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Effect of Glipizide on Insulin Secretion and Insulin Metabolism in Obese Type II Diabetic Patient

  1. Enzo Bonora, MD,
  2. Franco Pisani, MD,
  3. Rocco Micciolo, MD,
  4. Angela Corgnati, MD and
  5. Michele Muggeo, MD
  1. Department of Metabolic Diseases and Institute of Clinical Chemistry Trento, Italy
  2. University of Verona, Verona, and Institute of Statistics and Operation Research, University of Trento Trento, Italy
  1. Address correspondence and reprint requests to Dr. Enzo Bonora, Cattedra di Malattie del Metabolismo, Istituto di Patologia Medica, Policlinico di Borgo Roma, 1–37134 Verona, Italy.

Abstract

this study was designed to explore the short-term effect of glipizide on insulin secretion and metabolism. Plasma insulin and C-peptide levels in the fasting state and after a 100-g oral glucose load were measured in 17 obese newly diagnosed type II (non-insulin-dependent) diabetic subjects before and after 1 mo of treatment with glipizide (15 mg/day). Plasma glucose levels decreased significantly after treatment with glipizide. Plasma insulin and C-peptide concentrations in the fasting state did not change after glipizide treatment. Also, postglucose plasma insulin levels did not change after glipizide, whereas postglucose plasma C-peptide concentrations significantly increased. A significant relationship was found between the increase in C-peptide plasma levels and the decrease in glycemic profile after glucose load following glipizide treatment. The relation between plasma C-peptide and insulin incremental areas after the oral glucose load significantly increased after treatment. These results suggest that in obese type II diabetic patients, 1 mo of treatment with glipizide potentiates the (β-cell response to oral glucose load and increases insulin metabolism, probably within the liver.

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