Activating cAMP/PKA signaling in skeletal muscle suppresses the ubiquitin-proteasome-dependent proteolysis: implications for sympathetic regulation

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dc.contributor.authorSilveira, W. A.
dc.contributor.authorGoncalves, D. A.
dc.contributor.authorGraca, F. A.
dc.contributor.authorAndrade-Lopes, A. L. [UNIFESP]
dc.contributor.authorBergantin, L. B. [UNIFESP]
dc.contributor.authorZanon, N. M.
dc.contributor.authorGodinho, R. O. [UNIFESP]
dc.contributor.authorKettelhut, I. C.
dc.contributor.authorNavegantes, L. C. C.
dc.contributor.institutionUniversidade de São Paulo (USP)
dc.contributor.institutionUniversidade Federal de São Paulo (UNIFESP)
dc.date.accessioned2016-01-24T14:37:29Z
dc.date.available2016-01-24T14:37:29Z
dc.date.issued2014-07-01
dc.description.abstractAlthough we have recently demonstrated that plasma catecholamines induce antiproteolytic effects on skeletal muscle (Graca FA, Goncalves DAP, Silveira WA, Lira EC, Chaves VE, Zanon NM, Garofalo MAR, Kettelhut IC, Navegantes LCC. Am J Physiol Endocrinol Metab. 305: E1483-E1494, 2013), the role of the muscle sympathetic innervation and, more specifically, norepinephrine (NE) in regulating the ubiquitin (Ub)-proteasome system (UPS) remains unknown. Based on previous findings that chemical sympathectomy acutely reduces UPS activity, we hypothesized that muscle NE depletion induces adrenergic supersensitivity in rat skeletal muscles. We report that surgical sympathetic denervation (SDEN), a condition in which only muscle NE from both hindlimbs is depleted, transiently reduced the overall proteolysis and the UPS activity (similar to 25%) in both soleus and extensor digitorum longus muscles. This antiproteolytic response was accompanied by increased activity of adenylyl cyclase (112%), levels of cyclic adenosine monophosphate (cAMP; 191%), and the serine phosphorylation of cAMP response element-binding protein (32%). in extensor digitorum longus from normal rats, NE (10(-4) M) in vitro increased the levels of cAMP (115%) and the serine phosphorylation of both cAMP response element-binding protein (2.7-fold) and forkhead box class O1 transcription factor. Similar effects were observed in C2C12 cells incubated with forskolin (10 mu M). in parallel, NE significantly reduced the basal UPS (21%) activity and the mRNA levels of atrophy-related Ub-ligases. Similar responses were observed in isolated muscles exposed to 6-BNZ-cAMP (500 mu M), a specific PKA activator. the phosphorylation levels of Akt were not altered by SDEN, NE, forskolin or 6-BNZ-cAMP. Our results demonstrate that SDEN induces muscle adrenergic supersensitivity for cAMP leading to the suppression of UPS, and that the suppressive effects of NE on UPS activity and expression of Ubligases can be mediated by the activation of cAMP/PKA signaling, with the inhibition of forkhead box class O1 transcription factor.en
dc.description.affiliationUniv São Paulo, Ribeirao Preto Med Sch, Dept Physiol, BR-14049900 Ribeirao Preto, SP, Brazil
dc.description.affiliationUniv São Paulo, Ribeirao Preto Med Sch, Dept Biochem Immunol, BR-14049900 Ribeirao Preto, SP, Brazil
dc.description.affiliationUniversidade Federal de São Paulo UNIFESP, Dept Pharmacol, Div Cellular Pharmacol, São Paulo, Brazil
dc.description.affiliationUnifespUniversidade Federal de São Paulo UNIFESP, Dept Pharmacol, Div Cellular Pharmacol, São Paulo, Brazil
dc.description.sourceWeb of Science
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
dc.description.sponsorshipConselho Nacional de Pesquisa
dc.description.sponsorshipIDFAPESP: 08/06694-6
dc.description.sponsorshipIDFAPESP: 10/11083-6
dc.description.sponsorshipIDFAPESP: 12/18861-0
dc.description.sponsorshipIDFAPESP: 12/24524-6
dc.description.sponsorshipIDFAPESP: 10/11015-0
dc.description.sponsorshipIDConselho Nacional de Pesquisa: 140094/07-5
dc.description.sponsorshipIDConselho Nacional de Pesquisa: 306101/09-2
dc.description.sponsorshipIDConselho Nacional de Pesquisa: 303786/08-6
dc.format.extent11-19
dc.identifierhttp://dx.doi.org/10.1152/japplphysiol.01055.2013
dc.identifier.citationJournal of Applied Physiology. Bethesda: Amer Physiological Soc, v. 117, n. 1, p. 11-19, 2014.
dc.identifier.doi10.1152/japplphysiol.01055.2013
dc.identifier.issn8750-7587
dc.identifier.urihttp://repositorio.unifesp.br/handle/11600/37902
dc.identifier.wosWOS:000339169300002
dc.language.isoeng
dc.publisherAmer Physiological Soc
dc.relation.ispartofJournal of Applied Physiology
dc.rightsAcesso aberto
dc.subjectcatecholaminesen
dc.subjectsympathectomyen
dc.subjectproteolysisen
dc.subjectatrogin-1en
dc.subjectMuRF1en
dc.titleActivating cAMP/PKA signaling in skeletal muscle suppresses the ubiquitin-proteasome-dependent proteolysis: implications for sympathetic regulationen
dc.typeArtigo
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