Department of Emergency Medicine of First Affiliated Hospital and Department of Environmental Medicine, Zhejiang University School of Medicine, Hangzhou, China.
Center of Laboratory Medicine, Chongqing Prevention and Treatment Center for Occupational Diseases, Chongqing, China; Chongqing Key Laboratory of Prevention and Treatment for Occupational Diseases and Poisoning, Chongqing, China.
Environ Int. 2022 Nov;169:107512. doi: 10.1016/j.envint.2022.107512. Epub 2022 Sep 8.
Paraquat (PQ) is the most widely used herbicide in the world and a well-known potent neurotoxin for humans. PQ exposure has been linked to increase the risk of Parkinson's disease (PD). However, the mechanism underlying its neurotoxic effects in PD pathogenesis is unclear. In our present study, C57BL/6J mice treated with PQ manifested severe motor deficits indicated by the significant reductions in suspension score, latency to fall from rotarod, and grip strength at 8 weeks after PQ exposure. Pathological hallmarks of Parkinsonism in the midbrain such as dopaminergic neuron loss, increased α-synuclein protein, and dysregulated PD-related genes were observed. Non-targeted lipidome analysis demonstrated that PQ exposure alters lipid profile and abundance, increases pro-inflammatory lipids.27 significantly altered subclasses of lipids belonged to 6 different lipid categories. Glycerophospholipids, sphingolipids, and glycerides were the most abundant lipids. Abundance of pro-inflammatory lipids such as Cer, LPC, LPS, and LPI was significantly increased in the midbrain. mRNA expressions of genes regulating ceramide biosynthesis in the midbrain were markedly up-regulated. Moreover, PQ exposure increased serum pro-inflammatory cytokines and provoked neuroinflammation in the midbrain. Pro-inflammatory lipids and cytokines in the midbrain were positively correlated with motor deficits. PQ poisoning in humans significantly also elevated serum pro-inflammatory cytokines and induced an intense systemic inflammation. In summary, we presented initial investigations of PQ induced molecular events related to the PD pathogenesis, capturing aspects of disturbed lipid metabolism, neuroinflammation, impairment of dopaminergic neurons in the midbrain, and an intense systemic inflammation. These neurotoxic effects of PQ exposure may mechanistically contribute to the pathogenesis of PQ induced Parkinsonism. Results of this study also strongly support the hypothesis that ever-increasing prevalence of Parkinson's disease is etiologically linked to the health risk of exposure to neurotoxic environmental pollutants.
百草枯(PQ)是世界上应用最广泛的除草剂,也是一种众所周知的人类强效神经毒素。PQ 暴露已被证明会增加帕金森病(PD)的风险。然而,其在 PD 发病机制中的神经毒性作用的机制尚不清楚。在我们目前的研究中,PQ 处理的 C57BL/6J 小鼠表现出严重的运动功能障碍,表现在悬尾评分、从旋转棒上跌落的潜伏期和握力显著降低,在 PQ 暴露 8 周后。中脑帕金森病的病理标志,如多巴胺能神经元丧失、α-突触核蛋白增加和 PD 相关基因失调,也观察到。非靶向脂质组学分析表明,PQ 暴露改变了脂质谱和丰度,增加了促炎脂质。27 种显著改变的脂质亚类属于 6 种不同的脂质类别。甘油磷脂、鞘脂和甘油三酯是最丰富的脂质。中脑Cer、LPC、LPS 和 LPI 等促炎脂质的丰度显著增加。中脑调节神经酰胺生物合成的基因的 mRNA 表达明显上调。此外,PQ 暴露增加了中脑的促炎细胞因子并引发了神经炎症。中脑的促炎脂质和细胞因子与运动功能障碍呈正相关。人类 PQ 中毒也显著升高了血清促炎细胞因子,并引发了强烈的全身炎症。总之,我们初步研究了 PQ 诱导的与 PD 发病机制相关的分子事件,包括脂质代谢紊乱、神经炎症、中脑多巴胺能神经元损伤和强烈的全身炎症等方面。PQ 暴露的这些神经毒性作用可能从机制上导致 PQ 诱导的帕金森病的发病机制。本研究的结果也强烈支持这样一种假设,即帕金森病发病率的不断增加与接触神经毒性环境污染物的健康风险在病因上有关。