黄芪注射液对犬心脏双向变时作用的初步观察

为了观察黄芪注射液对正常犬和二尖瓣关闭不全病理模型 (MR)犬的变时作用 ,并探讨其机制 ,在异氟烷吸入麻醉下 ,对正常及外科方法制作的犬亚急性二尖瓣关闭不全模型 (术后 5 0天后 )一次性静脉推注含生药 2 g/ m L的黄芪注射液 1 .2 5 m L/ kg,通过体表心电图测定心率和 PQ、QRS、RR、QT,并计算 QTC(QT/ RR)间期。在正常犬 ,开始注射黄芪注射液后 ,心率出现先减少后恢复再持续减少和显著变化。 MR模型犬开始注射液后 ,心率出现先升高后恢复再持续升高的显著变化。 MR模型犬的心率减慢变化与 RR、PQ、QT、QTc呈高度显著负相关 (P<0 .0 1 )。表明黄芪注射液对正常比格犬 ,具有加快心率的正性变时作用。对二尖瓣闭锁不全 (MR)模型犬具有减缓心率的负性变时作用。黄芪注射液的变时作用似与机体的机能状态有关 ,呈现双向调节作用。     

沙拉沙星对实验性感染猪链球菌病及大肠杆菌病的药效学

为兽医临床合理应用沙拉星（Ｓarafloxacin）提供理论依据,就其对实验性感染猪链球菌 病及大肠杆菌病的药效学进行了研究。以试管２倍稀释法测得沙拉沙星对兰氏Ｃ群类马链球菌（Ｃ５５１２０）和猪大肠杆菌（Ｏ５５）的最小抑菌浓度（ＭＩＣ）分别是０．８mg/Ｌ及０．０５mg/Ｌ。肌注给药对猪链球菌病和大肠杆菌病的试验性治疗结果不明,低、中 高剂量沙拉沙星组２．５、５、１０mg/kg）及环丙沙星组（５mg/kg）用药５d（每隔１２     

乳胶凝集试验与血清中和试验检测猪伪狂犬病血清抗体的 …

应用血清中和试验（ＳＮＴ）和伪狂犬病乳胶凝集试验（ＬＡＴ）诊断试剂盒对两种伪狂犬病是性血清、伪狂犬病病毒（ＰＲＶ）高兔血甭及６０份被检猪血清进行了ＰＲＶ抗体效价测定和相关性分析,两种方法测得的抗体效价之间呈强相关性（ｒ＝０．９６）,且ＬＡＴ效价比ＳＮＴ一般高出一个滴度;能干为自３５个猪场的４１４份猪血清进行了ＰＲＶ抗体检测,并与ＳＮＴ检测结果进行了对比,结果在ＳＮＴ检测为阳笥的１７１份血清中,ＬＡ     

Vero E6细胞酵母双杂交cDNA文库的构建及鉴定

To seek out proteins which interact with structural proteins of porcine epidemic diarrhea virus （PEDV） in Vero E6 cells and study the mechanisms of viral infection.We created a Vero E6 cDNA yeast hybrid library. The total RNA of Vero E6 was extracted using Trizol method, and double strands cDNA was synthesized by SMART technique. We created a Vero E6 cDNA library by using homologous recombination in yeast. The results showed that the titer of cDNA library was 9.7×10⁸ CFU with the average of inserted fragments about 1.6 kb, and the recombination rate was 87%. These data indicated that the yeast two-hybrid cDNA library of Vero E6 was successfully constructed and might be useful for screening the host proteins interacting with structure protein of PEDV.     

放牧对西藏高寒嵩草草甸地上生物量空间分布的影响

以西藏自治区工布江达县的高寒嵩草（Kobresia）草甸为研究对象,利用地上生物量测定法对草地群落进行实地调查,并结合γ分布模型,从空间异质性角度来探索放牧对西藏高寒草甸地上生物量及其空间分布格局的影响,以期为高寒牧区退化草地的恢复及生产力的提高提供理论指导。结果表明：未放牧区（N）、适度放牧区（M）和重度放牧区（H）植物种地上生物量的空间分布与γ模型均具有很好的吻合性;样方内的平均生物量随着放牧强度的增大而减少,且适度放牧、重度放牧与未放牧区生物量之间均差异极显著（P<0.01）;群落的空间异质性表现为N>H>M,且草地植物种的生物量与其空间异质性负相关。因此在草地的管理与利用中,应有效控制植物群落的空间异质性来提高草地生产力,实现草畜平衡。     

Effect of Fermentation Bed with Spent Mushroom Substrate of Pleurotus eryngii on Weaning Piglets

[Objective] The paper was to investigate effects on fermentation bed temperature,growth performance,diarrhea rate and digestive en-zyme activity of weaning piglets by using spent mushroom substrate of Pleurotus eryngii as padding.[Method] A total of 120 weaning piglets(Duroc × Landrace ×Yorkshire) with average initial body weight of(8.0 ±0.5)kg were allocated to five dietary treatments in a randomized complete block design for 42 d,each of which was replicated three times with eight piglets per replicate(half male,half female).The padding for control group was(50% sawdust +50% rice husk);experimental group Ⅰ 100% spent mushroom substrate;experimental group Ⅱ(15% sawdust +15% rice husk +70% spent mushroom substrate);experimental group Ⅲ(25% sawdust +25% rice husk +50% spent mushroom substrate);experimental group Ⅳ(35% sawdust +35% rice husk +30% spent substrate).[Result] There was no significant difference in surface temperature of fermentation bed between experimental groups and control group(P0.05).Compared with the control group,the temperature under 20 cm of fermentation bed in ex-perimental groups I,Ⅱ and Ⅲ increased significantly(P0.05).Except for experimental group Ⅳ,other three experimental groups had higher aver-age daily gain(P0.05) and experimental group Ⅰ had higher average daily feed intake(P0.05) compared to the control group.The diarrhea rate and mortality of weaning piglets in experimental groups Ⅱ,Ⅲ and Ⅳ were significantly decreased compared with the control group(P0.05).Compared with the control group,other three experimental groups had higher digestive enzyme activity in duodenal contents except for experimental group Ⅳ(P0.05).[Conclusion] Spent mushroom substrate of P.eryngii can be used as fermentation bed padding,and the optimal proportion was experimental group Ⅲ.     

CDV、CPV和CPIV多重PCR检测方法的建立

为了建立一种快速诊断犬瘟热病毒、犬细小病毒和犬副流感病毒的多重PCR方法,参照GenBank中的犬瘟热病毒(CDV)、犬细小病毒(CPV)、犬副流感病毒(CPIV)基因序列,设计了3对引物分别用于特异扩增犬瘟热病毒F基因、犬细小病毒VP2基因和犬副流感病毒F基因上的目的片段.通过优化反应条件,建立同时扩增CDV(740 bp)、CPV(419 bp)和CPIV(559 bp)的多重PCR方法.结果表明特异性和敏感性良好,对CDV、CPV、CPIV3种病毒的最低核酸检测量为1 ng/μL.临床样品的多重PCR检测结果表明,建立的多重PCR方法能够对CDV、CPV、CPIV单个感染或混合感染的临床样品进行快速鉴别诊断.     

不同投喂方式对革胡子鲶消化酶的影响

在（25±1）℃水温、自然光照条件下,设3种投喂方式饲养革胡子鲶（clarias leath-er）：第1种连续投喂整个试验期间不间断,第2和3种分别连续投喂3、7 d 后饥饿1 d,3种方式分别以R0（对照组）、R1/3、R1/7表示,试验周期共45 d。结果显示：R0、R1/3和R1/7组胃、后肠和肝脏中蛋白酶活性影响差异不显著,但前肠和中肠内蛋白酶活性影响存在差异(P<0.05)。R0、R1/3、R1/7组的胃、前肠、中肠、后肠和肝脏中淀粉酶影响不显著,R0、R1/3、R1/7的胃、前肠和肝脏内脂肪酶活性影响差异显著(P<0.05),而R0、R1/3、R1/7组中肠和后肠中脂肪酶活性影响差异不显著(P>0.05)。     

《中华人民共和国兽药典》二O一O年版三部非禽源细胞及其制品外源病毒检验解读

对《中华人民共和国兽药典》二○一○年版三部中"非禽源细胞及其制品外源病毒检验"新变化和关键点进行了解读,为规范和完善非禽源外源病毒检验提供了参考。     

高致病性猪繁殖与呼吸综合征病毒非结构蛋白Nsp4的表达及其抗血清的制备

根据GenBank中已发表的高致病性猪繁殖与呼吸综合征病毒（Highly Pathogenic Porcine Reproductive and Respiratory Syndrome Virus,PRRSV）HuN4株全基因组序列,设计合成一对引物,对PRRSV HuN4株非结构蛋白Nsp4（Nonstructural protein 4基因进行RT-PCR扩增,克隆到原核表达载体pET30a（＋）中,构建重组表达载体pET30a-Nsp4,经酶切测序鉴定。将pET30a-Nsp4转化表达菌株BL21（DE3）,诱导可表达分子量约为27kDa重组蛋白。Westernblot显示其具有较好的反应原性,经镍离子亲和层析（Ni-NTA）纯化获得了高纯度的可溶性重组蛋白。将纯化的Nsp4蛋白免疫BALB／c小鼠,抗血清ELISA效价达1：16000,Western blot和IFA表明,所制备的抗血清能够特异性识别PRRSV自身表达的Nsp4蛋白。本研究获得了可溶性的PRRSV Nsp4蛋白,制备了Nsp4特异性多抗血清,为进一步研究Nsp4蛋白的亚细胞定位及功能奠定了基础。