饲粮中添加抗菌肽对肉鸭增重及血清尿素氮、总蛋白水平的影响   总被引：12，自引：1，他引：12  

陈晓生  张辉华  罗竞彪  温刘发  黄国庆  黄自然 《中国饲料》2005,(10):21-23

240只1日龄肉鸭随机成分4组,每组设3个重复,对照组用基础日粮,试验组在基础日粮上每千克分别添加1、2、3mL抗菌肽制剂。结果显示:1)2、3mL/kg添加量组增重效果显著(P<0.05),3mL/kg添加量组最佳;净肉率升高,达到显著水平(P<0.05),其中主要是胸肌率上升;腹脂率降低但差异不显著(P>0.05);料重比无显著变化(P>0.05)。2)血清总蛋白浓度差异不显著(P>0.05),但尿素氮浓度下降,2、3mL/kg添加量组达显著水平(P<0.05),3mL/kg添加量组最低。  相似文献   

反刍动物肽营养研究进展     

张香斋  李成会 《中国饲料》2005,(12):22-24

本文综述了反刍动物肽的吸收特点及影响因素,肽的吸收代谢机制,肽对瘤胃微生物的调控及对反刍动物生产性能发挥的作用,以及饲料蛋白源活性肽的开发应用。  相似文献   

酵母蛋白饲料培养条件的研究   总被引：4，自引：0，他引：4  

于荣  董颖超  秦玉昌 《中国饲料》2005,(18):20-21

对啤酒酵母进行发酵试验,结果表明:该酵母最优的培养条件是麦芽汁培养基稀释倍数2.5,培养时间20h,蔗糖添加量10Brix,尿素添加量0.02%,且酵母菌耐酸耐铜的性能好。  相似文献   

营养补偿初期苏尼特母羊对NDF、ADF消化能力的研究     

苗志国  侯先志  敖长金  吴庶青 《中国饲料》2005,(21):15-16

将45只处于妊娠后期(90～150d)的苏尼特母羊随机分成4组,以不同的营养水平(代谢能:0.20、0.33、0.44、0.86MJ/kgW0.75·d)分组饲养,分娩后进行补偿生长试验,研究妊娠后期不同营养限制程度的母羊在补偿初期(分娩后0～6周)对中性洗涤纤维(NDF)、酸性洗涤纤维(ADF)消化率的影响。结果表明:在补偿初期,各组母羊对ADF、NDF的消化率随着营养限制程度的增强而下降。  相似文献   

哺乳犊牛的消化特点与蛋白质需要   总被引：7，自引：0，他引：7  

李辉  刁其玉 《中国饲料》2005,(21):22-24

本文从犊牛的消化生理特点出发,综述了犊牛出生后的生理特征及蛋白质、必需氨基酸的需要量,并对代乳品中蛋白质原料进行了论述。  相似文献   

猪水泡病病毒结构蛋白基因的克隆及其蛋白二级结构和淋巴细胞表位的预测     

郑海学刘湘涛  尚佑军刘光清白兴文  罗静初谢庆阁 《中国兽医科技》2005,35(11):843-850

以免疫信息学和反向疫苗学为理论根据，利用RT-PCR法获得了猪水泡病病毒（SVDV）HK／70株的基因组序列并测序，应用生物信息学相关软件和方法，对SVDV结构蛋白的二级结构的不同方面及其抗原特异性淋巴细胞表位进行了预测，综合评价了SVDV结构蛋白的抗原特异性细胞表位，并计算出一些潜在的抗原位点。结果表明，VP1蛋白含有的细胞优势抗原表位最多，但其他结构蛋白也含有抗原特异性淋巴细胞表位，有的甚至有可能成为优势抗原表位或对优势抗原表位有协同作用。  相似文献   

不同月龄生长公牛日粮营养物质消化规律的研究     

周汉林  莫放  黄鸿威  徐萍 《家畜生态》2005,(4)

本试验选用3头6月龄左右断奶中国荷斯坦公牛,在试验全程喂以相对稳定的日粮,从2003年11月1日开始,到2004年6月20日结束,用以测定中国荷斯坦生长公牛在不同生长期对饲粮中各营养成分的代谢情况。试验结果表明:日粮中的DM、OM、NDF、ADF、淀粉和粗蛋白质的表观消化率随着生长犊牛的月龄的增加而增加(P<0.05);并且9月龄以后,DM、OM、NDF、ADF和粗蛋白质的表观消化率增长不明显(P>0.05),淀粉的表观消化率则在11月龄以后增长不明显(P>0.05)。氮的净吸收率随着生长犊牛的月龄的增加而下降(P<0.05),且在9月龄以后下降不明显(P>0.05)。  相似文献   

Role of p38MAPK in production of pro-inflammatory cytokines in Kupffer cells from severe acute pancreatitis rats     

REN Hong-bo  LI Zhao-shen  XU Guo-ming  TU Zheng-xing  JIA Yi-tao  SHI Xin-gang  GONG Yan-fang 《园艺学报》2003,19(7):923-926

AIM:To investigate the role of p38 mitogen-activated protein kinase (p38MAPK) signaling pathway in the Kupffer cells (KCs) production of pro-inflammatory cytokines, tumor necrosis factor-α(TNF-α) and interleukin-1β(IL-1β), in severe acute pancreatitis (SAP) rats.METHODS:Sprague-Dwaley rats were randomized into three groups:①sham operation rats, ②SAP rats, ③SAP rats given the p38 MAPK inhibitor CNI-1493(10 mg/kg, iv). The SAP model was induced by the bili-pancreatic duct infusion with 5% sterile soduim taurocholate solution. Rats from each group were killed at 12 h after sham operation or SAP and Kupffer cells (KCs) were isolated. The mRNA expressions of TNF-α and IL-1β (by quantitative real-time RT-PCR) and p38 MAPK activity (by Western blot analysis) in KCs were examined. The levels of TNF-α and IL-1β in plasma were determined by ELISA.RESULTS:There was a significant acvitation of p38 MAPK in KCs harvested from SAP rats than those from sham operation rats. SAP also promoted the mRNA expressions of TNF-α and IL-1β in KCs and the plasma levels of TNF-α and IL-1β. These events were significantly inhibited by treatment with CNI-1493.CONCLUSIONS:p38 MAPK activation is one important aspect of the signaling events that may mediate the KCs production of pro-inflammatory cytokines, TNF-α and IL-1β, in SAP rats. The inhibition of the p38 MAPK may be a potential target in the prevention and treatment of SAP.  相似文献   

Quick detection of sex determining region protein gene in mouse fetuses     

《园艺学报》2003,19(5):622-626

AIM: To detect quickly the Y-chromosome specific sex determining region protein (Sry) gene in mouse fetuses on embryonic day 14.5 with a PCR method. METHODS: We designed specific primers with the OLIGO 5. 0 software. Templates were prepared in 30 minutes by the following way. About 1 mg embryonic tissue but not fetal liver was suspended, and treated with 200μL of lysis buffer, consisting of PCR buffer containing 20 mg/L proteinase K, 0. 5% NP-40, and 0.05% Tween 40, at 60°C for 15 minutes, heated for 5 minutes at 100 °C, 10μL was used as template. The PCR react ion was performed in 50μL, using two sets of primers specific for Sry gene (chromosome Y) and IL-3 gene (chromosome 11) . PCR conditions and cycle numbers were optimized. The assessment of the results was done by electrophoresis in 3% agarose run at high voltage. The specificity of the method was conf irmed by fluorescent in situ hybridization (FISH) using a specific male probe on embryonic tissue cells. RESULTS: Electrophoresis showed that PCR product of male control DNA consisted of a 649 bp product representing the IL-3 gene and a 444 bp product representing the Y-specific Sry gene, female control DNA only one 649 bp product. Fetuses with two bands matching those as seen inmale control DNA are the presumpt ive male fetuses. Fetuses, only the IL-3-associated 649 bp band, are the presumptive female fetuses. These were confirmed by FISH. The ent ire procedure took <3. 5 h. CONCLUSION: The established PCR assay offers a quick, simple, accurate, and sensitive detection of sex determining region protein gene in mouse fetuses. This method allowed the preparation and culture of pure male and female hematopoietic stem cells from fetal tissue.  相似文献   

Rat urotensin-II-induced main pulmonary artery contractions are mediated by MAPK     

CHEN Shao-xian  XUE Bi-cheng  GONG Yong-sheng  FAN Xiao-fang  HU Liang-gang  CHEN Yan-fan  WANG Liang-xing 《园艺学报》2003,19(10):1365-1368

AIM: To investigate rat Urotensin-II(rat U-II)-induced vasoconstriction of rat main pulmonary arteries and the role of mitogen-activated protein kinase(MAPK). METHODS: The main pulmonary artery was dissected from the male Sprague-Dawley rats and artery ring width was 3-4 mm. Concentration-response curves were generated to rat U-II(0.03 nmol/L-30 nmol/L).Inhibitor of MAPK, PD 98059(0.1 μmol/L-10 μmol/L) were added into the medium after rat U-II(30 nmol/L)induced vasoconstriction had reached plateau to construct the relaxant concentration-response curves and their EC₅₀ and E_max. RESULTS：Rat U-II was a potent vasoconstrictor of isolated rat main pulmonary arteries [EC₅₀=7.95±0.40, E_max=(14.28±6.34)% of the response to 60 mmol/L KCl]; PD 98059 caused concentration-dependent relaxations of rat U-II precontracted arteries [EC₅₀=5.91±0.45, E_max=(81.39±13.65)%]. CONCLUSION: Rat U-II was a potent vasoconstrictor of rat main pulmonary arteries and this response was mediated through MAPK.  相似文献