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染锰大鼠生精细胞凋亡中caspase-3 mRNA、凋亡蛋白酶活化因子-1及多聚ADP核糖聚合酶的表达变化 被引量:3

Expression changes of caspase-3 mRNA,apoptosis protease activating factor-1 and poly ADP-ribose polymerase in apoptosis of spermatogenic cells of rats exposed to manganese
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摘要 目的:研究染锰诱导的大鼠生精细胞凋亡过程中,天冬氨酸特异性半胱氨酸酶-3(caspase-3)mRNA和凋亡蛋白酶活化因子-1(Apaf-1)、多聚ADP核糖聚合酶(PARP)的表达及其关系,探讨它们在生精细胞凋亡过程中的作用。方法:雄性SD大鼠,设立空白对照组、低剂量(15 mg/kg MnCl_2)和高剂量(30 mg/kg MnCl_2)组。实验组分别染锰4周和6周,空白对照组给予等容生理盐水,给药途径均为腹腔注射,TUNEL法检测生精细胞凋亡,原位杂交法和免疫组织化学法检测生精细胞caspase-3 mRNA、Apaf-1和PARP的表达。结果:与空白对照组比较,各染锰组生精细胞凋亡指数(AI)和caspase-3mRNA阳性细胞率均显著升高,Apaf-1和PARP阳性细胞率均显著降低。染锰剂量相同,6周与4周组比较,以及染锰时间相同,高剂量组与低剂量组比较,生精细胞AI和caspase-3 mRNA阳性细胞率均显著升高,Apaf-1和PARP阳性细胞率均显著降低。各组大鼠生精细胞AI与caspase-3 mRNA阳性细胞率呈正相关,与Apaf-1和PARP阳性细胞率呈负相关。结论:锰可影响大鼠生精细胞caspase-3 mRNA表达,促进Apaf-1和PARP分解,导致生精细胞凋亡,产生生殖毒性效应。 Objective: To determine the effect of caspase-3 mRNA and apoptosis protease activating factor-1 (Apaf-1), poly ADP-ribose polymerase (PARP) in apoptosis of spermatogenic cells of rats exposed to manganese. Methods: SD male rats were randomly divided into one control group and two manganese chloride (MnCl2) (15 mg/kg, 30 mg/kg) groups respectively. After being exposed to manganese for 4 and 6 weeks, the apoptosis of spermatogenic cells was examined by terminal deoxynucleotidyl transferase mediated dUTP nick end labeling (TUNEL) technique. The expression of caspase-3 mRNA in spermatogenic cells was investigated by in situ hybridization, and the expression of Apaf-1 and PARP was detected by immunohistochemistry. Results: Compared with the control group, AI and caspase-3 mRNA-positive-cell rates were L increased but the Apaf-1 and PARP-positive-celI rates were decreased. Among the same dose and same time manganese exposure groups, AI and caspase-3 mRNA-positive-cell rates were increased but the Apaf-1 and PARP-positive-cell rates were decreased in the 15 mg/kg MnC12 group compared to the 30 mg/kg MnCl2 group. There existed a positive correlation between AI and the caspase-3 mRNA-positive-cell rate and a negative correlation between AI and the Apaf-l-positive-cell rate and PARP-positive-cell rate. Conclusion: Manganese could upregulate the ,expression of caspase-3 mRNA, and decompose Apaf-1- positive-cell rate and PARP-positive-cell rate, which might be one of the important molecular mechanisms of reproductive toxicity of manganese.
出处 《解剖学杂志》 CSCD 北大核心 2017年第3期254-257,F0004,共5页 Chinese Journal of Anatomy
基金 遵义市科技项目基金(200707) 遵义市红花岗区科技项目基金(200622)
关键词 生精细胞 凋亡 天冬氨酸特异性半胱氨酸酶-3 MRNA 凋亡蛋白酶活化因子-1 多聚ADP核糖聚合酶 manganese spermatogenic cells apoptosis caspase-3 mRNA apoptosis protease activating factor-I poly ADP-ribose polymerase
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