乡土物种补播对青藏高原高寒草甸群落稳定性的影响

为了探究高寒草甸天然草地补播乡土物种对草地群落稳定性的影响，本试验以垂穗披碱草（Elymus nutans）、异针茅（Stipa aliena）、中华羊茅（Festuca sinensis）、溚草（Koeleria cristata）、星星草（Puccinellia tenuiflora）、扁蓿豆（Melissitus rutenica）、冷地早熟禾（Poa crymophila）为试验材料，设置5种混播组合，于2017年在青海省贵南县天然草地上进行补播。试验采用方差比率法（Variance ratio，VR）、M.Godron贡献定率法（Contribution law）以及生物量稳定性分析方法，结果表明：5种组合补播后使得群落联结性降低、生物量稳定性增大，群落整体稳定性增强，正向着稳定方向发展；5种组合中，组合D （扁蓿豆+星星草+垂穗披碱草+异针茅+溚草）的生物量稳定性最大，是对草地恢复最有效的物种组合。本试验筛选出了对草地生态修复最有效的物种组合，为草地保护及利用提供了科学依据。     

饲料中无机元素分析方法研究进展

饲料中所含的无机元素对动物生长具有重要意义。在饲料中过量添加无机元素会导致环境污染问题,也会通过食物链最终危害消费者的身体健康,因此,对饲料产品中的无机元素进行检测和动态监控尤为重要。综述了近年来饲料中无机元素含量检测主要应用的前处理方法及其含量检测技术,分析了不同前处理方法和含量检测技术的优点和不足,以期为饲料中无机元素分析方法的科学、合理应用提供参考。     

陈年六堡茶对高脂血症小鼠的调脂护肝作用研究

为了探讨陈年六堡茶的调脂保肝功效,比较分析了不同年代六堡茶的主要化学物质的差异,再以高脂高糖饮食建立高脂血症小鼠模型,并用选定的陈年六堡茶水提物灌胃小鼠,观察小鼠相关生理生化指标及组织形态的变化。结果表明,陈化15年茶样被选为陈年六堡茶的代表,用于后续试验。与模型组相比,陈年六堡茶尤其中高剂量条件下能有效减轻高脂血症小鼠体重、肝重和降低肝系数,显著提高高密度脂蛋白-胆固醇(HDL-C)含量,降低血清中总胆固醇(TC)、甘油三酯(TG)和低密度脂蛋白-胆固醇(LDL-C)含量,降低谷丙转氨酶(ALT)和谷草转氨酶(AST)活力,改善大鼠肝脏氧化应激状态,具有统计学意义(P0.05或P0.01)。肝脏和脂肪组织病理切片显示,陈年六堡茶能明显减少肝细胞中脂滴的形成和抑制脂肪细胞膨大,呈剂量依赖关系。综上表明,陈年六堡茶在正常剂量条件下能有效改善因高脂高糖饮食所致的小鼠脂质代谢紊乱和肝脏损伤。     

不同周龄大耳白兔血液生理生化指标的测定

为了明确大耳白兔中国兽药监察所封闭群的生物学特性，对其血液生理生化指标进行了测定。选5、10及13周龄的雄兔和雌兔。空腹采血测定红细胞、白细胞等16项血液生理指标和血糖、总蛋白等16项生化指标。10周龄的红细胞数、白细胞数、红细胞压积和平均红细胞血红蛋白含量高于5周龄和13周龄，雌雄间血液生理指标无明显差异，血清丙氨酸转氨酶含量随着周龄的增加而升高，碱性磷酸则随着周龄的增加而下降。与日本大耳白兔相比，主要血液生理指标比较接近，丙氨酸转氨酸、白蛋白、尿素氮、直接胆红素等血液生化指标相近，其他指标有所不同。测定结果表明，该封闭群具有不同于日本大耳白兔（Slc:JW/CSK)的生物学特性。     

苜蓿施用污泥效果的研究Ⅰ对苜蓿生长及元素含量的影响

将兰州市七里河污水处理厂生活污泥施用于人工种植的新疆大叶苜蓿草地，探讨了不同施用量对苜蓿生长及各元素含量的影响。研究结果表明，施用1.0-2.0kg/m^2污泥，苜蓿地上生物量显著增加，第一年增产23％－31％，第二年增产15％－31％。施用污泥苜蓿地上和地下部组织中N，P，Ca,Mg和Mn的含量总体呈增加趋势，Fe含量显著增加，而K和重金属元素Ni、Pb、As和Hg的含量与对照无显著差异，Zn和Cu的积累增多，但地上部组织中重金属元素均未超过植物中的平均含量，施用污泥未对新疆大叶苜蓿造成重金属污染。     

咯菌腈对草莓灰霉病Botrytis cinerea的毒力及防效研究初报

用生长速率法测定了咯菌腈、多菌灵、硫菌·霉威、苯醚甲环唑4种药剂对草莓灰霉病Botrytis cinerea的毒力。结果表明,4种药剂对草莓灰霉菌菌丝的生长都有不同程度的抑制作用,随药剂浓度增加抑制作用增强,其EC50值分别为0.0472、95.7193、0.4854、1.3611 mg/L,其中咯菌腈的毒力最强。田间防治试验结果表明:2.5%咯菌腈FC每667 m2施药量120 mL时防效为83.7%,80 mL时防效为67.7%;65%硫菌·霉威WP每667m2施药量100 g时防效为65.3%。     

Inhibitory effect of berberine on the activation and proliferation of T lymphocytes

AIM: To investigate the effect of berberine (Ber) on the activation and proliferation of T lymphocytes and its mechanism of action. METHODS: Whole peripheral blood from normal subjects was stimulated with phytohemagglutinin (PHA) or phorbol ester (PDB) plus ionomycin (Ion) and the expression levels of CD69 and CD25 were evaluated with flow cytometry after the staining with appropriate fluorescent monoclonal antibody. The distribution of cell cycles was analyzed by propidium iodide staining and dead cells by 7-aminoactinomycin live staining. RESULTS: 100 μmol/L and 50 μmol/L of Ber had significant inhibition of the expression of CD69 on T cells stimulated with PDB plus Ion or PHA, while effect of 25 μmol/L Ber was not significant. And as time of action extended, the extent of inhibition decreased. For the expression of CD25, Ber at the concentrations as above all exerted significant inhibitory effect in a dose-dependent manner. Moreover, Ber could block lymphocytes cell cycle progression from G₀/G₁ phase to S and G₂/M phase without phase specificity. Besides, live staining analysis revealed that Ber did not have significant cytotoxicity on lymphocytes. CONCLUSIONS: Ber significantly inhibits the expression of early and mid activation antigens of T cells and also blocks the progression of lymphocytes cell cycles. These results suggest that Ber exerts immunosuppression effect through inhibiting the activation and proliferation of T cells.     

Effect of EGFP gene transfection on the cell cycle distribution of primary cultured human chondrocytes

AIM: To investigate the effect of enhanced green fluorescence protein (EGFP) gene transfection on the cell cycle distribution of primary cultured human chondrocytes in order to establish a tracking method of cultured human nasoseptal chondrocytes. METHODS: pEGFP-N1 plasmid was amplified in E.coli, and purified by high purity kit. Primary cultured human chondrocytes,which were initially obtained from the nasoseptal cartilage, were cultured in vitro and transferred with pEGFP-N1 by means of electroporation with Amaxa nucleofector device. Transfering process and transient expression were evaluated by laser scanning confocal microscope (LSCM), the transfer efficiency and the cell cycle distribution were evaluated by flow cytometry. RESULTS: There was significant expression of EGFP at 24 h after transferring. The transfection efficiency of pEGFP-N1 into primary cultured human chondrocytes reached 35.37％ at 48 h. It didn't affect the process of cell adherance and had no effect on the cell cycle distribution. CONCLUSION: Primary cultured human chondrocytes, which were transfected with pEGFP, are alive in vitro, and the transferring process doesn't affect the cell cycle distribution. These results suggest that pEGFP-N1 is an ideal transient expression vector for primary cultured human chondrocytes and it might be a well tracer in construction tissue engineered cartilage.