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Involvement of Gut Microbial Metabolites Derived from Diet on Host Energy Homeostasis

Overview
Journal Int J Mol Sci
Publisher MDPI
Date 2022 May 28
PMID 35628369
Authors
Affiliations
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Abstract

Due to the excess energy intake, which is a result of a high fat and high carbohydrate diet, dysfunction of energy balance leads to metabolic disorders such as obesity and type II diabetes mellitus (T2DM). Since obesity can be a risk factor for various diseases, including T2DM, hypertension, hyperlipidemia, and metabolic syndrome, novel prevention and treatment are expected. Moreover, host diseases linked to metabolic disorders are associated with changes in gut microbiota profile. Gut microbiota is affected by diet, and nutrients are used as substrates by gut microbiota for produced metabolites, such as short-chain and long-chain fatty acids, that may modulate host energy homeostasis. These free fatty acids are not only essential energy sources but also signaling molecules via G-protein coupled receptors (GPCRs). Some GPCRs are critical for metabolic functions, such as hormone secretion and immune function in various types of cells and tissues and contribute to energy homeostasis. The current studies have shown that GPCRs for gut microbial metabolites improved host energy homeostasis and systemic metabolic disorders. Here, we will review the association between diet, gut microbiota, and host energy homeostasis.

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References
1.
Wan Y, Wang F, Yuan J, Li J, Jiang D, Zhang J . Effects of dietary fat on gut microbiota and faecal metabolites, and their relationship with cardiometabolic risk factors: a 6-month randomised controlled-feeding trial. Gut. 2019; 68(8):1417-1429. DOI: 10.1136/gutjnl-2018-317609. View

2.
Nagasumi K, Esaki R, Iwachidow K, Yasuhara Y, Ogi K, Tanaka H . Overexpression of GPR40 in pancreatic beta-cells augments glucose-stimulated insulin secretion and improves glucose tolerance in normal and diabetic mice. Diabetes. 2009; 58(5):1067-76. PMC: 2671040. DOI: 10.2337/db08-1233. View

3.
Jiang C, Xie C, Li F, Zhang L, Nichols R, Krausz K . Intestinal farnesoid X receptor signaling promotes nonalcoholic fatty liver disease. J Clin Invest. 2014; 125(1):386-402. PMC: 4382255. DOI: 10.1172/JCI76738. View

4.
Samuel B, Shaito A, Motoike T, Rey F, Backhed F, Manchester J . Effects of the gut microbiota on host adiposity are modulated by the short-chain fatty-acid binding G protein-coupled receptor, Gpr41. Proc Natl Acad Sci U S A. 2008; 105(43):16767-72. PMC: 2569967. DOI: 10.1073/pnas.0808567105. View

5.
Newgard C . Interplay between lipids and branched-chain amino acids in development of insulin resistance. Cell Metab. 2012; 15(5):606-14. PMC: 3695706. DOI: 10.1016/j.cmet.2012.01.024. View