ABSTRACT
The radioprotective effects of naturally occurring compounds have been investigated in vitro and in vivo considering their pharmacological role in prevention and treatment of cancer. Chitosan (CS) is a naturally occurring polymer that has been increasing attention in pharmaceutical and biomedical applications because of its biocompatibility, biodegradability, nontoxicity, cationic properties and bio adhesive characters. Lymphocytes were treated with different concentrations of chitosan for the period of 2 and 24 hr. Cell viability was determined by tryphan blue dye exclusion assay, single strand DNA damage by alkaline comet assay and in vitro cytogenetic damages were evaluated by micronucleus assays. Treatment of lymphocytes with chitosan before and after the exposure to 4Gy of electron beam radiation (EBR) resulted in the reduction of percentage of tail DNA in comet from 24.06±3.92 to 6.94±1.34 and olive tail moment (OTM) was reduced from 25.34±3.09 to 10.66±0.23 at 10μg/mL concentration. The micronucleus formation in radiation control group (13.75±0.37) was significantly reduced in chitosan pretreated groups 7.63±1.02. Cells treated with chitosan at 10μg/mL showed maximum viability after exposure to EBR. Present investigation data proves the protective effect of CS against EBR induced damage in lymphocyte. However, increase in concentration above 100 μg/mL though resulted in higher protection, an increased cell toxicity was also noticed.
ABSTRACT
Objectives: The aim of the study was to test the effect of whole body electron beam radiation on anxiety statein Swiss albino mice. Methods: Mice were irradiated with three different doses (2Gy,4Gy,6Gy)of electron beam radiations.After 24hours of radiation exposure animals were taken for testing level of anxiety using elevated plus maze and light dark arena apparatus. Results: Whole body electron beam irradiation at doses of 2, 4 and 6Gy lead to significant (p<0.001) anxiogenic activity in irradiated mice. Conclusions: Electron beam radiation has the potential to cause anxiety.
ABSTRACT
The aim of this study was to asses the DNA damage progression with days after single exposure of 6Gy electron beam radiation (EBR). Molecular DNA damage in lymphocytes of mice was assessed using alkaline comet assay and in bone marrow cells by micronucleus assay. In comet assay %DNA in tail, Comet length, Olive Tail Moment (OTM) served as a measure of DNA damage and in micronucleus test, frequency of micronucleus formation in bone marrow cells was measured to evaluate the DNA damage. The experiment was performed by taking 24 healthy Swiss albino mice with body weight 30+5g. The animals were grouped into four. Group1 served as control, Group 2, 3 and 4 were irradiated by 6Gy EBR. Animals of Group 2, 3 and 4 were sacrificed on 5th, 10th and 15th day post irradiation respectively. The comet assay procedure was carried out for all these groups by using lymphocytes separated from EDTA treated blood. The micronucleus test was performed in bone marrow cells (PCE-Poly chromatic erythrocytes, NCE-normochromatic erythrocytes). The slides prepared for this were scored for the measure of DNA damage. The results showed all comet parameter were significantly (P<0.05) affected by prolonging the post irradiation days from zero (control) to 5, 10 and 15. There was an alteration found in the PCE/PCE+NCE ratio in irradiated mice. A linear increase in the micronucleus formation was observed in post irradiated days. These results conclude a progression in DNA damage with days, post irradiation.
ABSTRACT
nges in standard square field.