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发育期接触百草枯和代森锰及帕金森病表型。

Developmental exposure to the pesticides paraquat and maneb and the Parkinson's disease phenotype.

作者信息

Thiruchelvam Mona, Richfield Eric K, Goodman Becky M, Baggs Raymond B, Cory-Slechta Deborah A

机构信息

Department of Environmental Medicine, University of Rochester School of Medicine and Dentistry, NY 14642, USA.

出版信息

Neurotoxicology. 2002 Oct;23(4-5):621-33. doi: 10.1016/s0161-813x(02)00092-x.

Abstract

Idiopathic Parkinson's disease (PD) is associated with advanced age, but it is still unclear whether dopaminergic neuronal death results from events initiated during development, adulthood, or represents a cumulative effect across the span of life. This study hypothesized that paraquat (PQ) and maneb (MB) exposure during critical periods of development could permanently change the nigrostriatal dopamine (DA) system and enhance its vulnerability to subsequent neurotoxicant challenges. C57BL/6 mice were treated daily with saline, 0.3 mg/kg PQ, 1 mg/kg MB or PQ + MB from post-natal (PN) days 5 to 19. At 6 weeks, a 20% decrease in activity was evident only in the PQ + MB group, with a further decline (40%) observed at 6 months. A subset of mice were re-challenged as adults with saline, 10 mg/kg PQ, 30 mg/kg MB, or PQ + MB 2 x a week for 3 weeks. Mice exposed developmentally to PQ + MB and rechallenged as adults were the most affected, showing a 70% reduction in motor activity 2 weeks following the last rechallenge dose. Striatal DA levels were reduced by 37% following developmental exposure to PQ + MB only, butfollowing adult re-challenge levels were reduced by 62%. A similar pattern of nigral dopaminergic cell loss was observed, with the PQ + MB treated group exhibiting the greatest reduction, with this loss being amplified by adult re-challenge. Developmental exposure to PQ or MB alone produced minimal changes. However, following adult re-challenge, significant decreases in DA and nigral cell counts were observed, suggesting that exposure to either neurotoxicant alone produced a state of silent toxicity that was unmasked following adult re-exposure. Taken together, these findings indicate that exposure to pesticides during the PN period can produce permanent and progressive lesions of the nigrostriatal DA system, and enhanced adult susceptibility to these pesticides, suggesting that developmental exposure to neurotoxicants may be involved in the induction of neurodegenerative disorders and/or alter the normal aging process.

摘要

特发性帕金森病(PD)与老年相关,但尚不清楚多巴胺能神经元死亡是源于发育过程、成年期启动的事件,还是代表了一生跨度中的累积效应。本研究假设,在发育关键期接触百草枯(PQ)和代森锰(MB)可永久性改变黑质纹状体多巴胺(DA)系统,并增强其对后续神经毒物挑战的易感性。从出生后(PN)第5天至19天,每天给C57BL/6小鼠注射生理盐水、0.3mg/kg PQ、1mg/kg MB或PQ + MB。在6周时,仅PQ + MB组的活动明显下降20%,在6个月时进一步下降(40%)。一部分小鼠成年后再次接受挑战,每周2次,持续3周,分别注射生理盐水、10mg/kg PQ、30mg/kg MB或PQ + MB。发育期间接触PQ + MB并成年后再次接受挑战的小鼠受影响最大,在最后一次再挑战剂量后2周,运动活动减少70%。仅在发育期间接触PQ + MB后,纹状体DA水平降低37%,但成年后再次接受挑战后,水平降低62%。观察到黑质多巴胺能细胞丢失有类似模式,PQ + MB处理组减少最多,成年后再次接受挑战会加剧这种丢失。单独发育期间接触PQ或MB产生的变化最小。然而,成年后再次接受挑战后,观察到DA和黑质细胞计数显著下降,表明单独接触任何一种神经毒物都会产生一种沉默毒性状态,成年后再次接触会使其显现出来。综上所述,这些发现表明,在PN期接触农药可导致黑质纹状体DA系统产生永久性和进行性损伤,并增强成年小鼠对这些农药的易感性,提示发育期间接触神经毒物可能参与神经退行性疾病的诱导和/或改变正常衰老过程。

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