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1.
Biomed Pharmacother ; 64(8): 534-40, 2010 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-19864106

RESUMEN

Obesity is widely recognized as cause of metabolic syndrome and cardiovascular disease. It is provoked by imbalance between the spending and consumption of energy associated with a chronic inflammatory condition due to excessive storage of fat tissue. Obese patients have an impaired inflammatory profile that contributes to the development of vascular complications, with fat tissue being partially responsible for controlling both processes: energy balance (through PPAR) and inflammatory condition (through inflammatory markers). White adipose tissue produces cytokines (IL-6, TNF-α, resistin, adiponectin, etc.) and participates in a broad spectrum of processes. Recently, glycine has been reported to have anti-inflammatory properties which reduce TNF-α and IL-6 levels and increase adiponectin in 3T3-L1 adipocytes and in fat tissue of obese mice. In this study, the possible regulatory role of glycine on some factors involved in storage and energy burning (PPAR-γ, PPAR-α, PPAR-δ and UCP-2) was analyzed in lean and monosodium glutamate-induced obese mice (MSG/Ob mice). Glycine clearly increased fat tissue PPAR-γ expression in lean but not in MSG/Ob mice. The PPAR-γ and PPAR-α liver expression was repressed in both groups of mice, while the expression of PPAR-δ decreased only in lean mice. Interestingly, glycine treatment also suppressed the expression of UCP-2, TNF-α and IL-6 in lean mice, and increased adiponectin and insulin serum levels. In conclusion, glycine regulates the production of inflammatory cytokines through PPAR-γ. These results provide clues on glycine signaling mechanisms as an anti-inflammatory agent that might be useful for treatment of metabolic and vascular complications associated to inflammation in obesity.


Asunto(s)
Antiinflamatorios/uso terapéutico , Citocinas/metabolismo , Metabolismo Energético/efectos de los fármacos , Glicina/uso terapéutico , Canales Iónicos/metabolismo , Proteínas Mitocondriales/metabolismo , Obesidad/prevención & control , Receptores Activados del Proliferador del Peroxisoma/metabolismo , Tejido Adiposo/efectos de los fármacos , Tejido Adiposo/inmunología , Tejido Adiposo/metabolismo , Animales , Antiinflamatorios/administración & dosificación , Antiinflamatorios/farmacología , Modelos Animales de Enfermedad , Glicina/administración & dosificación , Glicina/farmacología , Insulina/sangre , Interleucina-6/metabolismo , Leptina/sangre , Ratones , Obesidad/inmunología , Obesidad/metabolismo , Reacción en Cadena de la Polimerasa de Transcriptasa Inversa , Glutamato de Sodio , Factor de Necrosis Tumoral alfa/metabolismo , Proteína Desacopladora 2
2.
J Ethnopharmacol ; 82(2-3): 185-9, 2002 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-12241994

RESUMEN

Acute hypoglycemic effects of freeze-dried juice of Cucurbita ficifolia Bouché (Cucurbitaceae) fruits were studied in healthy and alloxan-diabetic mice. C. ficifolia fruit administered by intraperitoneal route produced, in a dose-dependent manner, a significant decrease of the glycemia in healthy mice. Although oral route of C. ficifolia fruit juice also caused significant reductions of blood glucose levels in healthy mice, the effect was minor. The juice administered by intraperitoneal route showed an acute hypoglycemic effect in alloxan-diabetic mice. In addition, daily oral administration of this preparation showed a highly significant reduction of the glycemia after 14 days of treatment. Freeze- dried juice caused acute toxicity when administered intraperitoneally, and also when it was administered daily by the oral route.


Asunto(s)
Cucurbitaceae , Diabetes Mellitus Experimental/tratamiento farmacológico , Hipoglucemiantes/administración & dosificación , Administración Oral , Animales , Glucemia/efectos de los fármacos , Glucemia/metabolismo , Cucurbita , Diabetes Mellitus Experimental/sangre , Relación Dosis-Respuesta a Droga , Evaluación Preclínica de Medicamentos/métodos , Frutas , Hipoglucemiantes/aislamiento & purificación , Inyecciones Intraperitoneales , Masculino , Ratones , Fitoterapia/métodos , Ratas , Ratas Wistar
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