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Modulator Effects of Astragals Polysaccharides on Duodenum Mucosal Immunity of Broilers

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  • College of Animal Science and Technology, Hebei North University, Zhangjiakou 075000, China

Received date: 2014-12-10

  Online published: 2015-05-13

Abstract

This experiment was conducted to investigate the modulator effects of astragals polysaccharides (APS) on duodenum mucosal immunity of broilers. Two hundred Arbor Acres broilers were randomly divided into four groups of 50 broilers per group: group Ⅰ was control group, while the other 3 groups were experimental groups which broilers were orally administered with 0.5 mL APS at 3 different concentrations (6, 4, 2 mg/mL) once per day for three days, and broilers in group Ⅰ were oral administratied the same volume of saline. All broilers at 7 days of age were vaccined with combined vaccine against Newcastle disease and infectious bronchitis with 2 times the volume by drop and nasal immunization. Duodenum mucosa was sampled on 8, 15, 22 days of age with ten broilers for detecting contents of immunoglobulin and interleukin-2 (IL-2), and for measurement of the numbers of mucosal immunity-associated cells, respectively. The results showed as follows: contents of immunoglobulin A, immunoglobulin G, immunoglobulin M of duodenum mucosa were significantly higher in broilers at age of 15 days drinking 6 and 4 mg/mL APS than the control (P<0.05). Content of IL-2 in duodenum mucosa and the numbers of intraepithelial lymphocyte, goblet cell and mast cell were significantly higher in broilers at age of 15 and 22 days drinking 6 and 4 mg/mL APS than the control (P<0.05 or P<0.01). It is concluded that oral administration of APS enhances duodenum mucosal immunity of broilers, and the proper concentration of APS was 6 and 4 mg/mL.

Cite this article

WANG Haifeng, GUO Bing . Modulator Effects of Astragals Polysaccharides on Duodenum Mucosal Immunity of Broilers[J]. Chinese Journal of Animal Nutrition, 2015 , 27(5) : 1534 -1539 . DOI: 10.3969/j.issn.1006-267x.2015.05.025

References

[1] 吕晓静,孟小宾,王小武,等.黄芪多糖的免疫作用机制研究进展[J].中国兽药杂志,2014(5):66-69.

[2] 孙波,陈静,吴娟,等.黄芪多糖对免疫抑制肉鸡生长性能、肠道菌群及免疫功能的影响[J].中国畜牧兽医,2014,41(8):101-106.

[3] 赵天章,李慧英,王志刚,等.黄芪多糖对肉仔鸡血清免疫细胞因子含量及小肠诱导型一氧化氮合成酶mRNA表达的影响[J].动物营养学报,2014,26(4):1011-1018.

[4] 常兰,张鹏飞,陈付菊,等.藏羚羊和藏绵羊小肠黏膜结构和黏膜免疫相关细胞的比较[J].中国病理生理杂志,2012,28(9):1658-1664.

[5] 朱惠玲,谢小利,刘玉兰,等.脂多糖应激对断奶仔猪肠黏膜免疫屏障的影响[J].中国畜牧杂志,2009,45(5):14-17.

[6] 黄其春,陈彤,郑新添,等.银杏叶提取物对肉仔鸡十二指肠黏膜免疫的调节作用[J].西北农林科技大学学报:自然科学版,2011,39(11):25-30.

[7] 余树民,甘梦,左之才,等.中药复方对免疫抑制模型小鼠细胞因子、免疫球蛋白及红细胞免疫黏附功能的影响[J].西北农林科技大学学报:自然科学版,2014,42(4):27-32.

[8] 王俊丽,章世元,徐春燕,等.黄芪多糖对肉仔鸡生产性能和部分免疫指标的影响[J].中国饲料,2010(7):18-21.

[9] 赵天章,李慧英.黄芪多糖对肉仔鸡生长性能和免疫功能的影响[J].饲料工业,2014,35(2):19-24.

[10] 吕健,李孟军.肠上皮内淋巴细胞研究进展[J].胃肠病学,2011,16(5):310-313.

[11] 胡艳艳,刘小伟.肠道杯状细胞结构和功能的研究进展[J].国际病理科学与临床杂志,2013,33(5):424-430.

[12] KALESNIKOFF J,GALLI S J.New developments in mast cell biology[J].Nature Immunology,2008,9(11):1215-1223.  

[13] 姜楠,胡易,陈耀星,等.肥大细胞在动物肠道黏膜免疫屏障中的作用[J].中国畜牧兽医,2011,38(8):167-170.

[14] 栾维民,杨树宝,顾玉宝,等.鸡肠相关性淋巴组织中IFN-γIL-2 mRNA表达的动态变化[J].中国兽医科学,2011,41(3):292-297.
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