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
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.