Micropropagation of Baccharis antioquensis (Asteraceae) and photoinduction of polyphenols by UV radiation / Micropropagación de Baccharis antioquensis (Asteraceae) y fotoinducción de polifenoles mediante radiación UV

Abstract Polyphenols are a large diversity of chemical types and interactions that can be responsible for a multiplicity of protective functions ranging from toxicity and light/UV shielding to signal transduction. Bacharis antioquensis has been described as a potential source of new photoprotective compounds with antioxidant capacity associated to polyphenols compounds. The aim of the present work was to develop a micropropagation protocol of B. antioquensis and evaluate the production of polyphenols by in vitro plants exposure to UVB radiation. Branches in juvenile stage of B. antioquensis were collected, desinfected and cultured on half strength Murashige and Skoog medium, supplemented or not with growth regulators (TDZ, BA or GA3) on light/darkness conditions and liquid/solid media. After UV treatments, the absorption coefficient in the UVA-UVB range, the antioxidant capacity and the total phenol content (TPC) from all tissue cultures and the wild tissue were evaluated. Growth regulators, light conditions and type of culture medium (solid or liquid) had a favorable effect on the response of explants. Treatments containing BA + GA3 regulators (2 and 0.5 mg/L respectively) and TDZ (0.5 mg/L) showed positive results in bud growth in liquid medium and darkness. Results showed that UVR exhibited promoting effects on the accumulation of polyphenols, enhancing the absorption coefficient in the UVA-UVB range, the antiradical capacity and the TPC of B. antioquensis in vitro plants. Rev. Biol. Trop. 66(2): 754-764. Epub 2018 June 01.

Resumen Los polifenoles son compuestos químicos con una diversidad de interacciones que pueden ser responsables de muchas funciones, que van desde la toxicidad hasta la protección y blindaje contra la luz/UV. Baccharis antioquensis es una fuente potencial de compuestos fotoprotectores con capacidad antioxidante. El objetivo del presente trabajo fue desarrollar un protocolo de micropropagación para B. antioquensis y evaluar la producción de polifenoles in vitro por exposición a la radiación UVB. Ramas juveniles fueron colectadas y cultivadas en medio de Murashige y Skoog (MS) y suplementadas o no con reguladores de crecimiento (TDZ, BA o GA3) en diferentes condiciones de luz/oscuridad y medios líquidos/sólidos. Después de los tratamientos UVR, se midió el espectro de absorción UV y se evaluó el coeficiente de absorción en la región UVA-UVB, la capacidad antioxidante y TPC tanto en las plantas in vitro como en las plantas silvestres. Los tratamientos que contenían reguladores BA + GA3 (2 y 0.5 mg / L respectivamente) y TDZ (0.5 mg / L) mostraron resultados positivos en el crecimiento del brote en medio líquido y en condiciones de oscuridad. Los resultados mostraron que la UVR tiene efectos promotores sobre la acumulación de metabolitos secundarios, aumentando el coeficiente de absorción en la región UVA-UVB, la capacidad antiradicalaria y TPC en las plantas in vitro.

Actividad tripanocida de Piper solmsianum C. DC. sobre formas epimastigota y tripomastigota de Trypanosoma cruzi / Trypanocidal activity of Piper solmsianum C. DC. against epimastigote and trypomastigote forms of Trypanosoma cruzi

Introducción: la infección por Trypanosoma cruzi, conocida como enfermedad de Chagas, es un problema importante de salud pública en países de América Central y Sudamérica.Objetivo: evaluar la actividad de extractos crudos de acetato de etilo de plantas in vitro de 6-8 meses y 10-12 meses de edad, de tallos leñosos y hojas de plantas silvestres maduras y el lignano tetrahidrofurano grandisina, aislados de Piper solmsianum, sobre las formas epimastigota y tripomastigota de T. cruzi in vitro.Métodos: en la evaluación del efecto de diversos extractos crudos de acetato de etilo y grandisina de P. solmsianum, sobre la viabilidad de las formas epimastigota y tripomastigota de T. cruzi, se utilizó el método MTT (3-(4,5-dimetiltiazol-2-il)-2,5-difeniltetrazolium bromuro).Resultados: en la forma epimastigota, el mejor resultado en la inhibición del crecimiento fue obtenido con 50 µg/mL de extracto de tallo y en la forma tripomastigota con 25 y 50 µg/mL de grandisina y plantas in vitro de 6-8 meses de edad, respectivamente. En todos los casos los valores de inhibición oscilaron entre 86 a 96 por ciento. Plantas in vitro de 6-8 meses de edad y grandisina fueron más activas sobre las formas epimastigota y tripomastigota de T. cruzi con valores de CI50 de 0,018 y 0,360 µg/mL, respectivamente.Conclusiones: se demuestra la actividad tripanocida de extractos de plantas silvestres y plantas in vitro de P. solmsianum(AU)

Introduction: the infection by Trypanosoma cruzi, known as Chagas' disease, poses a major public health problem in Central and South America countries.Objective: to evaluate the activity of crude ethyl acetate extracts from in vitro plants of 6-8 and 10-12 months of age, stem barks and mature wild plant leaves and tetrahydrofuran lignin grandisin isolated from Piper solmsianum against the epimastigote and trypomastigote forms of T. cruzi in vitro.Methods: in the evaluation of the effect of various crude ethyl acetate extracts and grandisin from P. solmsianum on the viability of epimastigote and trypomastigote forms of T. cruzi, the MTT method (3-(4,5-dimethylthiazol-2-il)-2,5-diphenyltetrazolium bromide) was used.Results: in the epimastigote form, the best results in growth inhibition was obtained with 50 µg/mL of stem extract, and in the trypomastigote form, with 25 and 50 µg/mL of grandisin and 6-8 months-old in vitro plants, respectively. The inhibition values in all cases ranged from 86 to 96 percent. 6-8 months old in vitro plants and grandisin were found to be active against the epimastigote and trypomastigote forms of T. cruzi with IC50 of 0.018 µg/mL and 0.360 µg/mL, respectively.Conclusions: the trypanocidal activity of extracts from wild plants and in vitro plants of P. solmsianum was proved(AU)

Micropropagation and production of camptothecin form in vitro plants of Ophiorrhiza mungos

Objective: To explore the biotechnological potential of Ophiorrhiza mungos for micropropagation and camptothecin (CPT) production from in vitro grown plants.Methods: Surface sterilized explants of O. mungos were transferred aseptically in MS media containing various combinations of phytohormones for callus initiation and multiple shoot proliferation. The content of CPT was quantified in the methanolic extract of O. mungos plants and in in vitro grown plants by using high performance liquid chromatography (HPLC). Results: Maximum fresh weight and dry weight biomass of O. mungos callus was obtained from MS medium supplemented with IAA (2 ppm)+ BAP (2 ppm) + GA (1 ppm). The maximum shoot proliferation (25) and elongation (6.5 cm) was found in MS medium supplemented with Picloram + Thidiazuron + Gibberellic Acid in 1:2:1 ratio after four weeks of incubation. The maximum content of CPT (0.0768 % w/w) was found in wholein vitro plants whereas the minimum CPT was observed in adventitious buds (0.0026 % w/w) as compared to the naturally grown O. mungos plants (0.0030% w/w).Conclusions: Present findings indicate that O. mungos plants respond favourably for in vitro propagation and also produce higher amount of CPT as compared to naturally grown plants.