Zuo Zhenzi, Li Jiayi, Zhang Bing, Hang Ai, Wang Qiaoxu, Xiong Guiya, Tang Liming, Zhou Zhijun, Chang Xiuli
School of Public Health and Key Laboratory of Public Health Safety of the Ministry of Education, Shanghai Medical College of Fudan University, Fudan University, Room 233, Building 8, 130 Dongan Road, Shanghai 200032, China.
Pharmacology and Toxicology Department, Shanghai Institute for Food and Drug Control, Shanghai 201203, China.
Toxics. 2023 Oct 7;11(10):842. doi: 10.3390/toxics11100842.
Early-life exposure to environmental neurotoxicants is known to have lasting effects on organisms. In this study, we aim to investigate the impacts of PQ exposure during early developmental stages and adult re-challenge in aged mice on non-motor neurobehavior. Two mouse models, which were exposed once during early life stage and re-exposure at adulthood, were created to explore the long-term effects of PQ on non-motor neurobehavior. As the results showed, early-life exposure to PQ caused impairment in working memory and cognitive ability in aged male mice, but not in female mice, exhibiting a sex-specific impairment. Moreover, male mice that were re-challenged with PQ at adulthood following early-life exposure also exhibited non-motor neurobehavioral disorders. Notably, re-exposure to PQ exacerbated neurobehavioral disorders and anxiety levels compared to single exposure during different life stages. Collectively, early-life exposure to PQ can result in irreversible impairments in non-motor neurobehavior and increase susceptibility to subsequent insults in male mice, but not in female mice, suggesting greater sensitivity in male rodents to PQ-induced non-motor neurobehavioral deficits.
已知早年暴露于环境神经毒物会对生物体产生持久影响。在本研究中,我们旨在调查早年发育阶段接触百草枯(PQ)以及老年小鼠成年后再次接触百草枯对非运动神经行为的影响。创建了两个小鼠模型,一个在生命早期阶段接触一次PQ并在成年期再次接触,以探究PQ对非运动神经行为的长期影响。结果显示,早年接触PQ会导致老年雄性小鼠的工作记忆和认知能力受损,但雌性小鼠未出现这种情况,表现出性别特异性损伤。此外,早年接触PQ后成年期再次接触PQ的雄性小鼠也表现出非运动神经行为障碍。值得注意的是,与不同生命阶段的单次接触相比,再次接触PQ会加剧神经行为障碍和焦虑水平。总体而言,早年接触PQ会导致雄性小鼠非运动神经行为出现不可逆损伤,并增加其对后续损伤的易感性,但雌性小鼠不会出现这种情况,这表明雄性啮齿动物对PQ诱导的非运动神经行为缺陷更为敏感。