Pharmaceutical Informatics Institute, College of Pharmaceutical Sciences, Zhejiang University, Hangzhou 310058, China.
Department of Neurology, Translational Research Institute of Brain and Brain-Like Intelligence, Shanghai Fourth People's Hospital Affiliated to Tongji University School of Medicine, Shanghai 200434, China.
Phytomedicine. 2022 Oct;105:154357. doi: 10.1016/j.phymed.2022.154357. Epub 2022 Jul 28.
Parkinson's disease (PD) is a progressive neurodegenerative disease, which brings increasing threaten for human health and is still lacking of satisfied treatment. Recently, numerous studies have also demonstrated the effect of particular subsets of CD4+ T cells on PD pathology. Th17 cells played an important role in the pathogenesis of PD. Traditional Chinese medicine has been widely used to treat PD clinically, and has a tremendous potential in clinical drug development.
The aim of this study was to verify the therapeutic effects of DHY on PD mice model, and investigate the underlying molecular mechanisms.
Herein, we verified the effects of a traditional Chinese medicine formula, named DiHuangYin (DHY), on the 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) induced mouse model of PD through behavioral and histopathological tests. High-resolution mass spectrometry combined with molecular networking was applied for substance profiling of DHY. Based on the chemical compositions of DHY, network pharmacology was performed. Immunofluorescence and ELISA were used to evaluate the expressions of cytokines in peripheral immune system. qPCR and immunofluorescence were used to detect the inflammation infiltration of central nervous system.
DHY improves the motor function and prevents the loss of dopaminergic neurons in the MPTP induced mouse model of PD. 118 components of DHY were identified or tentatively characterized based on the MS/MS data and molecular networking. Network pharmacology suggested IL-17 signaling pathway and neuroactive ligand-receptor interaction as the important targets. Compared to the MPTP-intoxicated mice, the DHY group showed a decreased number of Th17 cells from splenocytes and a decreased level of IL-17A in the serum. On the other hand, less inflammatory infiltration was found in the midbrain of DHY treatment mice which might be associated with the attenuated peripheral inflammation.
Though the underlying pharmacological mechanism of DHY is still lacking, we provided evidence that DHY decoction could protect dopaminergic neurons by mitigating peripheral inflammation.
帕金森病(PD)是一种进行性神经退行性疾病,它对人类健康造成的威胁日益增加,目前仍缺乏满意的治疗方法。最近,大量研究也表明,特定亚群的 CD4+T 细胞对 PD 病理有影响。Th17 细胞在 PD 的发病机制中起重要作用。中药在临床上已广泛用于治疗 PD,在临床药物开发方面具有巨大潜力。
本研究旨在验证 DHY 对 PD 小鼠模型的治疗作用,并探讨其潜在的分子机制。
在此,我们通过行为学和组织病理学测试验证了一种中药方剂地黄饮(DHY)对 1-甲基-4-苯基-1,2,3,6-四氢吡啶(MPTP)诱导的 PD 小鼠模型的作用。采用高分辨质谱结合分子网络对 DHY 的物质谱进行分析。基于 DHY 的化学成分,进行网络药理学分析。免疫荧光和 ELISA 用于评估外周免疫系统细胞因子的表达。qPCR 和免疫荧光用于检测中枢神经系统的炎症浸润。
DHY 改善了 MPTP 诱导的 PD 小鼠模型的运动功能并防止多巴胺能神经元丢失。基于 MS/MS 数据和分子网络,鉴定或初步表征了 DHY 的 118 个成分。网络药理学提示 IL-17 信号通路和神经活性配体-受体相互作用是重要靶点。与 MPTP 中毒组相比,DHY 组脾细胞中的 Th17 细胞数量减少,血清中 IL-17A 水平降低。另一方面,DHY 治疗组小鼠中脑的炎症浸润减少,这可能与外周炎症减轻有关。
尽管 DHY 的潜在药理机制尚不清楚,但我们提供的证据表明,DHY 汤可能通过减轻外周炎症来保护多巴胺能神经元。