» Articles » PMID: 31366145

Mitochondrial Uncoupling: A Key Controller of Biological Processes in Physiology and Diseases

Overview
Journal Cells
Publisher MDPI
Date 2019 Aug 2
PMID 31366145
Citations 164
Authors
Affiliations
Soon will be listed here.
Abstract

Mitochondrial uncoupling can be defined as a dissociation between mitochondrial membrane potential generation and its use for mitochondria-dependent ATP synthesis. Although this process was originally considered a mitochondrial dysfunction, the identification of UCP-1 as an endogenous physiological uncoupling protein suggests that the process could be involved in many other biological processes. In this review, we first compare the mitochondrial uncoupling agents available in term of mechanistic and non-specific effects. Proteins regulating mitochondrial uncoupling, as well as chemical compounds with uncoupling properties are discussed. Second, we summarize the most recent findings linking mitochondrial uncoupling and other cellular or biological processes, such as bulk and specific autophagy, reactive oxygen species production, protein secretion, cell death, physical exercise, metabolic adaptations in adipose tissue, and cell signaling. Finally, we show how mitochondrial uncoupling could be used to treat several human diseases, such as obesity, cardiovascular diseases, or neurological disorders.

Citing Articles

mTORC1 syndrome (TorS): unifying paradigm for PASC, ME/CFS and PAIS.

Bar-Tana J J Transl Med. 2025; 23(1):297.

PMID: 40059164 PMC: 11892318. DOI: 10.1186/s12967-025-06220-z.


Indole-3-propionic acid promotes hepatic stellate cells inactivation.

Ilha M, Sehgal R, Matilainen J, Rilla K, Kaminska D, Gandhi S J Transl Med. 2025; 23(1):253.

PMID: 40025530 PMC: 11871697. DOI: 10.1186/s12967-025-06266-z.


Weight loss-independent changes in human growth hormone during water-only fasting: a secondary evaluation of a randomized controlled trial.

Horne B, Anderson J, May H, Bair T, Le V, Iverson L Front Endocrinol (Lausanne). 2025; 15:1401780.

PMID: 39991046 PMC: 11842881. DOI: 10.3389/fendo.2024.1401780.


Dolutegravir induces endoplasmic reticulum stress at the blood-brain barrier.

Huang C, Qu Q, Hoque M, Bendayan R FASEB J. 2025; 39(4):e70377.

PMID: 39985305 PMC: 11846018. DOI: 10.1096/fj.202402677RR.


Novel mitochondrial-targeted alkyl chains act as fungal specific inhibitors of .

Edrich E, Young L, Spencer J, McGown A, Moore A, Gourlay C Front Microbiol. 2025; 15:1505308.

PMID: 39968045 PMC: 11832467. DOI: 10.3389/fmicb.2024.1505308.


References
1.
Dossi C, Tapia G, Espinosa A, Videla L, DEspessailles A . Reversal of high-fat diet-induced hepatic steatosis by n-3 LCPUFA: role of PPAR-α and SREBP-1c. J Nutr Biochem. 2014; 25(9):977-84. DOI: 10.1016/j.jnutbio.2014.04.011. View

2.
Urra F, Munoz F, Cordova-Delgado M, Ramirez M, Pena-Ahumada B, Rios M . FR58P1a; a new uncoupler of OXPHOS that inhibits migration in triple-negative breast cancer cells via Sirt1/AMPK/β1-integrin pathway. Sci Rep. 2018; 8(1):13190. PMC: 6123471. DOI: 10.1038/s41598-018-31367-9. View

3.
Kida R, Noguchi T, Murakami M, Hashimoto O, Kawada T, Matsui T . Supra-pharmacological concentration of capsaicin stimulates brown adipogenesis through induction of endoplasmic reticulum stress. Sci Rep. 2018; 8(1):845. PMC: 5770457. DOI: 10.1038/s41598-018-19223-2. View

4.
de Moraes R, Portari G, Soares Marreiros Ferraz A, da Silva T, Marocolo M . Effects of intermittent fasting and chronic swimming exercise on body composition and lipid metabolism. Appl Physiol Nutr Metab. 2017; 42(12):1341-1346. DOI: 10.1139/apnm-2017-0435. View

5.
Geisler J . 2,4 Dinitrophenol as Medicine. Cells. 2019; 8(3). PMC: 6468406. DOI: 10.3390/cells8030280. View