Huang Jianying, Cui Hengmin, Peng Xi, Fang Jing, Zuo Zhicai, Deng Junliang, Wang Xun, Wu Bangyuan
Key Laboratory of Animal Diseases and Environmental Hazards of Sichuan Province, Ya'an, Sichuan, China, 625014.
Biol Trace Elem Res. 2014 Jun;159(1-3):183-91. doi: 10.1007/s12011-014-0003-y. Epub 2014 May 8.
This study was designed to evaluate the effects of dietary nickel chloride (NiCl2) on the splenic immunity in broilers by observing changes of cytokine mRNA expression and protein levels, immunoglobulin (IgA, IgG, and IgM) contents, and IgA+ B cell and T-cell numbers using the methods of qRT-PCR, flow cytometry (FCM), and ELISA. A total of 240 1-day-old avian broilers were equally allocated into four groups and fed on a corn-soybean basal diet as the control diet or the same diet supplemented with 300, 600, and 900 mg/kg NiCl2 for 42 days. The mRNA expression and protein levels of IL-2, IL-6, IL-10, IL-12, TNF-α/LITAF, IFN-γ, and IgA, IgG, and IgM contents were significantly decreased (p<0.05 or p<0.01) in the 300-, 600-, and 900-mg/kg NiCl2 groups when compared with those of the control group, which was consistent with the reduction of T-cell subset percentages and IgA+ B cell numbers in the 300-, 600-, and 900-mg/kg NiCl2 groups. The abovementioned results showed that dietary NiCl2 in excess of 300 mg/kg caused damage on splenocytes and splenic immune function. The results of the present study provided new experimental evidences for further study on the effect mechanism of NiCl2 on splenic immunity.
本研究旨在通过采用实时荧光定量聚合酶链反应(qRT-PCR)、流式细胞术(FCM)和酶联免疫吸附测定(ELISA)等方法,观察细胞因子mRNA表达和蛋白水平、免疫球蛋白(IgA、IgG和IgM)含量以及IgA+B细胞和T细胞数量的变化,来评估日粮中氯化镍(NiCl₂)对肉鸡脾脏免疫的影响。总共240只1日龄肉仔鸡被平均分为四组,分别饲喂玉米-大豆基础日粮作为对照日粮,或饲喂添加300、600和900 mg/kg NiCl₂的相同日粮,持续42天。与对照组相比,300、600和900 mg/kg NiCl₂组中白细胞介素-2(IL-2)、白细胞介素-6(IL-6)、白细胞介素-10(IL-10)、白细胞介素-12(IL-12)、肿瘤坏死因子-α/脂多糖诱导肿瘤坏死因子-α(TNF-α/LITAF)、干扰素-γ(IFN-γ)的mRNA表达和蛋白水平以及IgA、IgG和IgM含量均显著降低(p<0.05或p<0.01),这与300、600和900 mg/kg NiCl₂组中T细胞亚群百分比和IgA+B细胞数量的减少一致。上述结果表明,日粮中NiCl₂超过300 mg/kg会对脾细胞和脾脏免疫功能造成损害。本研究结果为进一步研究NiCl₂对脾脏免疫的作用机制提供了新的实验证据。