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王琴, 刘轶群, 韩枫, 石丽丽, 韩超, 黄振武. 不同硒营养水平饲料对大鼠生殖功能影响[J]. 中国公共卫生, 2020, 36(11): 1563-1565. DOI: 10.11847/zgggws1123338
引用本文: 王琴, 刘轶群, 韩枫, 石丽丽, 韩超, 黄振武. 不同硒营养水平饲料对大鼠生殖功能影响[J]. 中国公共卫生, 2020, 36(11): 1563-1565. DOI: 10.11847/zgggws1123338
WANG Qin, LIU Yi-qun, HAN Feng, SHI Li-li, HAN Chao, . Influence of selenium content in fodder on reproductive function in male rats[J]. Chinese Journal of Public Health, 2020, 36(11): 1563-1565. DOI: 10.11847/zgggws1123338
Citation: WANG Qin, LIU Yi-qun, HAN Feng, SHI Li-li, HAN Chao, . Influence of selenium content in fodder on reproductive function in male rats[J]. Chinese Journal of Public Health, 2020, 36(11): 1563-1565. DOI: 10.11847/zgggws1123338

不同硒营养水平饲料对大鼠生殖功能影响

Influence of selenium content in fodder on reproductive function in male rats

  • 摘要:
      目的  观察适硒、低硒和缺硒三种饲料喂养对雄性大鼠生殖功能相关指标的影响。
      方法  36只4周龄断乳Wistar大鼠适应性饲养一周后,按体重随机分为三组:适硒、低硒和缺硒组。每周称量体重,饲养9周后戊巴比妥钠麻醉处死,迅速取一侧附睾尾,检测精子数量、活力和畸形。腹主动脉取血,检测全血硒含量,取肝脏和睾丸组织,检测两种组织硒含量以及睾丸GPx4活性。
      结果  适硒、低硒和缺硒组体重增加分别为207.88,204.05和198.24 g。适硒、低硒和缺硒组全血硒含量分别为421.57,365.35,126.05 ng/g,两两比较差异有统计学意义;肝脏硒含量分别为57.93,40.52,8.79 ng/g,两两比较差异有统计学意义;睾丸组织硒含量和精子数量无统计学差异。适硒组有活力精子百分比(63.07 %)高于低硒(53.91 %)和缺硒组(54.15 %),差异有统计学意义。适硒组未发现畸形精子,低硒组有1个无定型头精子,缺硒组有1个无钩头精子。与适硒(6.86 pmol/mL)和低硒(6.54 pmol/mL)组比较,缺硒组睾丸组织GPx4活性(5.09 pmol/mL)明显降低。
      结论  硒摄入可影响睾丸组织GPx4活性,进而影响精子活力并可能导致精子畸形。

     

    Abstract:
      Objective  To observe the influence of different selenium (Se) levels in fodder on reproductive function in male Wistar rats.
      Methods  Totally 36 four-week male weanling Wistar rats were randomly divided into three groups according to their body weight. After one week adaptive breeding, the rats of the three groups were fed with the fodder containing sufficient, low, and deficient Se content (S-, L-, and D-Se) for 9 weeks. The weight gains of the rats were recorded weekly. By the end of treatment, the rats were sacrificed and their cauda epididymidis specimens were sampled immediately for detections of sperm density, motility and malformation. Se content in blood, liver and testis samples of the rats were detected and glutathione peroxidase 4 (GPx4) in testis samples were determined.
      Results  For the rats of S-, L-, and D-Se group, the weight gain were 207.88, 204.05, and 198.24 grams; the blood Se concentration were 421.57, 365.35, and 126.05 ng/g; and the Se concentration of liver tissues were 57.93, 40.52, and 8.79 ng/g. There were significant differences in Se concentration of blood and liver tissues but there were no significant differences in Se concentration of testis tissue and sperm density among the rats of the three groups. The sperm motility ratio was 63.07%, 53.91%, and 54.15% for the rats of S-, L-, and D-Se group, with a significant difference. Sperm malformations were observed in the rats of L- and D-Se group but not in the rats of S-Se group. Significantly decreased GPx4 activity was detected in the rats of D-Se group compared to that in the rats of S- and L-Se group (5.09 vs. 6.86 and 6.54 pmol/ml).
      Conclusion  Dietary selenium intake could influence GPx4 activity in testis tissues, which could further impact sperm activity and may induce sperm malformation in rats.

     

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