Cistanche tubulosa improves peripheral neuropathy in MPTP-induced PD mice based on regulation of m6A methylation.

Q1 Health Professions
Yatan Li, Wei Jia, Junhua Hu, Borui Zhang, Xinxin Qi, Jianhua Yang, Xinling Yang
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引用次数: 0

Abstract

Background: This study aimed to discover whether Cistanche tubulosa affects the AKT/CASP3 pathway by regulating m6A methylation, to exert a protective effect against peripheral nerve injury in a Parkinson's Disease (PD) mouse model.

Methods: In this study, network pharmacology analysis and the molecular docking virtual screening technique was used to filter Acteoside (Act), a potential neuroprotective agent of active components in Cistanche tubulosa. A PD-related peripheral neuropathy mouse model was established by MPTP induction, followed by 21 days treatment of oral Act (25, 50, and 100 mg kg-1). Pole climbing, automatic avoidance ability and hot plate sensory tests were evaluated to determine behavioral changes caused by central and peripheral nerve injury. The pathological alterations of dorsal root ganglion tissue and the protein levels of IL-6, AKT, and CASP3 under Act intervention, as well as the dynamic changes of FTO, METTL3, and YTHDF2 which are closely related to m6A methylation, were comprehensively analyzed to observe the peripheral nerve protective efficacy of Act.

Results: The results showed that peripheral neuropathy occurring with PD in the mouse model, which could be verified by behavioral tests and pathological histological changes. In addition to the previously established protective effect of Act on dopaminergic neurons in substantia nigra (SN), extensive follow-up studies demonstrated that Act effectively induced m6A methylation, which could further regulate the AKT/CASP3 pathway to play a therapeutic role. In this study, medium and high doses of Act played more obvious therapeutic roles.

Conclusion: These findings suggest that Act may regulate the severity of peripheral nerve injury under the activation of the AKT/CASP3 signaling pathway by balancing the methylation level of m6A. These results provide a theoretical basis and experimental evidence for further research on the protective effect of Cistanche tubulosa on both the central and peripheral nerves in the treatment of PD.

肉苁梗通过调节m6A甲基化改善mptp诱导的PD小鼠周围神经病变。
背景:本研究旨在探讨肉苁梗是否通过调节m6A甲基化影响AKT/CASP3通路,从而对帕金森病(PD)小鼠模型周围神经损伤起到保护作用。方法:采用网络药理学分析和分子对接虚拟筛选技术,对肉苁蓉有效成分中潜在的神经保护剂牛蒡苷(actoside, Act)进行筛选。采用MPTP诱导建立pd相关周围神经病变小鼠模型,随后口服Act(25、50、100 mg kg-1)治疗21 d。通过攀竿、自动回避能力和热板感觉测试来判断中枢和周围神经损伤后的行为改变。综合分析Act干预下背根神经节组织病理改变及与m6A甲基化密切相关的IL-6、AKT、CASP3蛋白水平,以及FTO、METTL3、YTHDF2的动态变化,观察Act对周围神经的保护作用。结果:PD小鼠模型出现周围神经病变,行为学实验和病理组织学改变证实了这一点。除了先前确定的Act对黑质(SN)多巴胺能神经元的保护作用外,大量的后续研究表明,Act可有效诱导m6A甲基化,从而进一步调节AKT/CASP3通路发挥治疗作用。在本研究中,中、高剂量Act的治疗作用更为明显。结论:这些发现提示Act可能通过平衡m6A的甲基化水平,在AKT/CASP3信号通路激活的情况下调节周围神经损伤的严重程度。这些结果为进一步研究肉苁梗在PD治疗中对中枢和周围神经的保护作用提供了理论基础和实验依据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
5.50
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