Quantification of ethyl glucuronide, ethyl sulfate, nicotine, and its metabolites in human fetal liver and placenta

被引:4
作者
Swortwood, Madeleine J. [1 ,2 ]
Bartock, Sarah H. [1 ]
Scheidweiler, Karl B. [1 ]
Shaw, Sophie
Filis, Panagiotis [3 ]
Douglas, Alex [3 ]
O'Shaughnessy, Peter J. [4 ]
Soffientini, Ugo [4 ]
Lucendo-Villarin, Baltasar [5 ]
Iredale, John P. [6 ]
Hay, David C. [5 ]
Fowler, Paul A. [3 ]
Huestis, Marilyn A. [1 ,7 ,8 ]
机构
[1] NIDA, Chem & Drug Metab, Intramural Res Program, NIH, Baltimore, MD 21224 USA
[2] Sam Houston State Univ, Coll Criminal Justice, Dept Forens Sci, Huntsville, TX 77340 USA
[3] Univ Aberdeen, Sch Med Med Sci & Nutr, Inst Med Sci, Foresterhill, Aberdeen, Scotland
[4] Univ Glasgow, Inst Biodivers Anim Hlth & Comparat Med, Coll Med Vet & Life Sci, Glasgow G61 1QH, Lanark, Scotland
[5] Univ Edinburgh, MRC Ctr Regenerat Med, Edinburgh, Midlothian, Scotland
[6] Univ Bristol, Senate House,Tyndall Ave, Bristol BS8 1TH, Avon, England
[7] Univ Maryland, Sch Med, 655 W Baltimore St, Baltimore, MD 21201 USA
[8] 683 Shore Rd,Severna Pk, Severna Park, MD 21146 USA
基金
美国国家卫生研究院; 英国医学研究理事会;
关键词
Ethyl glucuronide; Nicotine; Human fetal liver; Placenta; Pregnancy; Prenatal exposure; TANDEM MASS-SPECTROMETRY; MATERNAL CIGARETTE-SMOKING; INFANT-DEATH-SYNDROME; NEUROBEHAVIORAL PROFILE; ALCOHOL-CONSUMPTION; ENZYME EXPRESSION; IN-VITRO; PREGNANCY; EXPOSURE; MECONIUM;
D O I
10.1007/s11419-017-0389-2
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
Purpose Tobacco and alcohol use during pregnancy is serious public health concerns and result in adverse developmental outcomes. Identifying in utero exposure is often achieved through meconium analysis or via maternal self-report. In this study, we analyzed fetal liver and placenta to examine second trimester alcohol and smoking exposure. Methods A validated liquid chromatography-tandem mass spectrometry method for simultaneous analysis of nicotine and its metabolites and alcohol markers (ethyl glucuronide: EtG and ethyl sulfate: EtS) was employed to analyze 193 fetal liver and 48 placenta (n = 47 paired) samples from electively terminated pregnancies. Results EtG, EtS, and nicotine markers' limits of detection were 0.7-20 ng/g in fetal samples. Ninety-eight fetal liver and 23 placenta samples were EtG/EtS-positive, while 137 liver and 25 placenta samples were positive for tobacco exposure. When both alcohol markers were present in samples, EtG/EtS ratios were 1.6-11.1 in 17 livers and 2.5-31.1 in 10 placentas. Median (range) summed tobacco marker concentrations were 422 (1.0-2776) and 154 (1.61621) ng/g in livers and placentas, respectively. Median EtG and nicotine marker concentrations were higher in liver than placenta in paired samples. Strong evidence of exposure occurred in 11 and 22 pairs, respectively, when both samples were positive for alcohol and/or tobacco markers. Conclusions These paired fetal liver and placenta alcohol and tobacco data provided a unique means for examining the effects of in utero exposure, a critical first step in selecting fetal samples for proteomic and RNA sequencing studies that could provide mechanisms for adverse developmental outcomes.
引用
收藏
页码:102 / 112
页数:11
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