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1.
Nutrients ; 13(6)2021 Jun 06.
Artículo en Inglés | MEDLINE | ID: mdl-34204042

RESUMEN

A randomized, double-blind, placebo-controlled study was conducted with the primary objective of assessing the effect of a natural extract of Sclerocarya birrea on glucose metabolism in subjects with prediabetes. The duration of the study was 90 days. Thirty-three subjects assigned to the experimental group (daily ingestion of 100 mg of the nutraceutical product) and 34 assigned to the placebo group completed the study. There were 36 men and 31 women with a mean age of 32.3 ± 14.1 years. In the area under the curve (AUC) of the oral glucose tolerance test (OGTT), statistically significant decreases in the experimental group at 40 and 90 days as compared with baseline were found, whereas significant changes in the placebo group were not observed. Within-group differences were statistically significant in favor of the experimental group for glucose peak at OGTT, serum insulin, insulin resistance markers, and flow-mediated dilation. Changes in lipid and anthropometric parameters were not observed, although there was a trend for lower cholesterol levels and a decrease in body weight in the experimental group. Decreases in systolic blood pressure were also higher among subjects in the experimental group. This exploratory study confirms the antidiabetic activity of Sclerocarya birrea in prediabetes. Further studies using better measurements of beta-cell function are needed to clarify the underlying mechanisms of the hypoglycemic effect of this natural compound.


Asunto(s)
Anacardiaceae , Suplementos Dietéticos , Hipoglucemiantes/administración & dosificación , Extractos Vegetales/administración & dosificación , Estado Prediabético/terapia , Adulto , Área Bajo la Curva , Biomarcadores/sangre , Glucemia/efectos de los fármacos , Presión Sanguínea/efectos de los fármacos , Peso Corporal/efectos de los fármacos , Colesterol/sangre , Método Doble Ciego , Femenino , Prueba de Tolerancia a la Glucosa , Control Glucémico/métodos , Humanos , Insulina/sangre , Resistencia a la Insulina , Masculino , Persona de Mediana Edad , Estado Prediabético/sangre
2.
Nutrients ; 12(5)2020 May 19.
Artículo en Inglés | MEDLINE | ID: mdl-32438719

RESUMEN

A single-center, randomized, double-blind controlled trial was conducted to assess the efficacy of a food supplement based on a combination of grapefruit, bitter orange, and olive extracts administered for eight weeks (n = 51) versus placebo (n = 45) on reduction of cardiovascular risk in healthy volunteers. Study variables included flow-mediated vasodilation (FMD), blood pressure (BP), lipid profile, thrombotic status, oxidative stress biomarkers, inflammation-related biomarkers, anthropometric variables, quality of life, and physical activity. The per-protocol data set was analyzed. In the active product group, there were statistically significant within-group differences at eight weeks as compared with baseline in FMD, systolic and diastolic BP, total cholesterol, LDL-C, LDL-oxidase, oxidized/reduced glutathione ratio, protein carbonyl, and IL-6. Significant between-group differences in these variables were also found. Significant changes in anthropometric variables and quality of life were not observed in the study groups. Changes in the level of physical activity were not recorded. Treatment with the active product was well tolerated. All these findings, taken together, support a beneficial effect of supplementation with a mixture of grapefruit, bitter orange fruits, and olive leaf extracts on underlying mechanisms that may interact each other to decrease the cardiovascular risk in healthy people.


Asunto(s)
Enfermedades Cardiovasculares/prevención & control , Citrus/química , Suplementos Dietéticos , Flavanonas/administración & dosificación , Flavonas/administración & dosificación , Olea/química , Polifenoles/administración & dosificación , Adulto , Antropometría , Presión Sanguínea/efectos de los fármacos , Citrus paradisi , Método Doble Ciego , Endotelio Vascular/efectos de los fármacos , Ejercicio Físico , Femenino , Voluntarios Sanos , Factores de Riesgo de Enfermedad Cardiaca , Humanos , Mediadores de Inflamación/sangre , Lípidos/sangre , Masculino , Persona de Mediana Edad , Estrés Oxidativo/efectos de los fármacos , Calidad de Vida , Vasodilatación/efectos de los fármacos
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