Carvedilol protects against apoptotic cell death induced by cisplatin in renal tubular epithelial cells


Autoria(s): Carvalho Rodrigues, M. A.; Gobe, G.; Santos, N. A. G.; Santos, A. C.
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

06/11/2013

06/11/2013

2012

Resumo

Cisplatin is a highly effective chemotherapeutic drug; however, its use is limited by nephrotoxicity. Studies showed that the renal injury produced by cisplatin involves oxidative stress and cell death mediated by apoptosis and necrosis in proximal tubular cells. The use of antioxidants to decrease cisplatin-induced renal cell death was suggested as a potential therapeutic measure. In this study the possible protective effects of carvedilol, a beta blocker with antioxidant activity, was examined against cisplatin-induced apoptosis in HK-2 human kidney proximal tubular cells. The mitochondrial events involved in this protection were also investigated. Four groups were used: controls (C), cisplatin alone at 25 mu M (CIS), cisplatin 25 mu M plus carvedilol 50 mu M (CV + CIS), and carvedilol alone 50 mu M (CV). Cell viability, apoptosis, caspase-9, and caspase-3 were determined. Data demonstrated that carvedilol effectively increased cell viability and minimized caspase activation and apoptosis in HK-2 cells, indicating this may be a promising drug to reduce nephrotoxicity induced by cisplatin.

Fundacao de Amparo a Pesquisa do Estado de Sao Paulo (FAPESP)

Coordenacao de Aperfeicoamento de Pessoal de Nivel Superior (CAPES)

Identificador

Journal of Toxicology and Environmental Health-Part A-Current Issues, Philadelphia, v. 75, n. 16-17, Special Issue, pp. 981-990, APR 19, 2012

1528-7394

http://www.producao.usp.br/handle/BDPI/42635

10.1080/15287394.2012.696512

http://dx.doi.org/10.1080/15287394.2012.696512

Idioma(s)

eng

Publicador

TAYLOR & FRANCIS INC

PHILADELPHIA

Relação

JOURNAL OF TOXICOLOGY AND ENVIRONMENTAL HEALTH-PART A-CURRENT ISSUES

Direitos

restrictedAccess

Copyright TAYLOR & FRANCIS INC

Palavras-Chave #RAT-KIDNEY MITOCHONDRIA #REDOX STATE UNBALANCE #HIGH-DOSE CISPLATIN #INDUCED NEPHROTOXICITY #ENERGETIC METABOLISM #OXIDATIVE STRESS #FAILURE #MECHANISMS #NECROSIS #OTOTOXICITY #ENVIRONMENTAL SCIENCES #PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH #TOXICOLOGY
Tipo

article

original article

publishedVersion