Department of Neurology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan Province, China.
iHuman Institute, ShanghaiTech University, Shanghai, China.
J Headache Pain. 2024 Sep 30;25(1):163. doi: 10.1186/s10194-024-01872-6.
Chronic migraine is closely related to the dysregulation of neurochemical substances in the brain, with metabolic imbalance being one of the proposed causes of chronic migraine. This study aims to evaluate the metabolic changes between energy metabolism and excitatory and inhibitory neurotransmitters in key brain regions of mice with chronic migraine-like state and to uncover the dysfunctional pathways of migraine.
A chronic migraine-like state mouse model was established by repeated administration of nitroglycerin (NTG). We used von Frey filaments to assess the mechanical thresholds of the hind paw and periorbital in wild-type and familial hemiplegic migraine type 2 mice. After the experiments, tissue was collected from five brain regions: the somatosensory cortex (SSP), hippocampus, thalamus (TH), hypothalamus, and the spinal trigeminal nucleus caudalis (TNC). Proton magnetic resonance spectroscopy (H-MRS) was employed to study the changes in brain metabolites associated with migraine, aiming to explore the mechanisms underlying metabolic imbalance in chronic migraine-like state.
In NTG-induced chronic migraine-like state model, we observed a significant reduction in energy metabolism during central sensitization, an increase in excitatory neurotransmitters such as glutamate, and a tendency for inhibitory neurotransmitters like GABA to decrease. The TNC and thalamus were the most affected regions. Furthermore, the consistency of N-acetylaspartate levels highlighted the importance of the TNC-TH-SSP pathway in the ascending nociceptive transmission of migraine.
Abnormal energy metabolism and neurotransmitter imbalance in the brain region of NTG-induced chronic migraine-like state model are crucial mechanisms contributing to the chronicity of migraine.
慢性偏头痛与大脑中神经化学物质的失调密切相关,代谢失衡是慢性偏头痛的一个潜在原因。本研究旨在评估慢性偏头痛样状态小鼠模型中关键脑区的能量代谢和兴奋性及抑制性神经递质的代谢变化,以揭示偏头痛的功能障碍途径。
通过重复给予硝化甘油(NTG)建立慢性偏头痛样状态小鼠模型。我们使用 von Frey 细丝评估野生型和家族性偏瘫性偏头痛 2 型小鼠后爪和眶周的机械阈值。在实验结束后,从五个脑区(体感皮层、海马体、丘脑、下丘脑和三叉神经脊束核尾侧部)采集组织。质子磁共振波谱(H-MRS)用于研究与偏头痛相关的脑代谢物变化,旨在探讨慢性偏头痛样状态下代谢失衡的机制。
在 NTG 诱导的慢性偏头痛样状态模型中,我们观察到在中枢敏化期间能量代谢显著降低,兴奋性神经递质如谷氨酸增加,而抑制性神经递质如 GABA 则呈下降趋势。三叉神经脊束核尾侧部和丘脑是受影响最严重的区域。此外,N-乙酰天冬氨酸水平的一致性突出了 TNC-TH-SSP 通路在偏头痛上行伤害性传递中的重要性。
NTG 诱导的慢性偏头痛样状态模型中脑区的异常能量代谢和神经递质失衡是偏头痛慢性化的关键机制。