Sharma Anjali, Choudhary Mayank Kumar, Gugulothu Dalapathi, Pandita Deepti, Verma Surajpal, Vora Lalitkumar K, Khatri Dharmendra Kumar, Garabadu Debapriya
Delhi Pharmaceutical Sciences and Research University (DPSRU), New Delhi, 110017, India.
CDSCO, FDA Bhawan, New Delhi, India.
Mol Neurobiol. 2025 Apr 3. doi: 10.1007/s12035-025-04868-8.
Multiple sclerosis (MS) is a complex autoimmune disease characterised by inflammation, demyelination, and neurodegeneration within the central nervous system (CNS). While the exact causes remain unclear, recent research highlights the significant role of epigenetic modifications and mitochondrial dysfunction in the disease's onset and progression. Epigenetic alterations, such as DNA methylation, histone modification, and microRNA regulation, influence gene expression without altering the DNA sequence, leading to immune dysregulation and inflammation. Similarly, mitochondrial dysfunction, marked by impaired oxidative phosphorylation, reduced adenosine triphosphate (ATP) production, and increased reactive oxygen species (ROS), contributes to neurodegeneration and impaired remyelination in MS. The growing interest in targeting these two interconnected mechanisms has opened new avenues for MS treatment. Herbal drugs, known for their multi-targeted effects, have shown potential in modulating epigenetic markers and enhancing mitochondrial function. Compounds such as resveratrol, curcumin, epigallocatechin-3-gallate (EGCG), quercetin, and omega-3 fatty acids demonstrate potential in regulating DNA methylation, histone deacetylation, and mitochondrial biogenesis. These natural agents offer dual-action therapies by reducing oxidative stress and inflammation while promoting neuronal survival and remyelination. This review explores the therapeutic potential of herbal drugs targeting epigenetic and mitochondrial pathways in MS, evaluating their mechanisms of action and highlighting their promise as novel therapeutic agents. While initial findings are encouraging, further research and clinical trials are required to validate the efficacy of these herbal treatments and fully understand their potential in slowing disease progression and improving patient outcomes in MS. Such exploration could pave the way for safer, multi-targeted therapies, offering new hope in the management of MS and other neurodegenerative diseases.
多发性硬化症(MS)是一种复杂的自身免疫性疾病,其特征是中枢神经系统(CNS)内存在炎症、脱髓鞘和神经退行性变。虽然确切病因尚不清楚,但最近的研究突出了表观遗传修饰和线粒体功能障碍在该疾病的发病和进展中的重要作用。表观遗传改变,如DNA甲基化、组蛋白修饰和微小RNA调节,在不改变DNA序列的情况下影响基因表达,导致免疫失调和炎症。同样,以氧化磷酸化受损、三磷酸腺苷(ATP)生成减少和活性氧(ROS)增加为特征的线粒体功能障碍,也促使了MS中的神经退行性变和髓鞘再生受损。针对这两种相互关联机制的兴趣日益浓厚,为MS治疗开辟了新途径。以多靶点作用著称的草药已显示出调节表观遗传标记和增强线粒体功能的潜力。白藜芦醇、姜黄素、表没食子儿没食子酸酯(EGCG)、槲皮素和ω-3脂肪酸等化合物在调节DNA甲基化、组蛋白去乙酰化和线粒体生物发生方面显示出潜力。这些天然药物通过减轻氧化应激和炎症,同时促进神经元存活和髓鞘再生,提供了双重作用疗法。本综述探讨了针对MS中表观遗传和线粒体途径的草药的治疗潜力,评估了它们的作用机制,并强调了它们作为新型治疗药物的前景。虽然初步研究结果令人鼓舞,但需要进一步的研究和临床试验来验证这些草药治疗的疗效,并充分了解它们在减缓MS疾病进展和改善患者预后方面的潜力。这样的探索可能为更安全的多靶点疗法铺平道路,为MS和其他神经退行性疾病的治疗带来新希望。