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Distinct glutamatergic projections of the posteroventral medial amygdala play different roles in arousal and anxiety
Ying Li, Yuchen Deng, Yifei Zhang, Dan Xu, Xuefen Zhang, Yue Li, Yidan Li, Ming Chen, Yuxin Wang, Jiyan Zhang, Like Wang, Yufeng Cang, Peng Cao, Linlin Bi, Haibo Xu
Ying Li, Yuchen Deng, Yifei Zhang, Dan Xu, Xuefen Zhang, Yue Li, Yidan Li, Ming Chen, Yuxin Wang, Jiyan Zhang, Like Wang, Yufeng Cang, Peng Cao, Linlin Bi, Haibo Xu
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Research Article Neuroscience

Distinct glutamatergic projections of the posteroventral medial amygdala play different roles in arousal and anxiety

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Abstract

Sleep disturbance usually accompanies anxiety disorders and exacerbates their incidence rates. The precise circuit mechanisms remain poorly understood. Here, we found that glutamatergic neurons in the posteroventral medial amygdala (MePVGlu neurons) are involved in arousal and anxiety-like behaviors. Excitation of MePVGlu neurons not only promoted wakefulness but also increased anxiety-like behaviors. Different projections of MePVGlu neurons played various roles in regulating anxiety-like behaviors and sleep-wakefulness. MePVGlu neurons promoted wakefulness through the MePVGlu/posteromedial cortical amygdaloid area (PMCo) pathway and the MePVGlu/bed nucleus of the stria terminals (BNST) pathway. In contrast, MePVGlu neurons increased anxiety-like behaviors through the MePVGlu/ventromedial hypothalamus (VMH) pathway. Chronic sleep disturbance increased anxiety levels and reduced reparative sleep, accompanied by the enhanced excitability of MePVGlu/PMCo and MePVGlu/VMH circuits but suppressed responses of glutamatergic neurons in the BNST. Inhibition of the MePVGlu neurons could rescue chronic sleep deprivation–induced phenotypes. Our findings provide important circuit mechanisms for chronic sleep disturbance–induced hyperarousal response and obsessive anxiety-like behavior and are expected to provide a promising strategy for treating sleep-related psychiatric disorders and insomnia.

Authors

Ying Li, Yuchen Deng, Yifei Zhang, Dan Xu, Xuefen Zhang, Yue Li, Yidan Li, Ming Chen, Yuxin Wang, Jiyan Zhang, Like Wang, Yufeng Cang, Peng Cao, Linlin Bi, Haibo Xu

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Figure 8

The effects of sleep deprivation on the activity of MePV neurons and the MePV-related neuronal circuits.

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The effects of sleep deprivation on the activity of MePV neurons and the...
(A) The expression of c-fos in the MePV of C57BL/6J mice following a 5-day sleep deprivation (SD) paradigm. Representative immunostaining images of c-fos+ cells in the MePV (A), VMH (B), PMCo (C), and BNST (D) of control and SD mice. (E) Left panel, experimental scheme of bilateral virus injection into the MePV and VMH. Middle panel, the heatmap for the calcium signal of VMH glutamatergic neurons before SD or after SD. The representative transitions (lights off to lights on) of the changes in color-coded fluorescence intensity before SD or after SD (n = 5, 50 trials). Right panel, the mean value (red trace or blue trace) represents the average responses of all the transitions (SEM: red shading or blue shading). (F) Left panel, experimental scheme of bilateral virus injection into the MePV and PMCo. Middle panel, color-coded fluorescence intensity changes of the representative shifts from the lights-off phase to the light-on phase before SD or after SD (n = 5, 45 trials). Right panel, the mean value (red trace or blue trace) represents the average responses of all the transitions (SEM: red shading or blue shading). (G) Left panel, experimental scheme of bilateral virus injection into the MePV and BNST. Middle panel, a shift in color-coded fluorescence intensity illustrates the representative transition from the lights-off phase to the light-on phase before SD or after SD (n = 5, 47 trials). Right panel, the mean value (red trace or blue trace) represents the average responses of all the transitions (SEM: red shading or blue shading). Data are presented as mean ± SEM.

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