Phenolic Compounds from Wild Plant and <i>In Vitro</i> Cultures of <i>Ageratina pichichensis</i> and Evaluation of Their Antioxidant Activity
Elizabeth Alejandra Motolinia-Alcántara,
Adrián Marcelo Franco-Vásquez,
Antonio Nieto-Camacho,
Roberto Arreguín-Espinosa,
Mario Rodríguez-Monroy,
Francisco Cruz-Sosa,
Angelica Román-Guerrero
Affiliations
Elizabeth Alejandra Motolinia-Alcántara
Departamento de Biotecnología, Universidad Autónoma Metropolitana-Iztapalapa, Av. Ferrocarril de San Rafael Atlixco 186, Col. Leyes de Reforma 1a. Sección, Alcaldía Iztapalapa, Ciudad de Mexico 09310, Mexico
Adrián Marcelo Franco-Vásquez
Departamento de Química de Biomacromoléculas, Instituto de Química, Universidad Nacional Autónoma de México, Coyoacán, Ciudad de Mexico 04510, Mexico
Antonio Nieto-Camacho
Laboratorio de Pruebas Biológicas, Instituto de Química, Universidad Nacional Autónoma de México, Coyoacán, Ciudad de Mexico 04510, Mexico
Roberto Arreguín-Espinosa
Departamento de Química de Biomacromoléculas, Instituto de Química, Universidad Nacional Autónoma de México, Coyoacán, Ciudad de Mexico 04510, Mexico
Mario Rodríguez-Monroy
Centro de Desarrollo de Productos Bióticos (CEPROBI), Departamento de Biotecnología, Instituto Politécnico Nacional (IPN), Yautepec 62731, Mexico
Francisco Cruz-Sosa
Departamento de Biotecnología, Universidad Autónoma Metropolitana-Iztapalapa, Av. Ferrocarril de San Rafael Atlixco 186, Col. Leyes de Reforma 1a. Sección, Alcaldía Iztapalapa, Ciudad de Mexico 09310, Mexico
Angelica Román-Guerrero
Departamento de Biotecnología, Universidad Autónoma Metropolitana-Iztapalapa, Av. Ferrocarril de San Rafael Atlixco 186, Col. Leyes de Reforma 1a. Sección, Alcaldía Iztapalapa, Ciudad de Mexico 09310, Mexico
Ageratina pichichensis, is commonly used in traditional Mexican medicine. In vitro cultures were established from wild plant (WP) seeds, obtaining in vitro plant (IP), callus culture (CC), and cell suspension culture (CSC) with the objective to determine total phenol content (TPC) and flavonoids (TFC), as well as their antioxidant activity by DPPH, ABTS and TBARS assays, added to the compound’s identification and quantification by HPLC, from methanol extracts obtained by sonication. CC showed significantly higher TPC and TFC than WP and IP, while CSC produced 2.0–2.7 times more TFC than WP, and IP produced only 14.16% TPC and 38.8% TFC compared with WP. There were identified compounds such as epicatechin (EPI), caffeic acid (CfA), and p-coumaric acid (pCA) in in vitro cultures that were not found in WP. The quantitative analysis shows gallic acid (GA) as the least abundant compound in samples, whereas CSC produced significantly more EPI and CfA than CC. Despite these results, in vitro cultures show lower antioxidant activity than WP, for DPPH and TBARS WP > CSC > CC > IP and ABTS WP > CSC = CC > IP. Overall, A. pichichensis WP and in vitro cultures produce phenolic compounds with antioxidant activity, especially CC and CSC, which are shown to be a biotechnological alternative for obtaining bioactive compounds.