Yamamoto H, Nakamura Y, Kunoh Y, Ichihara K, Nagasaka M, Asai H
Jpn J Pharmacol. 1986 Jul;41(3):283-92. doi: 10.1254/jjp.41.283.
Effects of (-) cis-2,3-dihydro-3-(4-methylpiperazinylmethyl)-2-phenyl-1,5-benz othiazepin-4-(5H ) -one hydrochloride (BTM-1086) on various experimental gastric and duodenal ulcers were studied in rats. In the pylorus-ligated ulcer, restraint and water immersion stress ulcer, and drug-induced ulcer (indomethacin, aspirin, reserpine, serotonin, cysteamine), BTM-1086 prevented the development of ulcer at a dose of 0.1 to 1 mg/kg, p.o., but only weakly inhibited the histamine-induced gastric ulcer. The inhibitory activities of BTM-1086 were significantly higher than those of atropine sulfate. In the healing experiment with the acetic acid-induced stomach ulcer, BTM-1086 (1 mg/kg/day, p.o., X 14) showed a significant healing effect, which was higher than that of propantheline bromide. BTM-1086 at a dose of 0.2 mg/kg, i.d., remarkably inhibited the gastric secretion 6 hr after pylorus ligation. The aspirin-induced reductions of the total acid and K+ as well as the increments of the volume and Na+ in the gastric secretion were prevented dose-dependently by pretreatment with BTM-1086.
研究了盐酸(-)顺式-2,3-二氢-3-(4-甲基哌嗪基甲基)-2-苯基-1,5-苯并硫氮杂䓬-4-(5H)-酮(BTM-1086)对大鼠各种实验性胃溃疡和十二指肠溃疡的影响。在幽门结扎性溃疡、束缚和水浸应激性溃疡以及药物诱导性溃疡(吲哚美辛、阿司匹林、利血平、血清素、半胱胺)模型中,BTM-1086以0.1至1mg/kg的口服剂量可预防溃疡的形成,但对组胺诱导的胃溃疡仅有微弱抑制作用。BTM-1086的抑制活性显著高于硫酸阿托品。在醋酸诱导的胃溃疡愈合实验中,BTM-1086(1mg/kg/天,口服,共14天)显示出显著的愈合效果,高于溴丙胺太林。BTM-1086以0.2mg/kg的腹腔注射剂量,可显著抑制幽门结扎6小时后的胃酸分泌。BTM-1086预处理可剂量依赖性地防止阿司匹林诱导的胃酸总量和钾离子减少以及胃酸分泌量和钠离子增加。