Fructose Alters Intermediary Metabolism of Glucose in Human Adipocytes and Diverts Glucose to Serine Oxidation in the One–Carbon Cycle Energy Producing Pathway

Increased consumption of sugar and fructose as sweeteners has resulted in the utilization of fructose as an alternative metabolic fuel that may compete with glucose and alter its metabolism. To explore this, human Simpson-Golabi-Behmel Syndrome (SGBS) preadipocytes were differentiated to adipocytes...

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Main Authors: Vijayalakshmi Varma, László G. Boros, Greg T. Nolen, Ching-Wei Chang, Martin Wabitsch, Richard D. Beger, Jim Kaput
Format: Article
Language:English
Published: MDPI AG 2015-06-01
Series:Metabolites
Subjects:
Online Access:http://www.mdpi.com/2218-1989/5/2/364
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spelling doaj-bca73f72e4cf4f20876af19b8e657fa92020-11-24T22:41:56ZengMDPI AGMetabolites2218-19892015-06-015236438510.3390/metabo5020364metabo5020364Fructose Alters Intermediary Metabolism of Glucose in Human Adipocytes and Diverts Glucose to Serine Oxidation in the One–Carbon Cycle Energy Producing PathwayVijayalakshmi Varma0László G. Boros1Greg T. Nolen2Ching-Wei Chang3Martin Wabitsch4Richard D. Beger5Jim Kaput6Biomarkers and Alternate Models branch, Division of Systems Biology, National Center for Toxicological Research, Jefferson, AR 72079, USASiDMAP LLC, Los Angeles, CA 90064, USABiomarkers and Alternate Models branch, Division of Systems Biology, National Center for Toxicological Research, Jefferson, AR 72079, USADivision of Bioinformatics and Biostatistics, National Center for Toxicological Research, Jefferson, AR 72079, USADivision of Pediatric Endocrinology and Diabetology, University of Ulm, Eythstr. 24, 89075 Ulm, GermanyBiomarkers and Alternate Models branch, Division of Systems Biology, National Center for Toxicological Research, Jefferson, AR 72079, USACurrent Address: Nestle Institute of Health Sciences, 1015 Lausanne, SwitzerlandIncreased consumption of sugar and fructose as sweeteners has resulted in the utilization of fructose as an alternative metabolic fuel that may compete with glucose and alter its metabolism. To explore this, human Simpson-Golabi-Behmel Syndrome (SGBS) preadipocytes were differentiated to adipocytes in the presence of 0, 1, 2.5, 5 or 10 mM of fructose added to a medium containing 5 mM of glucose representing the normal blood glucose concentration. Targeted tracer [1,2-13C2]-d-glucose fate association approach was employed to examine the influence of fructose on the intermediary metabolism of glucose. Increasing concentrations of fructose robustly increased the oxidation of [1,2-13C2]-d-glucose to 13CO2 (p < 0.000001). However, glucose-derived 13CO2 negatively correlated with 13C labeled glutamate, 13C palmitate, and M+1 labeled lactate. These are strong markers of limited tricarboxylic acid (TCA) cycle, fatty acid synthesis, pentose cycle fluxes, substrate turnover and NAD+/NADP+ or ATP production from glucose via complete oxidation, indicating diminished mitochondrial energy metabolism. Contrarily, a positive correlation was observed between glucose-derived 13CO2 formed and 13C oleate and doses of fructose which indicate the elongation and desaturation of palmitate to oleate for storage. Collectively, these results suggest that fructose preferentially drives glucose through serine oxidation glycine cleavage (SOGC pathway) one-carbon cycle for NAD+/NADP+ production that is utilized in fructose-induced lipogenesis and storage in adipocytes.http://www.mdpi.com/2218-1989/5/2/364human adipocytesfructoseglucose[1,2-13C2]-d-glucosetargeted tracer fate association study (TTFAS)SOGC pathway
collection DOAJ
language English
format Article
sources DOAJ
author Vijayalakshmi Varma
László G. Boros
Greg T. Nolen
Ching-Wei Chang
Martin Wabitsch
Richard D. Beger
Jim Kaput
spellingShingle Vijayalakshmi Varma
László G. Boros
Greg T. Nolen
Ching-Wei Chang
Martin Wabitsch
Richard D. Beger
Jim Kaput
Fructose Alters Intermediary Metabolism of Glucose in Human Adipocytes and Diverts Glucose to Serine Oxidation in the One–Carbon Cycle Energy Producing Pathway
Metabolites
human adipocytes
fructose
glucose
[1,2-13C2]-d-glucose
targeted tracer fate association study (TTFAS)
SOGC pathway
author_facet Vijayalakshmi Varma
László G. Boros
Greg T. Nolen
Ching-Wei Chang
Martin Wabitsch
Richard D. Beger
Jim Kaput
author_sort Vijayalakshmi Varma
title Fructose Alters Intermediary Metabolism of Glucose in Human Adipocytes and Diverts Glucose to Serine Oxidation in the One–Carbon Cycle Energy Producing Pathway
title_short Fructose Alters Intermediary Metabolism of Glucose in Human Adipocytes and Diverts Glucose to Serine Oxidation in the One–Carbon Cycle Energy Producing Pathway
title_full Fructose Alters Intermediary Metabolism of Glucose in Human Adipocytes and Diverts Glucose to Serine Oxidation in the One–Carbon Cycle Energy Producing Pathway
title_fullStr Fructose Alters Intermediary Metabolism of Glucose in Human Adipocytes and Diverts Glucose to Serine Oxidation in the One–Carbon Cycle Energy Producing Pathway
title_full_unstemmed Fructose Alters Intermediary Metabolism of Glucose in Human Adipocytes and Diverts Glucose to Serine Oxidation in the One–Carbon Cycle Energy Producing Pathway
title_sort fructose alters intermediary metabolism of glucose in human adipocytes and diverts glucose to serine oxidation in the one–carbon cycle energy producing pathway
publisher MDPI AG
series Metabolites
issn 2218-1989
publishDate 2015-06-01
description Increased consumption of sugar and fructose as sweeteners has resulted in the utilization of fructose as an alternative metabolic fuel that may compete with glucose and alter its metabolism. To explore this, human Simpson-Golabi-Behmel Syndrome (SGBS) preadipocytes were differentiated to adipocytes in the presence of 0, 1, 2.5, 5 or 10 mM of fructose added to a medium containing 5 mM of glucose representing the normal blood glucose concentration. Targeted tracer [1,2-13C2]-d-glucose fate association approach was employed to examine the influence of fructose on the intermediary metabolism of glucose. Increasing concentrations of fructose robustly increased the oxidation of [1,2-13C2]-d-glucose to 13CO2 (p < 0.000001). However, glucose-derived 13CO2 negatively correlated with 13C labeled glutamate, 13C palmitate, and M+1 labeled lactate. These are strong markers of limited tricarboxylic acid (TCA) cycle, fatty acid synthesis, pentose cycle fluxes, substrate turnover and NAD+/NADP+ or ATP production from glucose via complete oxidation, indicating diminished mitochondrial energy metabolism. Contrarily, a positive correlation was observed between glucose-derived 13CO2 formed and 13C oleate and doses of fructose which indicate the elongation and desaturation of palmitate to oleate for storage. Collectively, these results suggest that fructose preferentially drives glucose through serine oxidation glycine cleavage (SOGC pathway) one-carbon cycle for NAD+/NADP+ production that is utilized in fructose-induced lipogenesis and storage in adipocytes.
topic human adipocytes
fructose
glucose
[1,2-13C2]-d-glucose
targeted tracer fate association study (TTFAS)
SOGC pathway
url http://www.mdpi.com/2218-1989/5/2/364
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