Stanniocalcin 1 Enhances Carbon Flux from Glucose to Lipids in White Retroperitoneal Adipose Tissue in the Fed Rat

Lipids. 2016 Nov;51(11):1303-1307. doi: 10.1007/s11745-016-4202-5. Epub 2016 Oct 11.

Abstract

The present work assesses in vitro the role of human Stanniocalcin 1 (hSTC-1) in glucose metabolism in white retroperitoneal adipose tissue (WRAT) from fed rat. In the fed state, hSTC1 increases the incorporation of 14C from glucose into lipids in the rat WRAT. The increase in lipogenesis capacity supports the hypothesis that the activity of the glycerol-3-phosphate-generating pathway (glycolysis) from glucose is regulated by hSTC-1. The effect of hSTC-1 on de novo fatty acid synthesis and on glucose oxidation in WRAT is supported by an 85 % increase in 14CO2 production from 14C-glucose. The incubation of WRAT in the presence of hSTC-1 maintained the ADP/ATP ratio close to the control group. The presence of hSTC-1 in the incubation medium did not inhibit the lipolytic effect of epinephrine. In conclusion, hSTC-1 is one of the hormonal factors that control glucose metabolism in WRAT in the fed state.

Keywords: Endocrinology; Lipid metabolism.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenosine Triphosphate / metabolism
  • Adipose Tissue, White / metabolism*
  • Animals
  • Carbon Dioxide / metabolism
  • Fatty Acids / metabolism
  • Glucose / metabolism*
  • Glycoproteins / metabolism*
  • Humans
  • Lipid Metabolism*
  • Lipogenesis
  • Male
  • Oxidation-Reduction
  • Rats
  • Rats, Wistar

Substances

  • Fatty Acids
  • Glycoproteins
  • Carbon Dioxide
  • teleocalcin
  • Adenosine Triphosphate
  • Glucose