Positive correlation between rat brain glutamate concentrations and mitochondrial 2-oxoglutarate dehydrogenase activity
Abstract
Glutamate is a key metabolite and major excitatory neurotransmitter, degraded through transformation to 2-oxoglutarate which is further catabolized by 2-oxoglutarate dehydrogenase complex (OGDHC). Both the glutamate excitotoxicity and impaired OGDHC activity are hallmarks of neurodegeneration. This work quantifies a relationship between the brain OGDHC activity and glutamate levels, assessing its diagnostic value to characterize (patho)physiology. A moderate to strong positive correlation of the two parameters determined under varied physiological settings (brain regions, seasons, gender, pregnancy, rat line), is revealed. Mitochondrial impairment (OGDHC inhibition or acute hypobaric hypoxia) decreases the interdependence, even when the parameter means do not change significantly. Compared to the cortex, the cerebellum exhibits a lower inter-individual glutamate variation and a weaker glutamate-OGDHC interdependence. Specific metabolism of the brain regions is also characterized by a positive correlation between glutamate and γ-aminobutyric acid (GABA) concentrations in the cortex but not in the cerebellum. In contrast, a strong positive correlation between glutamate and glutamine is present in both the cortex and cerebellum. The differences in metabolic correlations are in line with transcriptomics data which suggest that glutamate distribution between competitive pathways contributes to the brain-region-specific features of the interdependences of glutamate and OGDHC or GAB…
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OGDHC is a limiting step in the process of glutamate uptake into the TCA cycle.
“This pathway mainly occurs in neurons (Dobolyi et al., 2020; Zhong et al., 2022), and OGDHC is a limiting step in this process (Mkrtchyan et al., 2018).”
From Toxic Concentrations of Glutamate Induce Ferroptosis without Affecting Mitochondrial Respiration in Rodent Brain Slice Cultures (2026) · cites this paper as Mkrtchyan et al., 2018
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Beyond the role of glutamate as a neurotransmitter
Nedergaard, M., Takano, T., & Hansen, A. J. (2002) · Nature Reviews Neuroscience · doi:10.1038/nrn916 · Cited by 450 · see citing works
Changes in cerebrospinal fluid neurochemistry during pregnancy
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Vaglio-Garro, A., Theuermann, M., Sweis, K. E., Zavadskis, S., Kokas, M., Környei, Z., Karas, M., Tretter, L., Komlódi, T., Weidinger, A., et al. (2026) · eneuro · doi:10.1523/eneuro.0439-25.2026
- Authors
- Mkrtchyan, G. V., Graf, A., Trofimova, L., Ksenofontov, A., Baratova, L., & Bunik, V.
- Affiliations
- Lomonosov Moscow State University (RU)
- Moscow Institute of Physics and Technology (RU)
- Corresponding author
- Bunik, Victoria
- Venue
- Analytical Biochemistry
- Publisher
- Elsevier BV
- Published
- 2018-07
- Volume
- 552
- Pages
- 100-109
- ISSN
- 0003-2697 (ISSN-L)
- OpenAlex
- W2784236692
- Cited by
- 21
- References
- 5
- Citations by year
- 2026: 2 · 2025: 1 · 2023: 2 · 2022: 4 · 2021: 5 · 2020: 3 · 2019: 3 · 2018: 1
- FWCI
- 1.30
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Analytical Biochemistry (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Biochemistry › Amino Acid Enzymes and Metabolism
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Biochemistry › Biochemical Acid Research Studies
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Keywords
- glutamate, 2-oxoglutarate dehydrogenase, mitochondrial metabolism, brain regions, cerebellum, cerebral cortex, glutamine, hypobaric hypoxia, neurodegeneration, glutamate excitotoxicity, interindividual variability, rats
- MeSH terms
- Animals, Brain, Female, Ketoglutarate Dehydrogenase Complex, Mitochondria, Rats, Sprague-Dawley, Rats, Wistar, Glutamic Acid, Rats
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