Oligodendrocytes use lactate as a source of energy and as a precursor of lipids
Abstract
Lactate is an important metabolic substrate for the brain during the postnatal period and also plays a crucial role in the traffic of metabolites between astrocytes and neurons. However, to date there are no clues with regard to lactate utilization by oligodendrocytes, the myelin‐forming cells in the brain. In the present work, lactate utilization by oligodendrocytes in culture was investigated and compared with its utilization by cultured neurons, type 1 and type 2 astrocytes. Our results clearly indicate that oligodendrocytes readily use lactate both as a metabolic fuel and as a precursor to build carbon skeletons. Oligodendrocytes oxidize lactate at a higher rate than that observed for neurons and astrocytes, and their rate of lipid synthesis from lactate was at least 6‐fold higher than that found in astrocytes or neurons. The rate of glucose utilization through different pathways was also investigated. The flux of glucose through the pentose phosphate pathway and the rate of lipid synthesis were at least 2‐fold higher in oligodendrocytes than in astrocytes or neurons. These findings indicate that oligodendrocyte metabolism is designed specifically for the synthesis of lipids, presumably those of myelin. GLIA 36:321–329, 2001. © 2001 Wiley‐Liss, Inc.
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In the presence of other nutrients, normal myelin thickness is reached in vivo without utilization of lactate.
“Thus, although oligodendrocytes use lactate as an energy source in vitro (Sánchez-Abarca et al., 2001), in the presence of other nutrients normal myelin thickness in reached in vivo without utilization of lactate.”
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 Sánchez-Abarca et al., 2001
Cultured oligodendrocytes in vitro express both LDHA and LDHB.
“we detected both LDHA and LDHB in these cells in vitro.”
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 Sánchez-Abarca et al., 2001
During developmental myelination, oligodendrocytes import and utilize lactate for ATP generation and the synthesis of myelin lipids, which requires functional expression of LDH.
“During developmental myelination, oligodendrocytes are thought to import and utilize lactate for ATP generation and the synthesis of myelin lipids (Amaral et al., 2016;Rinholm et al., 2011;Sánchez-Abarca et al., 2001), which requires functional expression of LDH.”
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 Sánchez-Abarca et al., 2001
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- Authors
- Sánchez‐Abarca, L. I., Tabernero, A., & Medina, J. M.
- Affiliations
- Universidad de Salamanca (ES)
- Corresponding author
- Medina, José M.
- Venue
- Glia
- Publisher
- Wiley
- Published
- 2001-10-09
- Volume
- 36
- Issue
- 3
- Pages
- 321-329
- ISSN
- 0894-1491 (ISSN-L)
- 1098-1136
- OpenAlex
- W1966661257
- Cited by
- 171
- References
- 0
- Citations by year
- 2026: 11 · 2025: 6 · 2024: 14 · 2023: 11 · 2022: 12 · 2021: 11 · 2020: 6 · 2019: 11 · 2018: 8 · 2017: 5 · 2016: 15 · 2015: 9 · 2014: 8 · 2013: 7 · 2012: 8
- FWCI
- 0.76
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Glia (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Fondo Investigacions Sanitarias (F.I.S.)
- Comision Interministerial Ciencia y Tecnologia (CICYT) (Spain)
- Topics
- Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Biochemistry › Lipid metabolism and biosynthesis
- Keywords
- oligodendrocytes, lactate utilization, lactate oxidation, glucose metabolism, pentose phosphate pathway, astrocytes, neurons, brain energy metabolism, myelin
- MeSH terms
- Aging, Animals, Astrocytes, Carbon Radioisotopes, Central Nervous System, Energy Metabolism, Female, Galactosylceramides, Glial Fibrillary Acidic Protein, Glucose, Immunohistochemistry, Lipids, Male, Neurons, Oligodendroglia, Rats, Wistar, Cell Culture Techniques, Lactic Acid, GAP-43 Protein, Rats
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