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1.
Arch Physiol Biochem ; 124(5): 410-417, 2018 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-29260581

RESUMEN

This study investigated the influence of caffeic, ferulic, gallic and protocatechuic acids on high-fructose diet-induced metabolic syndrome in rats. Oral administration of the phenolic acids significantly reversed high-fructose diet-mediated increase in body mass index and blood glucose. Furthermore, phenolic acids restored high-fructose diet-mediated alterations in metabolic hormones (insulin, leptin and adiponectin). Similarly, elevated tumour necrosis factor-α, interleukin-6 and -8 were significantly lowered. Administration of phenolic acids restored High-fructose diet-mediated increase in the levels of lipid parameters and indices of atherosclerosis, cardiac and cardiovascular diseases. High-fructose diet-mediated decrease in activities of antioxidant enzymes (superoxide dismutase, catalase, glutathione peroxidase, glutathione reductase and glucose 6-phosphate dehydrogenase) and increase in oxidative stress biomarkers (reduced glutathione, lipid peroxidation products, protein oxidation and fragmented DNA) were significantly restored by the phenolic acids. The result of this study shows protective influence of caffeic acid, ferulic acid, gallic acid and protocatechuic acid in high-fructose diet-induced metabolic syndrome.


Asunto(s)
Antioxidantes/uso terapéutico , Suplementos Dietéticos , Dislipidemias/prevención & control , Hiperglucemia/prevención & control , Resistencia a la Insulina , Síndrome Metabólico/terapia , Estrés Oxidativo , Animales , Fármacos Antiobesidad/uso terapéutico , Biomarcadores/sangre , Ácidos Cafeicos/uso terapéutico , Ácidos Cumáricos/uso terapéutico , Citocinas/sangre , Dieta de Carga de Carbohidratos/efectos adversos , Fructosa/efectos adversos , Ácido Gálico/uso terapéutico , Humanos , Hidroxibenzoatos/uso terapéutico , Síndrome Metabólico/etiología , Síndrome Metabólico/inmunología , Síndrome Metabólico/metabolismo , Obesidad/prevención & control , Fenoles/uso terapéutico , Distribución Aleatoria , Ratas Wistar
2.
Pharm Biol ; 55(1): 1662-1670, 2017 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-28447517

RESUMEN

CONTEXT: Leaves of Phyllanthus muellarianus (Kuntze) Exell. (Euphorbiacea) are widely used in the management of liver disorders in Nigeria. However, no there is no scientific validation to support this use. OBJECTIVE: Hepatoprotective effect of Phyllanthus muellarianus aqueous leaf extract was investigated in acetaminophen-induced liver injury mice. MATERIALS AND METHODS: Hepatoprotective effect of Phyllanthus muellarianus aqueous leaf extract was evaluated in acetaminophen-induced hepatic damage in Swiss albino mice using biomarkers of hepatocellular indices, oxidative stress, proinflammatory factors and lipid peroxidation. Mice received distilled water, 100, 200, or 400 mg/kg b.w of Phyllanthus muellarianus aqueous leaf extract, respectively, for seven days. Treatment groups were challenged with 300 mg/kg b.w of acetaminophen on the sixth day. RESULTS: Oral administration of Phyllanthus muellarianus aqueous leaf extract significantly (p < 0.05) attenuates acetaminophen-mediated alterations in serum alkaline phosphatase, alanine aminotransferase, aspartate aminotransferase, albumin and total bilirubin by 76.56, 85.41, 89.39, 82.77 and 78.38%. Similarly, acetaminophen-mediated decrease in activities of superoxide dismutase, catalase, glutathione peroxidase, glutathione reductase and glucose 6-phosphate dehydrogenase were significantly attenuated in the liver of mice by 85.10, 80.81, 80.45, 76.23 and 95.22%, respectively. Increased levels of conjugated dienes, lipid hydroperoxides, malondialdehyde, protein carbonyl, fragmented DNA, tumor necrosis factor-α, interleukin-6 and -8 were significantly lowered by Phyllanthus muellarianus aqueous leaf extract. CONCLUSION: Overall, results of this study show that Phyllanthus muellarianus halted acetaminophen-mediated hepatotoxicity due to its capability to enhance antioxidant enzymes.


Asunto(s)
Enfermedad Hepática Inducida por Sustancias y Drogas/prevención & control , Inflamación/tratamiento farmacológico , Phyllanthus/química , Extractos Vegetales/farmacología , Acetaminofén/toxicidad , Administración Oral , Animales , Antioxidantes/metabolismo , Biomarcadores/metabolismo , Enfermedad Hepática Inducida por Sustancias y Drogas/etiología , Enfermedad Hepática Inducida por Sustancias y Drogas/fisiopatología , Relación Dosis-Respuesta a Droga , Inflamación/patología , Peroxidación de Lípido/efectos de los fármacos , Hígado/efectos de los fármacos , Hígado/patología , Ratones , Nigeria , Estrés Oxidativo/efectos de los fármacos , Extractos Vegetales/administración & dosificación , Hojas de la Planta
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