Transplacental Transfer of Nitrosodimethylamine in Perfused Human Placenta

被引:26
作者
Annola, K. [1 ,3 ]
Heikkinen, A. T. [2 ,3 ]
Partanen, H. [1 ,3 ]
Woodhouse, H. [1 ,3 ]
Segerback, D. [4 ]
Vahakangas, K. [1 ,3 ]
机构
[1] Univ Kuopio, Dept Pharmacol & Toxicol, FIN-70211 Kuopio, Finland
[2] Univ Kuopio, Dept Pharmaceut, FIN-70211 Kuopio, Finland
[3] Bioctr Kuopio, Kuopio, Finland
[4] Karolinska Inst, Novum, Dept Biosci & Nutr, S-14157 Huddinge, Sweden
关键词
Fetal exposure; DNA-adducts; Xenobiotic metabolism; Food carcinogens; Human placental perfusion; N-NITROSO COMPOUNDS; CHILDHOOD BRAIN-TUMORS; CORD-BLOOD; CELL-LINES; RAT-LIVER; EXPOSURE; DNA; CONSUMPTION; METABOLISM; CARBAMAZEPINE;
D O I
10.1016/j.placenta.2008.12.012
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Nitrosodimethylamine (NDMA) is a carcinogenic compound present in tobacco smoke and food such as cured meat, smoked fish and beer. The O-6-methylguanine formed in human cord blood in mothers highly exposed to Such products implicates NDMA exposure of the fetus. Dual recirculating human placental perfusion was used to get direct evidence of the transplacental transfer of NDMA and DNA adduct formation in perfused human placenta. Eleven placentas from normal full-term pregnancies were collected immediately after delivery and an isolated lobule was perfused with 1 or 5 mu M of C-14-NDMA with a reference substance, antipyrine (0.1 mg/ml) added to the maternal circulation. Perfusate samples were collected from both maternal and fetal circulations every half an hour for the first two hours and once per hour from thereon. NDMA was analyzed by scintillation Counting and antipyrine by high performance liquid chromatography. The transfer of NDMA was comparable to that of antipyrine and probably occurred through passive diffusion, with the concentrations in maternal and fetal sides equilibrating in 2-3 h. No indication of any effect by efflux transporters on NDMA kinetics was noticed in the experiments utilizing Caco-2 or MDCK- MDCKII-MDR1 cell culture monolayer in a transwell system, either. Furthermore, no NDMA-DNA-adducts were found after the perfusions and no DNA-binding of NDMA was seen in in vitro incubations with human placental microsomes from 8 additional placentas. Thus, our study demonstrates that the human fetus can be exposed to NDMA from the maternal circulation. According to this study and the literature, NDMA is not metabolized in full-term human placenta front healthy non-smoking, non-drinking mothers. It remains to be studied whether NDMA concentrations high enough to evoke fetal toxicity can be obtained from dietary Sources. (C) 2008 Published by Elsevier Ltd.
引用
收藏
页码:277 / 283
页数:7
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