Wilson D E, Scruggs W, Birnbaum J E
Prostaglandins. 1981 Dec;22(6):971-8. doi: 10.1016/0090-6980(81)90025-3.
The efficacy of CL-115,574, a prostaglandin E1 analogue, as an acid antisecretory agent was evaluated in dogs. CL-115,574 inhibited acid secretion maximally at an oral dose of 20 micrograms/kg causing 100% inhibition of acid secretion up to one hour after administration, with significant inhibition of secretion (30%) still present nearly four hours after drug administration. The wide disparity between the maximally effective antisecretory dose 20 micrograms/kg and the dose at which reproducible side effects occurred (1 mg/kg) suggests that this compound may be developed as an antisecretory compound for use in man.
在犬类动物中评估了前列腺素E1类似物CL - 115,574作为一种胃酸分泌抑制剂的功效。CL - 115,574在口服剂量为20微克/千克时可最大程度地抑制胃酸分泌,给药后一小时内可导致胃酸分泌100%被抑制,给药近四小时后仍有显著的分泌抑制作用(30%)。最大有效抑酸剂量20微克/千克与出现可重复副作用的剂量(1毫克/千克)之间存在很大差异,这表明该化合物可能被开发用作人类胃酸分泌抑制剂。