S. Kojima et al., Mechanisms involved in the elevation of glutathione in RAW 264.7 cells exposed to low doses of gamma-rays, ANTICANC R, 20(3A), 2000, pp. 1589-1594
We examined the mechanisms of the elevation of glutathione level induced in
macrophage-like RAW 264.7 cells by low closes of gamma-rays. The level inc
reased soon after exposure of the cells to 50 cGy of gamma-rays, peaked bet
ween 3 hours and 6 hours and rearmed almost to the time 0 value by 24 hours
post-irradiation. Doses between 25 and 100 cGy significantly increased the
glutathione level at 4 hours post-irradiation. However there was no signif
icant elevation at doses of more than 100 cGy or less than 25 cGy. When the
effect of dose I-ate was examined at a constant absorbed dose of 50 cGy, d
ose rates Of more than 50 cGy/minute significantly increased the GSH level
at 4 hours post-irradiation. It was also shown that the elevation of glutat
hione level in cells irradiated with low doses of gamma-rays followed the i
nduction of mRNA coding for gamma-glutamylcysteine synthetase (gamma-GCS) a
rate-limiting enzyme of the de novo glutathione synthesis pathway When the
cells were exposed to the radiation in the presence of genistein, calphost
in C or nifedipine, the elevations of glutathione and gamma-GCS mRNA expres
sion were both mostly blocked. EGTA also strongly inhibited these elevation
s. These results suggest that the tyrosine kinase, calcium channel and prot
ein kinase C activities play an essential role in the law-dose-radiation-in
duced elevation of cellular glutathione.