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在外周和中枢神经系统的偏头痛相关关键区域中,大麻素水解酶 MAGL 和 FAAH 的活性不同。

Distinct Activity of Endocannabinoid-Hydrolyzing Enzymes MAGL and FAAH in Key Regions of Peripheral and Central Nervous System Implicated in Migraine.

机构信息

A. I. Virtanen Institute for Molecular Sciences, University of Eastern Finland, 70211 Kuopio, Finland.

Laboratory of Neurobiology, Kazan Federal University, 420008 Kazan, Russia.

出版信息

Int J Mol Sci. 2021 Jan 26;22(3):1204. doi: 10.3390/ijms22031204.

Abstract

In migraine pain, cannabis has a promising analgesic action, which, however, is associated with side psychotropic effects. To overcome these adverse effects of exogenous cannabinoids, we propose migraine pain relief via activation of the endogenous cannabinoid system (ECS) by inhibiting enzymes degrading endocannabinoids. To provide a functional platform for such purpose in the peripheral and central parts of the rat nociceptive system relevant to migraine, we measured by activity-based protein profiling (ABPP) the activity of the main endocannabinoid-hydrolases, monoacylglycerol lipase (MAGL) and fatty acid amide hydrolase (FAAH). We found that in trigeminal ganglia, the MAGL activity was nine-fold higher than that of FAAH. MAGL activity exceeded FAAH activity also in DRG, spinal cord and brainstem. However, activities of MAGL and FAAH were comparably high in the cerebellum and cerebral cortex implicated in migraine aura. MAGL and FAAH activities were identified and blocked by the selective and potent inhibitors JJKK-048/KML29 and JZP327A, respectively. The high MAGL activity in trigeminal ganglia implicated in the generation of nociceptive signals suggests this part of ECS as a priority target for blocking peripheral mechanisms of migraine pain. In the CNS, both MAGL and FAAH represent potential targets for attenuation of migraine-related enhanced cortical excitability and pain transmission.

摘要

在偏头痛疼痛中,大麻具有有前途的镇痛作用,但它与副作用的精神作用有关。为了克服外源性大麻素的这些不良反应,我们建议通过抑制降解内源性大麻素的酶来激活内源性大麻素系统 (ECS) 来缓解偏头痛疼痛。为了在与偏头痛相关的大鼠伤害感受系统的外周和中枢部分提供这样的目的的功能平台,我们通过基于活性的蛋白质谱 (ABPP) 测量了主要内源性大麻素水解酶,单酰基甘油脂肪酶 (MAGL) 和脂肪酸酰胺水解酶 (FAAH) 的活性。我们发现,在三叉神经节中,MAGL 的活性是 FAAH 的九倍。MAGL 的活性也超过了 DRG、脊髓和脑干中的 FAAH 活性。然而,在涉及偏头痛先兆的小脑和大脑皮层中,MAGL 和 FAAH 的活性都很高。MAGL 和 FAAH 活性分别被选择性和有效的抑制剂 JJKK-048/KML29 和 JZP327A 鉴定和阻断。在三叉神经节中产生痛觉信号的 MAGL 活性较高表明,这部分 ECS 是阻断偏头痛疼痛外周机制的优先靶点。在中枢神经系统中,MAGL 和 FAAH 都代表了减轻偏头痛相关皮质兴奋性增强和疼痛传递的潜在靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/111b/7865507/5d2a3b4a6c2b/ijms-22-01204-g001.jpg

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