Narotsky M G, Kavlock R J
ManTech Environmental Technology, Inc., Research Triangle Park, North Carolina, USA.
J Toxicol Environ Health. 1995 Jun;45(2):145-71. doi: 10.1080/15287399509531987.
As part of the validation of an integrated bioassay for systemic toxicity, neurotoxicity, and developmental toxicity, we evaluated the effects of four pesticides, four chlorinated solvents, and two other industrial chemicals in Fischer 344 rats. The pesticides included carbaryl, triadimefon, chlordane, and heptachlor; the solvents included dichloromethane (DCM), carbon tetrachloride, trichloroethylene (TCE), and tetrachloroethylene (perchloroethylene, PER); and the industrial chemicals were di(2-ethylhexyl)phthalate (DEHP) and phenol. In the developmental toxicity studies, timed-pregnant rats were treated by gavage with vehicle or 1 of 2 dose levels of each compound on gestation d 6-19. The dams were allowed to deliver and their litters were examined on postnatal d 1, 3, and 6. Litter weights were determined on postnatal d 1 and 6. Implants were also counted to determine prenatal loss. Maternal toxicity was evidenced by dose-related alterations in weight gain for all 10 compounds. Clinical signs of maternal toxicity were present for all chemicals except chlordane and heptachlor. DEHP exposure resulted in the most pronounced developmental toxicity (high levels of pre- and postnatal mortality), whereas chlordane induced extensive postnatal loss. Of the solvents, only DCM did not cause a high incidence of full-litter resorption. Phenol, heptachlor, triadimefon, and carbaryl showed only slight potential for developmental toxicity. Malformations suggestive of teratogenicity included kinked tail (phenol), microphthalmia (TCE, PER, DEHP), and cleft palate with renal agenesis (DEHP). Although several findings (eye defects caused by TCE and PER, full-litter resorption and delayed parturition caused by PER, and delayed parturition/dystocia associated with triadimefon) have not been previously reported, the results are generally consistent with previous reports and highlight the importance and relative ease of incorporation of developmental evaluations into a multidisciplinary screening battery.
作为对全身毒性、神经毒性和发育毒性综合生物测定法进行验证的一部分,我们评估了四种农药、四种氯化溶剂和两种其他工业化学品对Fischer 344大鼠的影响。农药包括西维因、三唑酮、氯丹和七氯;溶剂包括二氯甲烷(DCM)、四氯化碳、三氯乙烯(TCE)和四氯乙烯(全氯乙烯,PER);工业化学品为邻苯二甲酸二(2-乙基己基)酯(DEHP)和苯酚。在发育毒性研究中,对妊娠第6至19天的定时妊娠大鼠经口灌胃给予赋形剂或每种化合物的2个剂量水平之一。让母鼠分娩,并在出生后第1、3和6天检查它们的窝仔。在出生后第1天和第6天测定窝仔重量。还计算植入物数量以确定产前损失。所有10种化合物体重增加的剂量相关变化证明了母体毒性。除氯丹和七氯外,所有化学品均出现母体毒性的临床症状。DEHP暴露导致最明显的发育毒性(高水平的产前和产后死亡率),而氯丹导致广泛的产后损失。在溶剂中,只有DCM没有导致高比例的全窝吸收。苯酚、七氯、三唑酮和西维因仅显示出轻微的发育毒性潜力。提示致畸性的畸形包括扭结尾(苯酚)、小眼畸形(TCE、PER、DEHP)和伴有肾缺如的腭裂(DEHP)。尽管此前尚未报道一些研究结果(TCE和PER引起的眼部缺陷、PER引起的全窝吸收和分娩延迟,以及与三唑酮相关的分娩延迟/难产),但这些结果总体上与先前的报道一致,并突出了将发育评估纳入多学科筛查组合的重要性和相对简便性。