Johri Ashu, Yadav Sanjay, Dhawan Alok, Parmar Devendra
Developmental Toxicology Division, Industrial Toxicology Research Centre, M G Marg, Lucknow-226 001, UP, India.
Toxicol Appl Pharmacol. 2007 Dec 15;225(3):278-92. doi: 10.1016/j.taap.2007.08.006. Epub 2007 Aug 19.
Oral administration of different doses (0.0625, 0.125 or 0.25 mg/kg corresponding to 1/1400th, 1/700th or 1/350th of LD(50)) of lindane to the pregnant Wistar rats from gestation days 5 to 21 were found to produce a dose-dependent increase in the activity of cytochrome P450 (CYP)-dependent 7-ethoxyresorufin-O-deethylase (EROD), 7-pentoxyresorufin-O-dealkylase (PROD) and N-nitrosodimethylamine demethylase (NDMA-d) in brain and liver of offspring postnatally at 3 weeks. The increase in the activity of CYP monooxygenases was found to be associated with the increase in the mRNA and protein expression of xenobiotic metabolizing CYP1A, 2B and 2E1 isoenzymes in the brain and liver of offspring. Dose-dependent alterations in the parameters of spontaneous locomotor activity in the offspring postnatally at 3 weeks have suggested that increase in CYP activity may possibly lead to the formation of metabolites to the levels that may be sufficient to alter the behavioral activity of the offspring. Interestingly, the inductive effect on cerebral and hepatic CYPs was found to persist postnatally up to 6 weeks in the offspring at the relatively higher doses (0.125 and 0.25 mg/kg) of lindane and up to 9 weeks at the highest dose (0.25 mg/kg), though the magnitude of induction was less than that observed at 3 weeks. Alterations in the parameters of spontaneous locomotor activity in the offspring postnatally at 6 and 9 weeks, though significant only in the offspring at 3 and 6-week of age, have further indicated that due to the reduced activity of the CYPs during the ontogeny, lindane and its metabolites may not be effectively cleared from the brain. The data suggest that low dose prenatal exposure to the pesticide has the potential to produce overexpression of xenobiotic metabolizing CYPs in brain and liver of the offspring which may account for the behavioral changes observed in the offspring.
在妊娠第5天至21天,给怀孕的Wistar大鼠口服不同剂量(0.0625、0.125或0.25mg/kg,分别相当于LD(50)的1/1400、1/700或1/350)的林丹,结果发现,产后3周时,子代大鼠脑和肝中细胞色素P450(CYP)依赖的7-乙氧基异吩唑酮-O-脱乙基酶(EROD)、7-戊氧基异吩唑酮-O-脱烷基酶(PROD)和N-亚硝基二甲胺脱甲基酶(NDMA-d)的活性呈剂量依赖性增加。CYP单加氧酶活性的增加与子代大鼠脑和肝中参与外源性物质代谢的CYP1A、2B和2E1同工酶的mRNA和蛋白表达增加有关。产后3周时,子代大鼠自发运动活动参数的剂量依赖性改变表明,CYP活性的增加可能会导致代谢产物形成至足以改变子代行为活动的水平。有趣的是,在相对较高剂量(0.125和0.25mg/kg)的林丹作用下,子代大鼠脑和肝中CYP的诱导作用在出生后可持续至6周,在最高剂量(0.25mg/kg)下可持续至9周,尽管诱导程度低于3周时观察到的情况。产后6周和9周时,子代大鼠自发运动活动参数的改变,虽然仅在3周龄和6周龄的子代中显著,但进一步表明,由于个体发育过程中CYP活性降低,林丹及其代谢产物可能无法有效地从脑中清除。数据表明,产前低剂量接触该农药有可能使子代大鼠脑和肝中参与外源性物质代谢的CYP过表达,这可能是子代出现行为变化的原因。