Effect of fatty acids on energy coupling processes in mitochondria
Abstract
Long-chain fatty acids are natural uncouplers of oxidative phosphorylation in mitochondria. The protonophoric mechanism of this action is due to transbilayer movement of undissociated fatty acid in one direction and the passage of its anion in the opposite direction. The transfer of the dissociated form of fatty acid can be, at least in some kinds of mitochondrion, facilitated by adenine nucleotide translocase. Apart from dissipating the electrochemical proton gradient, long-chain fatty acids decrease the activity of the respiratory chain by mechanism(s) not fully understood. In intact cells and tissues fatty acids operate mostly as excellent respiratory substrates, providing electrons to the respiratory chain. This function masks their potential uncoupling effect which becomes apparent only under special physiological or pathological conditions characterized by unusual fatty acid accumulation. Short- and medium-chain fatty acids do not have protonophoric properties. Nevertheless, they contribute to energy dissipation because of slow intramitochondrial hydrolysis of their activation products, acyl-AMP and acyl-CoA. Long-chain fatty acids increase permeability of mitochondrial membranes to alkali metal cations. This is due to their ionophoric mechanism of action. Regulatory function of fatty acids with respect to specific cation channels has been postulated for the plasma membrane of muscle cells, but not demonstrated in mitochondria. Under cold stress, cold acclimation and arousal from hibernation the uncoupling effect of fatty acids may contribute to increased thermogenesis, especially in the muscle tissue. In brown adipose tissue, the special thermogenic organ of mammals, long-chain fatty acids promote operation of the unique natural uncoupling protein, thermogenin. As anionic amphiphiles, long-chain fatty acids increase the negative surface charge of biomembranes, thus interfering in their enzymic and transporting functions.
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FFAs are a required co-factor for UCP-1-catalyzed proton transport.
“Experiments performed on liposomes enriched in UCP-1 showed that FFAs are a required co-factor for UCP-1-catalyzed proton transport [29]”
From Mitochondrial Uncoupling: A Key Controller of Biological Processes in Physiology and Diseases (2019) · cites this paper as [29]
FFAs stimulate mitochondrial respiration directly, as seen in intact isolated brown adipocytes or mitochondria isolated from these cells.
“First, they stimulate directly mitochondrial respiration, as seen in intact isolated brown adipocytes or mitochondria isolated from these cells [28,29].”
From Mitochondrial Uncoupling: A Key Controller of Biological Processes in Physiology and Diseases (2019) · cites this paper as [29]
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“Experiments performed on liposomes enriched in UCP-1 showed that FFAs are a required co-factor for UCP-1-catalyzed proton transport [29], suggesting that the uncoupling effect of FFAs could depend on this channel.”
BackgroundMitochondrial Targets of Drug Toxicity
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- Authors
- Wojtczak, L., & Schönfeld, P.
- Affiliations
- Instytut Biologii Doświadczalnej im. Marcelego Nenckiego (PL)
- Corresponding author
- Wojtczak, Lech
- Venue
- Biochimica et Biophysica Acta (BBA) - Bioenergetics
- Publisher
- Elsevier BV
- Published
- 1993-11
- Volume
- 1183
- Issue
- 1
- Pages
- 41-57
- ISSN
- 0005-2728 (ISSN-L)
- OpenAlex
- W1967880167
- Cited by
- 363
- References
- 200
- Citations by year
- 2026: 4 · 2025: 6 · 2024: 8 · 2023: 8 · 2022: 13 · 2021: 9 · 2020: 8 · 2019: 10 · 2018: 4 · 2017: 13 · 2016: 20 · 2015: 22 · 2014: 17 · 2013: 12 · 2012: 8
- FWCI
- 0.81
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Biochimica et Biophysica Acta (BBA) - Bioenergetics (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Mitochondrial Function and Pathology
- Health Sciences › Medicine › Physiology › Adipose Tissue and Metabolism
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › ATP Synthase and ATPases Research
- Keywords
- long-chain fatty acids, mitochondrial uncoupling, adenine nucleotide translocase, electron transport inhibition, short- and medium-chain fatty acids, acyl-CoA, mitochondrial membrane permeability, alkali metal cations, thermogenesis, brown adipose tissue, thermogenin, membrane surface charge, fatty acid accumulation
- MeSH terms
- Uncoupling Protein 1, Animals, Adipose Tissue, Brown, Carrier Proteins, Fatty Acids, Ion Channels, Membrane Proteins, Mitochondria, Muscles, Oxidation-Reduction, Uncoupling Agents, Mitochondrial Proteins
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