PROTECTION AGAINST RADIATION-INDUCED CHROMOSOME-DAMAGE IN MOUSE BONE-MARROW BY OCIMUM-SANCTUM

Citation
A. Ganasoundari et al., PROTECTION AGAINST RADIATION-INDUCED CHROMOSOME-DAMAGE IN MOUSE BONE-MARROW BY OCIMUM-SANCTUM, Mutation research, 373(2), 1997, pp. 271-276
Citations number
16
Categorie Soggetti
Genetics & Heredity",Biology,"Biothechnology & Applied Migrobiology
Journal title
ISSN journal
00275107
Volume
373
Issue
2
Year of publication
1997
Pages
271 - 276
Database
ISI
SICI code
0027-5107(1997)373:2<271:PARCIM>2.0.ZU;2-K
Abstract
The radioprotective effect of the leaf extract of Ocimum sanctum (Ocim um extract, OE) was investigated by taking chromosome aberrations as t he end point. Adult Swiss mice were whole-body exposed to 1-6 Gy of ga mma radiation with/without pretreatment with 10 mg/kg b.wt. of OE intr aperitoneally for 5 consecutive days. Radiation was given 30 min after the last injection. Metaphase plates were prepared from femur marrow on days 1, 2, 7 and 14 post-treatment and the frequency of aberrant ce lls and individual aberrations were scored. OE alone did not have any significant effect on the chromosomes. Maximum percent of aberrant cel ls was observed at 24 h in all the exposed groups. The percent aberran t cells showed a linear quadratic increase with radiation dose, in bot h radiation alone (RT) and OE + RT-treated groups. Exchange (dicentric s and rings) and multiple (pulverized and severely damaged cells) aber rations also showed a similar response. However, the slopes of OE + RT was significantly shallower than RT groups (p < 0.05). A dose-modifyi ng factor of 2.63 was obtained taking percent aberrant cells for 2 Gy as the base. Progressive decline in the percent aberrant cells as well as the number of aberrations with time after irradiation was observed in both RT and OE + RT groups. OE treatment resulted in a faster reco very compared to RT alone group. At doses below 3 Gy, OE pretreatment almost completely eliminated the exchange aberrations from the cell po pulation by day 2. Studies on a chemical system demonstrated that OE s ignificantly reduced the generation of hydroxyl radical; a lower dose of OE (1 mg/ml) was more effective than 5 mg/ml and this effect was mo re pronounced than that produced by DMSO. These results show that OE a ffords in vivo protection against radiation-induced cytogenetic damage . Free radical scavenging is a likely mechanism of OE protection.