Assessment of micronucleus frequency in the peripheral blood of female rats in persistent estrus treated with selective estrogen receptor modulators


Autoria(s): Rodrigues Junior, Dorival Mendes; Santos, Alesse Ribeiro dos; Cavalcante, Ana Amelia de Carvalho Melo; Alencar, Airlane Pereira; Costa, Pedro Vitor Lopes; Silva, Benedito Borges da
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

15/10/2013

15/10/2013

01/01/2012

Resumo

The aim of this study was to evaluate micronucleus (MN) frequency in polychromatic erythrocytes (PCE) of female rats in persistent estrus (a model developed to mimic polycystic ovary syndrome) treated with selective estrogen receptor modulators (SERMs, tamoxifen, and raloxifene). Forty female Wistar-Hannover rats were divided into four groups of 10 animals each: Group I (normally cycling rats) and Group II (persistent estrus) both received only vehicle, while Group III (persistent estrus) was treated with tamoxifen (250 mu g/animal/day) and Group IV (persistent estrus) was treated with raloxifene (750 mu g/animal/day). Tamoxifen and raloxifene were given by oral gavage beginning on postnatal day 90 and continuing for 30 consecutive days. Peripheral blood samples were collected from tails 1 day following the last exposure. Blood smears were made on glass slides and stained with 10% Giemsa solution. ANOVA and a Tukey post-hoc test were used for data analysis. Mean percentages of MN were 1.82 +/- 0.13, 5.20 +/- 0.24, 3.32 +/- 0.13, and 3.04 +/- 0.12 in Groups I, II, III, and IV, respectively. The results indicate that tamoxifen and raloxifene similarly reduced the formation of MNPCE of female rats in persistent estrus (P < 0.0001 for Groups III and IV vs. Group II), using the dosages and time periods applied in the present study. The data suggest possibly antimutagenic effects of SERMs under high levels of estrogens. The findings also suggest that this is an interesting animal model for studying the genotoxicity of estrogens. Environ. Mol. Mutagen. 2012. (C) 2011 Wiley Periodicals, Inc.

Identificador

ENVIRONMENTAL AND MOLECULAR MUTAGENESIS, MALDEN, v. 53, n. 1, pp. 51-54, JAN, 2012

0893-6692

http://www.producao.usp.br/handle/BDPI/35134

10.1002/em.20676

http://dx.doi.org/10.1002/em.20676

Idioma(s)

eng

Publicador

WILEY-BLACKWELL

MALDEN

Relação

Environmental and Molecular Mutagenesis

Direitos

restrictedAccess

Copyright WILEY-BLACKWELL

Palavras-Chave #ESTROGENS #GENOTOXICITY #MICRONUCLEUS #PERSISTENT ESTRUS #RALOXIFENE #TAMOXIFEN #BREAST-CANCER CELLS #GENOMIC INSTABILITY #DNA-DAMAGE #TAMOXIFEN #ASSAY #PROLIFERATION #METABOLITES #PREVENTION #TISSUES #ENVIRONMENTAL SCIENCES #GENETICS & HEREDITY #TOXICOLOGY
Tipo

article

original article

publishedVersion