TY - JOUR
T1 - A comparative evaluation of the transport of H2-receptor antagonists by the human and baboon placenta
AU - Dicke, J. M.
AU - Johnson, R. F.
AU - Henderson, G. I.
AU - Kuehl, T. J.
AU - Schenker, S.
N1 - Funding Information:
From the ·Department of Obstetrics and Gynecology and the tDepartment of Medicine, Division of Gastroenterology and N utrition, University of Texas Health Science Center at San Antonio, San Antonio, Texas, the Audie L. Murphy Memorial Veterans' Hospital, San Antonio, Texas, and the :fDepartment of Physiology and Medicine, Southwest Foundation for Biomedical Research, San Antonio, Texas. Supported by NIH Grants Number NIAS 7R01ASS05814 and HL36536 and Eli Lilly & Co. Grant in Aid. Reprint requests: Jeffrey M. Dicke, MD, Department of Obstetrics and Gynecology, Washington 'University School of Medicine, The Jewish Hospital of St. Louis, 216 South Kingshighway, St. Louis, MO 63110.
PY - 1988
Y1 - 1988
N2 - 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, anti-pyrine. 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.
AB - 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, anti-pyrine. 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.
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U2 - 10.1097/00000441-198803000-00007
DO - 10.1097/00000441-198803000-00007
M3 - Article
C2 - 2895583
AN - SCOPUS:0023886587
VL - 295
SP - 198
EP - 206
JO - American Journal of the Medical Sciences
JF - American Journal of the Medical Sciences
SN - 0002-9629
IS - 3
ER -