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Evaluation of the toxicokinetics and apoptotic potential of ethanol extract from Echinodorus macrophyllus leaves in vivo.
Vaz, Márcia Soares Mattos; Vaz da Silva, Mário Sérgio; Oliveira, Rodrigo Juliano; da Silva Mota, Jonas; Brait, Débora Regina Hoff; de Carvalho, Luciana Noia Borges; Vani, Juliana Miron; Berno, Claudia Rodrigues; Araújo, Flávio Henrique Souza; de Barros, Márcio Eduardo.
Afiliação
  • Vaz MS; Faculty of Health Sciences, Federal University of Grande Dourados, Dourados, Mato Grosso do Sul, Brazil.
  • Vaz da Silva MS; Faculty of Health Sciences, Federal University of Grande Dourados, Dourados, Mato Grosso do Sul, Brazil.
  • Oliveira RJ; Federal University of Mato Grosso do Sul (UFMS), Campo Grande, MS, Brazil.
  • da Silva Mota J; Centre for Research on Biodiversity (CPBIO), State University of Mato Grosso do Sul (UEMS), Dourados, Mato Grosso do Sul, Brazil.
  • Brait DR; Faculty of Health Sciences, Federal University of Grande Dourados, Dourados, Mato Grosso do Sul, Brazil.
  • de Carvalho LN; Faculty of Health Sciences, Federal University of Grande Dourados, Dourados, Mato Grosso do Sul, Brazil.
  • Vani JM; Federal University of Mato Grosso do Sul (UFMS), Campo Grande, MS, Brazil.
  • Berno CR; Federal University of Mato Grosso do Sul (UFMS), Campo Grande, MS, Brazil.
  • Araújo FH; Federal University of Mato Grosso do Sul (UFMS), Campo Grande, MS, Brazil.
  • de Barros ME; Faculty of Health Sciences, Federal University of Grande Dourados, Dourados, Mato Grosso do Sul, Brazil; University Hospital of the Federal University of Grande Dourados, Dourados, Mato Grosso do Sul, Brazil. Electronic address: marciobarros@ufgd.edu.br.
Regul Toxicol Pharmacol ; 82: 32-38, 2016 Dec.
Article em En | MEDLINE | ID: mdl-27793745
ABSTRACT
This study evaluates the toxicological, genotoxic, mutagenic and apoptotic potential of an in vivo assay from Echinodorus macrophyllus extract (EEM). The acute toxicity test used 02 groups (n = 5) of female Wistar rats negative control group (saline) and experimental group (2000 mg/kg b.w. EEM), both orally administered (gavage) at single doses and monitored for 14 days. To assess the genotoxic, mutagenic and apoptotic potential, 50 male Swiss mice were divided into 5 groups (n = 10) Group I negative control (saline solution 0.1 ml/10 g b.w.); Group II positive control (cyclophosphamide 100 mg/kg b.w.) intraperitoneally administered; groups III-V received EEM at 500, 1000 and 2000 mg/kg b.w., respectively. Groups I, III-V received oral administrations (gavage). The results showed that there was no acute lethality or any signs of acute toxicity, indicating that LD50 is greater than 2000 mg/kg b.w. The groups treated with EEM showed no genotoxic or mutagenic activity and did not induce apoptosis in the liver and kidney. Therefore, EEM showed no acute toxicity and at doses of 500, 1000 and 2000 mg/kg b.w. absence of genotoxicity, mutagenicity and no apoptotic events were observed.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Solventes / Extratos Vegetais / Apoptose / Folhas de Planta / Alismataceae / Etanol / Toxicocinética / Rim / Fígado Tipo de estudo: Etiology_studies / Evaluation_studies Limite: Animals Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Solventes / Extratos Vegetais / Apoptose / Folhas de Planta / Alismataceae / Etanol / Toxicocinética / Rim / Fígado Tipo de estudo: Etiology_studies / Evaluation_studies Limite: Animals Idioma: En Ano de publicação: 2016 Tipo de documento: Article