Efeito protetor de proantocianidinas de sementes de Vitis vinifera L. (Vitaceae) contra efeitos genotóxicos do cloridrato de Doxorrubicina, em células somáticas de Drosophila melanogaster

Detalhes bibliográficos
Ano de defesa: 2008
Autor(a) principal: Rezende, Alexandre Azenha Alves de
Orientador(a): Não Informado pela instituição
Banca de defesa: Não Informado pela instituição
Tipo de documento: Dissertação
Tipo de acesso: Acesso aberto
Idioma: por
Instituição de defesa: Universidade Federal de Uberlândia
BR
Programa de Pós-graduação em Genética e Bioquímica
Ciências Biológicas
UFU
Programa de Pós-Graduação: Não Informado pela instituição
Departamento: Não Informado pela instituição
País: Não Informado pela instituição
Palavras-chave em Português:
Link de acesso: https://repositorio.ufu.br/handle/123456789/15781
Resumo: Proanthocyanidins (PAs), also known as condensed tannins, are naturally occurring oligomers and polymers of flavan-3-ol monomer units widely found in leaves, flowers, fruits, seeds, nuts and barks of many plants. Grape seeds proanthocyanidins (GSPs) has been used as nutritional supplements, as antioxidant, in preventing atherosclerosis, cardiovascular diseases and for dislipidemy treatment. The anthracycline antibiotic adriamycin (doxorubicin - DOX) is a cancer chemotherapeutic agent that interfere with topoisomerase II enzyme and generate free radicals. In the present study, GSPs (1.680; 3.375 or 6.750 mg/mL) alone were examined for genotoxicity and the same concentrations of GSPs in association with DOX (0.125 mg/mL) were examined for antigenotoxicity, using the standard (ST) and high bioactivation (HB) versions of the wing somatic mutation and recombination test in Drosophila melanogaster. The results observed in both crosses were rather similar. GSPs itself did not show genotoxicity at the doses used. GSPs suppressed the DNA damage induced by DOX in a dosedependent manner. Comparison of the frequencies of wing spots in the markerheterozygous (MH) flies and balancer-heterozygous (BH) flies, from both crosses, indicated that recombination was a major response for treatment with DOX alone. Simultaneous treatments demonstrated that GSPs has anti-mutagenic and antirecombinogenic activities. Nevertheless, the anti-recombinogenic activity was a major response.