REV-ERB nuclear receptors in the suprachiasmatic nucleus control circadian period and restrict diet-induced obesity

Marine Adlanmerini, Brianna M. Krusen, Hoang C.B. Nguyen, Clare W. Teng, Lauren N. Woodie, Michael C. Tackenberg, Caroline E. Geisler, Jane Gaisinsky, Lindsey C. Peed, Bryce J. Carpenter, Matthew R. Hayes, Mitchell A. Lazar

Producción científica: Articlerevisión exhaustiva

28 Citas (Scopus)

Resumen

Circadian disruption, as occurs in shift work, is associated with metabolic diseases often attributed to a discordance between internal clocks and environmental timekeepers. REV-ERB nuclear receptors are key components of the molecular clock, but their specific role in the SCN master clock is unknown. We report here that mice lacking circadian REV-ERB nuclear receptors in the SCN maintain free-running locomotor and metabolic rhythms, but these rhythms are notably shortened by 3 hours. When housed under a 24-hour light:dark cycle and fed an obesogenic diet, these mice gained excess weight and accrued more liver fat than controls. These metabolic disturbances were corrected by matching environmental lighting to the shortened endogenous 21-hour clock period, which decreased food consumption. Thus, SCN REV-ERBs are not required for rhythmicity but determine the free-running period length. Moreover, these results support the concept that dissonance between environmental conditions and endogenous time periods causes metabolic disruption.

Idioma originalEnglish
Número de artículoeabh2007
PublicaciónScience advances
Volumen7
N.º44
DOI
EstadoPublished - oct 2021

Nota bibliográfica

Publisher Copyright:
Copyright © 2021 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC).

Financiación

M.A. was supported by American Diabetes Association Training Grants (1-18-PDF-126). L.N.W. was supported by NIH T32DK007314-40. M.R.H. was supported by NIH R01DKDK021397. M.A.L. was supported by NIH R01DK45586, the JPB Foundation, and the Cox Institute for Medical Research.

FinanciadoresNúmero del financiador
Cox Institute for Medical Research
National Institutes of Health (NIH)R01DK45586, R01DKDK021397, T32DK007314-40
American Diabetes Association Inc1-18-PDF-126
JPB Foundation

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