A narrative review of autophagy in migraine.

IF 3.2 3区 医学 Q2 NEUROSCIENCES Frontiers in Neuroscience Pub Date : 2025-02-14 eCollection Date: 2025-01-01 DOI:10.3389/fnins.2025.1500189
Yanan Huang, Hongyan Li, Qijun Yu, Yonghui Pan
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Abstract

Background and objective: Autophagy is a natural process regulated by autophagy-related genes in eukaryotic cells that involves the degradation of cytoplasmic proteins and old or damaged organelles via the lysosomal pathway to help maintain cell homeostasis. Previous studies have suggested a potential association between autophagy and migraine, while the underlying mechanisms remain unclear. This review seeks to evaluate the possible involvement of autophagy in the pathophysiology of migraine, aiming to clarify its role and implications for future research and therapeutic strategies.

Methods: A search in PubMed was conducted for English-language articles until December 5, 2024. Key terms of "autophagy," "migraine," "microglia," "neurogenic inflammation," "central sensitization," "mitophagy" and "neuropathic pain" in different combinations.

Results: In the context of migraine, the activation of the phosphoinositide 3-kinase (PI3K)/protein kinase B (PKB/Akt) signaling pathway exerts a direct influence on the mammalian target of rapamycin (mTOR), leading to a reduction in autophagy levels. Moreover, the stimulation of purinergic ligand-gated ion channel type 7 receptor (P2X7R) in microglia can hinder autophagy by interfering with the fusion of autophagosomes and lysosomes, which impedes the degradation of substrates within the autophagolysosome. Increased levels of calcitonin gene-related peptide (CGRP) may also modulate autophagy through the Akt/mTOR or protein kinase A (PKA)/mTOR signaling pathways. Additionally, research indicates that mitophagy may be partially impaired in individuals suffering from migraine. Furthermore, autophagy could contribute to the dysregulation of synaptic plasticity by influencing the processes of long-term potentiation (LTP) and long-term depression (LTD), both of which are associated with central sensitization in chronic migraine.

Conclusion: These findings suggest that autophagy may play an important role in the pathophysiology of migraine, particularly in its development and central sensitization. Research on autophagy modulators related to migraine will provide valuable insights for treatment strategies.

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偏头痛中自噬的叙述性回顾。
背景和目的:自噬是真核细胞中由自噬相关基因调控的自然过程,通过溶酶体途径降解细胞质蛋白和老化或受损的细胞器,以帮助维持细胞稳态。先前的研究表明,自噬和偏头痛之间存在潜在的联系,但潜在的机制尚不清楚。本综述旨在评估自噬在偏头痛病理生理中的可能参与,旨在阐明其作用及其对未来研究和治疗策略的影响。方法:在PubMed检索2024年12月5日之前的英文文章。“自噬”、“偏头痛”、“小胶质细胞”、“神经源性炎症”、“中枢致敏”、“有丝噬”和“神经性疼痛”不同组合的关键词。结果:在偏头痛的情况下,磷酸肌苷3激酶(PI3K)/蛋白激酶B (PKB/Akt)信号通路的激活直接影响哺乳动物雷帕霉素(mTOR)靶点,导致自噬水平降低。此外,刺激小胶质细胞嘌呤能配体门控离子通道7型受体(P2X7R)可以通过干扰自噬体和溶酶体的融合来抑制自噬,从而阻碍自噬溶酶体内底物的降解。降钙素基因相关肽(CGRP)水平升高也可能通过Akt/mTOR或蛋白激酶A (PKA)/mTOR信号通路调节自噬。此外,研究表明,患有偏头痛的人的线粒体自噬可能部分受损。此外,自噬可能通过影响长期增强(LTP)和长期抑制(LTD)过程而导致突触可塑性失调,这两种过程都与慢性偏头痛的中枢致敏有关。结论:这些发现提示自噬可能在偏头痛的病理生理,特别是在其发展和中枢致敏中起重要作用。研究与偏头痛相关的自噬调节剂将为治疗策略提供有价值的见解。
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
Frontiers in Neuroscience
Frontiers in Neuroscience NEUROSCIENCES-
CiteScore
6.20
自引率
4.70%
发文量
2070
审稿时长
14 weeks
期刊介绍: Neural Technology is devoted to the convergence between neurobiology and quantum-, nano- and micro-sciences. In our vision, this interdisciplinary approach should go beyond the technological development of sophisticated methods and should contribute in generating a genuine change in our discipline.
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