4.7 Article

Curcumin induces brown fat-like phenotype in 3T3-L1 and primary white adipocytes

期刊

JOURNAL OF NUTRITIONAL BIOCHEMISTRY
卷 27, 期 -, 页码 193-202

出版社

ELSEVIER SCIENCE INC
DOI: 10.1016/j.jnutbio.2015.09.006

关键词

Anti-obesity; Curcumin; Adipocyte browning; Non-shivering thermogenesis; UCP1

资金

  1. Mid-career Researcher Program through NRF - Ministry of Science, ICT and Future Planning, Korea [2013R1A2A2A05004195]
  2. SRC Program (Center for Food & Nutritional Genomics) through NRF - Ministry of Science, ICT and Future Planning, Korea [2015R1A5A6001906]

向作者/读者索取更多资源

Recent advances have been made in the understanding of pharmacological and dietary agents that contribute to browning of white adipose tissue in order to combat obesity by promoting energy expenditure. Here, we show that curcumin induces browning of 3T3-L1 and primary white adipocytes via enhanced expression of brown fat-specific genes. Curcumin-induced browning in white adipocytes was investigated by determining expression levels of brown adipocyte-specific genes/proteins by realtime reverse transcriptase polymerase chain reaction, immunoblot analysis and immunocytochemical staining. Curcumin increased mitochondrial biogenesis, as evidenced by transmission electronic microscopic detection and enhanced expression of proteins involved in fat oxidation. Cucurmin also increased protein levels of hormone-sensitive lipase and p-acyl-CoA carboxylase, suggesting its possible role in augmentation of lipolysis and suppression of lipogenesis. Increased expression of UCP1 and other brown adipocyte-specific markers was possibly mediated by curcumin-induced activation of AMP-activated protein kinase (AMPK) based on the fact that inhibition of AMPK by dorsomorphin abolished expression of PRDM16, UCP1 and peroxisome proliferator-activated receptor gamma co-activator 1-alpha while the activator 5-Aminoimidazole-4-carboxamide ribonucleotide elevated expression of these brown marker proteins. Our findings suggest that curcumin plays a dual modulatory role in inhibition of adipogenesis as well as induction of the brown fat-like phenotype and thus may have potential therapeutic implications for treatment of obesity. (C) 2015 Elsevier Inc. All rights reserved.

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