The enhancement of fat oxidation during the active phase and suppression of body weight gain in glycerol-3-phosphate dehydrogenase 1 deficient mice
Abstract
We investigated whether the deletion of glycerol-3-phosphate dehydrogenase (GPD) 1 would affect carbohydrate oxidation, fat oxidation, and body weight by using the GPD1 null mice (BALB/cHeA (HeA)). We found that fat oxidation in HeA mice was significantly high during the early active phase than in BALB/cBy (By) mice used as a control under ad libitum conditions. Metabolic tracer experiment revealed that fatty acid oxidation in the skeletal muscle of HeA mice tended to be high. The energy expenditure and fat oxidation in HeA mice under fasting conditions were significantly higher than that in the By mice. Moreover, we monitored body weight gain in HeA mice under ad libitum feeding and found lower body weight gain. These data indicate that GPD1 deficiency induces enhancement of fat oxidation with suppression of weight gain. We propose that GPD1 deletion contributes to the reduction of body weight gain via enhancement of fat oxidation.
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Oligodendrocytes may benefit from coupling NAD+ regeneration to G3P generation as a phospholipid precursor in lipid biosynthesis.
“Since GPD1 connects glycolysis to lipid metabolism (Sato et al., 2020) oligodendrocytes may benefit from coupling the regeneration of NAD + to the generation of G3P as a phospholipid precursor in lipid biosynthesis.”
From Downregulated expression of lactate dehydrogenase in adult oligodendrocytes and its implication for the transfer of glycolysis products to axons (2024) · cites this paper as Sato et al., 2020
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Effect of Exercise Intensity on Skeletal Muscle AMPK Signaling in Humans
Chen, Z.-P., Stephens, T. J., Murthy, S., Canny, B. J., Hargreaves, M., Witters, L. A., Kemp, B. E., & McConell, G. K. (2003) · Diabetes · doi:10.2337/diabetes.52.9.2205 · Cited by 369 · see citing works
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Späte, E., Zhou, B., Sun, T., Kusch, K., Asadollahi, E., Siems, S. B., Depp, C., Werner, H. B., Saher, G., Hirrlinger, J., et al. (2024) · Glia · doi:10.1002/glia.24533 · Cited by 40 · see citing works
- Authors
- Sato, T., Sayama, N., Inoue, M., Morita, A., & Miura, S.
- Affiliations
- Shizuoka University (JP)
- Corresponding author
- Miura, Shinji
- Venue
- Bioscience, Biotechnology, and Biochemistry
- Publisher
- Informa UK Limited
- Published
- 2020-11-01
- Volume
- 84
- Issue
- 11
- Pages
- 2367-2373
- ISSN
- 0916-8451 (ISSN-L)
- 1347-6947
- OpenAlex
- W3043459054
- Cited by
- 4
- References
- 1
- Citations by year
- 2024: 2 · 2023: 1 · 2022: 1
- FWCI
- 0.29
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- academic.oup.com/journals/pages/open_access/funder_policies/chorus/standard_publication_model (vor)
- Locations
- Bioscience Biotechnology and Biochemistry (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Japan Society for the Promotion of Science (KAKENHI, numbers 15J10165)
- Mishima Kaiun Memorial Foundation (None)
- University of Shizuoka Grant for Scientific and Educational Research (None)
- Topics
- Health Sciences › Medicine › Physiology › Adipose Tissue and Metabolism
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Biochemistry › Lipid metabolism and biosynthesis
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Metabolism, Diabetes, and Cancer
- Keywords
- fat oxidation, fatty acid oxidation, skeletal muscle, weight gain, energy expenditure, fasting, carbohydrate oxidation, metabolic tracers
- MeSH terms
- Adipose Tissue, Animals, Body Weight, Glycerolphosphate Dehydrogenase, Oxidation-Reduction, Carbohydrate Metabolism, Mice
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