Issue 7, 2018

Dietary methionine restriction regulated energy and protein homeostasis by improving thyroid function in high fat diet mice

Abstract

Methionine-restricted diets (MRD) show an integrated series of beneficial health effects, including improving insulin sensitivity, limiting fat deposition, and decreasing oxidative stress, and inflammation responses. We aimed to explore the systemic responses to a MRD in mice fed with a high fat (HFD) and clarify the possible mechanism. Mice were fed with a control diet (0.86% methionine + 4% fat, CON), HFD (0.86% methionine + 20% fat), or MRD (0.17% methionine + 20% fat) for 22 consecutive weeks. HFD-fed mice showed widespread systemic metabolic disorders and thyroid dysfunction. A MRD significantly increased energy expenditure (e.g. fatty acid oxidation, glycolysis, and tricarboxylic acid cycle metabolism), regulated protein homeostasis, improved gut microbiota functions, prevented thyroid dysfunction, increased plasma thyroxine and triiodothyronine levels, decreased plasma thyroid stimulating hormone levels, increased type 2 deiodinase (DIO2) activity, and up-regulated mRNA and protein expression levels of DIO2 and thyroid hormone receptor α1 in the skeletal muscle. These results suggest that a MRD can improve the metabolic disorders induced by a HFD, and especially regulate energy and protein homeostasis likely through improved thyroid function. Thus, reducing methionine intake (e.g. through a vegan diet) may improve metabolic health in animals and humans.

Graphical abstract: Dietary methionine restriction regulated energy and protein homeostasis by improving thyroid function in high fat diet mice

Supplementary files

Article information

Article type
Paper
Submitted
11 Apr 2018
Accepted
15 Jun 2018
First published
19 Jun 2018

Food Funct., 2018,9, 3718-3731

Dietary methionine restriction regulated energy and protein homeostasis by improving thyroid function in high fat diet mice

Y. Yang, J. Zhang, G. Wu, J. Sun, Y. Wang, H. Guo, Y. Shi, X. Cheng, X. Tang and G. Le, Food Funct., 2018, 9, 3718 DOI: 10.1039/C8FO00685G

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