RESUMEN
Quinoa has acquired a great interest due to its high content of nutrients and biomolecules that have nutritional and medicinal properties. The aim of this study was to compare the total phenolic content (TPC), total flavonoids (TF), and the antioxidant capacity of 20 varieties of seeds and sprouts of quinoa extract. Quinoa seeds were germinated for 72 h and dried in an oven at 45 °C. The extracts were obtained by dynamic extraction using methanol. Phytochemical analysis with liquid chromatography coupled with mass spectrometry (LC-ESI-MS/MS), TPC, TF, and the antioxidant capacity was carried out and compared between both extracts. The TPC was determined with Folin-Ciocalteu reagent, TF with AlCl3, and the antioxidant capacity was determined according to the DPPH and ABTS assays. Sprout extracts showed high values of TPC (31.28 ± 0.42 mg GAE/g; Pasankalla variety), TF (14.31 ± 0.50 mg EQ/g; black Coito variety), and antioxidant capacity (IC50 (DPPH): 12.69 ± 0.29 µg/mL and IC50 (ABTS): 3.51 ± 0.04 µg/mL; Pasankalla). The extracts of the Pasankalla variety revealed 93 and 90 phytochemical constituents in the seeds and sprouts, respectively, such as amino acids, phenolic acids, flavonoids, fatty acids, and triterpene saponins, among others. Quinoa sprouts showed a high content of TPC and TF, and high antioxidant capacity compared with seed extracts, especially the Pasankalla variety.
RESUMEN
Jatropha macrantha Müll Arg. L is also known as "huanarpo macho" and used in the Peruvian traditional medicine as an aphrodisiac and erectile dysfunction (ED). The aim of this study was to determine the phytochemical constituents in leaves and stems ethyl acetate fraction (LEAF and SEAF) of J. macrantha and to compare the antioxidant activity and the ameliorative effect on ketamine-induced erectile dysfunction in rats. The phytochemical constituents were determined by LC-ESI-MS/MS, the total phenolic compounds and total flavonoids (TPC and TF) by Folin-Ciocalteu and aluminum chloride, respectively. The antioxidant activity was determined by DPPH, ABTS, and FRAP assays. Experimental groups were divided as follows: I: negative control; II: positive control (ketamine at 50 mg/ kg/d); III: sildenafil 5 mg/kg; IV, V, VI: LEAF at 25, 50 and 100 mg/kg, respectively, and VII, VIII, IX: SEAF at 25, 50, and 100 mg/kg, respectively. The phytochemical analysis revealed the presence mainly of coumarins, flavonoids, phenolic acids, and terpenes. TPC of LEAF and SEAF were 359 ± 5.21 mg GAE/g and 306 ± 1.93 mg GAE/g, respectively; TF in LEAF and SEAF were 23.7 ± 0.80 mg EQ/g, and 101 ± 1.42 mg EQ/g, respectively. The DPPH, ABTS, FRAP in SEAF were 647 ± 3.27; 668 ± 2.30; and 575 ± 2.86 µmol TE/g, respectively, whilst LEAF showed 796 ± 3.15; 679 ± 0.85; and 806 ± 3.42 µmol TE/g, respectively. Regarding sexual behavior, LEAF showed a better effect in mount frequency, intromission frequency, ejaculation frequency, mount latency, intromission latency, ejaculatory latency, and post ejaculatory latency than SEAF. As conclusion, LEAF of J. macrantha at 50 mg/kg showed a better effect on sexual behavior in male rats with erectile dysfunction than SEAF but not higher than sildenafil.
Asunto(s)
Disfunción Eréctil , Jatropha/química , Ketamina/efectos adversos , Fitoquímicos , Extractos Vegetales , Hojas de la Planta/química , Tallos de la Planta/química , Acetatos/química , Animales , Cromatografía Liquida , Disfunción Eréctil/inducido químicamente , Disfunción Eréctil/tratamiento farmacológico , Femenino , Ketamina/farmacología , Masculino , Espectrometría de Masas , Fitoquímicos/química , Fitoquímicos/farmacología , Extractos Vegetales/química , Extractos Vegetales/farmacología , Ratas , Ratas Sprague-DawleyRESUMEN
Objetivos: Evaluar el efecto neuroprotector del extracto hidroalcohólico de hojas de Satureja brevicalyx wayra muña en ratas sometidas a hiperoxia, y su progenie sometidas a hipoxia isquemia. Diseño: Experimental. Lugar: Área de Cirugía Experimental, Instituto Nacional de Salud del Niño, y Laboratorios del Centro de Investigación de Bioquímica y Nutrición, Facultad de Medicina, Universidad Nacional Mayor de San Marcos, Lima, Perú. Material biológico: Rattus novegicus de la cepa Holtzman, hojas secas de Satureja brevicalyx wayra muña. Intervenciones: Tratamiento con el extracto en dos modelos: hiperoxia en ratas hembras adultas, e hipoxia en la progenie de ratas madre tratadas. Se realiza ANOVA y prueba de Tukey. Principales medidas de resultados: Actividad de superóxido dismutasa (SOD), niveles de glutatión (GSH) total y niveles de sustancias reactivas al ácido tiobarbitúrico (TBARS). Resultados: En las ratas tratadas con el extracto se observó disminución significativa de TBARS y participación de GSH y SOD. Conclusiones: Nuestros resultados sugieren que el extracto hidroalcólico de Satureja brevicalyx ejerce efecto neuroprotector en condición de hiperoxia e hipoxia experimental, mediante la mitigación de la lipoperoxidación como parámetro de daño oxidativo, con participación del GSH y la actividad de SOD como mecanismos de defensa antioxidante.
Objectives: To determine Satureja brevicalyx wayra muna leaves hydroalcoholic extract neuroprotective effect in rats subjected to hyperoxia and its progeny to hypoxia ischemia. Design: Experimental. Setting: Department of Experimental Surgery, National Institute of Child Health, and Biochemistry and Nutrition Research Center Laboratory, Faculty of Medicine, Universidad Nacional Mayor de San Marcos, Lima, Peru. Biological material: Rattus novegicus Holtzman strain, Satureja brevicalyx wayra muna dry leaves. Interventions: Treatment with the extract had two models: hyperoxia in adult female rats and hypoxia in the offspring of rats treated. Both ANOVA and Tukey test were performed. Main outcome measures: Superoxide dismutase (SOD) activity, total glutathione (GSH) and thiobarbituric acid reactive substances (TBARS) levels. Results: Rats treated with the extract showed significant decrease in TBARS and participation of GSH and SOD. Conclusions: Our results suggest that Satureja brevicalyx hydroalcoholic extract exerts neuroprotective effect in hyperoxia and hypoxia conditions by alleviating experimental lipid peroxidation, an oxidative damage parameter, with participation of GSH and SOD activity as antioxidant defense mechanisms.