Loading…

The paraventricular thalamus is a critical thalamic area for wakefulness

Clinical observations indicate that the paramedian region of the thalamus is a critical node for controlling wakefulness. However, the specific nucleus and neural circuitry for this function remain unknown. Using in vivo fiber photometry or multichannel electrophysiological recordings in mice, we fo...

Full description

Saved in:
Bibliographic Details
Published in:Science (American Association for the Advancement of Science) 2018-10, Vol.362 (6413), p.429-434
Main Authors: Ren, Shuancheng, Wang, Yaling, Yue, Faguo, Cheng, Xiaofang, Dang, Ruozhi, Qiao, Qicheng, Sun, Xueqi, Li, Xin, Jiang, Qian, Yao, Jiwei, Qin, Han, Wang, Guanzhong, Liao, Xiang, Gao, Dong, Xia, Jianxia, Zhang, Jun, Hu, Bo, Yan, Junan, Wang, Yanjiang, Xu, Min, Han, Yunyun, Tang, Xiangdong, Chen, Xiaowei, He, Chao, Hu, Zhian
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:Clinical observations indicate that the paramedian region of the thalamus is a critical node for controlling wakefulness. However, the specific nucleus and neural circuitry for this function remain unknown. Using in vivo fiber photometry or multichannel electrophysiological recordings in mice, we found that glutamatergic neurons of the paraventricular thalamus (PVT) exhibited high activities during wakefulness. Suppression of PVT neuronal activity caused a reduction in wakefulness, whereas activation of PVT neurons induced a transition from sleep to wakefulness and an acceleration of emergence from general anesthesia. Moreover, our findings indicate that the PVT-nucleus accumbens projections and hypocretin neurons in the lateral hypothalamus to PVT glutamatergic neurons' projections are the effector pathways for wakefulness control. These results demonstrate that the PVT is a key wakefulness-controlling nucleus in the thalamus.
ISSN:0036-8075
1095-9203
DOI:10.1126/science.aat2512