Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
7
pubmed:dateCreated
2005-6-15
pubmed:abstractText
Adipocyte determination and differentiation-dependent factor 1 (ADD1) drives the expression of several lipogenic genes in mammals. Polyunsaturated fatty acids decrease ADD1 mRNA abundance in differentiating porcine adipocytes. The current study was designed to explore the mechanisms by which PUFA inhibit the expression of ADD1 in porcine adipocytes. Porcine preadipocytes were differentiated for 24 h with 0 or 100 microM of docosahexaenoic acid (DHA) and mixtures of different concentrations of antioxidants to investigate the effect of DHA and antioxidants on the ADD1 mRNA abundance. We found the relative mRNA abundance was decreased by the addition of 100 microM DHA to the medium for porcine differentiating adipocytes, and adding an antioxidant mixture to the medium prevented part of the decrease in ADD1 mRNA abundance. These data suggest that DHA decreased the steady-state transcription factor ADD1 mRNA through a mechanism related to fatty acid peroxidation. Indeed, adding 7.5 microM vitamin E (a natural antioxidant) also restored the concentrations of ADD1 and fatty acid synthase mRNA, which were decreased by DHA treatment; however, the DHA or the antioxidant treatment did not change the expression of antioxidation genes (superoxide dismutase 1 and glutathione peroxidase 1) in porcine stromal vascular cells. When supplemented with the eicosanoid synthesis pathway inhibitors, the inhibition of the expression of ADD1 by arachidonic acid was partially recovered. These results suggest that the mechanism by which PUFA decrease ADD1 mRNA is due to the metabolic product of eicosanoids and peroxidation of these PUFA.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Antioxidants, http://linkedlifedata.com/resource/pubmed/chemical/Arachidonic Acid, http://linkedlifedata.com/resource/pubmed/chemical/Docosahexaenoic Acids, http://linkedlifedata.com/resource/pubmed/chemical/Fatty Acid Synthetase Complex, http://linkedlifedata.com/resource/pubmed/chemical/Glutathione Peroxidase, http://linkedlifedata.com/resource/pubmed/chemical/RNA, Messenger, http://linkedlifedata.com/resource/pubmed/chemical/Sterol Regulatory Element Binding..., http://linkedlifedata.com/resource/pubmed/chemical/Superoxide Dismutase, http://linkedlifedata.com/resource/pubmed/chemical/Vitamin E, http://linkedlifedata.com/resource/pubmed/chemical/glutathione peroxidase GPX1, http://linkedlifedata.com/resource/pubmed/chemical/superoxide dismutase 1
pubmed:status
MEDLINE
pubmed:month
Jul
pubmed:issn
1525-3163
pubmed:author
pubmed:issnType
Electronic
pubmed:volume
83
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
1516-25
pubmed:meshHeading
pubmed-meshheading:15956459-Adipocytes, pubmed-meshheading:15956459-Animals, pubmed-meshheading:15956459-Antioxidants, pubmed-meshheading:15956459-Arachidonic Acid, pubmed-meshheading:15956459-Blotting, Northern, pubmed-meshheading:15956459-Cell Differentiation, pubmed-meshheading:15956459-Cells, Cultured, pubmed-meshheading:15956459-Docosahexaenoic Acids, pubmed-meshheading:15956459-Fatty Acid Synthetase Complex, pubmed-meshheading:15956459-Female, pubmed-meshheading:15956459-Gene Expression, pubmed-meshheading:15956459-Glutathione Peroxidase, pubmed-meshheading:15956459-Male, pubmed-meshheading:15956459-RNA, Messenger, pubmed-meshheading:15956459-Sterol Regulatory Element Binding Protein 1, pubmed-meshheading:15956459-Superoxide Dismutase, pubmed-meshheading:15956459-Swine, pubmed-meshheading:15956459-Vitamin E
pubmed:year
2005
pubmed:articleTitle
Effect of docosahexaenoic acid and arachidonic acid on the expression of adipocyte determination and differentiation-dependent factor 1 in differentiating porcine adipocytes.
pubmed:affiliation
Department of Animal Science, National Taiwan University, Taipei 106, Taiwan.
pubmed:publicationType
Journal Article, Comparative Study, Research Support, Non-U.S. Gov't