Arun Supatcharee, Burawat Jaturon, Sukhorum Wannisa, Sampannang Apichakan, Uabundit Nongnut, Iamsaard Sitthichai
Department of Anatomy, Faculty of Medicine, Khon Kaen University, Khon Kaen 40002, Thailand.
Center for Research and Development of Herbal Health Products, Faculty of Pharmaceutical Sciences, Khon Kaen University, Khon Kaen 40002, Thailand.
J Zhejiang Univ Sci B. 2016 Jan;17(1):21-9. doi: 10.1631/jzus.B1500174.
To investigate male reproductive parameters via changes of potential testicular protein markers in restraint-stress rats.
Male Sprague-Dawley rats were divided into two groups (non-immobilized control and restraint-immobilized/stress groups, n=8 each group). The stress animals were immobilized (12 h/d) by a restraint cage for 7 consecutive days. All reproductive parameters, morphology and histology were observed and compared between groups. In addition, the expression of steroidogenic acute regulatory (StAR) and phosphotyrosine proteins (previously localized in Sertoli and late spermatid cells) in testicular lysate was assayed by immuno-Western blotting.
Testosterone level, sperm concentration and sperm head normality of stress rats were significantly decreased while the corticosterone level was increased as compared with the control (P<0.05). Histologically, stress rats showed low sperm mass in epididymal lumen and some atrophy of seminiferous tubules. Although the expression of testicular StAR protein was not significantly different between groups, changed patterns of the 131, 95, and 75 kDa testicular phosphorylated proteins were observed in the stress group compared with the control group. The intensity of a testicular 95-kDa phosphorylated protein was significantly decreased in stress rats.
This study has demonstrated the alteration of testicular phosphorylated protein patterns, associated with adverse male reproductive parameters in stress rats. It could be an explanation of some infertility in stress males.
通过束缚应激大鼠睾丸潜在蛋白标志物的变化来研究雄性生殖参数。
将雄性Sprague-Dawley大鼠分为两组(非束缚对照组和束缚/应激组,每组n = 8)。应激组动物通过束缚笼连续7天每天束缚12小时。观察并比较两组之间的所有生殖参数、形态学和组织学。此外,通过免疫印迹法检测睾丸裂解物中类固醇生成急性调节蛋白(StAR)和磷酸化酪氨酸蛋白(先前定位于支持细胞和晚期精子细胞)的表达。
与对照组相比,应激大鼠的睾酮水平、精子浓度和精子头部正常率显著降低,而皮质酮水平升高(P<0.05)。组织学上,应激大鼠附睾管腔内精子数量减少,生精小管有一些萎缩。虽然两组之间睾丸StAR蛋白的表达没有显著差异,但与对照组相比,应激组观察到131、95和75 kDa睾丸磷酸化蛋白的变化模式。应激大鼠睾丸中95 kDa磷酸化蛋白的强度显著降低。
本研究证明了睾丸磷酸化蛋白模式的改变,这与应激大鼠不良的雄性生殖参数有关。这可能是应激男性不育的一种解释。