畜牧兽医学报 ›› 2010, Vol. 41 ›› Issue (6): 761-768.doi:

• 基础兽医 • 上一篇    下一篇

高钼对艾维茵肉鸡胸腺细胞周期和凋亡影响的研究

杨帆,崔恒敏*,肖杰,彭西,崔伟,程安春,陈涛,柏才敏   

  1. 四川农业大学动物医学院 环境公害与动物疾病四川省高校重点实验室,雅安 625014
  • 收稿日期:1900-01-01 修回日期:1900-01-01 出版日期:2010-06-25 发布日期:2010-06-25
  • 通讯作者: 崔恒敏

Effect of Dietary High Molybdenum on the Cell Cycle and Apoptosis of Thymus in Broilers

YANG Fan, CUI Heng-min*, XIAO Jie, PENG Xi, CUI Wei,CHENG An-chun, CHEN Tao, BAI Cai-min   

  1. Key Laboratory of Environmental Hazard and Animal Diseases of Sichuan Province,College of Veterinary Medicine, Sichuan Agricultural University, Ya′an 625014, China
  • Received:1900-01-01 Revised:1900-01-01 Online:2010-06-25 Published:2010-06-25

摘要: 本文旨在研究高钼对肉雏鸡胸腺的影响。300只1日龄艾维茵肉鸡健雏随机分为4组,分别饲以对照日粮(Mo 13 mg·kg-1)和高钼日粮(Mo 500 mg·kg-1,高钼Ⅰ组;Mo 1 000 mg·kg-1,高钼Ⅱ组;Mo 1 500 mg·kg-1,高钼Ⅲ组)6周,以实验病理学和流式细胞术的方法观察研究雏鸡胸腺变化。与对照组比较,高钼Ⅰ、Ⅱ、Ⅲ组胸腺淋巴细胞减少,胸腺小体增大增多,肌样细胞增多;胸腺绝对质量和脏器指数显著降低(P<0.05或P<0.01);流式细胞仪测定,高钼Ⅰ、Ⅱ、Ⅲ组胸腺细胞G0/G1期显著升高(P<0.05或P<0.01),S期、G2+M期和增殖指数(PI)显著降低(P<0.05或P<0.01),同时凋亡率显著高于对照组(P<0.01)。TUNUL染色观察结果与流式细胞仪检测结果一致。结果表明,日粮钼含量500 mg·kg-1及其以上可抑制胸腺的生长发育,导致雏鸡细胞免疫功能受损。

Abstract: The experiment was conducted with the objective of examining the effects of high molybdenum on the thymus in the broilers by the methods of experimental pathology and flow cytometry(FCM).360 one-day-old Avian broilers were randomly divided into four groups,and fed on diets as follows:Control diet (Mo 13 mg·kg-1) and High molybdenum diets(Mo 500 mg·kg-1, High molybdenum groupⅠ; Mo 1 000 mg·kg-1, High molybdenum groupⅡ; Mo 1 500 mg·kg-1, High molybdenum group Ⅲ) for 6 weeks. The results showed that decreased lymphocytes, enlarged Hassall′s corpuscles and increased myoid cells were observed in high molybdenum groupsⅠ,Ⅱand Ⅲ in comparison with those of control group histopathologically. The weight and the relative weight of thymus were decreased. The statistical analyses by FCM indicated that the G0/G1 phase of thymocyte was increased (P<0.05 or P<0.01) and the G2+M phase, S phase of thymocyte and the PI (Proliferating index) were decreased (P<0.05 or P<0.01) in high molybdenum groupsⅠ,Ⅱ and Ⅲ. Meanwhile, the percentage of cellular apoptosis was higher in high molybdenum groupsⅠ,Ⅱ and Ⅲ than that in control group. Also, the TUNEL staining was consistent with the result of FCM. It was concluded that dietary molybdenum in excess of 500 mg·kg-1 inhibited the development of thymus, caused pathological changes in the thymus and impaired the function of cellular immunity in broilers.