Dynamics of Polyphenol Biosynthesis by Calli Cultures, Suspension Cultures and Wild Specimens of the Medicinal Plant <i>Ligaria cuneifolia</i> (Ruiz & Pav.) Tiegh. (Loranthaceae). Analysis of Their Biological Activity
María Valeria Ricco,
Martín León Bari,
Alejandra Vanina Catalano,
Paula López,
Cecilia Beatriz Dobrecky,
Sergio Adrián Teves,
Ariana Posadaz,
Melina Laguia Becher,
Rafael Alejandro Ricco,
Marcelo Luis Wagner,
María Alejandra Álvarez
Affiliations
María Valeria Ricco
Centro de Estudios Biomédicos, Básicos, Aplicados y Desarrollo (CEBBAD), Facultad de Ciencias de la Salud, Universidad Maimónides, Hidalgo 775, Ciudad Autónoma de Buenos Aires 1405, Argentina
Martín León Bari
Centro de Estudios Biomédicos, Básicos, Aplicados y Desarrollo (CEBBAD), Facultad de Ciencias de la Salud, Universidad Maimónides, Hidalgo 775, Ciudad Autónoma de Buenos Aires 1405, Argentina
Alejandra Vanina Catalano
Cátedra de Farmacognosia, Facultad de Farmacia y Bioquímica, Universidad de Buenos Aires, Junín 956, Ciudad Autónoma de Buenos Aires 1113, Argentina
Paula López
Cátedra de Farmacognosia, Facultad de Farmacia y Bioquímica, Universidad de Buenos Aires, Junín 956, Ciudad Autónoma de Buenos Aires 1113, Argentina
Cecilia Beatriz Dobrecky
Cátedra de Farmacobotánica, Departamento de Farmacología, Facultad de Farmacia y Bioquímica, Universidad de Buenos Aires, Junín 956, Ciudad Autónoma de Buenos Aires 1113, Argentina
Sergio Adrián Teves
Cátedra de Microbiología, Facultad de Farmacia y Bioquímica, Universidad de Buenos Aires, Junín 956, Ciudad Autónoma de Buenos Aires 1113, Argentina
Ariana Posadaz
Facultad de Turismo y Urbanismo, Universidad Nacional de San Luis, Av. del Libertador s/n, Barranca Colorada, Villa de Merlo, San Luis 5881, Argentina
Melina Laguia Becher
Centro de Estudios Biomédicos, Básicos, Aplicados y Desarrollo (CEBBAD), Facultad de Ciencias de la Salud, Universidad Maimónides, Hidalgo 775, Ciudad Autónoma de Buenos Aires 1405, Argentina
Rafael Alejandro Ricco
Cátedra de Farmacobotánica, Departamento de Farmacología, Facultad de Farmacia y Bioquímica, Universidad de Buenos Aires, Junín 956, Ciudad Autónoma de Buenos Aires 1113, Argentina
Marcelo Luis Wagner
Cátedra de Farmacobotánica, Departamento de Farmacología, Facultad de Farmacia y Bioquímica, Universidad de Buenos Aires, Junín 956, Ciudad Autónoma de Buenos Aires 1113, Argentina
María Alejandra Álvarez
Centro de Estudios Biomédicos, Básicos, Aplicados y Desarrollo (CEBBAD), Facultad de Ciencias de la Salud, Universidad Maimónides, Hidalgo 775, Ciudad Autónoma de Buenos Aires 1405, Argentina
Ligaria cuneifolia (R. et P.) Tiegh. (Loranthaceae) is a South American hemiparasitic species with antioxidant, antitumoral, antimicrobial, and antilipidemic activities attributed to its polyphenolic content. We studied the polyphenolic pattern of L. cuneifolia during different phenological stages: flowering, fruiting, and post-fruiting. The highest total phenolic content was found in stems at post-fruiting (214 ± 12.1 mg gallic acid eq·g−1 DW) and fruiting (209 ± 13.7 mg gallic acid eq·g−1 DW), followed by post-fruiting leaves (207 ± 17.5 mg gallic acid eq·g−1 DW). Flavonoids accumulated at higher levels in leaves and hydroxycinnamic acids in leaves at flowering and post-fruiting. The polyphenolic pattern was similar between organs from wild plants and in vitro cultures, although at a significantly lower level in the latter ones. The performance of calli growing under a 16 h photoperiod in a modified White medium with 1-naphthalene acetic acid (2.50 μM) and Kinetin (9.20 μM) was better than in the dark. When calli grew in media only with auxins (IAA, NAA, and 2,4-D, all at 2.50 µM concentration), its growth and polyphenolic content improved. Cell suspensions with 2.50 µM NAA and 9.20 µM KIN grew slowly and produced very small amounts of polyphenols. As for the antioxidant activity, it was detected in all samples (approximately 1000 µmol trolox eq·g−1 DW) except fruits, where a lower value was found (328 µmol trolox eq·g−1 DW). In vitro cultures have the lowest antioxidant activity when compared to methanolic extracts from organs of wild specimens. Finally, antimutagenic or mutagenic activity in wild plants and in vitro culture extracts was not detected by the Ames test.