Medical School of Chinese PLA, Beijing, 100853, China.
Department of Neurology, International Headache Center, The First Medical Center of Chinese PLA General Hospital, Fuxing Road 28, Haidian District, Beijing, 100853, China.
J Headache Pain. 2024 Mar 8;25(1):29. doi: 10.1186/s10194-024-01739-w.
Energy metabolism disorders and neurogenic inflammation play important roles in the central sensitization to chronic migraine (CM). AMP-activated protein kinase (AMPK) is an intracellular energy sensor, and its activation regulates inflammation and reduces neuropathic pain. However, studies on the involvement of AMPK in the regulation of CM are currently lacking. Therefore, this study aimed to explore the mechanism underlying the involvement of AMPK in the central sensitization to CM.
Mice with recurrent nitroglycerin (NTG)-induced CM were used to detect the expression of AMPK protein in the trigeminal nucleus caudalis (TNC). Following intraperitoneal injection of the AMPK activator 5-aminoimidazole-4-carboxyamide ribonucleoside (AICAR) and inhibitor compound C, the mechanical pain threshold, activity level, and pain-like behaviors in the mice were measured. The expression of calcitonin gene-related peptide (CGRP) and cytokines, M1/M2 microglia, and NF-κB pathway activation were detected after the intervention.
Repeated NTG injections resulted in a gradual decrease in AMPK protein expression, and the negative regulation of AMPK by increased ubiquitin-like plant homeodomain and RING finger domain 1 (UHRF1) expression may counteract AMPK activation by increasing ADP/ATP. AICAR can reduce the hyperalgesia and pain-like behaviors of CM mice, improve the activity of mice, reduce the expression of CGRP, IL-1β, IL-6, and TNF-α in the TNC region, and increase the expression of IL-4 and IL-10. Moreover, AMPK in TNC was mainly located in microglia. AICAR could reduce the expression of inducible NO synthase (iNOS) in M1 microglia and increase the expression of Arginase 1 (Arg1) in M2 microglia by inhibiting the activation of NF-κB pathway.
AMPK was involved in the central sensitization of CM, and the activation of AMPK reduced neuroinflammation in NTG-induced CM mice. AMPK may provide new insights into interventions for energy metabolism disorders and neurogenic inflammation in migraine.
能量代谢紊乱和神经源性炎症在慢性偏头痛(CM)的中枢敏化中发挥重要作用。AMP 激活蛋白激酶(AMPK)是一种细胞内能量感受器,其激活可调节炎症并减轻神经性疼痛。然而,目前关于 AMPK 参与 CM 调节的研究尚缺乏。因此,本研究旨在探讨 AMPK 参与 CM 中枢敏化的机制。
使用反复给予硝化甘油(NTG)诱导的 CM 小鼠检测三叉神经尾核(TNC)中 AMPK 蛋白的表达。腹腔注射 AMPK 激活剂 5-氨基咪唑-4-甲酰胺核苷(AICAR)和抑制剂化合物 C 后,测量小鼠的机械痛阈、活动水平和痛样行为。干预后检测降钙素基因相关肽(CGRP)和细胞因子、M1/M2 小胶质细胞以及 NF-κB 通路的表达。
重复 NTG 注射导致 AMPK 蛋白表达逐渐下降,而 UHRF1 表达增加导致 AMPK 的负调控可能通过增加 ADP/ATP 来抵消 AMPK 的激活。AICAR 可减轻 CM 小鼠的痛觉过敏和痛样行为,提高小鼠的活动能力,降低 TNC 区域 CGRP、IL-1β、IL-6 和 TNF-α的表达,增加 IL-4 和 IL-10 的表达。此外,TNC 中的 AMPK 主要位于小胶质细胞中。AICAR 可通过抑制 NF-κB 通路的激活,减少 M1 小胶质细胞中诱导型一氧化氮合酶(iNOS)的表达,增加 M2 小胶质细胞中精氨酸酶 1(Arg1)的表达。
AMPK 参与 CM 的中枢敏化,激活 AMPK 可减轻 NTG 诱导的 CM 小鼠的神经炎症。AMPK 可能为偏头痛的能量代谢紊乱和神经源性炎症的干预提供新的思路。