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Repeated exposure to iron oxide nanoparticles causes testicular toxicity in mice
The aim of this study was to determine whether repeated exposure to iron oxide nanoparticles (Fe2O3-NPs) could be toxic to mice testis. Fe2O3-NPs (25 and 50 mg/kg) were intraperitoneally administered into mice once a week for 4 weeks. Our study showed that Fe2O3-NPs have the ability to cross the blood-testis barrier to get into the testis. The findings showed that exposure resulted in the accumulation of Fe2O3-NPs which was evidenced from the iron content and accumulation in the testis. Furthermore, 25 and 50 mg/kg Fe2O3-NPs administration increased the reactive oxygen species, lipid peroxidation, protein carbonyl content, glutathione peroxidase activity, and nitric oxide levels with a concomitant decrease in the levels of antioxidants--superoxide dismutase, catalase, glutathione, and vitamin C. Increased expression of Bax, cleaved-caspase-3, and cleaved-PARP confirms apoptosis. Serum testosterone levels increased with increased concentration of Fe2O3-NPs exposure. In addition, the histopathological lesions like vacuolization, detachment, and sloughing of germ cells were also observed in response to Fe2O3-NPs treatment. The data from our study entailed that testicular toxicity caused by Fe2O3-NPs exposure may be associated with Fe2O3-NPs accumulation leading to oxidative stress and apoptosis. Therefore, precautions should be taken in the safe use of Fe2O3-NPs to avoid complications in the fertility of males. Further research will unravel the possible molecular mechanisms on testicular toxicity of Fe2O3-NPs. © 2016 Wiley Periodicals, Inc. Environ Toxicol 32: 594-608, 2017.
Repeated exposure to iron oxide nanoparticles causes testicular toxicity in mice
The aim of this study was to determine whether repeated exposure to iron oxide nanoparticles (Fe2O3-NPs) could be toxic to mice testis. Fe2O3-NPs (25 and 50 mg/kg) were intraperitoneally administered into mice once a week for 4 weeks. Our study showed that Fe2O3-NPs have the ability to cross the blood-testis barrier to get into the testis. The findings showed that exposure resulted in the accumulation of Fe2O3-NPs which was evidenced from the iron content and accumulation in the testis. Furthermore, 25 and 50 mg/kg Fe2O3-NPs administration increased the reactive oxygen species, lipid peroxidation, protein carbonyl content, glutathione peroxidase activity, and nitric oxide levels with a concomitant decrease in the levels of antioxidants--superoxide dismutase, catalase, glutathione, and vitamin C. Increased expression of Bax, cleaved-caspase-3, and cleaved-PARP confirms apoptosis. Serum testosterone levels increased with increased concentration of Fe2O3-NPs exposure. In addition, the histopathological lesions like vacuolization, detachment, and sloughing of germ cells were also observed in response to Fe2O3-NPs treatment. The data from our study entailed that testicular toxicity caused by Fe2O3-NPs exposure may be associated with Fe2O3-NPs accumulation leading to oxidative stress and apoptosis. Therefore, precautions should be taken in the safe use of Fe2O3-NPs to avoid complications in the fertility of males. Further research will unravel the possible molecular mechanisms on testicular toxicity of Fe2O3-NPs. © 2016 Wiley Periodicals, Inc. Environ Toxicol 32: 594-608, 2017.
Repeated exposure to iron oxide nanoparticles causes testicular toxicity in mice
2017
Aufsatz (Zeitschrift)
Englisch
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