Abstract
The insulin-like growth factor system is intimately involved in renal development, growth, function and the pathophysiology of several disease states. Exogenous IGF-I increases GFR and RPF, perhaps mediated by nitric oxide (NO). In chronic renal failure, IGF-I, the binding proteins and their fragments decrease bioavailability. After transplantation, the levels of bioactive IGF-I increase likely due to better nutrition and increased clearance of the binding proteins and their fragments. In the nephritic syndrome, a similar mechanism may be active, in that the binding proteins and their fragments may inhibit IGF-I action.
Original language | English (US) |
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Pages (from-to) | 5-9 |
Number of pages | 5 |
Journal | Nephron |
Volume | 89 |
Issue number | 1 |
DOIs | |
State | Published - 2001 |
Externally published | Yes |
Keywords
- Chronic renal failure
- IGF-I
- IGFBPs
- Nephritic syndrome
- Renal development
ASJC Scopus subject areas
- Physiology
- Nephrology
- Physiology (medical)
- Urology