Journal
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE
Volume 1740, Issue 2, Pages 293-304Publisher
ELSEVIER SCIENCE BV
DOI: 10.1016/j.bbadis.2005.02.003
Keywords
brown adipose tissue; UCP1; PPAR gamma
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The effects of fatty acids and retinoic acid (carotene) on brown adipose tissue differentiation are mediated by activation of the transcription factors PPAR gamma and PPAR alpha in combination with RXR. There is good support for the idea that activated PPAR gamma promotes adipogenesis also in brown adipose tissue. However, the issue is more complex concerning the full differentiation to the brown adipocyte phenotype, particularly the expression of the brown -fat-specific marker UCPI. The effect of norepinephrine on PPAR- gene expression, at least in-vitro, is negative, PPAR gamma-ablated brown adipose tissue can express UCPI, and PGC-1 alpha coactivates other transcription factors (including PPAR alpha); thus, the significance of PPAR gamma for the physiological control of UCP1 gene expression is not settled. However, importantly, the effects of PPAR agonists demonstrate the existence of a pathway for brown adipose tissue recruitment that is not dependent on chronic adrenergic stimulation and may be active in recruitment conditions such as prenatal and prehibernation recruitment. The ability of chronic PPAR gamma agonist treatment to promote the occurrence of brown-fat features in white adipose tissue-like depots implies a role in antiobesity treatment, but this will only be effective if the extra thermogenic capacity is activated by adrenergic stimulation. (c) 2005 Elsevier B.V. All rights reserved.
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