中草药添加剂提高密蜂春繁效果的研究

在早春繁殖期,以中草药作为饲料添加剂,观察蜜蜂群势变化和蜂群健康情况.结果表明,试验组A和对照组CK的蜂群繁殖效果差异极显著,试验组蜂群健康、活动正常,蜂群繁殖率提高了12.1%.     

高寒地区不同建植期人工草地群落垂直结构和生产力变化的研究

对高寒地区不同建植期人工草地群落垂直结构和生产力的变化研究结果表明：（1）随着人工草地建植时间的延长,人工草地群落垂穗披碱草高度异质性逐渐减小.（2） 不同建植期（1999、1998、1997年建植）人工草地垂穗披碱草和群落平均地上生物量均主要分布在0 ～20cm冠层中,约占平均地上生物量的61.03%、90.64%、84.55%和67.47%、92.54%、86.08%.（3） 不同建植期 （1999、1998、1997年建植）人工草地群落平均地下生物量均主要分布在0～10cm土层中,约占地下总生物量的85.97%、81.73%和78.47%.（4） 建植的人工草地如果其组分单一,即物种的丰富度很低时,均匀度增加,物种对环境资源的竞争力和利用率提高,导致土壤资源库中某些营养成分缺乏,草地群落初级生产力因此而降低。     

重庆市江北区城乡交错带土地利用规划探讨

特殊的经济地理位置使得城乡交错带成为土地利用规划和土地利用管理的重点和难点区域。本文以重庆市江北区为例，分析了城乡交错带土地利用的基本特性，并根据现状和未来15年国民经济和社会发展的预测。提出了土地利用总体规划的重点。     

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

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.     

Influence of ischemia-reperfusion on apoptosis of sinoatrial node cells in rabbits in vivo

AIM:To study influence of ischemia-reperfusion(IR) on apoptosis and expression of apoptosis-related genes Fas-L, Bax and Bcl-2 of sinoatrial node(SAN) cells in rabbits in vivo. METHODS:Ninety healthy adult rabbits were divided randomly into control group, ischemia groups (I_{10 min}, I_{30 min}, I_{60 min} and I_{120 min}) and IR groups (I_{10 min}R_4h, I_{30 min}R_4h, I_{60 min}R_4hand I_{120 min}R_4h). IR injury model of SAN was established by occluding and loosening the start section of right coronary artery. The apoptosis of SAN cells was detected by TUNEL staining. The expression of Fas-L, Bax and Bcl-2 of SAN cells was detected by immunohistochemistry. RESULTS:①No obvious apoptosis of SAN cells was observed in control group, I_{10 min} and I_{30 min} groups. Apoptosis of different degrees in SAN cells were found in 68.3%(41/60) rabbits in I_{60 min}, I_{120 min} and 4 subgroups of IR. ②The highest expression of Fas-L and Bax was observed in I_{120 min} group and that of Bcl-2 was in I_{60 min} group. ③The highest expression of Fas-L and Bax was observed in I_{60 min}R_4h group. The peak level of Bcl-2 was observed in I_{30 min}R_4h group. ④The expression of Fas-L and Bax was significant higher in IR group than that in ischemic group at the same time point. CONCLUSION:Ischemia and IR induced apoptosis of SAN cells in rabbit in vivo. Fas-L、Bax、Bcl-2 may participate in the regulation of apoptosis and the injury during IR aggravates the apoptosis of SAN cells.     

中国斜纹夜蛾寄生蜂名录

根据浙江大学应用昆虫学研究所收藏的寄生蜂标本和国内外报道，对我国寄生斜纹夜蛾的原寄生蜂和重寄生蜂进行系统整理研究。我出我国斜纹夜蛾寄生蜂40种，其中包括原寄生蜂29种，重寄生蜂11种，同时还以附录的形式列出了我国已报道过但有存疑的寄生蜂7种及国外已有报道但在我国还未采集到标本的寄生蜂61种。     

农作物病虫预报可视化发展与应用前景

农作物病虫预报可视化具有形象生动、信息传递快捷、覆盖面广等优点,是更好发挥预报作用的最佳方式。大范围实施这种预报发布形式的条件,目前已基本成熟,经过努力,必然会在不长的时间内取得长足进展。     

月季切花乙烯受体ETR1 cDNA克隆及其序列分析*

 根据乙烯受体基因ETR1 保守区设计引物, 分别以瓶插寿命差异显著的月季切花品种‘德克萨斯’和‘维亚蒂’为材料, 通过RT-PCR 从花瓣中扩增出了797 bp 的cDNA 片段, 它编码265 个氨基酸。测序和序列分析表明,‘德克萨斯’重组质粒中插入片段的核苷酸序列之间完全相同, 命名为pRT-ETR1。而‘维亚蒂’所获得的重组质粒中插入片段的核苷酸和氨基酸序列之间存在差异, 同源性分别为85. 2 %和92. 1 % , 分别命名为pRV-ETR1-V4 和pRV-ETR1-V5。pRV2 ETR12V5 的核苷酸和氨基酸序列与‘德克萨斯’pRT2 ETR1 的同源性均达99 %以上; pRV-ETR1-V4 中的核苷酸和氨基酸序列与‘德克萨斯’pRT-ETR1 的同源性分别为85. 0 %和92. 5 %。上述插入片段与桃、苹果、天竺葵、拟南芥等植物的ETR1相应区域高度同源, 其氨基酸同源性均大于90 %。     

Analysis of the distribution and clonality of TCR Vβ T cells in cord blood

AIM:To investigate the distribution and clonality of TCR Vβ subfamily T cells in cord blood. METHODS:The CDR3 of TCR Vβ 24 subfamily genes were amplified in mononuclear cells from 13 cases of cord blood. To observe the usage of TCR Vβ repertoire, the PCR products were further labeled with fluorescent and analyzed by genescan technique for the CDR3 size, to evaluate clonality of the detectable TCR Vβ T cells. Peripheral bloods from 10 cases of normal individuals and T cell line Molt-4 and Jurkat served as controls. RESULTS:Only 38.78%±16.26% of 24 Vβ subfamily T cell were selectively expressed in cord blood, predominantly in Vβ 3, 5, 8, 9 and 13, whereas all 24 Vβ subfamilies could be detected in T cells from peripheral blood of normal individuals. Genescan analysis showed that all PCR products of TCR Vβ subfamilies from cord blood or normal individual peripheral blood displayed multi-peaks. CONCLUSION:Some TCR Vβ subfamily T cells were absent in cord blood. All TCR Vβ subfamily T cells in cord blood displayed polyclonality.     

Effect of Jiawei Sini Decoction on glucocorticoid receptor in thymocytes of chronic psychological stress rats

AIM: To observe the effect of Jiawei Sini Decoction (JWSND) on glucocorticoid receptor (GCR) in thymocytes of chronic psychological stress rats. METHODS: The rats were randomly divided into 4 groups, control group (C), model group (M), group treated by JWSND C₁, group treated by ginsenosides C₂. The number of thymocyte GCR sites and the GCR nuclear thanslocation rate were detected by radioimmunoassay. RESULTS: Compared with the control group, in the model group, the thymocyte weight index lowered significantly ( P<0.05 ), and the GCR nuclear thanslocation rate was increased significantly ( P<0.01 ), but the number of thymocyte GCR sites was unchanged. Compared with the model group, thymus gland weight indexes of C₁ and C₂ were increased significantly ( P<0.05 ), while the GCR nuclear thanslocation rate lowered significantly ( P<0.01 ). Moreover, no significant difference was found in all indexes between C₁ and control group. CONCLUSION: The inhibitory effect of glucocorticoid on the thymus could be significantly reversed by JWSND via suppressing the thanslocation of GCR from cytoplasm to nucleus in chronic psychological stress rats.