We studied the effect of the acute administration of gliclazide at 160 mg on insulin
release during hyperglycaemic clamps in 12 type 2 diabetes patients, age 50 ± 9.0
years, diabetes duration 5.5 ± 4.8 years, fasting blood glucose 9.6 ± 2.1 mmol/L (means
± SD). After a 210 min of hyperinsulinaemic euglycaemic clamp (blood glucose 4.6 ±
0.14 mmol/L), gliclazide or placebo (randomised, double-blind, cross-over) was administered;
60 minutes later, a hyperglycaemic clamp (4 hr) at 8 mmol/L was started. Plasma C-peptide
levels increased significantly after the administration of gliclazide (increment 0.17
± 0.15 vs. 0.04 ± 0.07 nmol/L, p = 0.024) before the clamp. After the start of the
hyperglycaemic clamp, the areas under the curve (AUC) for insulin and C-peptide did
not differ from 0 - 10 min (first phase) with gliclazide. However, second-phase insulin
release (30 - 240 min) was markedly enhanced by gliclazide. AUC plasma insulin (30
to 240 min) was statistically significantly higher after gliclazide (12.3 ± 13.9 vs.
- 0.56 ± 9.4 nmol/L × 210 min, p = 0.022); similarly, AUC plasma C-peptide (30 to
240 min) was also higher: 128 ± 62 vs. 63 ± 50 nmol/L × 210 min, p = 0.002). In conclusion,
in long-standing type 2 diabetes the acute administration of gliclazide significantly
enhances second phase insulin release at a moderately elevated blood glucose level.
In contrast to previous findings in mildly diabetic subjects, these 12 type 2 diabetes
patients who had an inconsiderable first phase insulin release on the placebo day,
only showed an insignificant increase in first phase with gliclazide.
Key words:
Gliclazide - Insulin Secretion - Type 2 Diabetes
References
- 1
Yki-Jarvinen H.
Pathogenesis of non-insulin-dependent diabetes mellitus.
Lancet.
1994;
343
91-95
- 2
Van Haeften T W, Boonstra E, Veneman T F, Gerich J E, Van der Veen E A.
Dose-response characteristics for glucose-stimulated insulin release in man and the
assessment of influence of glucose on arginine stimulated insulin release.
Metabolism.
1990;
39
1292-1299
- 3
Van Haeften T W, Van Maarschalkerweerd W WA, Gerich J E, Van der Veen E A.
Decreased insulin secretory capacity and normal pancreatic B-cell glucose sensitivity
in non-obese patients with NIDDM.
Eur J Clin Invest.
1991;
21
168-174
- 4
Wolffenbuttel B HR, Van Haeften T W.
Non-insulin-dependent diabetes mellitus: defects in insulin secretion.
Eur J Clin Invest.
1993;
23
69-79
- 5
Gerich J E.
Oral hypoglycemic agents.
N Engl J Med.
1989;
321
1231-1245
- 6
Groop L C.
Sulfonylureas in NIDDM.
Diabetes Care.
1992;
15
737-754
- 7
Wolffenbuttel B HR, Van Haeften T W.
Prevention of complications in non-insulin-dependent diabetes mellitus (NIDDM).
Drugs.
1995;
50
263-288
- 8
Van Haeften T W, Veneman T F, Gerich J E, Van der Veen E A.
Influence of gliclazide on glucose-stimulated insulin release in man.
Metabolism.
1991;
40
751-755
- 9
Hosker J P, Rudenski A S, Burnett M A, Matthews D R, Turner R C.
Similar reductions of first and second phase-cell responses at three different glucose
levels in type II diabetes and the effect of gliclazide therapy.
Metabolism.
1989;
38
767-772
- 10
Liu D, Moberg E, Kollind M, Lins P, Adamson U, Macdonald I A.
Arterial, arterialized venous, venous and capillary blood glucose measurements in
normal man during hyperinsulinaemic euglycemia and hypoglycemia.
Diabetologia.
1992;
35
287-290
- 11
Wahren J, Johansson B L.
Ernst-Friedich-Pfeiffer Memorial Lecture. New aspects of C-peptide physiology.
Horm Metab Res.
1998;
30
A2-A5
- 12
Metz S A, Halter J B, Robertson R P.
Paradoxical inhibition of insulin secretion by glucose in human diabetes mellitus.
J Clin Endocrinol Metab.
1979;
48
827-835
- 13
Nesher R, Cerasi E.
Biphasic insulin release as the expression of combined inhibitory and potentiating
effects of glucose.
Endocrinology.
1987;
121
1017-1024
- 14
Ligtenberg J JM, Sluiter W J, Reitsma W D, Van Haeften T W.
Effect of glibenclamide on insulin release at moderate and high blood glucose levels
in normal man.
Eur J Clin Invest.
1997;
27
685-689
- 15
Johnson A B, Argyraki M, Thow J C, Jones I R, Broughton D, Miller M, Taylor R.
The effect of sulphonylurea therapy on skeletal muscle glycogen synthase activity
and insulin secretion in newly presenting type 2 (non-insulin-dependent) diabetic
patients.
Diabetic Medicine.
1991;
8
243-253
- 16
Widstrom A, Cerasi E.
On the action of tolbutamide in normal man. Modulation of glucose-induced insulin
release by tolbutamide.
Acta Endocrinol.
1973;
72
519-531
- 17
Groop L C, Melander A, Groop P, Ratheiser K, Simonson D C, DeFronzo R A.
Different effects of glyburide and glipizide on insulin secretion and hepatic glucose
production in normal and NIDDM subjects.
Diabetes.
1987;
36
1320-1328
- 18
Hosker J P, Burnett M A, Davies E G, Harris E A, Turner R C.
Sulfonylurea therapy doubles B-cell response to glucose in type 2 diabetic patients.
Diabetologia.
1985;
28
809-814
- 19
Clark H E, Matthews D R.
The effect of glimepiride on pancreatic β cell function under hyperglycaemic clamp
and hyperinsulinaemic, euglycaemic clamp conditions in NIDDM.
Horm Metab Res.
1996;
28
445-450
- 20
Ashcroft F M.
Mechanisms of the glycaemic effects of sulfonylureas.
Horm Metab.
Res1996;
28
456-463
- 21
Eliasson L, Renstroom E, Ammala C, Berggren P O, Bertorello A M, Bokvist K, Chibalin A,
Deeney J T, Flatt P R, Gabel J, Gromada J, Larsson O, Lindstrom P, Rhodes C J, Rorsman P.
PKC-dependent stimulation of exocytosis by sulfonylureas in pancreatic ß cells.
Science.
1996;
276
813-815
J. J. M. LigtenbergM.D.
Dept. of Internal Medicine
Groningen University Hospital
P.O. Box 30.001
9700 RB Groningen
The Netherlands
Phone: Phone:+ 31 (59) 3616161
Fax: Fax:+ 31 (59) 3613216
Email: E-mail:j.j.m.ligtenberg@int.azg.nl