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1.
National Journal of Andrology ; (12): 126-130, 2011.
Article in Chinese | WPRIM | ID: wpr-266201

ABSTRACT

<p><b>OBJECTIVE</b>To study the effects of polychlorinated biphenyl (PCB) on the phenotype of the testis tissue and the testis tissue and the expression c-fos, c-Myc and beta-catenin in the rat testis.</p><p><b>METHODS</b>Forty-five Wistar male rats were divided into a control and three perimental groups, the former fed normally, and the latter with PCB at 0.1, 1 and 10 mg/kg respectively for 90 days. Then the effects of PCB on the phenotype of the testis tissue and the expressions of c-fos, c-Myc and p-catenin were determined by histopathology and immunohistochemistry.</p><p><b>RESULTS</b>Histopathological examinations revealed testis edema, damage of the mesenchymal phenotype, morphological changes of the contorted seminiferous tubules, absence of stromal cells, spermiocytes and prespermatids, and decreased number of sperm. The expressions of c-fos and c-Myc were significantly higher in the 1 and 10 mg/kg PCB groups than in the control and 0.1 mg/kg PCB groups (P < 0.01). The expression of beta-catenin was downregulated in the 0.1 mg/kg PCB group, with significant differences from the other groups (P < 0.01), but it was higher in the 1 mg/kg PCB than in the control and 10 mg/kg PCB groups (P < 0.01).</p><p><b>CONCLUSION</b>PCB causes changes in the phenotype of the testis tissue, and the abnormal expressions of c-fos, c-Myc and beta-catenin are closely related to the PCB-induced testis injury.</p>


Subject(s)
Animals , Male , Rats , Polychlorinated Biphenyls , Proto-Oncogene Proteins c-fos , Metabolism , Proto-Oncogene Proteins c-myc , Metabolism , Rats, Wistar , Testis , Metabolism , Pathology , beta Catenin , Metabolism
2.
National Journal of Andrology ; (12): 116-123, 2005.
Article in Chinese | WPRIM | ID: wpr-267742

ABSTRACT

<p><b>OBJECTIVE</b>To study the effects of polychlorinated biphenyl (PCB) on bcl-2 and TGFbeta1 expression in rat testes.</p><p><b>METHODS</b>Forty male Wistar rats were divided into 4 groups at random: Group A (normal control), Group B (fed on 10(-8) mol/L PBC), Group C (feb on 10(-7) mol/L) and Group D (feb on 10(-6) mol/L). After three months, all the rats were killed, the animal model established, and observations made on the expression of bcl2 and TGFbeta1 in the rat testis using the optical microscope and immunohistochemical techniques.</p><p><b>RESULTS</b>The damage to the structure of the testis was related to the dosage of PCB: the higher the dodage, the more serious the damage. PCB induced the expression of bcl-2 and TGFbeta1. The TGFbeta1 expression was significantly higher in the highest dosage group than in others (P < 0.01 ), and the bcl-2 expression was dramatically higher in Group C than in other groups (P < 0.01).</p><p><b>CONCLUSION</b>PCB can cause injury in rat testes.</p>


Subject(s)
Animals , Male , Rats , Dose-Response Relationship, Drug , Polychlorinated Biphenyls , Toxicity , Proto-Oncogene Proteins c-bcl-2 , Random Allocation , Rats, Wistar , Testis , Metabolism , Pathology , Transforming Growth Factor beta1
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