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Pravastatin, simvastatin, and atorvastatin did not improve OGTT-induced blood glucose or plasma insulin changes in diabetic Goto-Kakizaki rats.
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Demonstrates that statin therapy fails to improve glucose intolerance or insulin response in diabetic rats, indicating no glycemic benefit.
We examined whether 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) reductase inhibitors (statins) improve glucose intolerance in spontaneously diabetic Goto-Kakizaki (GK) rats or not. The fasting blood glucose, plasma insulin, and serum cholesterol levels were significantly higher in GK rats than those in age-matched Wistar rats. All rats were given orally once a day 0.5% carboxymethylcellulose, pravastatin 8 mg/kg, simvastatin 8 mg/kg, or atorvastatin 8 mg/kg. An oral glucose tolerance test (OGTT) was performed before and 3, 6 and 12 weeks after statin treatments. The hyperglycemic response to OGTT in GK rats significantly exceeded that in Wistar rats. The plasma insulin level in GK rats increased with age until 14-week-old (treated for 6 weeks), and then decreased. Glucose intake significantly increased the plasma insulin in almost all rats. The increment of plasma insulin due to OGTT in GK rats appeared to be less than that in Wistar rats, because the basal level was already high in GK rats. Pravastatin, simvastatin, and atorvastatin did not modify changes in blood glucose and plasma insulin induced by glucose intake. In conclusion, long-term treatments of GK rats with statins did not improve glucose intolerance observed during OGTT.
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Satoh et al. (2005) studied Glucose intolerance in spontaneous diabetes (Goto-Kakizaki rats). Pravastatin, simvastatin, or atorvastatin vs. 0.5% carboxymethylcellulose was evaluated on Changes in blood glucose and plasma insulin during oral glucose tolerance test (OGTT). Pravastatin, simvastatin, and atorvastatin did not improve OGTT-induced blood glucose or plasma insulin changes in diabetic Goto-Kakizaki rats.
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