A Systems Approach Dissociates Fructose-Induced Liver Triglyceride from Hypertriglyceridemia and Hyperinsulinemia in Male Mice

Nutrients. 2021 Oct 18;13(10):3642. doi: 10.3390/nu13103642.

Abstract

The metabolic syndrome (MetS), defined as the co-occurrence of disorders including obesity, dyslipidemia, insulin resistance, and hepatic steatosis, has become increasingly prevalent in the world over recent decades. Dietary and other environmental factors interacting with genetic predisposition are likely contributors to this epidemic. Among the involved dietary factors, excessive fructose consumption may be a key contributor. When fructose is consumed in large amounts, it can quickly produce many of the features of MetS both in humans and mice. The mechanisms by which fructose contributes to metabolic disease and its potential interactions with genetic factors in these processes remain uncertain. Here, we generated a small F2 genetic cohort of male mice derived from crossing fructose-sensitive and -resistant mouse strains to investigate the interrelationships between fructose-induced metabolic phenotypes and to identify hepatic transcriptional pathways that associate with these phenotypes. Our analysis indicates that the hepatic transcriptional pathways associated with fructose-induced hypertriglyceridemia and hyperinsulinemia are distinct from those that associate with fructose-mediated changes in body weight and liver triglyceride. These results suggest that multiple independent mechanisms and pathways may contribute to different aspects of fructose-induced metabolic disease.

Keywords: ChREBP; SREPB1c; Tlr4; fructose; hyperinsulinemia; hypertriglyceridemia; obesity; steatosis; transcriptomics.

MeSH terms

  • Animals
  • Cohort Studies
  • Fructose / adverse effects*
  • Gene Expression Regulation
  • Gene Regulatory Networks
  • Haplotypes
  • Hyperinsulinism / blood
  • Hyperinsulinism / complications*
  • Hypertriglyceridemia / blood
  • Hypertriglyceridemia / complications*
  • Insulin / blood
  • Liver / metabolism*
  • Male
  • Mice
  • Mice, Inbred C3H
  • Mice, Inbred C57BL
  • Mutation, Missense / genetics
  • Phenotype
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Systems Analysis*
  • Triglycerides / blood
  • Triglycerides / metabolism*

Substances

  • Insulin
  • RNA, Messenger
  • Triglycerides
  • Fructose