Why does Brain Metabolism not Favor Burning of Fatty Acids to Provide Energy? - Reflections on Disadvantages of the Use of Free Fatty Acids as Fuel for Brain
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It is puzzling that hydrogen-rich fatty acids are used only poorly as fuel in the brain. The long-standing belief that a slow passage of fatty acids across the blood-brain barrier might be the reason. However, this has been corrected by experimental results. Otherwise, accumulated nonesterified fatty acids or their activated derivatives could exert detrimental activities on mitochondria, which might trigger the mitochondrial route of apoptosis. Here, we draw attention to three particular problems: (1) ATP generation linked to β-oxidation of fatty acids demands more oxygen than glucose, thereby enhancing the risk for neurons to become hypoxic; (2) β-oxidation of fatty acids generates superoxide, which, taken together with the poor anti-oxidative defense in neurons, causes severe oxidative stress; (3) the rate of ATP generation based on adipose tissue-derived fatty acids is slower than that using blood glucose as fuel. Thus, in periods of extended continuous and rapid neuronal firing, fatty acid oxidation cannot guarantee rapid ATP generation in neurons. We conjecture that the disadvantages connected with using fatty acids as fuel have created evolutionary pressure on lowering the expression of the β-oxidation enzyme equipment in brain mitochondria to avoid extensive fatty acid oxidation and to favor glucose oxidation in brain.
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Injured neurons and oligodendrocytes have a low capacity for consuming FFAs and sequestering them into lipid droplets, making them more vulnerable to lipid-induced cytotoxicity in chronic inflammation.
“Injured neurons and oligodendrocytes have a low capacity for consuming FFAs and sequestering them into LDs61, making them more vulnerable to lipid-induced cytotoxicity in chronic inflammation62,63.”
From Amyloid-β induces lipid droplet-mediated microglial dysfunction via the enzyme DGAT2 in Alzheimer’s disease (2025) · cites this paper as [61]
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References 87 · Cited by 457
- Authors
- Schönfeld, P., & Reiser, G.
- Affiliations
- Otto-von-Guericke-Universität Magdeburg (DE)
- Corresponding author
- Schönfeld, Peter
- Venue
- Journal of Cerebral Blood Flow & Metabolism
- Publisher
- SAGE Publications
- Published
- 2013-08-07
- Volume
- 33
- Issue
- 10
- Pages
- 1493-1499
- ISSN
- 0271-678X (ISSN-L)
- 1559-7016
- PMC
- PMC3790936
- OpenAlex
- W1981287677
- Cited by
- 457
- References
- 87
- Citations by year
- 2026: 33 · 2025: 45 · 2024: 51 · 2023: 54 · 2022: 51 · 2021: 50 · 2020: 43 · 2019: 34 · 2018: 25 · 2017: 25 · 2016: 19 · 2015: 14 · 2014: 10 · 2013: 1
- FWCI
- 1.61
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Journal of Cerebral Blood Flow & Metabolism (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Physiology › Diet and metabolism studies
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Mitochondrial Function and Pathology
- Health Sciences › Nursing › Nutrition and Dietetics › Fatty Acid Research and Health
- Keywords
- brain energy metabolism, fatty acid oxidation, fatty acid beta-oxidation, free fatty acids, blood-brain barrier, mitochondrial apoptosis, neuronal hypoxia, superoxide, oxidative stress, ATP production, glucose oxidation, brain mitochondria, evolutionary pressure
- MeSH terms
- Adenosine Triphosphate, Animals, Brain, Energy Metabolism, Fatty Acids, Glucose, Humans, Mitochondria, Neurons, Oxidation-Reduction, Oxygen, Oxidative Stress
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