Genotoxic studies in hypertensive and normotensive rats treated with amiodarone


Autoria(s): ALMEIDA, Mara Ribeiro; LIMA, Estela de Oliveira; SILVA, Valdo Jose Dias da; CAMPOS, Mateus Gandra; ANTUNES, Lusania M. G.; SALMAN, Ana Karina Dias; DIAS, Francisca L.
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

19/10/2012

19/10/2012

2008

Resumo

Amiodarone, a benzofuran derivative. is a very effective antiarrhythmic medication, but has potential to cause side effects. Although its cytotoxicity potential is very well-known, there are few reports about its genotoxicity effects. Since amiodarone has not been investigated in genotoxicity studies, and the spontaneously hypertensive rat (SHR) is a well-characterized model for hypertension, the aim of the present study was to perform cytogenetic analysis on chromosome aberrations in bone marrow cells of SHRs and normotensive Wistar-Kyoto rats (WKYs) that received oral amiodarone treatment for 4 weeks. Amiodarone activity was also monitored using electrocardiograms. The presence of bradycardia in amiodarone-treated rats confirmed that this drug was really active. Metaphase analysis on bone marrow cells showed that there were significant differences in total chromosomal damage and percentage abnormal metaphase between WKY and SHR negative controls. In the SHR negative control, the frequencies of basal chromosomal aberrations and abnormal metaphases were significantly higher (p < 0.05). There were high numbers of chromosomal aberrations in all amiodarone-treated groups, compared with negative controls. In amiodarone-treated groups, the most frequent chromosomal aberration was chromatid breaks. More chromosomal aberrations were found in WKYs that received amiodarone, with a statistically significant difference in comparison with negative controls (p < 0.05). However, in SHR rats there was no significant difference between the amiodarone and negative groups regarding chromosomal damage induction. These results showed that treatment with amiodarone was genotoxic in WKYs, but not in SHRs. Further studies are needed to confirm whether amiodarone is genotoxic or efficient and harmless, among humans undergoing therapy. (c) 2008 Published by Elsevier B.V.

PIBIC/CNPq (Conselho Nacional de Desenvolvimento Cientifico a Tecnologico)

BIC/FAPEMIG (Fundaqao de Apoio a Pesquisa do Estado de Minas Gerais)

Identificador

MUTATION RESEARCH-GENETIC TOXICOLOGY AND ENVIRONMENTAL MUTAGENESIS, v.657, n.2, p.155-159, 2008

1383-5718

http://producao.usp.br/handle/BDPI/20438

10.1016/j.mrgentox.2008.09.005

http://dx.doi.org/10.1016/j.mrgentox.2008.09.005

Idioma(s)

eng

Publicador

ELSEVIER SCIENCE BV

Relação

Mutation Research-genetic Toxicology and Environmental Mutagenesis

Direitos

restrictedAccess

Copyright ELSEVIER SCIENCE BV

Palavras-Chave #Chromosomal aberrations #Arterial hypertension #DNA damage #Bone marrow cells #Wistar rats #OXIDATIVE DNA-DAMAGE #CHROMOSOME-ABERRATIONS #FREE-RADICALS #INDUCTION #TOXICITY #TISSUES #Biotechnology & Applied Microbiology #Genetics & Heredity #Toxicology
Tipo

article

original article

publishedVersion