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J Med Food ; 15(5): 453-60, 2012 May.
Article in English | MEDLINE | ID: mdl-22439875

ABSTRACT

Chitosan is a natural product derived from chitin. To investigate the hypoglycemic and anti-obesity effects of chitosan, male Sprague-Dawley rats were divided into four groups: normal control, diabetic, and diabetic fed 5% or 7% chitosan. Diabetes was induced in rats by injecting streptozotocin/nicotinamide. After 10 weeks of feeding, the elevated plasma glucose, tumor necrosis factor-α, and interleukin-6 and lower adiponetin levels caused by diabetes were effectively reversed by chitosan treatment. In addition, 7% chitosan feeding also elevated plasma glucagon-like peptide-1 levels and lowered the insulin resistance index (homeostasis model assessment) in diabetic rats. Lower adipocyte granular intensities and higher lipolysis rates in adipose tissues were noted in the 7% chitosan group. Moreover, chitosan feeding reduced hepatic triglyceride and cholesterol contents and increased hepatic peroxisomal proliferator-activated receptor α expression in diabetic rats. Our results indicate that long-term administration of chitosan may reduce insulin resistance through suppression of lipid accumulation in liver and adipose tissues and amelioration of chronic inflammation in diabetic rats.


Subject(s)
Adiponectin/blood , Adipose Tissue/drug effects , Chitosan/therapeutic use , Diabetes Mellitus, Experimental/drug therapy , Insulin Resistance , Lipid Metabolism/drug effects , Liver/drug effects , Adipose Tissue/cytology , Adipose Tissue/metabolism , Animals , Biological Products/pharmacology , Biological Products/therapeutic use , Blood Glucose/metabolism , Chitosan/pharmacology , Cholesterol/metabolism , Diabetes Mellitus, Experimental/metabolism , Glucagon-Like Peptide 1/blood , Hypoglycemic Agents/pharmacology , Hypoglycemic Agents/therapeutic use , Inflammation/drug therapy , Inflammation/metabolism , Insulin/metabolism , Interleukin-6/blood , Liver/metabolism , Male , PPAR alpha/metabolism , Rats , Rats, Sprague-Dawley , Triglycerides/metabolism , Tumor Necrosis Factor-alpha/blood
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