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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 1

The effects of NREM-to-REM transitions, NREM-to-unusual wake transitions, and REM-to-wake transitions on the activity of MePVGlu neurons.

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The effects of NREM-to-REM transitions, NREM-to-unusual wake transitions...
(A) Top: The in vivo recording arrangement; Bottom: Illustrations of the MePV from a mouse expressing the rAAV-CaMKIIa-GCaMP6f virus (n = 6 mice/group), displaying virus expression as well as the position of the fiber tip above the MePV. (B) The heatmap for the calcium signal of MePVGlu neurons. The representative transitions (closed arm-open arm, 87 trials) of the changes in color-coded fluorescence intensity. (C) The color-coded fluorescence intensity changes of the representative shifts from the open arm to the closed arm (45 trials). (D) A shift in color-coded fluorescence intensity illustrating the representative transition from NREM to forced wakeup (16 trials). (E) Changes in color-coded fluorescence intensity indicating the representative transitions from NREM to REM (132 trials). (F) The representative shifts in fluorescence intensity during the transitions from REM to normal wakefulness (20 trials). (G) Representative shift in color-coded fluorescence intensity (83 trials) depicting the transition from NREM to natural wake. (H) Color changes representing shifts in fluorescence intensity from REM to microarousal (119 trials). (I) A shift in the intensity of the color-coded fluorescence indicating the representative transition from NREM to microarousal (257 trials). Mean (red trace) ± SEM (red shading) represents the average responses of all the transitions.

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ISSN 2379-3708

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