DOI QR코드

DOI QR Code

Zinc-chelated Vitamin C Stimulates Adipogenesis of 3T3-L1 Cells

  • Ghosh, Chiranjit (Animal Environment Division, National Institute of Animal Science, RDA) ;
  • Yang, Seung Hak (Animal Environment Division, National Institute of Animal Science, RDA) ;
  • Kim, Jong Geun (Animal Environment Division, National Institute of Animal Science, RDA) ;
  • Jeon, Tae-Il (Department of Animal Science, College of Agriculture & Life Science, Chonnam National University) ;
  • Yoon, Byung Hyun (FeedBEST CORP) ;
  • Lee, Jai Young (Department of Chemistry, Konyang University) ;
  • Lee, Eun Young (Department of Environmental Energy Engineering, Suwon University) ;
  • Choi, Seok Geun (Department of Animal Life and Environmental Science, Hankyong National University) ;
  • Hwang, Seong Gu (Department of Animal Life and Environmental Science, Hankyong National University)
  • 투고 : 2013.04.01
  • 심사 : 2013.05.15
  • 발행 : 2013.08.01

초록

Adipose tissue development and function play a critical role in the regulation of energy balance, lipid metabolism, and the pathophysiology of metabolic syndromes. Although the effect of zinc ascorbate supplementation in diabetes or glycemic control is known in humans, the underlying mechanism is not well described. Here, we investigated the effect of a zinc-chelated vitamin C (ZnC) compound on the adipogenic differentiation of 3T3-L1 preadipocytes. Treatment with ZnC for 8 d significantly promoted adipogenesis, which was characterized by increased glycerol-3-phosphate dehydrogenase activity and intracellular lipid accumulation in 3T3-L1 cells. Meanwhile, ZnC induced a pronounced up-regulation of the expression of glucose transporter type 4 (GLUT4) and the adipocyte-specific gene adipocyte protein 2 (aP2). Analysis of mRNA and protein levels further showed that ZnC increased the sequential expression of peroxisome proliferator-activated receptor gamma ($PPAR{\gamma}$) and CCAAT/enhancer-binding protein alpha (C/$EBP{\alpha}$), the key transcription factors of adipogenesis. These results indicate that ZnC could promote adipogenesis through $PPAR{\gamma}$ and C/$EBP{\alpha}$, which act synergistically for the expression of aP2 and GLUT4, leading to the generation of insulin-responsive adipocytes and can thereby be useful as a novel therapeutic agent for the management of diabetes and related metabolic disorders.

키워드

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