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C57BL/6N小鼠暴露于2,3,7,8-四氯二苯并对二恶英后诱导肾积水的敏感性高峰期的特征分析。

Characterization of the peak period of sensitivity for the induction of hydronephrosis in C57BL/6N mice following exposure to 2,3,7, 8-tetrachlorodibenzo-p-dioxin.

作者信息

Couture L A, Harris M W, Birnbaum L S

机构信息

Experimental Toxicology Branch, National Institute of Environmental Health, Sciences, Research Triangle Park, North Carolina 27709.

出版信息

Fundam Appl Toxicol. 1990 Jul;15(1):142-50. doi: 10.1016/0272-0590(90)90171-f.

Abstract

2,3,7,8-Tetrachlorodibenzo-p-dioxin (TCDD) is an extremely potent teratogen in mice. Hydronephrosis and cleft palate are the most sensitive measures of teratogenicity in mice following exposure to TCDD and other structurally related polyhalogenated aromatic hydrocarbons. Despite a relatively long half-life, investigators have identified a critical window for the induction of cleft palate in C57BL/6N mice. To characterize the critical period for renal teratogenesis, pregnant C57BL/6N mice were treated once by gavage with 0-24 micrograms TCDD/kg body wt on Gestation Day (GD) 6, 8, 10, 12, or 14. All dams were killed on GD 18, and the fetuses were examined for the presence of hydronephrosis and cleft palate. Maternal liver-to-body weight ratios were significantly elevated above controls on all days, while maternal weight gain was unaffected. Fetal mortality was increased relative to controls only at 24 micrograms TCDD/kg on GD 6. There was no significant difference in fetal body weights between control and TCDD-treated fetuses. The incidence of cleft palate increased in a dose-related fashion from GD 6 to GD 12, and identification of GD 12 as the critical window for induction of clefting of the hard palate was confirmed. Hydronephrosis was observed at all dose levels, regardless of exposure day, and the incidence was close to 100% at 3 micrograms TCDD/kg and higher doses on GD 12 and earlier. At all doses on GD 14, both the incidence and severity of hydronephrosis were decreased relative to all other days. There was a dose-related increase in the severity of the renal lesion on each day, but between GD 6 and 12 severity was constant. Thus, while palatal sensitivity to TCDD increased with gestational age between GD 6 and 12, there was no difference among these days in development of hydronephrosis. The data suggest, however, that on GD 14 the urinary tract may be less sensitive to TCDD.

摘要

2,3,7,8-四氯二苯并-对-二恶英(TCDD)是一种对小鼠极具致畸性的物质。肾盂积水和腭裂是小鼠暴露于TCDD及其他结构相关的多卤代芳烃后最敏感的致畸性指标。尽管TCDD的半衰期相对较长,但研究人员已确定了C57BL/6N小鼠腭裂诱导的关键窗口期。为了明确肾脏致畸的关键时期,在妊娠第6、8、10、12或14天,对怀孕的C57BL/6N小鼠经口灌胃给予0至24微克TCDD/千克体重,仅处理一次。所有母鼠均在妊娠第18天处死,检查胎儿是否存在肾盂积水和腭裂。所有给药日母鼠肝脏与体重之比均显著高于对照组,而母鼠体重增加未受影响。仅在妊娠第6天给予24微克TCDD/千克时,胎儿死亡率相对于对照组有所增加。对照组和经TCDD处理的胎儿体重之间无显著差异。腭裂发生率从妊娠第6天到第12天呈剂量相关增加,且确定妊娠第12天为硬腭裂诱导的关键窗口期。无论暴露日如何,在所有剂量水平均观察到肾盂积水,在妊娠第12天及更早时间,当TCDD剂量为3微克/千克及更高时,发生率接近100%。在妊娠第14天的所有剂量下,肾盂积水的发生率和严重程度相对于其他所有日期均有所降低。每天肾脏病变的严重程度均呈剂量相关增加,但在妊娠第6天至第12天严重程度保持不变。因此,虽然在妊娠第6天至第12天腭部对TCDD的敏感性随胎龄增加,但这些天之间肾盂积水的发展无差异。然而,数据表明,在妊娠第14天,尿路对TCDD的敏感性可能较低。

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