An evaluation, using the comet assay and the micronucleus test, of the antigenotoxic effects of chlorophyll b in mice


Autoria(s): SERPELONI, Juliana Mara; GROTTO, Denise; AISSA, Alexandre Ferro; MERCADANTE, Adriana Zerlotti; BIANCHI, Maria de Lourdes Pires; ANTUNES, Lusania Maria Greggi
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

19/10/2012

19/10/2012

2011

Resumo

We investigated the effects of the dietary pigment chlorophyll b (CLb) on cisplatin (cDDP)-induced oxidative stress and DNA damage, using the comet assay in mouse peripheral blood cells and the micronucleus (MN) test in bone marrow and peripheral blood cells. We also tested for thiobarbituric acid reactive substances (TBARS) and reduced glutathione (GSH) in liver and kidney tissues, as well as catalase (CAT) activity and GSH in total blood. CLb (0.2 and 0.5 mg/kg b.w.) was administrated by gavage every day for 13 days. On the 14th day of the experiment, 6 mg/kg cDDP or saline was delivered intraperitoneally. Treatment with cDDP led to a significant decrease in DNA migration and an increase in MN frequency in both cell types, bone marrow and peripheral blood cells. In the kidneys of mice treated with cDDP, TBARS levels were increased, whereas GSH levels were depleted in kidney and liver. In mice that were pretreated with CLb and then treated with cDDP, TBARS levels maintained normal concentrations and GSH did not differ from cDDP group. The improvement of oxidative stress biomarkers after CLb pre-treatment was associated with a decrease in DNA damage, mainly for the highest dose evaluated. Furthermore, CLb also slightly reduced the frequency of chromosomal breakage and micronucleus formation in mouse bone marrow and peripheral blood cells. These results show that pre-treatment with CLb attenuates cDDP-induced oxidative stress, chromosome instability, and lipid peroxidation. (C) 2011 Elsevier B.V. All rights reserved.

Fundacao de Amparo a Pesquisa do Estado de Sao Paulo (FAPESP)[05/59552-6]

Fundacao de Amparo a Pesquisa do Estado de Sao Paulo (FAPESP)[2008/06793-4]

Fundacao de Amparo a Pesquisa do Estado de Sao Paulo (FAPESP)[2010/05096-8]

Conselho Nacional para o Desenvolvimento Cientifico e Tecnologico (CNPq)

Coordenacao de Aperfeicoamento de Pessoal de Ensino Superior (CAPES/DS)

Identificador

MUTATION RESEARCH-GENETIC TOXICOLOGY AND ENVIRONMENTAL MUTAGENESIS, v.725, n.1/Fev, p.50-56, 2011

1383-5718

http://producao.usp.br/handle/BDPI/20205

10.1016/j.mrgentox.2011.06.009

http://dx.doi.org/10.1016/j.mrgentox.2011.06.009

Idioma(s)

eng

Publicador

ELSEVIER SCIENCE BV

Relação

Mutation Research-genetic Toxicology and Environmental Mutagenesis

Direitos

restrictedAccess

Copyright ELSEVIER SCIENCE BV

Palavras-Chave #Chlorophyll b #Cisplatin #Genotoxicity #Antioxidant #Nephrotoxicity #CISPLATIN-INDUCED NEPHROTOXICITY #BONE-MARROW-CELLS #IN-VIVO #INDUCED CLASTOGENESIS #SULFHYDRYL GROUPS #DNA-DAMAGE #VITAMIN-C #GENOTOXICITY #ANTIOXIDANTS #GLUTATHIONE #Biotechnology & Applied Microbiology #Genetics & Heredity #Toxicology
Tipo

article

original article

publishedVersion