Role of diets and exercise in ameliorating obesity-related hepatic steatosis: Insights at the microRNA-dependent thyroid hormone synthesis and action

Life Sci. 2020 Feb 1:242:117182. doi: 10.1016/j.lfs.2019.117182. Epub 2019 Dec 18.

Abstract

Aims: The present study was designed to compare the effects of a low-fat diet (LF), calorie restriction (CR), quercetin (Que) and exercise (Ex) on hepatic steatosis in a high-fat (HF) diet-induced obesity prone (OP) model in the perspective of microRNA (miR)-dependent thyroid hormone (TH) synthesis and action.

Main methods: Male C57BL/6J mice were administered a HF diet for 10 weeks to induce OP phenotype and then divided into 5 groups, HF diet (OP-HF), LF diet (OP-LF), 70% CR (OP-CR), 0.05% Que (OP-Que) and a treadmill exercise regimen (OP-Ex); one additional group fed LF diet served as control (LF). 7 weeks later, serum indexes, metabolic alterations, redox status and histological appearance in the thyroid and liver, and TH related miRs with their targets expressions were determined.

Key findings: No significance on T3 levels was observed among the six groups. LF, CR, Que and Ex significantly ameliorated HF-induced hepatic steatosis to varying degrees, inhibited T4 production via differentially elevating miR-339, miR-383 and miR-146b to decrease NIS expression and regulating miR-200a/Nrf2 to maintain redox status in the thyroid. Furthermore, these four interventions differentially and significantly decreased miR-383 and miR-146b to elevate TRb and DIO1 expression, and subsequent TH responsive lipid metabolism genes regulation. Among them, the effects of CR on hepatic steatosis were the most prominent.

Significance: Our data indicated that amelioration of hepatic steatosis by LF, CR, Que and Ex resulted in many shared, but also many differential changes in the miR-dependent TH production and action.

Keywords: Calorie restriction; Exercise; Hepatic steatosis; Low-fat diet; Quercetin; Thyroid; microRNA.

MeSH terms

  • Animals
  • Caloric Restriction
  • Diet, Fat-Restricted*
  • Fatty Liver / diet therapy
  • Fatty Liver / etiology
  • Fatty Liver / therapy*
  • Hypolipidemic Agents / therapeutic use
  • Lipids / analysis
  • Liver / chemistry
  • Male
  • Mice, Inbred C57BL
  • MicroRNAs / metabolism
  • MicroRNAs / physiology*
  • Obesity / complications*
  • Oxidative Stress
  • Physical Conditioning, Animal*
  • Quercetin / therapeutic use
  • Thyroid Hormones / metabolism*

Substances

  • Hypolipidemic Agents
  • Lipids
  • MicroRNAs
  • Thyroid Hormones
  • Quercetin