Adiponectin Expression Is Induced by Vitamin E via a Peroxisome Proliferator-Activated Receptor (cid:1) -Dependent Mechanism
Adiponectin Expression Is Induced by Vitamin E via a Peroxisome Proliferator-Activated Receptor (cid:1) -Dependent Mechanism
复制标题
维生素 E 通过过氧化物酶体增殖物激活受体 (cid:1) 诱导脂联素表达 - 依赖性机制
DOI:
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发表时间:
2009
期刊:
影响因子:
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通讯作者:
M. Amiot
中科院分区:
文献类型:
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作者:
J. Landrier;E. Gouranton;Claire El Yazidi;C. Malezet;P. Balaguer;P. Borel;M. Amiot
Adiponectin is a well-known adipokine secreted by adipocytes that presents insulin-sensitizing properties. The regulation of expression of this adipokine by micronutrients is largely unknown. We dem-onstrateherethatadiponectinexpressionisinducedinadipocytesafterexposuretotocopherolsviathe peroxisome proliferator-activated receptor (cid:1) (PPAR (cid:1) ) pathway. Vitamin E force feeding resulted in an induction of adiponectin in mice at both mRNA and protein levels. Adiponectin mRNA and protein secretion were also increased by vitamin E ( (cid:2) - and (cid:1) -tocopherol) in 3T3-L1 cells, together with PPAR (cid:1) mRNA,independentofanantioxidanteffect.Intransienttransfections,both (cid:2) -and (cid:1) -vitamersinduced theluciferasegenereporterunderthecontrolofahumanadiponectinpromoterviaaPPAR-responsive element. The induction of adiponectin by tocopherols seems to be PPAR (cid:1) dependent, because it was blocked by the specific antagonist GW9662. Finally, we showed that intracellular concentrations of a PPAR (cid:1) endogenous ligand, 15-deoxy- (cid:1) 12,14-prostaglandin J2, increased after treatment with toco-pherolsin3T3-L1cells.Insummary,vitaminEup-regulatesadiponectinexpressionviaamechanismthat implicates PPAR (cid:1) together with its endogenous ligand 15-deoxy- (cid:1) 12,14-prostaglandin J2. The induction of adiponectin via an original molecular mechanism could be considered as the basis for the beneficial effect of vitamin E on insulin sensitivity. ( Endocrinology 150: 5318–5325, 2009) The performed in triplicate and repeated at least two times independently.
影响因子:
16.2
作者:
Mayer-Davis, EJ;Costacou, T;Bell, RA
通讯作者:
Bell, RA