Effect of metformin on glucagon-like peptide 1 (GLP-1) and leptin levels in obese nondiabetic subjects

被引:258
作者
Mannucci, E
Ognibene, A
Cremasco, F
Bardini, G
Mencucci, A
Pierazzuoli, E
Ciani, S
Messeri, G
Rotella, CM
机构
[1] Univ Florence, Dipartimento Fisiopatol Clin, Insegnamento Malattie Metab & Ricambio, Endocrinol Sect, I-50134 Florence, Italy
[2] Careggi Gen Hosp, Clin Chem Lab, Florence, Italy
关键词
D O I
10.2337/diacare.24.3.489
中图分类号
R5 [内科学];
学科分类号
1002 [临床医学]; 100201 [内科学];
摘要
OBJECTIVE - To evaluate the effects of metformin on glucagon-like peptide 1 (GLP-1) and leptin levels. RESEARCH DESIGN AND METHODS - A total of 10 obese nondiabetic male patients were studied before and after a. 14-day treatment with 2,550 mg/day metformin and were compared with 10 untreated obcsr control subjects. On days 0 and 15, leptin and GLP-1(7-36)amide/(7-37) levels were assessed before and after an oral glucose load during a euglycemic hyprrinsulinemic clamp to avoid the interference of variations of insulinemia and glycemia on GLP-1 and leptin secretion. The effects of metformin on GLP-(7-36)amide degradation in human plasma and in a buffer solution containing dipeptidyl peptidase IV (DPP-IV) were also studied. RESULTS - Leptin levels were not affected by the oral glucose load, and they were not modified after metformin tr treatment. Metformin induced a significant (P < 0.05) increase of GLP-1(7-36)amide/(7-37) at 30 and 60 min after the oral glucose load (63.8 +/- 29.0 vs. 50.3 +/- 15.6 pmol/l and 75.8 +/- 35.4 vs. 46.9 +/- 20.0 pmol/l, respectively), without affecting baseline GLP-1 levels. No variations of GLP-1 levels were observed in the control group. In pooled human plasma, metformin (0.1-0.5 <mu>g/ml) significantly inhibited degradation of GLP-1(7-36)amide after a 30-min incubation at 37 degreesC; similar results were obtained in a buffer solution containing DPP-IV. CONCLUSIONS - Metformin significantly increases GLP-1 levels after an oral glucose load in obese nondiabetic subjects; this effect could be due to an inhibition of GLP-1 degradation.
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收藏
页码:489 / 494
页数:6
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