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Inhibiting neuronal AC1 for treating anxiety and headache in the animal model of migraine.

Abstract
Migraines are a common medical condition. From a basic science point of view, the central mechanism for migraine and headache is largely unknown. In the present study, we demonstrate that cortical excitatory transmission is significantly enhanced in the anterior cingulate cortex (ACC)-a brain region which is critical for pain perception. Biochemical studies found that the phosphorylation levels of both the NMDA receptor GluN2B and AMPA receptor GluA1 were enhanced in ACC of migraine rats. Both the presynaptic release of glutamate and postsynaptic responses of AMPA receptors and NMDA receptors were enhanced. Synaptic long-term potentiation (LTP) was occluded. Furthermore, behavioral anxiety and nociceptive responses were increased, which were reversed by application of AC1 inhibitor NB001 within ACC. Our results provide strong evidence that cortical LTPs contribute to migraine-related pain and anxiety. Drugs that inhibit cortical excitation such as NB001 may serve as potential medicines for treating migraine in the future.
AuthorsRen-Hao Liu, Mingjie Zhang, Man Xue, Tao Wang, Jing-Shan Lu, Xu-Hui Li, Yu-Xin Chen, Kexin Fan, Wantong Shi, Si-Bo Zhou, Qi-Yu Chen, Li Kang, Qian Song, Shengyuan Yu, Min Zhuo
JournaliScience (iScience) Vol. 26 Issue 6 Pg. 106790 (Jun 16 2023) ISSN: 2589-0042 [Electronic] United States
PMID37235050 (Publication Type: Journal Article)
Copyright© 2023 The Author(s).

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