Fukuda T, Setoguchi M, Inaba K, Shoji H, Tahara T
Research Laboratories, Yoshitomi Pharmaceutical Industries Ltd., Fukuoka, Japan.
Eur J Pharmacol. 1991 Apr 24;196(3):299-305. doi: 10.1016/0014-2999(91)90443-t.
Y-25130( (+/-)N-(1-azabicyclo[2.2.2]oct-3-yl)-6-chloro-4-methyl-3-oxo-3,4-dihydro - 2H-1,4-benzoxazine-8-carboxamide hydrochloride) is a potent and selective 5-HT3 receptor antagonist free of dopamine receptor blocking activity. This compound was effective against emesis induced in animals by cytotoxic drugs or by total body X-radiation. When given prophylactically, the doses required to completely inhibit cisplatin-induced emesis in dogs and doxorubicin and cyclophosphamide-induced emesis in ferrets were 0.1 and 0.3 mg/kg i.v., respectively. Y-25130, at the dose of 0.3 mg/kg i.v., almost completely inhibited X-radiation-induced emesis in ferrets. When given during emesis, the doses required to completely inhibit cisplatin-induced emesis in dogs and doxorubicin- and cyclophosphamide-induced emesis in ferrets were 0.1 and 0.3 mg/kg i.v., respectively. The i.v. dose of 0.3 mg/kg of Y-25130 was enough to almost completely inhibit cisplatin-induced emesis in dogs for 24 h. From these results, it is suggested that Y-25130 may become an effective antiemetic drug against emesis induced by anticancer therapy.
Y - 25130((±)N - (1 - 氮杂双环[2.2.2]辛 - 3 - 基)- 6 - 氯 - 4 - 甲基 - 3 - 氧代 - 3,4 - 二氢 - 2H - 1,4 - 苯并恶嗪 - 8 - 甲酰胺盐酸盐)是一种强效且具有选择性的5 - HT3受体拮抗剂,无多巴胺受体阻断活性。该化合物对细胞毒性药物或全身X射线辐射诱导的动物呕吐有效。预防性给药时,完全抑制顺铂诱导的犬呕吐以及阿霉素和环磷酰胺诱导的雪貂呕吐所需的静脉注射剂量分别为0.1和0.3 mg/kg。静脉注射剂量为0.3 mg/kg的Y - 25130几乎完全抑制了雪貂的X射线辐射诱导的呕吐。在呕吐期间给药时,完全抑制顺铂诱导的犬呕吐以及阿霉素和环磷酰胺诱导的雪貂呕吐所需的静脉注射剂量分别为0.1和0.3 mg/kg。静脉注射0.3 mg/kg的Y - 25130足以在24小时内几乎完全抑制犬的顺铂诱导的呕吐。从这些结果表明,Y - 25130可能成为一种有效的抗癌治疗诱导呕吐的止吐药物。