In many patients treated with cisplatin a peripheral sensory neuropathy dev
elops. This side-effect is considered dose-limiting, and therefore restrict
s the total dose of cisplatin that can be administered. Recent in vitro and
in vivo studies suggest that recombinant human Glial Growth Factor 2 (rhGG
F2) has neuroprotective effects. This prompted us to investigate in a vat m
odel whether rhGGF2 ameliorates cisplatin neuropathy. A total of 48 rats we
re randomly divided into four groups of 12 rats each. Three groups received
cisplatin and were treated with either 0.1 mg/kg rhGGF2, 0.3 mg/kg rhGGF2
or placebo. The fourth group (saline/placebo) sewed as age-matched controls
. In the cisplatin/placebo treated vats a neuropathy developed, as determin
ed by measurements of the nerve conduction velocity (NCV). Treatment with r
hGGF2 dose-dependently protected against the neuropathy. Histological exami
nation and morphometric analysis revealed that rhGGF2 also protects against
cisplatin-induced changes in the morphology and size of DRG satellite cell
nuclei. In a control study rhGGF2 did not affect normal NCV development. W
e conclude that rhGGF2 treatment is of benefit in the treatment of cisplati
n neuropathy in the vat. (C) 2000 Wiley-Liss, Inc.