Mechanisms involved in the elevation of glutathione in RAW 264.7 cells exposed to low doses of gamma-rays

Citation
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
Citations number
35
Categorie Soggetti
Onconogenesis & Cancer Research
Journal title
ANTICANCER RESEARCH
ISSN journal
02507005 → ACNP
Volume
20
Issue
3A
Year of publication
2000
Pages
1589 - 1594
Database
ISI
SICI code
0250-7005(200005/06)20:3A<1589:MIITEO>2.0.ZU;2-L
Abstract
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.