2008Journal of environmental healthRequires access

Antagonism of Glutathione to Antioxidative Capacity Decrease Induced by Manganese Exposure in Rats

Qianxing Wang

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Abstract

Objective To study the antagonism of glutathione(GSH) to antioxidative capacity decrease induced by manganese exposure in rats.Methods 48 healthy male SD rats were randomly divided into six groups: the blank control,GSH control,MnCl2.4H2O(15 mg/kgand 30 mg/kg),15 mg/kgMnCl2.4H2O+1 mmol/kgGSH and 30 mg/kg MnCl2.4H2O+1 mmol/kg GSH,the treatment was conducted through peritoneal injection.The activity of superoxide dismutase(SOD),catalase(CAT) and glutathione peroxidase(GSH-Px)in the serumand the testis were determined bycolorimetric analysis.Results Compared with the blank control group,the activity of SOD,CAT and GSH-Px in the serum and testis in 30 mg/kg groups significantly decreased(P 0.01).The activity of SOD and CAT in the serum and testis in 30 mg/kg+GSH group decreased significantly(P0.01).Compared with the single manganese treated groups,all antioxidase activities in the serum and testis in 15 mg/kg+ GSH group increased significantly(P0.01).All antioxidase activities in the serum increased significantly(P0.01) and SOD and GSH-Px in the testis increased significantly(P0.01)in 30 mg/kg+GSH group.Pathological examination showed the different degree of denaturation in seminiferous tubule and the decrease of spermatogenic epithelium and spermiogenesis in 15 mg/kg and 30 mg/kg groups.The testicular lesions returned to the normal level in histopathology in 15 mg/kg+GSH group.It was shown that the seminiferous tubule was denatured and the spermiogenesis decreased in 30 mg/kg+GSH group.Conclusion GSH can antagonize antioxidative capacitydecrease induced bymanganese exposure in rats.

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Objective To study the antagonism of glutathione(GSH) to antioxidative capacity decrease induced by manganese exposure in rats.Methods 48 healthy male SD rats were randomly divided into six groups: the blank control,GSH control,MnCl2.4H2O(15 mg/kgand 30 mg/kg),15 mg/kgMnCl2.4H2O+1 mmol/kgGSH and 30 mg/kg MnCl2.4H2O+1 mmol/kg GSH,the treatment was conducted through peritoneal injection.The activity of superoxide dismutase(SOD),catalase(CAT) and glutathione peroxidase(GSH-Px)in the serumand the testis were determined bycolorimetric analysis.Results Compared with the blank control group,the activity of SOD,CAT and GSH-Px in the serum and testis in 30 mg/kg groups significantly decreased(P 0.01).The activity of SOD and CAT in the serum and testis in 30 mg/kg+GSH group decreased significantly(P0.01).Compared with the single manganese treated groups,all antioxidase activities in the serum and testis in 15 mg/kg+ GSH group increased significantly(P0.01).All antioxidase activities in the serum increased significantly(P0.01) and SOD and GSH-Px in the testis increased significantly(P0.01)in 30 mg/kg+GSH group.Pathological examination showed the different degree of denaturation in seminiferous tubule and the decrease of spermatogenic epithelium and spermiogenesis in 15 mg/kg and 30 mg/kg groups.The testicular lesions returned to the normal level in histopathology in 15 mg/kg+GSH group.It was shown that the seminiferous tubule was denatured and the spermiogenesis decreased in 30 mg/kg+GSH group.Conclusion GSH can antagonize antioxidative capacitydecrease induced bymanganese exposure in rats.

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Available abstract

Objective To study the antagonism of glutathione(GSH) to antioxidative capacity decrease induced by manganese exposure in rats.Methods 48 healthy male SD rats were randomly divided into six groups: the blank control,GSH control,MnCl2.4H2O(15 mg/kgand 30 mg/kg),15 mg/kgMnCl2.4H2O+1 mmol/kgGSH and 30 mg/kg MnCl2.4H2O+1 mmol/kg GSH,the treatment was conducted through peritoneal injection.The activity of superoxide dismutase(SOD),catalase(CAT) and glutathione peroxidase(GSH-Px)in the serumand the testis were determined bycolorimetric analysis.Results Compared with the blank control group,the activity of SOD,CAT and GSH-Px in the serum and testis in 30 mg/kg groups significantly decreased(P 0.01).The activity of SOD and CAT in the serum and testis in 30 mg/kg+GSH group decreased significantly(P0.01).Compared with the single manganese treated groups,all antioxidase activities in the serum and testis in 15 mg/kg+ GSH group increased significantly(P0.01).All antioxidase activities in the serum increased significantly(P0.01) and SOD and GSH-Px in the testis increased significantly(P0.01)in 30 mg/kg+GSH group.Pathological examination showed the different degree of denaturation in seminiferous tubule and the decrease of spermatogenic epithelium and spermiogenesis in 15 mg/kg and 30 mg/kg groups.The testicular lesions returned to the normal level in histopathology in 15 mg/kg+GSH group.It was shown that the seminiferous tubule was denatured and the spermiogenesis decreased in 30 mg/kg+GSH group.Conclusion GSH can antagonize antioxidative capacitydecrease induced bymanganese exposure in rats.

Key concepts: Glutathione, Chemistry, Glutathione peroxidase, Superoxide dismutase, Endocrinology, Internal medicine, Catalase, Seminiferous tubule

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