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Título : Antioxidant and oxidative stress modulation properties of azorella pedunculata methanolic extract on A549 cancel cells
Autor: Cazar Ramirez, Maria Elena
Grijalva, Marcelo
Gómez, Nayara
Salazar Anchundia, Lizeth Andrea
Castillo Elsitdié, Luis Gerardo
Vallejo Lopez, Maria Jose
Jara Bermeo, Adriana Paola
Correspondencia: Grijalva, Marcelo, rmgrijalva@espe.edu.ec
Palabras clave : DPPH
Azorella pedunculata
Oxidative stress
Antioxidant capacity
Área de conocimiento FRASCATI amplio: 1. Ciencias Naturales y Exactas
Área de conocimiento FRASCATI detallado: 1.6.11 Ciencias de las Plantas
Área de conocimiento FRASCATI específico: 1.6 Ciencias Biológicas
Área de conocimiento UNESCO amplio: 09 - Salud y Bienestar
ÁArea de conocimiento UNESCO detallado: 0916 - Farmacia
Área de conocimiento UNESCO específico: 091 - Salud
Fecha de publicación : 2019
Volumen: Volumen 9, número 4
Fuente: International Journal of Pharmaceutical and Phytopharmacological Research
Tipo: ARTÍCULO
Abstract: 
Species of the genus Azorella have been widely studied for the presence of secondary metabolites with biological activities. Azorella pedunculata is the most common species of Azorella genus in Ecuadorian moors.The present study evaluated the oxidative stress-protective and antioxidant effects of methanolic extract from A. pedunculata on A549 cells treated with hydrogen peroxide (for induction of oxidative stress). The DPPH assay (2,2-diphenyl-1-picrylhydrazyl) was used to assess the antioxidant activity of the extract. Cell viability for extract-treated cells was assessed by the 3-(4, 5- dimethylthiazol-2-yl)-2, 5-diphenyltetrazolium bromide (MTT) assay. The protective activity against oxidative stress in A549 cells pretreated with the extract and then exposed to H2O2 was evaluated by flow cytometry. In addition, gene expression analysis for oxidative stress related genes superoxide dismutase 2 (SOD-2), and catalase (CAT) was performed with real-time quantitative reverse transcription PCR (RT-qPCR). The extract was cytotoxic at concentrations above 500μg/mL. Pretreatment with methanolic extract at concentrations of 100 and 250µg/mL significantly decreased ROS (+) cell population, in comparison with the H2O2 treatment control. The mRNA levels of assessed genes were also modulated when cells were pretreated with the extract. In comparison with the H2O2 control, SOD-2 was upregulated when cells were pre-treated with the methanolic extract at 100 µg/mL, and CAT was down-regulated when cells were pre-treated with 100 and 250 µg/mL of extract. The methanolic extract of A. pedunculata might exert a protective effect against oxidative stress. Further studies are required to elucidate the molecular mechanisms involved. The findings of this study might be, however, of value for potential biological and medical applications
URI : http://dspace.ucuenca.edu.ec/handle/123456789/37392
https://eijppr.com/fFUL10x
URI Fuente: https://eijppr.com/
ISSN : 2250-1029, e 2249-6084
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