Nephrol Dial Transplant (2003) 18: 1293-1298
© 2003 European Renal Association-European Dialysis and Transplant Association
Role of insulin and the IGF system in renal hypertrophy in diabetic Psammomys obesus (sand rat)
1 Diabetes Center and Department of Internal Medicine, Hadassah University Hospital, Jerusalem, Israel, 2 Institute of Experimental Clinical Research, Aarhus University Hospital, Aarhus C, Denmark and 3 Soroka University Hospital, Ben-Gurion University of the Negev, Beer Sheva, Israel
Background. Diabetic nephropathy is caused by multiple factors related to the altered metabolic environment in diabetes mellitus (DM). Experimental diabetic kidney disease is characterized by renal hypertrophy associated with increased tissue concentrations of insulin-like growth factor I (IGF-I). To assess the specific roles of serum insulin and glucose in mediating the development of diabetic nephropathy, the effects of both hyperinsulinaemic and hypoinsulinaemic DM were studied in Psammomys obesus (sand rat), a model of type 2 DM.
Methods. The IGF-I system was studied in normal Psammomys obesus gerbils and at 5, 15 and 70 days after the induction of either hyper- or hypoinsulinaemic DM. To induce hyperinsulinaemic DM, Psammomys were raised on a high-energy diet. Hypoinsulinaemic DM was induced by either administration of streptozotocin or a specially designed diet.
Results. Hyperinsulinaemic hyperglycaemic Psammomys did not exhibit renal hypertrophy (unchanged kidney/body-weight ratio) and renal IGF-I levels were in the normal range on days 5, 15 and 70. In contrast, Psammomys with hypoinsulinaemic hyperglycaemia induced either by streptozotocin injection or by pancreas exhaustion brought on by a long-term caloric excess diet, had significant increases in kidney/body-weight ratio which were associated with elevated renal IGF-I and mRNA and protein levels of kidney IGF binding protein I.
Conclusions. This study shows that serum insulin levels in the presence of hyperglycaemia have an important role in the development of experimental diabetic nephropathy in the Psammomys model. The implication of this finding is that the pathophysiological mechanisms for diabetic kidney disease in experimental models may be different for type 1 and type 2 DM.
Keywords: diabetic kidney disease; insulin; insulin-like growth factor binding proteins; insulin-like growth factor I; Psammomys obesus
Correspondence and offprint requests to: Mogher Khamaisi, MD, PhD, Diabetes Center and Department of Internal Medicine, Hadassah University Hospital, POB 12000, Jerusalem, Israel 91120. Email: murir{at}hadassah.org.il