Ps. Heijmen et al., Cisplatin ototoxicity and the possibly protective effect of alpha-melanocyte stimulating hormone, HEARING RES, 128(1-2), 1999, pp. 27-39
It is known that adrenocorticotrophic hormone (ACTH)-derived peptides, the
so-called melanocortins, can reduce cisplatin-induced neurotoxicity. Recent
ly, our group has found that cisplatin-induced ototoxicity can also be redu
ced or prevented by treatment with the synthetic melanocortin-like peptide,
ORG 2766 (Hamers et al., 1994; De Groot et al., 1997). The present study w
as designed to investigate the possibly ameliorating effects of the physiol
ogically more relevant naturally occurring neuropeptide alpha-melanocyte st
imulating hormone (alpha-MSH) upon cisplatin ototoxicity and to compare its
protective effects to those of ORG 2766. For eight consecutive days guinea
pigs were treated with cisplatin at a concentration of either 1.5 mg/kg/da
y or 2 mg/kg/day. Animals were co-treated with either alpha-MSH (75 mu g/kg
/day), ORG 2766 (75 mu g/kg/day), or a sham injection containing physiologi
cal saline. Electrocochleography and hair cell counts were performed. Treat
ment with 1.5 mg/kg/day cisplatin resulted in a large variability of the mo
rphological and electrophysiological data, a variability that might have ma
sked possible effects of ORG 2766 and alpha-MSH. Treatment with 2 mg/kg/day
cisplatin caused less variable, severe reductions in the compound action p
otentials and cochlear microphonics combined with basal and middle-turn out
er hair cell loss in five out of six animals. However, in the alpha-MSH co-
treated groups, two out of six animals could be classified as normal, two a
nimals as moderately affected and two animals as severely affected. In the
ORG 2766 co-treated group we found three animals that were not affected and
three animals that were severely affected. We conclude that the protective
effects of alpha-MSH and ORG 2766 co-treatment are comparable and that alp
ha-MSH might be clinically useful in protecting against cisplatin-induced o
totoxicity. (C) 1999 Elsevier Science B.V. All rights reserved.