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Gastric bypass alters diurnal feeding behavior and reprograms the hepatic clock to regulate endogenous glucose flux
Yuanchao Ye, Marwa Abu El Haija, Reine Obeid, Hussein Herz, Liping Tian, Benjamin Linden, Yi Chu, Deng Fu Guo, Daniel C. Levine, Jonathan Cedernaes, Kamal Rahmouni, Joseph Bass, Mohamad Mokadem
Yuanchao Ye, Marwa Abu El Haija, Reine Obeid, Hussein Herz, Liping Tian, Benjamin Linden, Yi Chu, Deng Fu Guo, Daniel C. Levine, Jonathan Cedernaes, Kamal Rahmouni, Joseph Bass, Mohamad Mokadem
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Research Article Endocrinology Metabolism

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

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Abstract

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 (mPer2Luc), 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 ClockΔ19 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.

Authors

Yuanchao Ye, Marwa Abu El Haija, Reine Obeid, Hussein Herz, Liping Tian, Benjamin Linden, Yi Chu, Deng Fu Guo, Daniel C. Levine, Jonathan Cedernaes, Kamal Rahmouni, Joseph Bass, Mohamad Mokadem

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Figure 4

RYGB induces a phase shift in hepatic clock gene oscillation but not the SCN.

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RYGB induces a phase shift in hepatic clock gene oscillation but not the...
mPer2Luc mice were placed on either HFD or regular CHOW diet, and RYGB versus sham surgery was performed on both groups. Tissue analysis was implemented at day 10, when RYGB mice and their sham counterparts had similar body weights. Average background-subtracted bioluminescence showing circadian profiles of mPER2 expression in (A) liver, (B) SCN, (C) mWAT, and (D) soleus muscle from mPer2Luc knockin mice after surgeries. The first 1–3 days of traces were excluded due to nonlinear background. Phase map, period values of mPER2 rhythms, amplitude, and damping were shown for central and peripheral circadian oscillators of mPer2Luc knockin mice in RYGB and Sham-operated mice on CHOW and HFD. Values reported as means ± SD. Box plots show the interquartile range (box), median (line), and minimum and maximum (whiskers). One-way ANOVA was used to compare 4 groups together. **P < 0.01. N, Sham Chow n= 3–4, RYGB Chow = 3–4, Sham HFD = 4–6, RYGB HFD = 4–6.

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