Pontine control of rapid eye movement sleep and fear memory

Author:

Wen Yu Jun12ORCID,Yang Wen Jia23,Guo Chun Ni24,Qiu Mei Hong25,Kroeger Daniel26,Niu Jian Guo12,Zhan Shu Qin27,Yang Xi Fei28,Gisabella Barbara29,Vetrivelan Ramalingam2,Lu Jun210

Affiliation:

1. Ningxia Key Laboratory of Craniocerebral Diseases, Department of Anatomy, Histology and Embryology, School of Basic Medicine Ningxia Medical University Yinchuan Ningxia China

2. Department of Neurology Beth Israel Deaconess Medical Center and Harvard Medical School Boston Massachusetts USA

3. Shanghai Yueyang Integrated Medicine Hospital Shanghai China

4. Department of Neurology, Shanghai First People's Hospital Shanghai Jiaotong University Shanghai China

5. Department of Neurobiology, School of Basic Medical Science, Shanghai Medical College Fudan University Shanghai China

6. Department of Anatomy, Physiology & Pharmacology, College of Veterinary Medicine Auburn University Auburn Alabama USA

7. Department of Neurology, Xuanwu Hospital Capital Medical University Beijing China

8. Shenzhen Center for Disease Control and Prevention Shenzhen Guangdong China

9. Department of Psychiatry and Human Behavior University of Mississippi Medical Center Jackson Mississippi USA

10. Stroke Center, Department of Neurology 1st Hospital of Jilin University Changchun Jilin China

Abstract

AbstractAimsWe often experience dreams of strong irrational and negative emotional contents with postural muscle paralysis during rapid eye movement (REM) sleep, but how REM sleep is generated and its function remain unclear. In this study, we investigate whether the dorsal pontine sub‐laterodorsal tegmental nucleus (SLD) is necessary and sufficient for REM sleep and whether REM sleep elimination alters fear memory.MethodsTo investigate whether activation of SLD neurons is sufficient for REM sleep induction, we expressed channelrhodopsin‐2 (ChR2) in SLD neurons by bilaterally injecting AAV1‐hSyn‐ChR2‐YFP in rats. We next selectively ablated either glutamatergic or GABAergic neurons from the SLD in mice in order to identify the neuronal subset crucial for REM sleep. We finally  investigated the role of REM sleep in consolidation of fear memory using rat model with complete SLD lesions.ResultsWe demonstrate the sufficiency of the SLD for REM sleep by showing that photo‐activation of ChR2 transfected SLD neurons selectively promotes transitions from non‐REM (NREM) sleep to REM sleep in rats. Diphtheria toxin‐A (DTA) induced lesions of the SLD in rats or specific deletion of SLD glutamatergic neurons but not GABAergic neurons in mice completely abolish REM sleep, demonstrating the necessity of SLD glutamatergic neurons for REM sleep. We then show that REM sleep elimination by SLD lesions in rats significantly enhances contextual and cued fear memory consolidation by 2.5 and 1.0 folds, respectively, for at least 9 months. Conversely, fear conditioning and fear memory trigger doubled amounts of REM sleep in the following night, and chemo‐activation of SLD neurons projecting to the medial septum (MS) selectively enhances hippocampal theta activity in REM sleep; this stimulation immediately after fear acquisition reduces contextual and cued fear memory consolidation by 60% and 30%, respectively.ConclusionSLD glutamatergic neurons generate REM sleep and REM sleep and SLD via the hippocampus particularly down‐regulate contextual fear memory.

Funder

National Institutes of Health

National Natural Science Foundation of China

Publisher

Wiley

Subject

Pharmacology (medical),Physiology (medical),Psychiatry and Mental health,Pharmacology

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