Aim: To find out the effect of lindane on testicular antioxidant system and testicular steroidogenesis in adult malerats. Methods: Adult male rats were orally administered with lindane at a dose of 5.0 mg/kg body weig...Aim: To find out the effect of lindane on testicular antioxidant system and testicular steroidogenesis in adult malerats. Methods: Adult male rats were orally administered with lindane at a dose of 5.0 mg/kg body weight per dayfor 30 days. Twenty-four hours after the last treatment the rats were killed using anesthetic ether. Testes, epididymis,seminal vesicles and ventral prostate were removed and weighed. A 10% testicular homogenate was prepared and cen-trifuged at 4℃. The supernatant was used for various biochemical estimations. Results; The body weight and theweights of testes, epididymis, seminal vesicles and ventral prostate were reduced in lindane-treated rats. There was asignificant decline in the activities of antioxidant enzymes superoxide dismutase (SOD), catalase and glutathione reduc-tase while an increase in hydrogen peroxide (H_2O_2) generation was observed. The specific activities of testicularsteroidogenic enzymes 3β-hydroxysteroid dehydrogenase and 17β-hydroxysteroid dehydrogenase were decreased. Thelevels of DNA, RNA and protein were also decreased in lindane-treated rats. Conclusion: Lindane induces oxida-tive stress and decreases antioxidant enzymes in adult male rats.展开更多
Aim: To find out the changes induced by lindane on the antioxidant enzymes in epididymis and epididymal sperm ofadult rats. Methods: Adult male rats were orally administered lindane at a dose of 5.0 mg/kg body weight ...Aim: To find out the changes induced by lindane on the antioxidant enzymes in epididymis and epididymal sperm ofadult rats. Methods: Adult male rats were orally administered lindane at a dose of 5.0 mg/kg body weight per dayfor 30 days. At the end of the treatment, the rats were sacrificed. The epididymis was removed and weighed and spermwere collected for sperm count, motility and biochemical studies. A 1% homogenate of epididymis was prepared andused for biochemical estimations. Results; In lindane-treated rats, there were significant reductions in the epididy-mal weight, epididymal sperm count and motility compared with the controls. Significant decreases in the superoxidedismutase (SOD), catalase, glutathione reductase and glutathione peroxidase activities and significant increases in theH_2O_2 generation and lipid peroxidation were also observed in the epididymis and epididymal sperm of lindane-treatedrats. Conclusion; Lindane decreases the levels of antioxidant enzymes in the epididymis and epididymal sperm ofadult rats thereby inducing oxidative stress. (Asian J Androl 2001 Sep; 3 : 205 - 208)展开更多
Aim: To find out the toxic effect of endosulfan on the testicular function of pubertal rats. Methods: Male rats of pu-bertal age were orally administered endosulfan at a dose of 1.0 mg/kg body weight for 30 days. Twen...Aim: To find out the toxic effect of endosulfan on the testicular function of pubertal rats. Methods: Male rats of pu-bertal age were orally administered endosulfan at a dose of 1.0 mg/kg body weight for 30 days. Twenty-four hours af-ter the last treatment, the rats were sacrificed and the testis, epididymis, seminal vesicles and ventral prostate were re-moved and weighed. A 10 % testicular homogenate was prepared for biochemical estimations. Results: In endosul-fan-treated rats, there were a reduction in the body weight and the weights of testis and accessory sex organs, a de-crease in the testicular lactate and pyruvate activities, and in the testicular DNA and RNA concentrations, whereas thetesticular protein concentration was slightly increased; the specific activity of testicular steroidogenic enzyme, 3β-OH-steroid dehydrogenase and the ascorbic acid level were decreased, which were correlated with a decrease in steroidoge-nesis. The lysosomal enzyme acid phosphatase and brash-border enzyme alkaline phosphatase activities were also de-creased in the testis of treated rats. Conclusion: In pubertal rats, endosulfan treatment inhibits the testicular functions.(Asian J Androl 1999 Dec; 1: 203-206)展开更多
Aim: To study the effect of bisphenol A on the epididymis and epididymal sperm of rats and the possible amelioration action of co-administration with vitamin C. Methods: Male Wistar rats were orally administered bisph...Aim: To study the effect of bisphenol A on the epididymis and epididymal sperm of rats and the possible amelioration action of co-administration with vitamin C. Methods: Male Wistar rats were orally administered bisphenol A (0.2 μg·kg-1·day-1, 2 μg·kg-1·day-1 and 20 μg·kg-1·day-1) and 0.2 μg, 2μg and 20 μg bisphenol A + 40 mg vitamin C·kg-1·day-1 for 60 days. On day 61, rats were killed with anesthetic ether and sperm collected from epididymis were used for assessment of sperm count, motility and viability and biochemical studies. A 1 % homogenate of epididymis was prepared and used for biochemical estimations. Caput, corpus and cauda epididymis were fixed in Bouin's fixative for histological studies. Results: Administration of bisphenol A caused a reduction in the epididymal sperm motility and count and the sperm viability remained unchanged. The activities of superoxide dismutase and glu-tathione peroxidase decreased, while the levels of lipid peroxidation increased in epididymal sperm and epididymis at all doses. Co-administration with vitamin C reversed the effect of bisphenol A-induced oxidative stress in epididymal sperm and epididymis. A complete degeneration of epididymal epithelium in caput, corpus and cauda regions with reduction in the number of sperms were observed at all doses of bisphenol A-treated rats. Conclusion: Bisphenol A induced oxidative stress in epididymis and caused degeneration of the epididymal epithelium of rats. Co-administration with vitamin C had a protective effect against the bisphenol A-induced toxicity in epididymal sperm and epididymis.展开更多
文摘Aim: To find out the effect of lindane on testicular antioxidant system and testicular steroidogenesis in adult malerats. Methods: Adult male rats were orally administered with lindane at a dose of 5.0 mg/kg body weight per dayfor 30 days. Twenty-four hours after the last treatment the rats were killed using anesthetic ether. Testes, epididymis,seminal vesicles and ventral prostate were removed and weighed. A 10% testicular homogenate was prepared and cen-trifuged at 4℃. The supernatant was used for various biochemical estimations. Results; The body weight and theweights of testes, epididymis, seminal vesicles and ventral prostate were reduced in lindane-treated rats. There was asignificant decline in the activities of antioxidant enzymes superoxide dismutase (SOD), catalase and glutathione reduc-tase while an increase in hydrogen peroxide (H_2O_2) generation was observed. The specific activities of testicularsteroidogenic enzymes 3β-hydroxysteroid dehydrogenase and 17β-hydroxysteroid dehydrogenase were decreased. Thelevels of DNA, RNA and protein were also decreased in lindane-treated rats. Conclusion: Lindane induces oxida-tive stress and decreases antioxidant enzymes in adult male rats.
文摘Aim: To find out the changes induced by lindane on the antioxidant enzymes in epididymis and epididymal sperm ofadult rats. Methods: Adult male rats were orally administered lindane at a dose of 5.0 mg/kg body weight per dayfor 30 days. At the end of the treatment, the rats were sacrificed. The epididymis was removed and weighed and spermwere collected for sperm count, motility and biochemical studies. A 1% homogenate of epididymis was prepared andused for biochemical estimations. Results; In lindane-treated rats, there were significant reductions in the epididy-mal weight, epididymal sperm count and motility compared with the controls. Significant decreases in the superoxidedismutase (SOD), catalase, glutathione reductase and glutathione peroxidase activities and significant increases in theH_2O_2 generation and lipid peroxidation were also observed in the epididymis and epididymal sperm of lindane-treatedrats. Conclusion; Lindane decreases the levels of antioxidant enzymes in the epididymis and epididymal sperm ofadult rats thereby inducing oxidative stress. (Asian J Androl 2001 Sep; 3 : 205 - 208)
文摘Aim: To find out the toxic effect of endosulfan on the testicular function of pubertal rats. Methods: Male rats of pu-bertal age were orally administered endosulfan at a dose of 1.0 mg/kg body weight for 30 days. Twenty-four hours af-ter the last treatment, the rats were sacrificed and the testis, epididymis, seminal vesicles and ventral prostate were re-moved and weighed. A 10 % testicular homogenate was prepared for biochemical estimations. Results: In endosul-fan-treated rats, there were a reduction in the body weight and the weights of testis and accessory sex organs, a de-crease in the testicular lactate and pyruvate activities, and in the testicular DNA and RNA concentrations, whereas thetesticular protein concentration was slightly increased; the specific activity of testicular steroidogenic enzyme, 3β-OH-steroid dehydrogenase and the ascorbic acid level were decreased, which were correlated with a decrease in steroidoge-nesis. The lysosomal enzyme acid phosphatase and brash-border enzyme alkaline phosphatase activities were also de-creased in the testis of treated rats. Conclusion: In pubertal rats, endosulfan treatment inhibits the testicular functions.(Asian J Androl 1999 Dec; 1: 203-206)
文摘Aim: To study the effect of bisphenol A on the epididymis and epididymal sperm of rats and the possible amelioration action of co-administration with vitamin C. Methods: Male Wistar rats were orally administered bisphenol A (0.2 μg·kg-1·day-1, 2 μg·kg-1·day-1 and 20 μg·kg-1·day-1) and 0.2 μg, 2μg and 20 μg bisphenol A + 40 mg vitamin C·kg-1·day-1 for 60 days. On day 61, rats were killed with anesthetic ether and sperm collected from epididymis were used for assessment of sperm count, motility and viability and biochemical studies. A 1 % homogenate of epididymis was prepared and used for biochemical estimations. Caput, corpus and cauda epididymis were fixed in Bouin's fixative for histological studies. Results: Administration of bisphenol A caused a reduction in the epididymal sperm motility and count and the sperm viability remained unchanged. The activities of superoxide dismutase and glu-tathione peroxidase decreased, while the levels of lipid peroxidation increased in epididymal sperm and epididymis at all doses. Co-administration with vitamin C reversed the effect of bisphenol A-induced oxidative stress in epididymal sperm and epididymis. A complete degeneration of epididymal epithelium in caput, corpus and cauda regions with reduction in the number of sperms were observed at all doses of bisphenol A-treated rats. Conclusion: Bisphenol A induced oxidative stress in epididymis and caused degeneration of the epididymal epithelium of rats. Co-administration with vitamin C had a protective effect against the bisphenol A-induced toxicity in epididymal sperm and epididymis.
