Uncoupling Protein 1 Decreases Superoxide Production in Brown Adipose Tissue Mitochondria *
Journal of Biological Chemistry, ISSN: 0021-9258, Vol: 285, Issue: 29, Page: 21961-21968
2010
- 76Citations
- 83Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
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Metrics Details
- Citations76
- Citation Indexes76
- 76
- CrossRef59
- Captures83
- Readers83
- 83
Article Description
In thermogenic brown adipose tissue, uncoupling protein 1 (UCP1) catalyzes the dissipation of mitochondrial proton motive force as heat. In a cellular environment of high oxidative capacity such as brown adipose tissue (BAT), mitochondrial uncoupling could also reduce deleterious reactive oxygen species, but the specific involvement of UCP1 in this process is disputed. By comparing brown adipose tissue mitochondria of wild type mice and UCP1 -ablated litter mates, we show that UCP1 potently reduces mitochondrial superoxide production after cold acclimation and during fatty acid oxidation. We address the sites of superoxide production and suggest diminished probability of “reverse electron transport” facilitated by uncoupled respiration as the underlying mechanism of reactive oxygen species suppression in BAT. Furthermore, ablation of UCP1 represses the cold-stimulated increase of substrate oxidation normally seen in active BAT, resulting in lower superoxide production, presumably avoiding deleterious oxidative damage. We conclude that UCP1 allows high oxidative capacity without promoting oxidative damage by simultaneously lowering superoxide production.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S0021925820602319; http://dx.doi.org/10.1074/jbc.m110.122861; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=77954606816&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/20466728; http://www.jbc.org/lookup/doi/10.1074/jbc.M110.122861; https://syndication.highwire.org/content/doi/10.1074/jbc.M110.122861; https://linkinghub.elsevier.com/retrieve/pii/S0021925820602319; https://dx.doi.org/10.1074/jbc.m110.122861; https://www.jbc.org/content/285/29/21961; http://www.jbc.org/article/S0021925820602319/abstract; http://www.jbc.org/article/S0021925820602319/fulltext; http://www.jbc.org/article/S0021925820602319/pdf; https://www.jbc.org/article/S0021-9258(20)60231-9/abstract; http://www.jbc.org/cgi/doi/10.1074/jbc.M110.122861; http://www.jbc.org/content/285/29/21961.abstract; http://www.jbc.org/content/285/29/21961.full; http://www.jbc.org/content/285/29/21961.full.pdf; http://www.jbc.org/content/285/29/21961
American Society for Biochemistry & Molecular Biology (ASBMB)
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