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Abnormal Food Timing and Predisposition to Weight Gain: Role of Barrier Dysfunction and Microbiota

Overview
Journal Transl Res
Publisher Elsevier
Specialty Pathology
Date 2020 Nov 22
PMID 33221482
Citations 10
Authors
Affiliations
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Abstract

Obesity has become a common rising health care problem, especially in "modern" societies. Obesity is considered a low-grade systemic inflammation, partly linked to leaky gut. Circadian rhythm disruption, a common habit in modern life, has been reported to cause gut barrier impairment. Abnormal time of eating, defined by eating close to or during rest time, is shown to cause circadian rhythm disruption. Here, using a non-obesogenic diet, we found that abnormal feeding time facilitated weight gain and induced metabolic dysregulation in mice. The effect of abnormal time of eating was associated with increased gut permeability, estimated by sucralose and/or lactulose ratio and disrupted intestinal barrier marker. Analysis of gut microbiota and their metabolites, as important regulators of barrier homeostasis, revealed that abnormal food timing reduced relative abundance of butyrate-producing bacteria, and the colonic butyrate level. Overall, our data supported that dysbiosis was characterized by increased intestinal permeability and decreased beneficial barrier butyrate-producing bacteria and/or metabolite to mechanistically link the time of eating to obesity. This data provides basis for noninvasive microbial-targeted interventions to improve intestinal barrier function as new opportunities for combating circadian rhythm disruption induced metabolic dysfunction.

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References
1.
Wehrens S, Christou S, Isherwood C, Middleton B, Gibbs M, Archer S . Meal Timing Regulates the Human Circadian System. Curr Biol. 2017; 27(12):1768-1775.e3. PMC: 5483233. DOI: 10.1016/j.cub.2017.04.059. View

2.
Kelly C, Zheng L, Campbell E, Saeedi B, Scholz C, Bayless A . Crosstalk between Microbiota-Derived Short-Chain Fatty Acids and Intestinal Epithelial HIF Augments Tissue Barrier Function. Cell Host Microbe. 2015; 17(5):662-71. PMC: 4433427. DOI: 10.1016/j.chom.2015.03.005. View

3.
Summa K, Voigt R, Forsyth C, Shaikh M, Cavanaugh K, Tang Y . Disruption of the Circadian Clock in Mice Increases Intestinal Permeability and Promotes Alcohol-Induced Hepatic Pathology and Inflammation. PLoS One. 2013; 8(6):e67102. PMC: 3688973. DOI: 10.1371/journal.pone.0067102. View

4.
Liu W, Zhou X, Li Y, Zhang S, Cai X, Zhang R . Serum leptin, resistin, and adiponectin levels in obese and non-obese patients with newly diagnosed type 2 diabetes mellitus: A population-based study. Medicine (Baltimore). 2020; 99(6):e19052. PMC: 7015632. DOI: 10.1097/MD.0000000000019052. View

5.
Ivanov I, Honda K . Intestinal commensal microbes as immune modulators. Cell Host Microbe. 2012; 12(4):496-508. PMC: 3516493. DOI: 10.1016/j.chom.2012.09.009. View