Cited by 457Diet and metabolism studiesMitochondrial Function and PathologyFatty Acid Research and Health

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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Schönfeld, Peter, Reiser, Georg·2013·Journal of Cerebral Blood Flow & Metabolism

Abstract

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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Crossref · 10.1038/jcbfm.2013.128

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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.”

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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
Published
2013-08-07
Volume
33
Issue
10
Pages
1493-1499
ISSN
  • 0271-678X (ISSN-L)
  • 1559-7016
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
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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