茎花葱臭木化学成分的研究

从茎花葱臭木种子中分离得到5个化合物,经理化与波谱分析鉴定为β-谷甾醇(1)、没食子酸乙酯(2)、胡萝卜苷(3)、1-O-β-D-吡喃葡萄糖基-(2S,3S,4R,8Z)-2-N-(2 ′-羟基二十四烷酰氨基)十八二氧鞘氨-8-烯(4)和2,3,2″,3″-四氢穗花杉双黄酮(5).这5个化合物均首次从该植物中分离得到.其中化合物5进行细胞毒活性测试,没有显示抑制活性.     

若尔盖人-狼冲突现状与管理研究

大中型食肉动物肇事事件导致人类与野生动物关系恶化,给生物多样性保护工作带来巨大的挑战。若尔盖湿地是我国三大湿地之一,湿地、草原分布广泛,生物多样性丰富,畜牧业发达,但近年来狼(Canis lupus)捕杀牲畜的肇事事件时有发生。为了解若尔盖野生狼肇事件的空间分布以及牧民对人-狼冲突管理的看法,本研究于2022年对若尔盖县13个乡镇83个行政村进行走访调查。结果表明：(1)多数受访者(66.0%)认为在过去5年内,若尔盖县野生狼数量有所增加;(2)狼肇事事件具有明显的空间分异性,最严重的是包座乡。包座乡临近山区,该区域牧场面积广阔、牧民饲养牲畜数量多等原因导致该镇发生狼肇事事件较多;(3)对于狼肇事,绝大多数牧民(85.0%)更希望采取经济补偿或者驱赶措施,只有少数牧民(9.4%)希望采取捕杀的措施;(4)影响牧民对狼肇事管理措施的偏好因子中,受教育程度、年龄、民族以及被杀牲畜数量有显著影响。建议加强狼种群监测管理,采取措施减少狼捕杀牲畜,优化补偿机制,缓解当地牧民与狼之间的矛盾。本研究为当前若尔盖县野生动物保护和管理决策提供了依据,对其他地区大型食肉动物与当地居民冲突管理具有借鉴意义。     

利用恒河婴猴模型对肠道病毒71型传播感染特征的生物学分析

本文在前期工作基础上,进一步对肠道病毒71型(EV71)从恒河婴猴的感染个体向其他未感染个体传播的可能性及相关生物学特性做了初步分析.通过喷雾形式经呼吸道感染1~2月龄恒河婴猴(A组);在观察临床症状同时,于感染后第7天,取该组动物粪便处理后,将上清液以喷雾形式经呼吸道感染新的婴猴个体(B组),随后对该次代感染个体进行...     

基于Voronoi图的丹顶鹤巢址空间格局分析

依据1996年、2003—2007年扎龙保护区丹顶鹤巢址数据,利用Voronoi图理论,分析了巢址的空间分布特征,计算了其拓扑指数—Voronoi图面积。结果表明,丹顶鹤巢址空间分布具有明显的空间聚类特征。以扎龙保护区的2006年巢址、居民点、国道和铁路为对象,构成其Voronoi图,较好地说明了人类活动对丹顶鹤巢址的空间格局的影响,研究结果对丹顶鹤栖息地的保护将起到重要作用。     

益生菌对调节脑梗死后大鼠运动功能的机制研究

探讨在脑梗死后康复期使用益生菌治疗促进大鼠运动功能恢复的机制。

成年雄性SPF级7～8周龄Wistar大鼠,体重200～250 g,共35只。25只大鼠颅内注射内皮素制作脑缺血模型,模型制作后5只大鼠死亡,剩余20只大鼠按照随机数表法分为缺血组（ISC组）和缺血+益生菌组（ISC+PB组）,每组10只。另外10只大鼠作为假手术组（SHAM组）。SHAM组大鼠仅使用生理盐水按照上述造模流程进行。各组均喂食普通大鼠饲料。ISC+PB组大鼠第7天开始使用益生菌VSL#3溶液进行灌胃,0.25 mL/(只•d)。采用原位末端转移酶标记（TdT-mediated dUTP nick-end labeling,TUNEL）凋亡试剂盒检测凋亡细胞。采用蛋白质免疫印迹法检测各组大鼠海马与梗死周边皮层脑源性神经营养因子（brain derived neurotrophic factor,BDNF）的蛋白水平变化。使用梯形平衡木测试大鼠的肢体运动功能。

ISC组大鼠TUNEL阳性细胞数量较SHAM组显著增多（t=3.278,P=0.016）,ISC+PB组大鼠的TUNEL阳性细胞数量低于ISC组（t=2.721,P=0.037）。ISC组大鼠海马与梗死周边BDNF蛋白表达水平高于SHAM组（t=2.012,P=0.032）,ISC+PB组大鼠海马与梗死周边皮层BDNF水平较ISC组进一步提高（t=1.892,P=0.021）。梯形平衡木行走实验显示ISC组大鼠产生明显的运动功能损伤（t=3.425,P=0.041）,而ISC+PB组错误率低于ISC组（t=4.131,P=0.024）。

脑梗死后益生菌通过调控BDNF水平,抑制细胞凋亡,改善运动功能。

     

HOME: highly optimized microscope environment.

The Highly Optimized Microscope Environment (HOME) is a computerized microscope designed to assist pathologists and cytotechnicians in clinical routine tasks. The prototype system consists of a IBM-PC compatible computer and a light microscope in which a built-in high-resolution computer display image is superimposed on the optical image of the specimen. Also, a manually operated encoding stage and objective turret encoder are used to provide continuous monitoring of the stage coordinates and microscope magnification to the computer. This allows any position on a slide to be uniquely defined and makes it possible to measure interactively lengths and areas larger than the size of the microscope field. Software, written in the C language and operating under the MS-DOS/MS-Windows environment, is controlled by means of a mouse-driven cursor moving over menu light-buttons displayed on the microscope image. The HOME microscope workstation is potentially useful in a wide range of applications such as i) tagging information on particular cells and tissue structures that can thus be accurately located and relocated, ii) performing morphometric measurement, differential counting, and stereological assessment of biological specimens, and iii) training and educating laboratory personnel. Finally, HOME will offer in the near future a user-friendly interface for automatic image processing of cells and tissue entities in interactively selected specimen areas.     

Increment of hFIX expression with endogenous intron 1 in Vitro

This paper probes into the feasibility of increasing expression level of hFIX gene with endogenous intron 1 sequence.hFIX minigene was obtained with middle sequence truncated intron 1 inserted into the relative site of hFIX cDNA,and plasmid vector pKG5i‘IX,retroviral vector G1NaCi‘IX were constructed.These vectors were transduced into target cells of PA317,C2C12,primary rabbit skin fibroblasts (RSF) and primary human skin fibroblasts (HSF).The expression level of mixed colonies are PA317/pKG5i‘IX,151 ng/10^6 cells/24h;PA317/G1NaCi‘IX,308 ng/10^6 cells/24 h;C2C12/G1NaCi‘IX,186 ng/10^6 cells/24 h;RSF/G1NaCi‘IX,1929 ng/10^6 cells/24 h;HSF/G1NaCi‘IX,1646 ng/10^6 cells/24 h.These results indicated that hFIX minigene with intron l is able to increase the expression level to about 3 times of that of hFIX cDNA.Meanwhile,in order to study the application of hFIX minigene in the retroviral-mediated gene transfer system and refrain from intron splicing during viral production,a retroviral vector G1NaCi‘IXR with reversely inserted hFIX minigene expression cassette was constructed.The expression level of reverse constructor in PA317 cells was 390 ng/10^6 cells/24 h with 79% of bioactivity.PCR detection of HT/G1NaCi‘IXR cells infected with PA317/G1NaCi‘IXR supernatant confirmed the existence of intron 1 sequence.These results suggested that expression vector with forward-inserted intronl-carrying hFIX expression cassette can be used in directed gene transfer,but when using the retroviral-mediated gene transfer system,reversely-inserted intronl-carrying hFIX expression cassette should be considered.     

康氏木霉纤维素酶系中C_x酶多分子型的分离纯化及某些性质

从康氐木霉(Trichoderma k(?)ningii)白色变异株As 3.4001的粗酶制剂中,获得了纤维素酶系中的一组C_x酶(C_(x1) C_(x2) C_(x3) C_(x4))。分离步骤包括Sephadex G-75凝胶过滤,DEAESephadex A-50离子交换层析,ConA-Sepharose亲合层析,SE-Sephadex C-50离子交换层析及聚丙烯酰胺凝胶电泳。C_(x1)与C_(x2)的分子量不同而所带电荷相同,它们的分子量各自为44,500和34,000。C_(x2)—C_(x4)的分子量相同而所带电荷不同。纯化的C_(x1)—C_(x4)经聚丙烯酰胺凝胶电泳鉴定为单带。比较它们对羧甲基纤维素钠(CMC-Na)的糖化力及液化力表明在作用方式的随机性上C_(x2)>C_(x3)>C_(x1)>C_(x4)。     

Changes in structure of tissues and in plasma cortisol during the spawning migration of pink salmon, Oncorhynchus gorbucha (Walbaum)

Changes in the structure of the gonad, skin, interrenal, liver, kidney, stomach, gill and pituitary gland, as well as blood cortisol and haematocrit values were investigated in adult pink salmon during their migration through the Fraser and Thompson Rivers to the spawning grounds. At the commencement of their freshwater migration the gonads of both males and females were in an advanced state of development, the pituitary contained a large complement of well-granulated gonadotrops, and hypertrophy was evident in the interrenal tissue and in the epidermis of the skin. At this time, no change from the normal sexually immature salmon was evident in the structure of the gill, liver or stomach. Sclerosis of the glomeruli was noted in the kidney. The plasma cortisol level was consistent with concentrations in unstressed salmon.
Migration of the fish through a turbulent section of the Fraser River evoked a marked increase in both blood cortisol concentration and in interrenal nuclear diameters.
On arrival at the spawning grounds, 10–15 days after entry into fresh water, a general but not marked deterioration of the tissues was evident. The results are discussed in relation to the spawning migration of other species of Pacific salmon.