Literature DB >> 31473062

A Rare Mutation of β1-Adrenergic Receptor Affects Sleep/Wake Behaviors.

Guangsen Shi1, Lijuan Xing1, David Wu1, Bula J Bhattacharyya1, Christopher R Jones2, Thomas McMahon1, S Y Christin Chong1, Jason A Chen3, Giovanni Coppola3, Daniel Geschwind3, Andrew Krystal4, Louis J Ptáček5, Ying-Hui Fu6.   

Abstract

Sleep is crucial for our survival, and many diseases are linked to long-term poor sleep quality. Before we can use sleep to enhance our health and performance and alleviate diseases associated with poor sleep, a greater understanding of sleep regulation is necessary. We have identified a mutation in the β1-adrenergic receptor gene in humans who require fewer hours of sleep than most. In vitro, this mutation leads to decreased protein stability and dampened signaling in response to agonist treatment. In vivo, the mice carrying the same mutation demonstrated short sleep behavior. We found that this receptor is highly expressed in the dorsal pons and that these ADRB1+ neurons are active during rapid eye movement (REM) sleep and wakefulness. Activating these neurons can lead to wakefulness, and the activity of these neurons is affected by the mutation. These results highlight the important role of β1-adrenergic receptors in sleep/wake regulation.
Copyright © 2019 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  ADRB1; dorsal pons; familial natural short sleep; sleep duration

Year:  2019        PMID: 31473062      PMCID: PMC6763376          DOI: 10.1016/j.neuron.2019.07.026

Source DB:  PubMed          Journal:  Neuron        ISSN: 0896-6273            Impact factor:   17.173


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