Orexin/hypocretin receptor 2 signaling in MCH neurons regulates REM sleep and insulin sensitivity

Orexin/hypocretin receptor type 2 (Ox2R), which is widely expressed in the brain, receives orexin signals and modulates sleep and metabolism. Ox2R selective agonists are currently under clinical trials for narcolepsy treatment. Here, we focused on Ox2R expression and function in melanin-concentrating hormone (MCH) neurons, which have opposite roles to orexin neurons in sleep and metabolism regulation. Ox2R-expressing MCH neurons showed heterogeneity of RNA expression, and orexin B application in brain slices induced both excitatory and inhibitory responses in distinct MCH neuron populations. Ox2R inactivation in MCH neurons reduced transitions from non-rapid eye movement (NREM) to REM sleep and impaired insulin sensitivity with excessive feeding after a fasting period in female mice. In conclusion, Ox2R mediates excitatory and inhibitory responses in MCH neuron sub-populations in vivo, which regulate sleep and metabolism in female mice.

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Publication Details

Journal
Cell Reports
Published
2025-02-01
DOI
https://doi.org/10.1016/j.celrep.2025.115277
Citations
8
Primary Topic
Sleep and Wakefulness Research
Type
article
Field-Weighted Citation Impact
11.45

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article

Orexin/hypocretin receptor 2 signaling in MCH neurons regulates REM sleep and insulin sensitivity

Peter Kloppenburg, Christian Heilinger, Shuntaro Izawa, Debora Fuscà et al.
8 citations
Cell Reports
Sleep and Wakefulness Research
11.45
article

Orexin/hypocretin receptor 2 signaling in MCH neurons regulates REM sleep and insulin sensitivity

Peter Kloppenburg, Christian Heilinger, Shuntaro Izawa, Debora Fuscà, F. Thomas Wunderlich, Lukas Steuernagel, A. Christine Hausen, Hong Jiang, Jens C. Brüning
article en
8 citations

Abstract

Orexin/hypocretin receptor type 2 (Ox2R), which is widely expressed in the brain, receives orexin signals and modulates sleep and metabolism. Ox2R selective agonists are currently under clinical trials for narcolepsy treatment. Here, we focused on Ox2R expression and function in melanin-concentrating hormone (MCH) neurons, which have opposite roles to orexin neurons in sleep and metabolism regulation. Ox2R-expressing MCH neurons showed heterogeneity of RNA expression, and orexin B application in brain slices induced both excitatory and inhibitory responses in distinct MCH neuron populations. Ox2R inactivation in MCH neurons reduced transitions from non-rapid eye movement (NREM) to REM sleep and impaired insulin sensitivity with excessive feeding after a fasting period in female mice. In conclusion, Ox2R mediates excitatory and inhibitory responses in MCH neuron sub-populations in vivo, which regulate sleep and metabolism in female mice.

Cell ReportsVol. 44(2)
University of Cologne (DE), Peking University (CN), Max Planck Institute for Metabolism Research (DE), Cologne Excellence Cluster on Cellular Stress Responses in Aging Associated Diseases (DE), University Hospital Cologne (DE), German Center for Diabetes Research (DE)
Manpei Suzuki Diabetes Foundation, H2020 European Research Council
Zero hunger
Openalex Percentile: Top 1%
Sleep and Wakefulness Research
11.45
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