辛)诱导呕吐的能力及其作用机制。腹腔注射哇巴因可引起呕吐,且呈剂量依赖性,而洋地黄皂苷和地高辛则不会。然而,将哇巴因注入脑室不会引起呕吐。手术切断腹部迷走神经可部分预防哇巴因诱导的呕吐。用选择性5-羟色胺3(5-HT3)受体拮抗剂托烷司琼预处理,不影响哇巴因引起的呕吐反应。这些结果表明,哇巴因通过外周机制发挥催吐作用,但5-HT3受体不参与该途径。