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Effects of dietary selenium on apoptosis of germ cells in the testis during spermatogenesis in roosters

机译:日粮硒对公鸡精子发生过程中睾丸生殖细胞凋亡的影响

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摘要

The aim of this study was to determine the effects of dietary selenium (Se) supplementation on apoptosis of germ cells in the testis during spermatogenesis in roosters. Eighty 12-week-old Hy-Line Variety white roosters with an averaged body weight of 1.38 +/- 0.2 kg were selected and randomly divided into four experimental groups. They were fed the basal diet (0.044 mg/kg Se dry matter) supplemented with 0 (control), 0.5, 1.0, or 2.0 mg/kg of Se dry matter from sodium selenite). After the 45-day feeding experiment, testis samples were collected from the roosters of each treatment group to detect the population of apoptotic germ cells using the terminal deoxynucleotidyl transferase dUTP nick end labeling assay. The protein expression of cell cycle-related genes and the messenger RNA (mRNA) expression of apoptosis and cell cycle-related genes had also been detected. The results show that the population of apoptotic germ cells in the control and 2.0 mg/kg groups was increased (P 0.05) compared with that in the 0.5 mg/kg and 1.0 mg/kg groups. Expressions of CDC2 and CCNB1 protein in the control and 2.0 mg/kg groups were lower (P 0.05) than those in the 0.5 mg/kg and 1.0 mg/kg groups. The mRNA level of CDC2 in the 0.5 mg/kg group was higher (P 0.05) than that in other groups. The lowest (P 0.05) mRNA expressions of apoptosis-related genes (BCL-2, CASPASE 3, CASPASE 8) were also obtained in the 0.5 mg/kg group. These results show that dietary Se of roosters can affect apoptosis of germ cells by regulating the mRNA expressions of apoptosis- and cell cycle-related genes in the testis during spermatogenesis. (C) 2015 Elsevier Inc. All rights reserved.
机译:这项研究的目的是确定日粮中添加硒对公鸡精子发生过程中睾丸生殖细胞凋亡的影响。选择八十只平均体重为1.38 +/- 0.2公斤的12周龄Hy-Line品种白公鸡,并将其随机分为四个实验组。给他们喂基础饮食(0.044 mg / kg硒干物质),辅以0(对照),0.5、1.0或2.0 mg / kg的亚硒酸钠硒干物质。在为期45天的喂养实验后,从每个治疗组的公鸡收集睾丸样本,以使用末端脱氧核苷酸转移酶dUTP缺口末端标记测定法检测凋亡的生殖细胞群。还检测了细胞周期相关基因的蛋白表达以及凋亡和细胞周期相关基因的信使RNA(mRNA)表达。结果表明,与0.5 mg / kg和1.0 mg / kg组相比,对照组和2.0 mg / kg组的凋亡生殖细胞数量增加(P <0.05)。对照和2.0 mg / kg组的CDC2和CCNB1蛋白表达低于0.5 mg / kg和1.0 mg / kg组的表达(P <0.05)。 0.5 mg / kg组的CDC2 mRNA水平高于其他组(P <0.05)。 0.5 mg / kg组的凋亡相关基因(BCL-2,CASPASE 3,CASPASE 8)的mRNA表达最低(P <0.05)。这些结果表明,饮食中的硒可以通过调节生精过程中睾丸细胞凋亡和细胞周期相关基因的mRNA表达来影响生殖细胞的凋亡。 (C)2015 Elsevier Inc.保留所有权利。

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