Qiu Sheng-Hua, Zhuang Hui-Yi, Zhang Hua-Feng, Li Chang-Ling
Department of Pediatric Surgery, Yishui Central Hospital of Linyi City, Yishui, Shandong 276400, China.
Zhonghua Nan Ke Xue. 2013 Jul;19(7):612-6.
To explore the effects of glial cell-derived neurotrophic factor (GDNF) on the stem cell factor (SCF), superoxide dismutase (SOD), catalase (CAT) and malondialdehyde (MDA) in the undescended testis tissue of rats.
Models of left cryptorchidism were made in 48 healthy male rats weighing (200 +/- 20) g and randomly divided into four groups: model control, GDNF 7 d, GDNF 14 d and GDNF 21 d. The rats in the latter three groups were killed at 7, 14 and 21 days after intravenous injection of GDNF, their left testes harvested for measurement of the activities of SOD and CAT and the content of MDA. The apoptosis index of spermatogenic cells was detected by TUNEL, the histological changes of the testis tissue observed under the light microscope, and the gene and protein expressions of SCF determined by real-time quantitative PCR and Western blotting, respectively.
The apoptosis indexes of spermatogenic cells were obviously decreased in the GDNF 7 d, GDNF 14 d and GDNF 21 d groups (8.42 +/- 0.16, 4.45 +/- 0.34 and 7.32 +/- 0.09) as compared with that of the model control (13.5 +/- 0.64), with statistically significant difference between the GDNF 14 d and control groups (P < 0.01). The SCF expression and SOD activity were remarkably increased while the MDA content markedly reduced in the GDNF groups in comparison with those in the model control (P < 0.01).
GDNF had a protective effect on the spermatogenic function of rat testes with unilateral cryptorchidism. It could enhance the antioxidant enzyme activity of the antioxidant enzyme system, elevate the expression of SCF and thus improve the testicular reproductivity, which were best indicated in the GDNF 14 d group.
探讨胶质细胞源性神经营养因子(GDNF)对大鼠隐睾组织中干细胞因子(SCF)、超氧化物歧化酶(SOD)、过氧化氢酶(CAT)和丙二醛(MDA)的影响。
选取48只体重(200±20)g的健康雄性大鼠制作左侧隐睾模型,并随机分为四组:模型对照组、GDNF 7天组、GDNF 14天组和GDNF 21天组。后三组大鼠在静脉注射GDNF后的第7、14和21天处死,取其左侧睾丸测定SOD和CAT活性以及MDA含量。采用TUNEL法检测生精细胞凋亡指数,光镜下观察睾丸组织学变化,分别用实时定量PCR和Western blotting法检测SCF的基因和蛋白表达。
与模型对照组(13.5±0.64)相比,GDNF 7天组、GDNF 14天组和GDNF 21天组生精细胞凋亡指数明显降低(分别为8.42±0.16、4.45±0.34和7.32±0.09),GDNF 14天组与对照组比较差异有统计学意义(P<0.01)。与模型对照组相比,GDNF组SCF表达和SOD活性显著升高,MDA含量显著降低(P<0.01)。
GDNF对单侧隐睾大鼠睾丸的生精功能具有保护作用。它可增强抗氧化酶系统的抗氧化酶活性,提高SCF表达,从而改善睾丸生殖能力,其中以GDNF 14天组效果最佳。