Direct measurement of oxidative metabolism in the living brain by microdialysis: a review

• Published in: Journal of neurochemistry 2009-05, Vol.109 (s1), p.24-29
• Main Authors: Ronald Zielke, H, Zielke, Carol L, Baab, Peter J
• Format: Article
• Language: English
• Subjects: Animals; Biochemistry; Brain; Brain Chemistry - physiology; Cellular biology; compartmentation; energy metabolism; Energy Metabolism - physiology; fluorocitrate; Humans; Lactates - metabolism; Metabolism; microdialysis; Microdialysis - methods; Neurology; oxidation; Oxidation-Reduction
• ISSN: 0022-3042; 1471-4159
• DOI: 10.1111/j.1471-4159.2009.05941.x

This review summarizes microdialysis studies that address the question of which compounds serve as energy sources in the brain. Microdialysis was used to introduce ¹⁴C-labeled glucose, lactate, pyruvate, glutamate, glutamine, and acetate into the interstitial fluid of the brain to observe their metabolism to ¹⁴CO₂. Although glucose uptake from the systemic system supplies the carbon source for these compounds, compounds synthesized from glucose by the brain are subject to recycling including complete metabolism to CO₂. Therefore, the brain utilizes multiple compounds in its domain to provide the energy needed to fulfill its function. The physiological conditions controlling metabolism and the contribution of compartmentation into different brain regions, cell types, and subcellular spaces are still unresolved. The aconitase inhibitor fluorocitrate, with a lower inhibition threshold in glial cells, was used to identify the proportion of lactate and glucose that was oxidized in glial cells versus neurons. The fluorocitrate data suggest that glial and neuronal cells are capable of utilizing both lactate and glucose for energy metabolism.