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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...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Clinical Investigation
2023
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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. |
format | Online Article Text |
id | pubmed-10070113 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Society for Clinical Investigation |
record_format | MEDLINE/PubMed |
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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