羔羊期和性成熟期奶山羊下丘脑中催产素的表达

采用免疫组化链霉素抗生物素蛋白-过氧化物酶法(SP法),检测羔羊期和性成熟期雌性奶山羊下丘脑中催产素表达的变化规律.结果显示,催产素免疫反应阳性神经元在羔羊和性成熟羊的视上核、室旁核、乳头体内侧核等核团均有分布,在羔羊的室周核、视前内侧核等核团广泛分布,但在性成熟羊的这些核团却未见分布.在视上核、室旁核、乳头体内侧核等核团的催产素免疫阳性神经元数量,性成熟羊显著高于羔羊(P＜0.01);这些核团中催产素免疫阳性产物的平均灰度值,羔羊显著低于性成熟羊(P＜0.01),在其他核团则羔羊高于性成熟羊,且大部分差异明显(P＜0.01).结果提示,性成熟羊下丘脑中除室周核、视前内侧核等核团外,室旁核、视上核、乳头体内侧核、乳头体后核等核团,催产素的表达高于羔羊,说明这些核团对生殖系统的发育成熟可能有重要作用.     

H5N1亚型禽流感灭活疫苗免疫鸵鸟后抗体消长规律及免疫程序的研究

为了探讨鸵鸟对H5亚型禽流感灭活疫苗的免疫原性,做好鸵鸟禽流感的防控工作,采用哈尔滨兽医研究所研制的重组H5N1亚型禽流感疫苗,不同剂量免疫鸵鸟,用HI方法检测母源抗体和免疫抗体,根据母源抗体的衰减和免疫抗体的消长规律确定首免和再免日龄.结果表明,雏鸵鸟母源抗体能维持约3周～8周;8周龄时分组首免,C1组产生的免疫反应优于C2组,抗体峰值能达到7.50 log2,维持时间为9周左右;17周龄时C1组以3.0 mL/羽进行二免,2周后抗体达到7.40log2,3周～7周抗体维持在高峰值,最高达8.80log2,以后逐渐下降,有效抗体水平能维持至接种后25周左右.二免后25周进行三免,以5 mL/羽三免后2周抗体可达到9.80log2,2周～4周抗体维持在最高峰,以后缓慢下降,期间抗体时有起伏,但有效抗体水平约可维持1年时间.三免后45周内抗体水平合格率均在70%以上.根据抗体消长规律,初步推荐了鸵鸟的免疫程序.     

奶牛乳汁孕酮免疫检测方法研究进展

有关乳汁孕酮的放射免疫检测技术和酶联免疫检测技术,近几十年来不断有报道,并逐渐成熟.但是测试费用、技术人员培养及方法本身的弊端等因素,使得这些项技术的普及受到了限制.这就要求从业人员不断创新,开发更有市场价值、老百姓更易接受的测试方法.胶体金试纸条在医学上应用广泛,已经呈现出了它应用于动物医学中,在激素测定方面乐观的应用前景.     

水产动物精氨酸需求的研究进展

精氨酸是水产动物必需氨基酸之一,在水产饲料中添加适量的精氨酸,可以提高饲料蛋白质的营养价值,促进水产健康养殖的发展。本文就近年来国内外关于水产动物对精氨酸需求的研究进展作一综述。     

氮素水平与光强互作对‘蓝伞’玉簪生长和光合特性的影响

 以蓝灰类型玉簪‘蓝伞’（Hosta 'Blue Umbrella'）为材料，研究了4种光强（自然光照的100%、50%、30%、10%）和4种氮素水平（盆栽土施尿素量0、0.5、1.5和2.5 g·kg^-1）处理对玉簪生长和光合特性的影响。结果表明：‘蓝伞’玉簪的生长和光合特性受光强、氮素水平以及光氮互作的影响。在同一氮素水平下，随着光照强度的减弱，玉簪的生物量、叶面积、叶片数、光合速率及可溶性蛋白含量均表现先上升后下降的趋势，在30%～50%光强下达到最大值；叶绿素含量则随光强的减弱而增加。在同一光照强度下，随着氮素水平的升高，玉簪的生物量、叶面积、叶片数、光合速率及叶绿素和可溶性蛋白含量均呈先上升后下降的趋势，在0.5 g·kg^-1氮素水平下达到最大值。     

遮光对青榨械光合速率及叶绿素荧光参数的影响

研究了遮光15％、35％、50％和全光照处理对青榨槭新梢生长、叶片色素含量、净光合速率以及叶绿素荧光参数的影响。结果表明，随着遮光度增加，叶片色素含量增加，叶绿素a／b减小；叶片净光合速率（Pn）、初始荧光（Fo）、原初光能转化效率（Fv／Fm）和光化学猝灭系数（qP）增加，但非光化学猝灭系数（qN）降低。全光照和遮光15％处理条件下，Pn日变化呈双峰曲线，而35％和50％处理条件下呈单峰曲线；遮光35％和50％处理条件下Fv／Fm日变化幅度较小，15％和全光照处理条件下Fv／Fm日变化呈先上升后下降再上升趋势。50％遮光处理青榨槭幼苗Pn最高，新梢年生长量最大，可在育苗生产中应用。     

The anticancer activity of genistein on implanted tumor of human primary gastric carcinoma cells in nude mice

AIM: To investigate the apoptosis of implanted tumor of primary human gastric cancer cells in nude mice induced by genistein and the relation between this apoptosis and expression of bcl-2 and bax.METHODS: Establishing a transplanted tumor model by injecting human primary gastric cancer cells into subcutaneous tissue of nude mice.The different doses of genistein (0.5mg/kg,1mg/kg and 1.5 mg/kg ) were directly injected beside tumor body respectively,for six times at an interval of two days.Then changes of tumor volume were measured continuously and tumor inhibition rate of each group was calculated.We observed the morphologic alteration by electron microscope,measured the apoptotic rate by TUNEL staining method,detected the expression of apoptosis-regulated gene bcl-2 and bax by immunohistochemical staining and RT-PCR.RESULTS: Genistein could significantly inhibit carcinoma growth when it was injected near the carcinoma.Genistein induced implanted tumors cells to undergo apoptosis with apoptotic characteristics by transmission electron microscope.The apoptosis index of above three groups was increased progressively.Positive rate of Bcl-2 protein of above three groups was decreased progressively and positive rate of Bax protein of above three groups was increased progressively by immunohistochemical staining.The density of bcl-2 mRNA decreased progressively and the density of bax mRNA increased progressively with elongation of time by RT-PCR.CONCLUSION: Genistein is able to induce the apoptosis of transplanted tumor cells.This apoptosis may be mediated by down-regulating bcl-2 and up-regulating bax mRNA and its protein.     

Effects of PDS on rat brain cortical nuclear factor kappa B in LPS shock

AIM:To explore the molecular mechanism of brain tissue injury induced by lipopolysaccharide (LPS),the effects of panaxadiol (PDS) on the expression of nuclear factor kappa B (NF-κB) in cerebral cortex of rat with LPS shock were studied. METHODS:Rats were randomly divided into LPS roup,LPS+dexamethasone group,LPS+PDS group and control group. The DNA binding activity and protein expression of NF-κB were observed. These indices were assayed at 1 h and 4 h after intravenous injection of LPS (4 mg·kg^-1). RESULTS:EMSA showed that PDS inhibited NF-κB DNA-binding activity in nuclear extracts at both 1 h and 4 h after LPS injection,compared with the LPS group (P<0.01). Western blotting showed that PDS down-regulated the expression of p65 and p50 protein in the nuclear extracts compared with the LPS group. However,the expression of p65 and p50 protein from cytosolic extracts did not show any significant change. CONCLUSION:PDS may alleviate brain injury by inhibiting NF-κB activation.