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Cyclic adenosine monophosphate protects renal cell lines against amphotericin B toxicity in a PKA-independent manner

dc.contributor.authorFerreira, A. F.
dc.contributor.authorFranca, F. D.
dc.contributor.authorRossoni, J. V.
dc.contributor.authorViana, P. H. L.
dc.contributor.authorMoraes, K. C. M. [UNESP]
dc.contributor.authorGomes, D. A.
dc.contributor.authorCosta, D. C.
dc.contributor.authorTagliati, C. A.
dc.contributor.authorChaves, M. M.
dc.contributor.institutionUniversidade Federal de Minas Gerais (UFMG)
dc.contributor.institutionUniv Fed Ouro Preto
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2018-11-26T16:19:15Z
dc.date.available2018-11-26T16:19:15Z
dc.date.issued2016-01-02
dc.description.abstractAmphotericin B is the gold standard agent in the management of serious systemic fungal infections. However, this drug can cause nephrotoxicity, which contributes up to 25% of all acute kidney injuries in critically ill patients. Cyclic adenosine monophosphate can protect kidney cells from death due to injury or drug exposure in some cases. Hence, the objective of this work was to evaluate if cAMP could prevent cell death that occurs in renal cell lines subjected to AmB treatment and, if so, to assess the involvement of PKA in the transduction of this signal. Two different renal cell lines (LLC-PK1 and MDCK) were used in this study. MTT and flow cytometry assays showed increased cell survival when cells were exposed to cAMP in a PKA-independent manner, which was confirmed by western blot. This finding suggests that cAMP (db-cAMP) may prevent cell death caused by exposure to AmB. This is the first time this effect has been identified when renal cells are exposed to AmB's nephrotoxic potential.en
dc.description.affiliationUniv Fed Minas Gerais, Inst Ciencias Biol, Dept Bioquim & Imunol, BR-30161970 Belo Horizonte, MG, Brazil
dc.description.affiliationUniv Fed Ouro Preto, Inst Ciencias Exatas & Biol, Dept Ciencias Biol, Mouro Preto, MG, Brazil
dc.description.affiliationUniv Estadual Paulista, Inst Biociencias, Dept Biol, Rio Claro, SP, Brazil
dc.description.affiliationUniv Fed Minas Gerais, Dept Anal Clin & Toxicol, Fac Farm, Bioquim, BR-30161970 Belo Horizonte, MG, Brazil
dc.description.affiliationUnespUniv Estadual Paulista, Inst Biociencias, Dept Biol, Rio Claro, SP, Brazil
dc.description.sponsorshipUFMG (Universidade Federal de Minas Gerais)
dc.description.sponsorshipUFOP (Universidade Federal de Ouro Preto)
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de Minas Gerais (FAPEMIG)
dc.description.sponsorshipCoordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)
dc.description.sponsorshipConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
dc.description.sponsorshipIdFAPEMIG: APQ-00596-08
dc.format.extent28-34
dc.identifierhttp://dx.doi.org/10.3109/01480545.2015.1012210
dc.identifier.citationDrug And Chemical Toxicology. Abingdon: Taylor & Francis Ltd, v. 39, n. 1, p. 28-34, 2016.
dc.identifier.doi10.3109/01480545.2015.1012210
dc.identifier.fileWOS000368195900004.pdf
dc.identifier.issn0148-0545
dc.identifier.urihttp://hdl.handle.net/11449/161130
dc.identifier.wosWOS:000368195900004
dc.language.isoeng
dc.publisherTaylor & Francis Ltd
dc.relation.ispartofDrug And Chemical Toxicology
dc.relation.ispartofsjr0,460
dc.rights.accessRightsAcesso aberto
dc.sourceWeb of Science
dc.subjectcAMP
dc.subjectcell protection
dc.subjectnephrotoxicity
dc.titleCyclic adenosine monophosphate protects renal cell lines against amphotericin B toxicity in a PKA-independent manneren
dc.typeArtigo
dcterms.licensehttp://journalauthors.tandf.co.uk/permissions/reusingOwnWork.asp
dcterms.rightsHolderTaylor & Francis Ltd
dspace.entity.typePublication
unesp.campusUniversidade Estadual Paulista (Unesp), Instituto de Biociências, Rio Claropt
unesp.departmentBiologia - IBpt

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