Increased Glucose Sensitivity of Stimulus-Secretion Coupling in Islets From Psammomys obesus After Diet Induction of Diabetes
- Jose A.G. Pertusa1,
- Rafael Nesher2,
- Nurit Kaiser2,
- Erol Cerasi2,
- Jean-Claude Henquin1 and
- Jean-Christophe Jonas1
- 1Unit of Endocrinology and Metabolism, Faculty of Medicine, University of Louvain, Brussels, Belgium
- 2Endocrinology and Metabolism Service and the Hadassah Diabetes Center, the Hebrew University-Hadassah Medical Center, Jerusalem, Israel
Abstract
When fed a high-energy (HE) diet, diabetes-prone (DP) Psammomys obesus develop type 2 diabetes with altered glucose-stimulated insulin secretion (GSIS). β-Cell stimulus-secretion coupling was investigated in islets isolated from DP P. obesus fed a low-energy (LE) diet (DP-LE) and after 5 days on a HE diet (DP-HE). DP-LE islets cultured overnight in 5 mmol/l glucose displayed glucose dose-dependent increases in NAD(P)H, mitochondrial membrane potential, ATP/(ATP + ADP) ratio, cytosolic calcium concentration ([Ca2+]c), and insulin secretion. In comparison, DP-HE islets cultured overnight in 10 mmol/l glucose were 80% degranulated and displayed an increased sensitivity to glucose at the level of glucose metabolism, [Ca2+]c, and insulin secretion. These changes in DP-HE islets were only marginally reversed after culture in 5 mmol/l glucose and were not reproduced in DP-LE islets cultured overnight in 10 mmol/l glucose, except for the 75% degranulation. Diabetes-resistant P. obesus remain normoglycemic on HE diet. Their β-cell stimulus-secretion coupling was similar to that of DP-LE islets, irrespective of the type of diet. Thus, islets from diabetic P. obesus display an increased sensitivity to glucose at the level of glucose metabolism and a profound β-cell degranulation, both of which may affect their in vivo GSIS.
Footnotes
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Address correspondence and reprint requests to Jean-Christophe Jonas, Endocrinology and Metabolism, UCL 55.30, Avenue Hippocrate, 55 B-1200 Brussels, Belgium. E-mail: jonas{at}endo.ucl.ac.be.
Received for publication 21 December 2001 and accepted in revised form 15 May 2002.
[Ca2+]c, cytosolic calcium concentration; DP, diabetes prone; DR, diabetes resistant; GSIS, glucose-stimulated insulin secretion; HE, high energy; LE, low energy.
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