Diabetic neuropathy is a common and disabling complication of diabetes
mellitus whose pathogenesis remains unknown. Insulin-like growth fact
ors (IGFs) have been recently implicated in the development and mainte
nance of the peripheral nervous system, and circulating IGF levels are
decreased in experimental and clinical diabetes. Therefore, we tested
the hypothesis that IGF gene expression is reduced in peripheral nerv
es early after the onset of diabetes. Sciatic nerves from nondiabetic
and streptozotocin-treated rats were removed 5-7 days after the induct
ion of diabetes. RNA was isolated and analyzed by Northern and slot bl
ots. IGF-I mRNA content was significantly decreased per milligram wet
weight nerve (P < 0.025) as well as per poly(A)(+) RNA (P < 0.01) in d
iabetic vs nondiabetic nerves. Likewise, the amount of IGF-II mRNA was
significantly decreased per milligram wet weight nerve (P < 0.01) as
well as per poly(A)(+) RNA (P < 0.005). These effects were selective b
ecause histone 3.3 mRNA content, as well as poly(A)(+) mRNA content, p
er milligram nerve were unchanged. Insulin treatment partially prevent
ed this decline in IGF-I and IGF-II mRNA levels. The diminished IGF mR
NA content is one of the earliest biochemical abnormalities to be obse
rved in the diabetic nerve, supporting the hypothesis that a reduction
in IGF activity in diabetic nerves precedes and contributes to the de
velopment of neuropathy, (C) 1994 Academic Press, Inc.