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J Cell Biochem ; 120(10): 17312-17325, 2019 10.
Article in English | MEDLINE | ID: mdl-31111540

ABSTRACT

The current study was conducted to assess the relationship between testicular cells in spermatogenesis, through which the production of healthy and mature sperm is essential. However, it seems necessary to obtain more information about the three-dimensional pattern of the testis cells arrangement, which is directly related to the function of the testis after induction of diabetes. Twelve adult mice (28-30 g) were assigned into two experimental groups: (1) control and (2) diabetic (40 mg/kg STZ). The epididymal sperm collected from the tail of the epididymis and testes samples were taken for stereology, immunocytochemistry and RNA extraction. Our data showed that diabetes could notably decrease the number of testicular cells, together with a reduction of total sperm count. In addition, the results from the second-order stereology indicated the significant changes in the spatial arrangement of Sertoli cells and spermatogonial cells in the diabetic groups, in comparison with the control (P < .05). Moreover, the immunohistochemistry results showed a significant reduction in Sex-determining Region Y (SRY) box 9 gene (SOX9), vimentin, occludin, and connexin-43 positive cells in the diabetic groups compared with the control (P < .05). Furthermore, our data showed that the expression of steroidogenic acute regulatory protein steroidogenic acute regulatory protein (StAR) and peripheral benzodiazepine receptor peripheral benzodiazepine receptor (PBR) was significantly reduced in the diabetic groups, in comparison with the control (P < .05). These findings suggest that structural and functional changes of testis cells after induction of diabetes cause the alterations in the spatial arrangement of Sertoli and spermatogonial cells, ultimately influencing the normal spermatogenesis in mice.


Subject(s)
Apoptosis , Diabetes Mellitus, Experimental/complications , Infertility, Male/pathology , Leydig Cells/pathology , Sertoli Cells/pathology , Spermatogenesis , Spermatogonia/pathology , Animals , Cell Proliferation , Cells, Cultured , Infertility, Male/etiology , Infertility, Male/metabolism , Leydig Cells/metabolism , Male , Mice , Sertoli Cells/metabolism , Spatial Analysis , Spermatogonia/metabolism
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