SUBCUTANEOUS GLUCAGON-LIKE PEPTIDE-I IMPROVES POSTPRANDIAL GLYCEMIC CONTROL OVER A 3-WEEK PERIOD IN PATIENTS WITH EARLY-TYPE-2 DIABETES

1. Glucagon-like peptide-1 (7-36) amide (GLP-1) is released into the c irculation after meals and is the most potent physiological insulinotr opic hormone in man. GLP-1 has the advantages over other therapeutic a gents for Type 2 diabetes of also suppressing glucagon secretion and d elaying gastric emptying. One of the initial abnormalities of Type 2 d iabetes is the loss of the first-phase insulin response, leading to po stprandial hyperglycaemia. 2. To investigate the therapeutic potential of GLP-1 in Type 2 diabetes, six patients were entered into a 6-week, double-blind crossover trial during which each received 3 weeks treat ment with subcutaneous GLP-1 or saline, self-ad ministered th ree ti m es a day immediately before meals. A standard test meal was given at t he beginning and end of each treatment period. 3. GLP-1 reduced plasma glucose area under the curve (AUC) after the standard test meal by 58 % (AUC, 0-240 min : GLP-1 start of treatment, 196 +/- 141 mmol.min(-1) .l(-1); saline start of treatment, 469 +/- 124 mmol.min(-1).l(-1); F = 16.4, P < 0.05). The plasma insulin excursions were significantly hig her with GLP-1 compared with saline over the initial postprandial 30 m in, the time period during which the GLP-1 concentration was considera bly elevated. The plasma glucagon levels were significantly lower over the 240-min postprandial period with GLP-1 treatment. The beneficial effects of GLP-1 on plasma glucose, insulin and glucagon concentration s were fully maintained for the 3-week treatment period. 4. We have de monstrated a significant improvement in postprandial glycaemic control with subcutaneous GLP-1 treatment. GLP-1 improves glycaemic control p artially by restoring the first-phase insulin response and suppressing glucagon and is a potential treatment for Type 2 diabetes.