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      Effects of myricetin on glycemia and glycogen metabolism in diabetic rats.

      Life Sciences
      Animals, Blood Glucose, drug effects, Body Weight, Diabetes Mellitus, Experimental, blood, drug therapy, metabolism, Dose-Response Relationship, Drug, Eating, Flavonoids, pharmacology, Glucose-6-Phosphate, Glycogen, Glycogen Synthase, Hindlimb, Hyperglycemia, Hypertriglyceridemia, Hypoglycemic Agents, Liver, enzymology, Liver Glycogen, Male, Muscle, Skeletal, Phosphorylase a, Rats, Rats, Wistar

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          Abstract

          In our previous study, we found that myricetin, a naturally occurring bioflavonoid, was able to stimulate glucose transport in rat adipocytes and enhance insulin-stimulated lipogenesis. We report here that after 2 days of treatment with myricetin (3 mg/12 h), hyperglycemia in diabetic rats was reduced by 50% and the hypertriglyceridemia that is often associated with diabetes was normalised. Treatment with myricetin increased hepatic glycogen and glucose-6-phosphate content. It increased hepatic glycogen synthase I activity without having any effect on total glycogen synthase nor phosphorylase a activity. It lowered phosphorylase a activity in the muscle. Thus, the hypoglycemic effect of myricetin is likely to be due to its effect on glycogen metabolism. There was no indication of serious hepatotoxicity with myricetin treatment and therefore, myricetin could be of therapeutic potential in diabetes.

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