K. Namikawa et al., EFFECT OF THE LIPID PEROXIDE REACTION CAUSED BY REPEATED COLD STRESS ON CISPLATIN-INDUCED NEPHROTOXICITY, Biological trace element research, 63(3), 1998, pp. 213-220
The peroxide reaction in mouse kidney was examined in order to determi
ne the relationship between the lipid peroxide reaction caused by SART
(specific alternation of rhythm in temperature) stress and that cause
d by drug administration After exerting SART stress for one wk on 6-wk
-old male ddY mice (stress group), the peroxide reaction generated by
the administration of a single dose of cis-diamminedichloroplatinum (c
isplatin: CDDP, 10 mg/kg, ip) into SART-stressed mice (stress + CDDP g
roup) was compared with the reaction of CDDP-administered nonstressed
mice (CDDP group), saline-administered nonstressed mice (saline group)
, and saline-administered SART-stressed mice (stress + saline group).
Lipid peroxidation in the kidneys was significantly higher in the stre
ss group upon cessation of stress exertion than in the normal group. H
owever, no significant difference in the lipid peroxide level after ad
ministration of CDDP was observed between the CDDP groups. The renal g
lutathione levels were significantly different between the CDDP groups
and the saline administered groups. These results indicate that the p
eroxide reaction is generated in the kidneys by stress, but stress has
no effect on the peroxide damage caused by CDDP administration. Howev
er, the contribution of stress to renal function impairment requires f
urther evaluation.