Carbendazim and Chlorpyrifos are some of the most widespread environmental contaminants of major concern to human and animal reproductive health. Acute toxicity test results for pesticides were evaluated by the Probit analysis method and 96 h LC50 values for C. chanos exposed to chlorpyrifos was 3.73 and 11.5 mg l-1 for carbendazim. Chlorpyrifos and carbendazim significantly decreased total protein, catalase, glutathione S-transferase and acetyl choline esterase and induced lipid peroxidation. Maximum effects of protein, catalase, lipid peroxidation, acetyl choline esterase and glutathione s-transferase were obtained in response to 23.68 mg l-1 of chlorpyrifos and 43.68 mg l-1 of carbendazim. Micronuclei assay results have shown increased abnormality with increasing doses of chlorpyrifos and carbendazim. Maximum increasing in micronuclei was observed in chlorpyrifos exposed C. chanos. This study showed that chlorpyrifos and carbendazim induced alterations in the activity of antioxidant enzymes and could induce clastogenicity.

Protection of biological systems against radiation damage is of paramount importance during accidental and unavoidable exposure to radiation. Several physico-chemical and biological factors collectively contribute to the damage caused by radiation and are, therefore, targets for developing radioprotectors. Chemicals capable of scavenging free radicals, relieving oxidative stress, promoting antioxidant activity and modulating immune response have been some of the radioprotectors extensively investigated with limited success. It has long been known that some of the most effective radioprotective agents are those which contain sulphydryl groups. 4-amino-5-mercapto-3-methyl-1, 2, 4-triazole (AMMT) is one of the well-known 1, 2, 4 triazole derivatives with functional sulphydryl group. The present study reports an evaluation of radical scavenging and radioprotective properties of sulphydryl group containing triazole derivative. The lethal dose of electron beam radiation (EBR) was studied by survival assay. The dose reduction factor (DRF) of AMMT was calculated using the ratio between LD50 of EBR with and without AMMT treatment. Radical scavenging property of AMMT was assessed by DPPH radical scavenging assay. The clastogenic effects of EBR were recorded by Micronucleus test in bone marrow cells and DNA fragmentation assay in mice hepatic cells. The survival assay results showed that the LD50 of EBR was 10 Gy. The calculated DRF for AMMT was found to be 1.2. DPPH radical scavenging assay showed a positive result when it was compared with the standard glutathione. Treatment of mice with 100 mg of AMMT for 15 days before irradiation significantly (P<0.05) reduced the frequency of micronucleus formation in bone marrow cells and also reduced the DNA fragmentation in hepatic cells. The results obtained in the present study indicated that AMMT has a protective effect against the EBR-induced mortality and clastogenicity.