INSULIN-LIKE GROWTH-FACTOR IMPROVES RENAL ARCHITECTURE OF FETAL KIDNEYS WITH COMPLETE URETERAL OBSTRUCTION

Citation
Gf. Steinhardt et al., INSULIN-LIKE GROWTH-FACTOR IMPROVES RENAL ARCHITECTURE OF FETAL KIDNEYS WITH COMPLETE URETERAL OBSTRUCTION, The Journal of urology, 154(2), 1995, pp. 690-693
Citations number
21
Categorie Soggetti
Urology & Nephrology
Journal title
ISSN journal
00225347
Volume
154
Issue
2
Year of publication
1995
Part
2
Pages
690 - 693
Database
ISI
SICI code
0022-5347(1995)154:2<690:IGIRAO>2.0.ZU;2-7
Abstract
Others have previously demonstrated that the administration of insulin -like growth factor-I accelerates recovery from ischemic acute tubular necrosis in the rat kidney. We investigated the effect of insulin-lik e growth factor-I on the histology of unilaterally obstructed kidneys in the pouch young of the North American opossum, Didelphis virginiana . In this model complete unilateral ureteral obstruction reliably indu ces statistically significant degrees of caliceal dilatation, tubular cystic change, and cortical and medullary fibrosis in kidneys examined 1 week after the creation of complete obstruction. Cortical and medul lary inflammation is also increased after 1 week of obstruction in thi s model but not to a degree that is statistically different than contr ol (sham operated) animals. We administered insulin-like growth factor -I to opossum pups with complete unilateral obstruction created at a l ength of 5 cm. (age 25 days, human equivalent 18 to 20 weeks). Insulin -like growth factor-I (400 mcg./kg.) was injected subcutaneously on th e day of operation and again on days 2 and 4 postoperatively. The anim als were sacrificed 1 week after obstruction and the formalin fixed, p araffin embedded kidneys were assessed histologically. In the obstruct ed kidney insulin-like growth factor-I ameliorated the development of fibrosis (cortical and medullary) and caliceal dilatation such that th ese characteristics did not differ significantly from those of sham op erated animals. Tubular cystic change in the obstructed kidneys was al so decreased by insulin-like growth factor-I administration but not to significant levels. Insulin-like growth factor-I treatment in obstruc ted animals resulted in significantly more inflammation (cortical and medullary) than in the sham operated animals. We also administered ins ulin-like growth factor-I to normal pups with no other intervention. T hese insulin-like growth factor-I treated pups did not differ from sha m pups for any characteristic studied. Our study suggests that there i s a protective effect of insulin-like growth factor-I on renal archite cture when administered in the setting of experimental fetal ureteral obstruction.