Department of Toxicology, Public Health School, Harbin Medical University, 150081, No 157, Baojian Road, Nangang District, Harbin City, Heilongjiang Province, China.
Department of Acupuncture, Heilongjiang Academy of Chinese Medical Sciences, 150036, No 142, Sanfu Street, Xiangfang District, Harbin City, Heilongjiang Province, China.
Food Chem Toxicol. 2022 Jun;164:113018. doi: 10.1016/j.fct.2022.113018. Epub 2022 Apr 14.
Activated microglia play an active role in the pathogenesis of PD and paraquat (PQ) induces PD. The study was to understand the time relationship between microglial activation and dopaminergic neuron loss in the substantia nigra (SN) of PQ-induced PD mice. Male C57BL/6 mice were injected intraperitoneally with PQ, twice a week for six weeks. Some mice underwent behavioral assessments each week and were sacrificed for SN tissues, in which histopathological analysis, dopaminergic neuron loss, microglial activation and phenotypic characteristics were evaluated. The results showed that motor retardation, coordination disorders and limb stiffness occurred four weeks after PQ exposure, as well as the degeneration and loss of dopaminergic neurons in the SN. Activated microglia and increased CD68 expression appeared two weeks after PQ exposure in time-dependent manners. Increased CD86 and decreased CD206 expression were observed four weeks after PQ exposure, accompanied by increased TNF-α and IL-6 levels and decreased IL-10 and TGF-β levels. These results indicate that PQ can activate microglia in vivo, and microglial activation precedes neuronal loss in the SN. Activated microglia are characterized by mixed M1/M2 polarization in the early stage and M1 polarization in the late stage of PQ-induced PD development.
激活的小胶质细胞在 PD 的发病机制中发挥积极作用,百草枯(PQ)可诱导 PD。本研究旨在了解 PQ 诱导 PD 小鼠黑质(SN)中小胶质细胞激活和多巴胺能神经元丢失之间的时间关系。雄性 C57BL/6 小鼠每周两次腹膜内注射 PQ,持续 6 周。一些小鼠每周进行行为评估,并进行 SN 组织切除,用于进行组织病理学分析、多巴胺能神经元丢失、小胶质细胞激活和表型特征评估。结果显示,PQ 暴露 4 周后出现运动迟缓、协调障碍和肢体僵硬,以及 SN 中多巴胺能神经元的变性和丢失。PQ 暴露后 2 周,小胶质细胞激活和 CD68 表达增加呈时间依赖性。PQ 暴露 4 周后,观察到 CD86 增加和 CD206 减少,同时 TNF-α 和 IL-6 水平升高,IL-10 和 TGF-β 水平降低。这些结果表明,PQ 可以在体内激活小胶质细胞,且小胶质细胞的激活先于 SN 中的神经元丢失。激活的小胶质细胞在 PQ 诱导 PD 发展的早期表现为 M1/M2 混合极化,晚期表现为 M1 极化。