研究简报

γ-氨基丁酸对断喙雏鸡血清细胞因子含量及脾脏中 Bcl-2和Fas基因mRNA表达量的影响

  • 谢婉莹 ,
  • 侯新燕 ,
  • 闫峰宾 ,
  • 韩瑞丽 ,
  • 孙桂荣 ,
  • 康相涛
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  • 河南农业大学牧医工程学院, 河南省家禽种质资源工程研究中心, 郑州 450002

收稿日期: 2012-02-01

  网络出版日期: 2012-07-05

基金资助

现代农业产业技术体系建设专项资金(CARS-41-K04)及河南省重大科技攻关项目(112101110800)

γ-Aminobutyric Acid Affects Serum Cytokine Contents and mRNA Expression Levels of Bcl-2 and Fas genes in Spleen of Chicks under Beak Trimming Stress

  • XIE Wanying ,
  • HOU Xinyan ,
  • YAN Fengbin ,
  • HAN Ruili ,
  • SUN Guirong ,
  • KANG Xiangtao
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  • College of Livestock Husbandry and Veterinary Engineering, Henan Agricultural University, Henan Innovative Engineering Research Center of Poultry Germplasm Resource, Zhengzhou 450002, China

Received date: 2012-02-01

  Online published: 2012-07-05

摘要

本试验旨在研究γ-氨基丁酸(GABA)对断喙应激条件下雏鸡生长性能、血清细胞因子含量及脾脏中细胞凋亡相关基因B细胞淋巴瘤/白血病2(B-cell lympoma/leukemia-2,Bcl-2)和Fas基因mRNA表达量的影响。选取1日龄体重相近的健康固始鸡公雏360只,随机分为5个组,每组6个重复,每个重复12只鸡。其中A、B、C组均为断喙组,饮水中分别添加40、60和80 mg/kg的GABA;D组不断喙,不添加GABA;E组断喙,不添加GABA。结果表明:1)断喙应激导致雏鸡采食量减少、体重下降,添加GABA可以提高采食量和体重;2)断喙应激引起了血清白细胞介素1β(IL-1β)、白细胞介素6(IL-6)和肿瘤坏死因子α(TNF-α)含量的升高,第1、5天E组血清IL-1β含量显著高于D组(P<0.05),添加80 mg/kg GABA显著降低了血清IL-1β含量(P<0.05);与D组相比,断喙后第1、7天E组血清TNF-α和IL-6含量均显著升高(P<0.05),添加80 mg/kg GABA后显著降低(P<0.05);3)E组第1、3、7天脾脏中促凋亡基因Fas mRNA表达量显著高于D组,添加GABA后下降,且随着GABA剂量加大而进一步降低(P<0.05),添加80 mg/kg GABA可轻度上调抗凋亡基因Bcl-2 mRNA表达量(P>0.05)。由此可知,GABA在改善断喙应激雏鸡生长性能方面具有良好效果,同时添加GABA抑制了断喙应激后雏鸡血清细胞因子含量以及脾脏中促凋亡基因Fas的mRNA表达量的升高,且添加80 mg/kg效果较好。

本文引用格式

谢婉莹 , 侯新燕 , 闫峰宾 , 韩瑞丽 , 孙桂荣 , 康相涛 . γ-氨基丁酸对断喙雏鸡血清细胞因子含量及脾脏中 Bcl-2和Fas基因mRNA表达量的影响[J]. 动物营养学报, 2012 , 24(7) : 1352 -1360 . DOI: 10.3969/j.issn.1006-267x.2012.07.021

Abstract

This experiment was conducted to investigate the effects of γ-aminobutyric acid (GABA) on growth performance, serum cytokine contents and mRNA expression levels of apoptosis-related gene B-cell lympoma/leukemia-2 (Bcl-2) and Fas gene in spleen of chicks under beak trimming stress. A total of 360 one-day-old healthy Gu-shi male chicks were randomly divided into 5 groups (A, B, C, D and E) with 6 replicates per group and 12 chicks per replicate. Groups A, B and C were supplemented with 40, 60 and 80 mg/kg GABA in drinking water, group D was not supplemented with GABA, and group E was supplemented with GABA. The results showed as follows: 1) beak trimming induced FI and BW to decrease, whereas supplemented with GABA could increased FI and BW of chicks under beak trimming stress (P<0.05). 2) The contents of interleukin-1β (IL-1β), interleukin-6 (IL-6)and tumor necrosis factor-α (TNF-α)in serum were increased by beak trimming stress, the serum IL-1β content in group E was significantly higher than that in group D on the first and fifth days (P<0.05), and the supplementation of 80 mg/kg GABA significantly decreased the serum IL-1β content. Compared with group D, the contents of TNF-α and IL-6 in serum in group E were significantly increased on the first and seventh days (P<0.05), and supplementation of 80 mg/kg GABA significantly decreased the contents of TNF-α and IL-6 in serum (P<0.05). 3) The splenetic Fas gene mRNA expression level in group E was significantly higher than that in group D on the first, third and seventh days (P<0.05), and the splenetic Fas gene mRNA expression level was decreased with GABA supplementation (P<0.05), the supplementation of 80 mg/kg GABA could increase the splenetic Bcl-2 gene mRNA expression level (P>0.05). In conclusion, GABA can improve the growth performance of chick under beak trimming stress, and it also inhibit serum cytokines contents and splenetic Fas gene mRNA expression under beak trimming stress, and the optimum supplemention level of GABA is 80 mg/kg.

参考文献

[1] HESTER P Y,SHEA-MOORE M.Beak trimming egg-laying strains of chickens[J].World’s Poultry Science,2003,59:458-474.
[2] GENTLE M J,WADDINGTON D,HUNTER L H,et al.Behavioural evidence for persistent pain following partial beak amputation in chickens[J].Applied Animal Behaviour Science,1990,27:149-157.
[3] GENTLE M J,HUNTER L N,WADDINGTON D.The onset of pain related behaviours following partial beak amputation in the chicken[J].Neuroscience Letters,1991,128:113-116.
[4] GONG C,HOFF J T,KEEP R F.Acute inflammatory reaction following experimental intracerebral hemorrhage in rat[J].Brain Research,2000,871(1):57-65.  
[5] CASTILLO J,OAVALOS A,ALVAREZ-SABIN J,et al.Molecular signatures of brain injury after intracerebral hemorrhage[J].Neurology,2002,58(4):624-629.  
[6] 吴家幂,马领松,周向阳,等.补体在脑出血后脑组织损伤机制中的作用[J].中华神经医学杂志,2006,5(2):152-154.
[7] 孙桂荣,李燕,康相涛,等.断喙应激对雏鸡胸腺细胞凋亡及相关凋亡蛋白表达的影响[J].畜牧兽医学报,2011,42(7):1000-1006.
[8] GENTLE M J.Cutaneous sensory afferents recorded from the nervus intramandibularis of Gallus gallus var domesticus[J].Comparative Physiology A,1989,164:763-774.
[9] XU X G,YANG Z F,HUANG S H,et al.Promotive effects of GABA on acid secretion from isolated mouse stomach in vitro[J].Acta Zoologica Sinica,2001,47:170-175.
[10] ZAKUSOV W,OATROVSKAYA R U,BULAYEV V M.GABA-opiates interactions in the activity of analgesics[J].Archives Internationales de Pharmacodynamie et de Therapie,1983,265:61-75.
[11] CHERUBINI E,GAIARSA J L,BEN-ARI Y.GABA:an excitatory transmitter in early postnatal life[J].Trends in Neurosciences,1991,12:515-519.
[12] FAN Z Y,DENG J P,LIU G H,et al.Effects of γ-aminobutyric acid on the performance and internal hormone levels in growing pigs[J].Chinese Journal of Animal Nutrition,2007,19(4):350-356.
[13] PIGUERAS L,VICENTE M.Peripheral GABA-β agonists stimulate gastric acid secretion in mice[J].British Journal of Pharmacology,2004,142:1038-1048.
[14] KATO S,ARAKI H,KAWAUCHI S.Body temperature dependence in baclofen-induced gastric acid secretion in rats relation to capsaicin sensitive affront neurons[J].Life Sciences,2001,68:1951-1963.
[15] SHUYE P U,JAIN M R,HORVATH T L.Interactions between neuropeptide Y and γ-ammobutyric acid in stimulation of feeding:a morphological and pharmacological analysls[J].Endocrinology,1999,140:933-940.
[16] KHANSARI D N,MURGO A J,FAITH R E.Effects of stress on the immune system[J].Immunol Today,1990,11:170-175.
[17] CUNHA F Q,FERREIRA S H.Peripheral hyperalgesic cytokines[J].Advances in Experimental Medicine and Biology,2003,521:22-39.
[18] ARRUDA J,SWEITZER L S,RUTKOWSKI M D,et al.Intrathecal anti-IL-6 antibody and IgG attenuates peripheral nerve injury-induced mechanical allodynia in the rat:possible immune modulation in neuropathic pain[J].Brain Research,2000,879:216-225.
[19] FRISEN J,RISLING M,FRIED K.Distribution and axonal relations of macrophages in a neuroma[J].Neuroscience,1993,55:1003-1013.
[20] SPANGELO B L,HORRELL S,GOODWIN A L,et al.Somatostatin and gamma-aminobutyric acid inhibit interleukin-1β-stimulated release of interleukin-6 from rat c6 glioma cells[J].Neuroimmunomodulation,2004,11:332-340.
[21] JOSEPH D,ROACH J D,AGUINALDO G T,et al.γ-aminobutyric acid inhibits synergistic interleukin-6 releases but not transcriptional activation in astrocytoma cells[J].Neuroimmunomodulation,2008,15:117-124.
[22] ITOH N,NAGATA S.A novel protein domain required for apoptosis[J].Biological Chemistry,1993,268:10932-10939.
[23] WILLIAMS G T,SMITH C A.Molecular of apoptosis: genetic controls on cell death[J].Cell,1993,74:777-779.
[24] 胡书超,张建祥.脑出血后的神经细胞凋亡机制及治疗策略[J].国外医学脑血管疾病分册,2004,12(7):524-526.
[25] XUE M,DELBIGIOL M R.Acute tissue damage after injections of thrombin and plasmin into rat striatum[J].Stroke,2001,32(9):2164-2169.  
[26] HOLMIN S,MATHIESAN T.Intracerebral administration of interleukin 1 beta and induction of inflammation,apoptosis and vasogenic edema[J].Neurosurg,2000,92(1):108-120.  
[27] MAYNE M,NI W,YAN H J,et al.Antisense oligodeoxynucleotide inhibition of tumor necrosis factor-alpha expression is neuropotective after intraerbral hemorrhage[J].Stroke,2001,32(1):240-248.  
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