Abbott B D, Birnbaum L S, Diliberto J J
Reproductive Toxicology Division, U.S. Environmental Protection Agency, Research Triangle Park, North Carolina 27711, USA.
Toxicol Appl Pharmacol. 1996 Nov;141(1):256-63. doi: 10.1006/taap.1996.0282.
2,3,7,8-Tetracholoridbenzo-p-dioxin (TCDD) is a developmentally toxic environmental contaminant capable of inducing cleft palate and hydronephrosis in embryonic C57BL/6N mice. In this study, the disposition of TCDD was determined in pregnant C57BL/6N mice in the 24 hr immediately following oral administration on Gestation Day (GD) 12. TCDD was detected in maternal blood, liver, and fat and in the placenta, embryonic liver, and palate within 30 min after dosing on GD 12. The levels peaked in blood and placenta at 3 hr and in the other tissues at 8 hr. Levels of TCDD decreased slightly after 8 hr in embryonic liver and palate. In vitro systems were used to study the mechanisms of action of TCDD and in these models exposure is typically reported as concentration of TCDD in the culture medium. The present study is the first to allow a direct comparison of the level of TCDD in embryonic tissue after in vivo and in vitro exposures. Uptake of TCDD was determined in embryonic palatal organ culture and tissue levels were then expressed in comparable units for both in vivo and in vitro exposures. The data provide new information on distribution in the pregnant mouse and the embryo and also show that the palatal organ culture model provides a reasonable dosimetric representation of in utero exposure.
2,3,7,8-四氯二苯并对二噁英(TCDD)是一种具有发育毒性的环境污染物,能够在胚胎期的C57BL/6N小鼠中诱发腭裂和肾积水。在本研究中,于妊娠第12天(GD 12)口服给药后24小时内,测定了妊娠C57BL/6N小鼠体内TCDD的处置情况。在GD 12给药后30分钟内,在母体血液、肝脏、脂肪以及胎盘、胚胎肝脏和腭部均检测到了TCDD。其水平在血液和胎盘于3小时达到峰值,在其他组织于8小时达到峰值。在胚胎肝脏和腭部,8小时后TCDD水平略有下降。利用体外系统研究TCDD的作用机制,在这些模型中,暴露通常以培养基中TCDD的浓度来报告。本研究首次对体内和体外暴露后胚胎组织中TCDD的水平进行了直接比较。在胚胎腭器官培养中测定了TCDD的摄取情况,然后以可比单位表示体内和体外暴露后的组织水平。这些数据提供了关于在妊娠小鼠和胚胎中分布的新信息,并且还表明腭器官培养模型为子宫内暴露提供了合理的剂量学表征。