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Role of TNF-related apoptosis-inducing ligand (TRAIL) in the pathogenesis of varicocele-induced testicular dysfunction

机译:TNF相关凋亡诱导配体(TRAIL)在精索静脉曲张引起的睾丸功能障碍的发病机理中的作用

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摘要

The higher frequency of varicocele in men with infertility has drawn attention and resulted in increased research at the molecular level towards treatments. The aim of this study was to investigate the role of tumor necrosis factor (TNF)-related apoptosis-inducing ligand (TRAIL) and its receptors in varicocele-induced testicular dysfunction in an experimental rat model. The rats were divided into three groups: control, sham and varicocele. Varicoceles in rats were induced by partial ligation of the left renal vein and left testes. The rats were analyzed 13 weeks after surgery. The degree of DNA fragmentation within cells in the testis was determined using terminal deoxynucleotidyl transferase deoxyuridine triphosphate nick end labeling (TUNEL) assay. Tubule degeneration was evaluated using the Johnsen score. The expression of TRAIL and its receptors was detected by immunohistochemical and Western blotting techniques. The apoptotic index, Johnsen score and the expression of TRAIL and TRAIL receptors were examined. The data are presented as the mean±s.d. and were analyzed using computer software. The Kruskal–Wallis and Dunn's multiple comparison tests were used in the statistical analyses. The germ cell apoptotic index was increased in rats with varicoceles when compared with the sham and control groups (P=0.0031). The Johnsen score was significantly decreased in the varicocele group when compared with the sham and control groups (P<0.0001). Immunohistochemical and Western blotting analyses showed that after varicocele induction, the expression of TRAIL-R1 and TRAIL-R4 in germ cells was increased and the expression of TRAIL-R2 was decreased. There are no significant differences among the groups in terms of TRAIL and TRAIL-R3 receptor expression. The results of this study indicate that TRAIL and its receptors may have a potential role in the pathogenesis of varicocele-induced testicular dysfunction.
机译:不育男性精索静脉曲张的发病率较高,引起了人们的注意,并导致在分子水平上对治疗的研究增多。这项研究的目的是在实验大鼠模型中研究肿瘤坏死因子(TNF)相关的凋亡诱导配体(TRAIL)及其受体在精索静脉曲张诱发的睾丸功能障碍中的作用。将大鼠分为三组:对照组,假手术和精索静脉曲张。大鼠左肾静脉和左睾丸部分结扎可诱发精索静脉曲张。术后13周对大鼠进行分析。使用末端脱氧核苷酸转移酶脱氧尿苷三磷酸缺口末端标记(TUNEL)测定法确定睾丸细胞内DNA片段化的程度。使用Johnsen评分评估小管变性。 TRAIL及其受体的表达通过免疫组织化学和Western印迹技术检测。检查细胞凋亡指数,Johnsen评分以及TRAIL和TRAIL受体的表达。数据表示为平均值±s.d。并使用计算机软件进行了分析。统计分析中使用了Kruskal–Wallis和Dunn的多重比较检验。与假手术组和对照组相比,精索静脉曲张大鼠的生殖细胞凋亡指数增加(P = 0.0031)。与假手术和对照组相比,精索静脉曲张组的约翰森评分显着降低(P <0.0001)。免疫组织化学和蛋白质印迹分析表明,精索静脉曲张诱导后,生殖细胞中TRAIL-R1和TRAIL-R4的表达增加,而TRAIL-R2的表达则降低。在TRAIL和TRAIL-R3受体表达方面,各组之间没有显着差异。这项研究的结果表明,TRAIL及其受体可能在精索静脉曲张引起的睾丸功能障碍的发病机理中具有潜在作用。

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