Dicke J M, Johnson R F, Henderson G I, Kuehl T J, Schenker S
Department of Obstetrics and Gynecology, University of Texas Health Science Center, San Antonio.
Am J Med Sci. 1988 Mar;295(3):198-206. doi: 10.1097/00000441-198803000-00007.
Using a single cotyledon perfusion model, the placental transport of four H2-receptor antagonists, cimetidine, famotidine, nizatidine, and ranitidine, was determined and compared using normal term human and normal preterm baboon placentas. In both the human and baboon placentas, the transport of each agent was similar whether administered singly or in combination with the other drugs. Drug transport was the same in both directions, maternal-to-fetal and vice versa, indicating a lack of preferential transfer. The H2-receptor antagonists were transported at about 40% the rate of the freely diffusable reference compound, antipyrine. There were no significant differences between the human and baboon in any of the parameters of placental function evaluated. Placental glucose and oxygen consumptions, and lactate production were comparable in the human and baboon preparations. The transport and clearance of each of the H2-antagonists were similar in each species.
采用单叶灌注模型,使用足月正常人类胎盘和早产正常狒狒胎盘,测定并比较了四种H2受体拮抗剂(西咪替丁、法莫替丁、尼扎替丁和雷尼替丁)的胎盘转运情况。在人类和狒狒胎盘中,每种药物单独给药或与其他药物联合给药时,其转运情况相似。药物在母胎和胎母两个方向上的转运相同,表明不存在优先转运。H2受体拮抗剂的转运速率约为可自由扩散的参考化合物安替比林的40%。在所评估的胎盘功能的任何参数方面,人类和狒狒之间均无显著差异。人类和狒狒制剂中的胎盘葡萄糖和氧气消耗以及乳酸生成相当。每种H2拮抗剂在每个物种中的转运和清除情况相似。