Ameliorative effect of myricetin on insulin resistance in mice fed a high-fat, high-sucrose diet
Nutrition Research and Practice
;
: 544-549, 2014.
Artículo
en Inglés
| WPRIM
| ID: wpr-51346
ABSTRACT
BACKGROUND/OBJECTIVES:
Obesity-associated insulin resistance is a strong risk factor for type 2 diabetes mellitus. The aim of this study was to investigate the effect of myricetin on adiposity, insulin resistance, and inflammatory markers in mice with diet-induced insulin resistance. MATERIALS/METHODS:
Five-week-old male C57BL/6J mice were fed a basal diet, a high-fat, high-sucrose (HFHS) diet, or the HFHS diet containing 0.06% myricetin or 0.12% myricetin for 12 weeks after a 1-week adaptation, and body weight and food intake were monitored. After sacrifice, serum lipid profiles, glucose, insulin, adipocyte-derived hormones, and proinflammatory cytokines were measured. The homeostasis model assessment for insulin resistance (HOMA-IR) was determined.RESULTS:
Myricetin given at 0.12% of the total diet significantly reduced body weight, weight gain, and epidydimal white adipose tissue weight, and improved hypertriglyceridemia and hypercholesterolemia without a significant influence on food intake in mice fed the HFHS diet. Serum glucose and insulin levels, as well as HOMA-IR values, decreased significantly by 0.12% myricetin supplementation in mice fed the HFHS diet. Myricetin given at 0.12% of the total diet significantly reduced serum levels of leptin, tumor necrosis factor-alpha (TNF-alpha) and interleukin-6 (IL-6) in mice fed the HFHS diet.CONCLUSIONS:
These findings suggest that myricetin may have a protective effect against diet-induced obesity and insulin resistance in mice fed HFHS diet, and that alleviation of insulin resistance could partly occur by improving obesity and reducing serum proinflammatory cytokine levels.
Texto completo:
Disponible
Índice:
WPRIM (Pacífico Occidental)
Asunto principal:
Glucemia
/
Peso Corporal
/
Resistencia a la Insulina
/
Hipertrigliceridemia
/
Aumento de Peso
/
Factores de Riesgo
/
Citocinas
/
Interleucina-6
/
Factor de Necrosis Tumoral alfa
/
Leptina
Tipo de estudio:
Estudio de etiología
/
Estudio pronóstico
/
Factores de riesgo
Límite:
Animales
/
Humanos
/
Masculino
Idioma:
Inglés
Revista:
Nutrition Research and Practice
Año:
2014
Tipo del documento:
Artículo
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