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The protective effect of vitamin E against oxidative damage caused by formaldehyde in the testes of adult rats
Author(s) -
Zhou DangXia,
Qiu ShuDong,
Zhang Jie,
Tian Hong,
Wang HaiXue
Publication year - 2006
Publication title -
asian journal of andrology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.701
H-Index - 74
eISSN - 1745-7262
pISSN - 1008-682X
DOI - 10.1111/j.1745-7262.2006.00198.x
Subject(s) - malondialdehyde , glutathione peroxidase , oxidative stress , glutathione , endocrinology , vitamin e , medicine , superoxide dismutase , sperm , h&e stain , vitamin c , chemistry , spermatogenesis , andrology , antioxidant , immunohistochemistry , biochemistry , enzyme
Aim : To investigate the effect of formaldehyde (FA) on testes and the protective effect of vitamin E (VE) against oxidative damage by FA in the testes of adult rats. Methods : Thirty rats were randomly divided into three groups: (1) control; (2) FA treatment group (FAt); and (3) FAt + VE group. FAt and FAt + VE groups were exposed to FA by inhalation at a concentration of 10 mg/m 3 for 2 weeks. In addition, FAt + VE group were orally administered VE during the 2‐week FA treatment. After the treatment, the histopathological and biochemical changes in testes, as well as the quantity and quality of sperm, were observed. Results : The testicular weight, the quantity and quality of sperm, the activities of superoxide dismutase (SOD), glutathione peroxidase (GSH‐Px) and glutathione (GSH) were significantly decreased whereas the level of malondialdehyde (MDA) was significantly increased in testes of rats in FAt group compared with those in the control group. VE treatment restored these parameters in FAt + VE group. In addition, microscopy with hematoxylin‐eosin (HE) staining showed that seminiferous tubules atrophied, seminiferous epithelial cells disintegrated and shed in rats in FAt group and VE treatment significantly improved the testicular structure in FAt + VE group. Conclusion : FA destroys the testicular structure and function in adult rats by inducing oxidative stress, and this damage could be partially reversed by VE.

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