中国神经再生研究(英文版) ›› 2026, Vol. 21 ›› Issue (4): 1468-1482.doi: 10.4103/NRR.NRR-D-24-01371

• 综述:退行性病与再生 • 上一篇    下一篇

PPARα在神经系统疾病中的潜在治疗作用

  

  • 出版日期:2026-04-15 发布日期:2025-07-26
  • 基金资助:
    天津市卫计委中医药重点领域科研项目(2024012);天津市教委项目(2021KJ217)。天津市卫计委中医药重点领域科研项目(2024012);天津市教委项目(2021KJ217)。

Role of peroxisome proliferator-activated receptor alpha in neurodegenerative diseases and other neurological disorders: Clinical application prospects

Zijun Wu1, 2, #, Yuying Zhao1, 2, #, Shujing Hao1, 2, #, Mengyao An1, 2, Chengcheng Song1, 2, Jing Li1, 2, *   

  1. 1 Department of Anesthesiology, Tianjin Medical University General Hospital, Tianjin, China;  2 Tianjin Research Institute of Anesthesiology, Tianjin, China
  • Online:2026-04-15 Published:2025-07-26
  • Contact: Jing Li, PhD, xtjing@163.com.
  • Supported by:
    This work was supported by grants from Tianjin Scientific Research Project in Key Areas of Traditional Chinese Medicine, Tianjin Municipal Health Commission, No. 2024012 (to JL); Tianjin Municipal Education Commission Project, No. 2021KJ217 (to CS).

摘要:

过氧化物酶体增殖激活受体α(PPARα)是核激素受体超家族的成员之一,作为转录因子参与细胞代谢的调节。据报道,PPARα在神经退行性疾病的发生和发展中起着关键作用。因此,PPARα激动剂在治疗神经系统疾病方面受到越来越多的关注。文章的目的是综述PPARα 在神经系统疾病中的研究进展。PPARα 是一种在成年小鼠和成年神经组织中与所有细胞类型共定位的同工酶。传统上认为 PPARα 主要定位于细胞核,但 PPARα 的功能可能受细胞质和细胞核之间动态平衡的调节。PPARα 内源性和外源性激动剂与过氧化物酶体增殖激活反应元件(PPRE)结合,发挥其生物效应。PPARα 在神经退行性疾病中发挥着重要的治疗作用。PPARα 激动剂吉非罗齐可通过自噬-溶酶体途径降低阿尔茨海默病小鼠模型海马中可溶性和不可溶性 Aβ 的水平。PPARα 对黑质的正常发育和功能维持至关重要,并能减轻帕金森病小鼠模型的运动功能障碍。此外,PPARα 可以减轻多种神经系统疾病中的神经炎症和氧化应激。因此,PPARα在多种神经系统疾病中的发生发展起着重要作用,而PPARα激动剂有望成为治疗神经退行性疾病的新治疗药物,为患者提供新的治疗选择。

https://orcid.org/0000-0002-8863-4790 (Jing Li)

关键词: 阿尔茨海默病, 激动剂, 非诺贝特, PPARα, 吉非罗齐, 胶质母细胞瘤, 肠道微生物群, 多发性硬化, 神经变性, 神经炎症, 帕金森病, 神经系统疾病, 神经退行性疾病

Abstract: Peroxisome proliferator-activated receptor alpha is a member of the nuclear hormone receptor superfamily and functions as a transcription factor involved in regulating cellular metabolism. Previous studies have shown that PPARα plays a key role in the onset and progression of neurodegenerative diseases. Consequently, peroxisome proliferator-activated receptor alpha agonists have garnered increasing attention as potential treatments for neurological disorders. This review aims to clarify the research progress regarding peroxisome proliferator-activated receptor alpha in nervous system diseases. Peroxisome proliferator-activated receptor alpha is present in all cell types within adult mouse and adult neural tissues. Although it is conventionally believed to be primarily localized in the nucleus, its function may be regulated by a dynamic balance between cytoplasmic and nuclear shuttling. Both endogenous and exogenous peroxisome proliferator-activated receptor alpha agonists bind to the peroxisome proliferator-activated response element to exert their biological effects. Peroxisome proliferator-activated receptor alpha plays a significant therapeutic role in neurodegenerative diseases. For instance, peroxisome proliferator-activated receptor alpha agonist gemfibrozil has been shown to reduce levels of soluble and insoluble amyloid-beta in the hippocampus of Alzheimer’s disease mouse models through the autophagy-lysosomal pathway. Additionally, peroxisome proliferator-activated receptor alpha is essential for the normal development and functional maintenance of the substantia nigra, and it can mitigate motor dysfunction in Parkinson’s disease mouse models. Furthermore, peroxisome proliferator-activated receptor alpha has been found to reduce neuroinflammation and oxidative stress in various neurological diseases. In summary, peroxisome proliferator-activated receptor alpha plays a crucial role in the onset and progression of multiple nervous system diseases, and peroxisome proliferator-activated receptor alpha agonists hold promise as new therapeutic agents for the treatment of neurodegenerative diseases, providing new options for patient care.

Key words: agonists, Alzheimer’s disease, gut microbiota, multiple sclerosis, nervous system disease, neurodegeneration, neurodegenerative disease, neuroinflammation, Parkinson’s disease, peroxisome proliferator-activated receptor alpha