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dc.creatorSantos, Gustavo A.-
dc.creatorPereira, Vinícius D.-
dc.creatorRoman, Erika A. F. R.-
dc.creatorIgnacio-Souza, Leticia-
dc.creatorVitorino, Daniele C.-
dc.creatorMoura, Rodrigo Ferreira de-
dc.creatorRazolli, Daniela S.-
dc.creatorTorsoni, Adriana S.-
dc.creatorVelloso, Licio A-
dc.creatorTorsoni, Marcio A.-
dc.date.accessioned2020-12-18T17:14:16Z-
dc.date.available2020-12-18T17:14:16Z-
dc.date.issued2013-04-
dc.identifier.citationSANTOS, G. A. et al. Hypothalamic inhibition of acetyl-CoA carboxylase stimulates hepatic counter-regulatory response independent of AMPK activation in rats. PLoS ONE, [S. l.], v. 8, n. 4, e62669, Apr. 2013. DOI: https://doi.org/10.1371/journal.pone.0062669.pt_BR
dc.identifier.urihttp://repositorio.ufla.br/jspui/handle/1/45943-
dc.description.abstractBackground Hypothalamic AMPK acts as a cell energy sensor and can modulate food intake, glucose homeostasis, and fatty acid biosynthesis. Intrahypothalamic fatty acid injection is known to suppress liver glucose production, mainly by activation of hypothalamic ATP-sensitive potassium (K(ATP)) channels. Since all models employed seem to involve malonyl-CoA biosynthesis, we hypothesized that acetyl-CoA carboxylase can modulate the counter-regulatory response independent of nutrient availability. Methodology/Principal Findings In this study employing immunoblot, real-time PCR, ELISA, and biochemical measurements, we showed that reduction of the hypothalamic expression of acetyl-CoA carboxylase by antisense oligonucleotide after intraventricular injection increased food intake and NPY mRNA, and diminished the expression of CART, CRH, and TRH mRNA. Additionally, as in fasted rats, in antisense oligonucleotide-treated rats, serum glucagon and ketone bodies increased, while the levels of serum insulin and hepatic glycogen diminished. The reduction of hypothalamic acetyl-CoA carboxylase also increased PEPCK expression, AMPK phosphorylation, and glucose production in the liver. Interestingly, these effects were observed without modification of hypothalamic AMPK phosphorylation. Conclusion/Significance Hypothalamic ACC inhibition can activate hepatic counter-regulatory response independent of hypothalamic AMPK activation.pt_BR
dc.languageen_USpt_BR
dc.publisherPLoS ONEpt_BR
dc.rightsAttribution 4.0 International*
dc.rightsacesso abertopt_BR
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.sourcePLoS ONEpt_BR
dc.subjectHomeostasispt_BR
dc.subjectHypothalamic AMPK activationpt_BR
dc.subjectACC inhibitionpt_BR
dc.titleHypothalamic inhibition of acetyl-CoA carboxylase stimulates hepatic counter-regulatory response independent of AMPK activation in ratspt_BR
dc.typeArtigopt_BR
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