Can Brown Fat Win the Battle Against White Fat?
- PMID: 25760392
- PMCID: PMC4481171
- DOI: 10.1002/jcp.24986
Can Brown Fat Win the Battle Against White Fat?
Abstract
A rapid growth in the overweight and obese population in the last few decades suggest that the current diet, exercise, awareness or drug strategies are still not effectively restraining the obesity epidemic. Obesity results from increased energy intake, and the body's energy balance shifts towards energy abundance. Therefore, current research is focused on developing new strategies aimed at increasing energy expenditure. As a result, brown adipose tissue (BAT) is receiving tremendous attention since the major function of BAT is to dissipate energy as heat. For example, mouse models that have increased BAT activity or increased numbers of brown-like adipocytes within the white adipose tissue (WAT) are lean and protected from obesity. Alternatively, mouse models that lack BAT activity are more susceptible to age and diet-induced obesity. However, a significant loss of BAT mass during the natural growth process in humans has created enormous challenges in effectively utilizing this tissue to increase energy expenditure. New strategies are primarily focused on expanding the BAT mass and/or activating the existing BAT. In this regard, recent finding that expression of early B cell factor-2 (Ebf2) reprograms the white pre-adipocytes into brown adipocytes is a significant break-through in developing BAT-mediated strategies to treat obesity. Here we review the major biological functions of WAT and BAT, which play critical but opposing roles in the energy spectrum, energy storage versus energy expenditure, and we evaluate whether activation and/or expansion of BAT is practically achievable to treat obesity in humans.
© 2015 Wiley Periodicals, Inc.
Conflict of interest statement
The authors declare no competing financial conflicts of interest.
Figures
Similar articles
-
Endogenous ways to stimulate brown adipose tissue in humans.Ann Med. 2015 Mar;47(2):123-32. doi: 10.3109/07853890.2013.874663. Epub 2014 Feb 13. Ann Med. 2015. PMID: 24521443 Review.
-
Brown adipose tissue and thermogenesis.Horm Mol Biol Clin Investig. 2014 Jul;19(1):25-37. doi: 10.1515/hmbci-2014-0022. Horm Mol Biol Clin Investig. 2014. PMID: 25390014 Review.
-
Chronic l-menthol-induced browning of white adipose tissue hypothesis: A putative therapeutic regime for combating obesity and improving metabolic health.Med Hypotheses. 2016 Aug;93:21-6. doi: 10.1016/j.mehy.2016.05.006. Epub 2016 May 11. Med Hypotheses. 2016. PMID: 27372851
-
Differentiation and characterization in primary culture of white adipose tissue brown adipocyte-like cells.Int J Obes (Lond). 2009 Jun;33(6):680-6. doi: 10.1038/ijo.2009.46. Epub 2009 Mar 10. Int J Obes (Lond). 2009. PMID: 19274054
-
Role of PRDM16 in the activation of brown fat programming. Relevance to the development of obesity.Histol Histopathol. 2013 Nov;28(11):1411-25. doi: 10.14670/HH-28.1411. Epub 2013 Jun 17. Histol Histopathol. 2013. PMID: 23771475 Review.
Cited by
-
Metabolic and genomic adaptations to winter fattening in a primate species, the grey mouse lemur (Microcebus murinus).Int J Obes (Lond). 2018 Feb;42(2):221-230. doi: 10.1038/ijo.2017.195. Epub 2017 Aug 14. Int J Obes (Lond). 2018. PMID: 28925409
-
Lecithin:Cholesterol Acyltransferase (LCAT) Deficiency Promotes Differentiation of Satellite Cells to Brown Adipocytes in a Cholesterol-dependent Manner.J Biol Chem. 2015 Dec 18;290(51):30514-29. doi: 10.1074/jbc.M115.676056. Epub 2015 Oct 22. J Biol Chem. 2015. PMID: 26494623 Free PMC article.
-
Angiotensin(1-7) attenuates visceral adipose tissue expansion and lipogenesis by suppression of endoplasmic reticulum stress via Mas receptor.Nutr Metab (Lond). 2022 Dec 16;19(1):82. doi: 10.1186/s12986-022-00716-x. Nutr Metab (Lond). 2022. PMID: 36527093 Free PMC article.
-
Two-Pore Channels: Lessons from Mutant Mouse Models.Messenger (Los Angel). 2015 Jun;4(1):4-22. doi: 10.1166/msr.2015.1041. Messenger (Los Angel). 2015. PMID: 27330869 Free PMC article.
-
Genetic Polymorphisms Complicate COVID-19 Therapy: Pivotal Role of HO-1 in Cytokine Storm.Antioxidants (Basel). 2020 Jul 18;9(7):636. doi: 10.3390/antiox9070636. Antioxidants (Basel). 2020. PMID: 32708430 Free PMC article. Review.
References
-
- Arch JR. beta(3)-Adrenoceptor agonists: potential, pitfalls and progress. European journal of pharmacology. 2002;440:99–107. - PubMed
-
- Arch JR, Ainsworth AT, Ellis RD, Piercy V, Thody VE, Thurlby PL, Wilson C, Wilson S, Young P. Treatment of obesity with thermogenic beta-adrenoceptor agonists: studies on BRL 26830A in rodents. Int J Obes 8 Suppl. 1984;1:1–11. - PubMed
-
- Attele AS, Shi ZQ, Yuan CS. Leptin, gut, and food intake. Biochemical pharmacology. 2002;63:1579–1583. - PubMed
-
- Austin S, St-Pierre J. PGC1alpha and mitochondrial metabolism--emerging concepts and relevance in ageing and neurodegenerative disorders. Journal of cell science. 2012;125:4963–4971. - PubMed
Publication types
MeSH terms
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical
Research Materials
Miscellaneous