Sortilin 1 knockout alters basal adipose glucose metabolism but not diet-induced obesity in mice

FEBS Lett. 2017 Apr;591(7):1018-1028. doi: 10.1002/1873-3468.12610. Epub 2017 Mar 16.

Abstract

Sortilin 1 (Sort1) is a trafficking receptor that has been implicated in the regulation of plasma cholesterol in humans and mice. Here, we use metabolomics and hyperinsulinemic-euglycemic clamp approaches to obtain further understanding of the in vivo effects of Sort1 deletion on diet-induced obesity as well as on adipose lipid and glucose metabolism. Results show that Sort1 knockout (KO) does not affect Western diet-induced obesity nor adipose fatty acid and ceramide concentrations. Under the basal fasting state, chow-fed Sort1 KO mice have decreased adipose glycolytic metabolites, but Sort1 deletion does not affect insulin-stimulated tissue glucose uptake during the insulin clamp. These results suggest that Sort1 loss-of-function in vivo does not affect obesity development, but differentially modulates adipose glucose metabolism under fasting and insulin-stimulated states.

Keywords: cholesterol; diabetes; hyperlipidemia; obesity.

MeSH terms

  • Adaptor Proteins, Vesicular Transport / deficiency*
  • Adaptor Proteins, Vesicular Transport / genetics
  • Adipose Tissue / metabolism*
  • Animals
  • Basal Metabolism
  • Ceramides / metabolism
  • Diet, Western / adverse effects
  • Fasting
  • Fatty Acids / metabolism
  • Glucose / metabolism*
  • Glucose Clamp Technique
  • Glycolysis
  • Hypoglycemic Agents / administration & dosage
  • Hypoglycemic Agents / metabolism
  • Insulin / administration & dosage
  • Insulin / metabolism
  • Male
  • Mice, 129 Strain
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Obesity / etiology
  • Obesity / genetics
  • Obesity / metabolism*

Substances

  • Adaptor Proteins, Vesicular Transport
  • Ceramides
  • Fatty Acids
  • Hypoglycemic Agents
  • Insulin
  • Glucose
  • sortilin