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Gastric bypass alters diurnal feeding behavior and reprograms the hepatic clock to regulate endogenous glucose flux

The molecular clock machinery regulates several homeostatic rhythms, including glucose metabolism. We previously demonstrated that Roux-en-Y gastric bypass (RYGB) has a weight-independent effect on glucose homeostasis and transiently reduces food intake. In this study we investigate the effects of R...

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Autores principales: Ye, Yuanchao, Abu El Haija, Marwa, Obeid, Reine, Herz, Hussein, Tian, Liping, Linden, Benjamin, Chu, Yi, Guo, Deng Fu, Levine, Daniel C., Cedernaes, Jonathan, Rahmouni, Kamal, Bass, Joseph, Mokadem, Mohamad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Clinical Investigation 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10070113/
https://www.ncbi.nlm.nih.gov/pubmed/36787197
http://dx.doi.org/10.1172/jci.insight.166618
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author Ye, Yuanchao
Abu El Haija, Marwa
Obeid, Reine
Herz, Hussein
Tian, Liping
Linden, Benjamin
Chu, Yi
Guo, Deng Fu
Levine, Daniel C.
Cedernaes, Jonathan
Rahmouni, Kamal
Bass, Joseph
Mokadem, Mohamad
author_facet Ye, Yuanchao
Abu El Haija, Marwa
Obeid, Reine
Herz, Hussein
Tian, Liping
Linden, Benjamin
Chu, Yi
Guo, Deng Fu
Levine, Daniel C.
Cedernaes, Jonathan
Rahmouni, Kamal
Bass, Joseph
Mokadem, Mohamad
author_sort Ye, Yuanchao
collection PubMed
description The molecular clock machinery regulates several homeostatic rhythms, including glucose metabolism. We previously demonstrated that Roux-en-Y gastric bypass (RYGB) has a weight-independent effect on glucose homeostasis and transiently reduces food intake. In this study we investigate the effects of RYGB on diurnal eating behavior as well as on the molecular clock and this clock’s requirement for the metabolic effects of this bariatric procedure in obese mice. We find that RYGB reversed the high-fat diet–induced disruption in diurnal eating pattern during the early postsurgery phase of food reduction. Dark-cycle pair-feeding experiments improved glucose tolerance to the level of bypass-operated animals during the physiologic fasting phase (Zeitgeber time 2, ZT2) but not the feeding phase (ZT14). Using a clock gene reporter mouse model (mPer2(Luc)), we reveal that RYGB induced a liver-specific phase shift in peripheral clock oscillation with no changes to the central clock activity within the suprachiasmatic nucleus. In addition, we show that weight loss effects were attenuated in obese Clock(Δ19) mutant mice after RYGB that also failed to improve glucose metabolism after surgery, specifically hepatic glucose production. We conclude that RYGB reprograms the peripheral clock within the liver early after surgery to alter diurnal eating behavior and regulate hepatic glucose flux.
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spelling pubmed-100701132023-04-05 Gastric bypass alters diurnal feeding behavior and reprograms the hepatic clock to regulate endogenous glucose flux Ye, Yuanchao Abu El Haija, Marwa Obeid, Reine Herz, Hussein Tian, Liping Linden, Benjamin Chu, Yi Guo, Deng Fu Levine, Daniel C. Cedernaes, Jonathan Rahmouni, Kamal Bass, Joseph Mokadem, Mohamad JCI Insight Research Article The molecular clock machinery regulates several homeostatic rhythms, including glucose metabolism. We previously demonstrated that Roux-en-Y gastric bypass (RYGB) has a weight-independent effect on glucose homeostasis and transiently reduces food intake. In this study we investigate the effects of RYGB on diurnal eating behavior as well as on the molecular clock and this clock’s requirement for the metabolic effects of this bariatric procedure in obese mice. We find that RYGB reversed the high-fat diet–induced disruption in diurnal eating pattern during the early postsurgery phase of food reduction. Dark-cycle pair-feeding experiments improved glucose tolerance to the level of bypass-operated animals during the physiologic fasting phase (Zeitgeber time 2, ZT2) but not the feeding phase (ZT14). Using a clock gene reporter mouse model (mPer2(Luc)), we reveal that RYGB induced a liver-specific phase shift in peripheral clock oscillation with no changes to the central clock activity within the suprachiasmatic nucleus. In addition, we show that weight loss effects were attenuated in obese Clock(Δ19) mutant mice after RYGB that also failed to improve glucose metabolism after surgery, specifically hepatic glucose production. We conclude that RYGB reprograms the peripheral clock within the liver early after surgery to alter diurnal eating behavior and regulate hepatic glucose flux. American Society for Clinical Investigation 2023-03-22 /pmc/articles/PMC10070113/ /pubmed/36787197 http://dx.doi.org/10.1172/jci.insight.166618 Text en © 2023 Ye et al. https://creativecommons.org/licenses/by/4.0/This work is licensed under the Creative Commons Attribution 4.0 International License. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Article
Ye, Yuanchao
Abu El Haija, Marwa
Obeid, Reine
Herz, Hussein
Tian, Liping
Linden, Benjamin
Chu, Yi
Guo, Deng Fu
Levine, Daniel C.
Cedernaes, Jonathan
Rahmouni, Kamal
Bass, Joseph
Mokadem, Mohamad
Gastric bypass alters diurnal feeding behavior and reprograms the hepatic clock to regulate endogenous glucose flux
title Gastric bypass alters diurnal feeding behavior and reprograms the hepatic clock to regulate endogenous glucose flux
title_full Gastric bypass alters diurnal feeding behavior and reprograms the hepatic clock to regulate endogenous glucose flux
title_fullStr Gastric bypass alters diurnal feeding behavior and reprograms the hepatic clock to regulate endogenous glucose flux
title_full_unstemmed Gastric bypass alters diurnal feeding behavior and reprograms the hepatic clock to regulate endogenous glucose flux
title_short Gastric bypass alters diurnal feeding behavior and reprograms the hepatic clock to regulate endogenous glucose flux
title_sort gastric bypass alters diurnal feeding behavior and reprograms the hepatic clock to regulate endogenous glucose flux
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10070113/
https://www.ncbi.nlm.nih.gov/pubmed/36787197
http://dx.doi.org/10.1172/jci.insight.166618
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