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.
Abbreviations
- G3P:
-
Glycerol 3 Phosphate
- hSTC-1:
-
Human Stanniocalcin 1
- KH:
-
Krebs Henseleit
- NADPH:
-
Nicotinamide adenine dinucleotide phosphate
- TAG:
-
Triacylglycerols
- WAT:
-
White adipose tissue
- WRAT:
-
White retroperitoneal adipose tissue
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Acknowledgments
This work was supported by grants from Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq), and Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES), Brazil. RSMS and LCK are PQ-CNPq fellows, and AGC and JFAM are CNPq fellows, and VS is a PNPD-CAPES fellow. The experiments were performed according to the current Brazilian laws.
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Cozer, A.G., Trapp, M., Vieira Marques, C. et al. Stanniocalcin 1 Enhances Carbon Flux from Glucose to Lipids in White Retroperitoneal Adipose Tissue in the Fed Rat. Lipids 51, 1303–1307 (2016). https://doi.org/10.1007/s11745-016-4202-5
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DOI: https://doi.org/10.1007/s11745-016-4202-5