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Cytotoxic, genotoxic and mutagenic evaluation of Alibertia edulis (rich.) a. Rich. ex DC: an indigenous species from Brazil.
Tolouei, Sara Emilia Lima; Traesel, Giseli Karenina; Freitas de Lima, Fernando; Souza de Araújo, Flávio Henrique; Honaiser Lescano, Caroline; Cardoso, Claudia Andrea Lima; Oesterreich, Silvia Aparecida; Vieira, Maria do Carmo.
Afiliación
  • Tolouei SEL; Department of Pharmacology, Universidade Federal do Paraná, Curitiba, Paraná, Brazil.
  • Traesel GK; Faculty of Health Sciences, Universidade Federal da Grande Dourados, Dourados, Mato Grosso do Sul, Brazil.
  • Freitas de Lima F; Faculty of Health Sciences, Universidade Federal da Grande Dourados, Dourados, Mato Grosso do Sul, Brazil.
  • Souza de Araújo FH; Center of Biological and Health Sciences, Universidade Federal do Mato Grosso do Sul, Campo Grande, Mato Grosso do Sul, Brazil.
  • Honaiser Lescano C; Faculty of Medicinal Sciences, Universidade Estadual de Campinas, Campinas, São Paulo, Brazil.
  • Cardoso CAL; Department of Chemistry, Universidade Estadual do Mato Grosso do Sul, Dourados, Mato Grosso do Sul, Brazil.
  • Oesterreich SA; Faculty of Health Sciences, Universidade Federal da Grande Dourados, Dourados, Mato Grosso do Sul, Brazil.
  • Vieira MDC; Faculty of Agricultural Sciences, Universidade Federal da Grande Dourados, Dourados, Mato Grosso do Sul, Brazil.
Drug Chem Toxicol ; 43(2): 200-207, 2020 Mar.
Article en En | MEDLINE | ID: mdl-30044655
ABSTRACT
Tea leaves of Alibertia edulis is popularly used in folk medicine. However, studies on the genotoxicity of this plant are not available. We aimed to investigate the in vivo and in vitro cytotoxic, genotoxic and mutagenic potentials of the aqueous extract of A. edulis leaves (AEAE). Antioxidant assays, the Artemia salina test, MTT in human platelets, micronucleus in bone marrow and comet in peripheral blood were performed. Animals received four different doses of the AEAE by oral gavage for 30 days. Saline and cyclophosphamide were used as controls. The AEAE exhibited a maximal inhibition at 100 and 250 µg/mL, according to the ABTS and DPPH methods, respectively. The A. salina assay showed that the AEAE presented some toxicity at doses of 100, 250 and 500 µg/mL. Through the MTT assay, the AEAE showed no toxic effects on human platelets during the incubation period. The alkaline comet assay showed that all doses of the AEAE were statistically similar to the negative control group since they did not induce any significant increase of the overall number of damaged cells nor the severity of the cell damage. In the micronucleous assay, results demonstrate that the AEAE did not increase the production of micronucleated polychromatic erythrocytes and was statistically similar to the negative control. The four doses of the plant extract did not affect the production of new erythrocytes and were statistically similar to the negative control groups. Furthermore, the AEAE demonstrated no cytotoxicity, genotoxicity and mutagenicity at the doses tested in rats.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Extractos Vegetales / Rubiaceae / Eritrocitos Límite: Animals / Female / Humans / Male País/Región como asunto: America do sul / Brasil Idioma: En Año: 2020 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Extractos Vegetales / Rubiaceae / Eritrocitos Límite: Animals / Female / Humans / Male País/Región como asunto: America do sul / Brasil Idioma: En Año: 2020 Tipo del documento: Article