dc.creatorJOSE, A. A. F. B. V.
dc.creatorGAMA, M. A. S.
dc.creatorLANNA, D. D. P.
dc.date.accessioned2012-04-17T22:47:38Z
dc.date.accessioned2018-07-04T14:33:20Z
dc.date.available2012-04-17T22:47:38Z
dc.date.available2018-07-04T14:33:20Z
dc.date.created2012-04-17T22:47:38Z
dc.date.issued2008
dc.identifierGENETICS AND MOLECULAR RESEARCH, v.7, n.2, p.284-294, 2008
dc.identifier1676-5680
dc.identifierhttp://producao.usp.br/handle/BDPI/14791
dc.identifierhttp://www.geneticsmr.com//year2008/vol7-2/pdf/gmr417.pdf
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1611639
dc.description.abstractThe objective of the present study was to determine the effects of trans-10, cis-12 conjugated linoleic acid (CLA) in adipose tissue explant cultures of growing pigs on the following responses: lipogenesis (measured as rate of C-14-labeled glucose incorporation over a subsequent 2-h incubation in the presence or absence of insulin), lipolysis (release of non-esterified fatty acid over a 2-h incubation in the presence or absence of isoproterenol), activities of lipogenic enzymes, and mRNA abundance of fatty acid synthase (FAS). Adipose tissue explants from nine growing pigs (78 +/- 3 kg) were cultured in 199 medium with insulin, dexamethasone and antibiotics for 4, 12, 24, and 48 h. The treatments were 1) control: 100 mu M polyvinyl alcohol (PVA); 2) pGH: 100 ng/mL porcine growth hormone (pGH) plus 100 mu M PVA; 3) CLA200: 200 mu M trans-10, cis-12 CLA; 4) CLA50: 50 mu M trans-10, cis-12 CLA, and 5) LA: 200 mu M linoleic acid. Fatty acids were added along with PVA (2: 1), respectively, for 24 h. Explants were collected after each culture period and assayed for lipogenesis. Transcripts of FAS mRNA were quantified by real-time RT-PCR after 24 and 48 h. Lipolysis and activities of FAS, glucose 6-phosphate dehydrogenase, 6-phosphogluconate dehydrogenase, and NADP-malate dehydrogenase were determined after 48 h. As expected, glucose incorporation was decreased (P < 0.05) in response to pGH treatment (positive control). LA had no effect on any parameter evaluated. Treatment with trans-10, cis-12 CLA decreased FAS activity (P < 0.05), but NADPH-generating enzymes were unaffected by treatments. Consistent with reduction in FAS activity, both lipid synthesis and FAS mRNA abundance were reduced with chronic CLA treatment, pGH increased baseline and stimulated lipolysis (P < 0.05) after 48 h of culture, while CLA treatment had no effect on non-esterified fatty acid release. Results of this study showed that trans-10, cis-12 CLA alters lipogenesis but has no effect on lipolysis in cultures of pig adipose tissue.
dc.languageeng
dc.publisherFUNPEC-EDITORA
dc.relationGenetics and Molecular Research
dc.rightsCopyright FUNPEC-EDITORA
dc.rightsopenAccess
dc.subjectconjugated linoleic acid
dc.subjectadipose tissue explants
dc.subjectlipogenesis
dc.subjectbioactive fatty acid
dc.subjectswine
dc.titleEffects of trans-10, cis-12 conjugated linoleic acid on gene expression and lipid metabolism of adipose tissue of growing pigs
dc.typeArtículos de revistas


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