Astrocytic activation in the anterior cingulate cortex is critical for sleep disorder under neuropathic pain

神经病理性疼痛 扣带回前部 神经科学 坐骨神经 谷氨酸受体 星形胶质细胞 医学 化学 麻醉 心理学 内科学 中枢神经系统 受体 认知
作者
Akira Yamashita,Asami Hamada,Yuki Suhara,Rui Kawabe,Makoto Yanase,Naoko Kuzumaki,Michiko Narita,Ryosuke Matsui,Hideyuki Okano,Minoru Narita
出处
期刊:Synapse [Wiley]
卷期号:68 (6): 235-247 被引量:82
标识
DOI:10.1002/syn.21733
摘要

Insomnia, depression, and anxiety disorder are common problems for people with neuropathic pain. In this study, mild noxious heat stimuli increased the duration and number of spontaneous pain-like behaviors in sciatic nerve-ligated mice. We used functional magnetic resonance imaging to visualize the increased blood oxygenation level-dependent signal intensity in the anterior cingulate cortex (ACC) of mice with sciatic nerve ligation under mild noxious stimuli. Such stimuli significantly increased the release of glutamate in the ACC of nerve-ligated mice. In addition, sciatic nerve ligation and mild noxious stimuli changed the morphology of astrocytes in the ACC. Treatment of cortical astrocytes with glutamate caused astrocytic activation, as detected by a stellate morphology. Furthermore, glutamate induced the translocation of GAT-3 to astrocyte cell membranes using primary cultured glial cells from the mouse cortex. Moreover, the GABA level at the synaptic cleft in the ACC of nerve-ligated mice was significantly decreased exposure to mild noxious stimuli. Finally, we investigated whether astrocytic activation in the ACC could directly mediate sleep disorder. With the optogenetic tool channel rhodopsin-2 (ChR2), we demonstrated that selective photostimulation of these astrocytes in vivo triggered sleep disturbance. Taken together, these results suggest that neuropathic pain-like stimuli activated astrocytes in the ACC and decreased the extracellular concentration of GABA via an increase in the release of glutamate. Furthermore, these findings provide novel evidence that astrocytic activation in the ACC can mimic sleep disturbance in mice.
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