Deleterious effects of polynuclear aromatic hydrocarbon on blood vascular system of the rat fetus

被引:23
作者
Sanyal, Mrinal K. [1 ]
Li, You-Lan [1 ]
机构
[1] Yale Univ, Sch Med, Dept Obstet & Gynecol, New Haven, CT 06510 USA
关键词
pregnancy; fetus-placenta; vascular disruption; brain and skin hemorrhage; growth retardation; 7,12-dimethylbenz[alpha]anthracene; benzo[alpha]pyrene;
D O I
10.1002/bdrb.20122
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Polynuclear aromatic hydrocarbons (PAH), benzo[alpha]pyrene (B[alpha]P) and 7,12-dimethylbenz[alpha]anthracene (DMBA) are toxic environmental agents distributed widely. The relative deleterious effects of these agents on growth and blood vasculature of fetus and placental tissues of the rat were studied. METHODS: Pregnant rats (Day I sperm positive) with implantation sites confirmed by laparotomy were treated intraperitoneally (i.p.) on Pregnancy Days 10, 12, and 14 with these agents dissolved in corn oil at cumulated total doses 50, 100, and 200 mg/kg/rat, and control with corn oil only (3-20 dams/group). Fetal growth, tissue hemorrhage, and placental pathology were evaluated by different parameters on Pregnancy Day (PD) 20 in treated and control rats. RESULTS: DMBA was relatively more deleterious compared to B[a]P indicated by increased lethality and progressive reduction of body weight of the mother with increasing doses. At 200 mg/kg/rat doses of these agents, maternal survival was 45% and 100% and body weight reduced 24% and 52% of controls, respectively. The fetal survival rates in live mothers were similar to that of controls. They induced marked fetal growth retardation and necrosis of placental tissues. B[a]P and DMBA produced significant toxicity to differentiating fetal blood vascular system as exhibited by rupture of blood vessels and hemorrhage, especially in the skin, cranial, and brain tissues. CONCLUSIONS: Maternal PAH exposure induced placental toxicity and associated adverse fetal development and hemorrhage in different parts of the fetal body, in particular, marked intradermal and cranial hemorrhage, showing that developing fetal blood vasculature is a target of PAH toxicity. Birth Defects Res (PartB) 80:367-373, 2007. (c) 2007 Wiley-Liss, Inc.
引用
收藏
页码:367 / 373
页数:7
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