纳米微粒材料生物学活性研究进展   总被引：1，自引：0，他引：1  

亓立峰  许梓荣  江霞  胡彩虹 《中国兽药杂志》2004,38(8):25-28

综述了纳米微粒的生物学效应及其免疫调节、抗菌、抗肿瘤等多种生物学活性.  相似文献   

对虾的免疫机制及其疾病预防策略的研究   总被引：5，自引：0，他引：5  

魏克强  许梓荣 《中国兽药杂志》2004,38(9):25-29

在对虾的细胞免疫中血细胞是主要的作用因素,而体液免疫是血淋巴中的一些酶和调节因子,机体还可以被诱导产生特殊的免疫保护反应.应用免疫增强剂、疫苗和基因工程技术为预防对虾病害提供了有效的途径.本文根据国内外的有关资料,就对虾的免疫机制和疾病预防策略进行了综述.  相似文献   

亚热带牧用草地中威提特东非狼尾草的种子繁殖研究   总被引：4，自引：0，他引：4  

匡崇义 徐驰薛世明  吴文荣 《四川草原》2004,(10):8-10

在3月和4月对全日制放牧的东非狼尾草草地上的风干牛粪取样,进行发芽试验,分别测定其中的东非狼尾草发芽种子数量。结果,3月取样平均432.5 g的牛粪中东非狼尾草平均发芽种子数量为118.25粒,4月取样平均437.8 g的牛粪中东非狼尾草平均发芽种子数量为52.8粒,二者平均牛粪重为435.15 g,平均发芽种子为85.5粒,说明牛粪中东非狼尾草种子数量较多,是其繁殖扩展较快的主要原因;3月取样的种子数量为4月取样数量的1.38倍,说明人工利用牛粪进行东非狼尾草繁殖时,需在有降雨来临前准备,即1～3月进行牛粪的准备工作。  相似文献   

散养湘黄鸡常见病的临床表现特点及其防制     

何华西  许美解  廖仁彩  艾国良 《畜牧兽医杂志》2004,23(3):4-7

湘黄鸡进行专业户(场)散养时，由于生产方式不同于舍饲群养，其生产环境、食物结构和易感病种类都必然发生变化。对此，笔者结合临床所遇病例进行了研究总结，对散养湘黄鸡的几种常发病的病因、病理、临床表现及防治特点等方面进行了介绍。  相似文献   

利用紫茎泽兰栽培田头菇的研究   总被引：9，自引：0，他引：9  

田果廷  徐学忠  杨琼芬  徐雨然 《中国食用菌》2004,23(4):13-15

利用紫茎泽兰作为原料栽培田头菇 ,同时利用稻草和棉籽壳为原料栽培田头菇作对照。研究结果表明 ,代料熟料栽培田头菇的培养基配方中 ,以紫茎泽兰为主要原料的配方A效果最好 ,生物学效率比对照的稻草培养基平均增产 80 %以上。利用紫茎泽兰鲜草和干草作培养基的单产量差异不明显。  相似文献   

三尖杉枝叶粉末防治花生根结线虫病   总被引：6，自引：0，他引：6  

文艳华  冯志新  陈立  徐汉虹 《植物保护学报》2004,31(2):161-165

采用盆栽及大田小区试验,研究了三尖杉Cephalotaxus fortunei枝叶干粉末对花生根结线虫病的防治效果.盆栽试验结果表明,每盆(2kg土)施用三尖杉枝叶干粉末10、15及20 g三种处理,与对照组相比,初侵染相应推迟4、6、10天,并能减少侵染量,降低根结增长率,显著减轻花生根结线虫病病情.大田小区试验结果与盆栽试验结果相似,每小区(5m2)沟施三尖杉枝叶干粉末120、80、50 g,处理后34及53天的2次平均防治效果分别为89%、82%及50%,施药对照10%益舒宝颗粒剂25g处理(相当于45kg/hm2)为74%.综合使用剂量及花生生长情况,建议沟施150kg/hm2三尖杉枝叶干粉为宜.  相似文献   

Role of potassium channels in the regulation of intracellular free Ca²⁺ concentration of pulmonary artery smooth muscle cells in rats     

FAN Zai-wen  ZHANG Zhen-xiang  XU Yong-jian 《园艺学报》2004,20(2):150-153

AIM: To investigate the role of potassium channels in the regulation of intracellular free calcium concentration ( [Ca²⁺]_i) of pulmonary artery smooth muscle cells (PASMCs) in rats. METHODS: The fluorescence Ca²⁺ indicator Fura-2/AM was used to observe [Ca²⁺]_i of rat PASMCs in normal and chronic hypoxic condition. The influences of potassium channels on PASMCs proliferation were assessed by MTT assay. RESULTS: 1. In normoxic condition, [Ca²⁺]_i was (156.91±8.60) nmol/L, and in hypoxic condition, [Ca²⁺]_i was (294.01±16.81) nmol/L. 2. In normoxic condition, the voltage-dependent K⁺-channel antagonist 4-aminopyridine (4AP), but not the Ca²⁺-activated K⁺-channel antagonist tetraethylammonium (TEA) and the ATP-sensitive K⁺-channel antagonist glibenclamide (Glib) increased [Ca²⁺]_i. 3. In hypoxic condition, 4AP and TEA caused the rise in [Ca²⁺]_i , but Glib had no effect on [Ca²⁺]_i. 4. MTT assay showed that 4AP increased the value of absorbing light degree (A value) in normoxic and hypoxic condition (0.582±0.062,0.873±0.043,respectively, P＜0.01), TEA increased A value only in hypoxic condition, and Glib had no effect on the proliferation of PASMCs. CONCLUSIONS: K_V plays an important role in the regulation of [Ca²⁺]_i and proliferation of PASMCs. K_Ca serves as distinct responsive roles in the regulation of proliferation of PASMCs in hypoxic condition. K_ATP has no effect on [Ca²⁺]_i and proliferation of PASMCs in normoxic and hypoxic conditions.  相似文献   

Cortical gene expression pattern in rat focal cerebral ischemia     

ZHANG Zhan-jun  YING Kang  WANG Zhong  ZHANG Xiao-yan  LIU Jian-xun  HUANG Yan  XU Li  WEI Cui-e  WANG Yong-yan 《园艺学报》2004,20(8):1427-1433

AIM: To investigate the genes differential expression in cortex during rat focal cerebral ischemia.METHODS: cDNA microarray chips containing numerous cDNAs were used to investigate the gene expression pattern between samples of focal cerebral ischemia and sham-control operation rats. RESULTS: Two hundred and eleven genes differentially expressed were screened out, among these genes, up-and down-regulated genes were 199 and 12, respectively. CONCLUSIONS: The analysis of gene expression pattern of focal cerebral ischemia based on cDNA microarray can realize high-throughput screening of the genes associated with the focal cerebral ischemia. The differential expression of genes may be related to the pathogenesis of focal cerebral ischemic diseases.  相似文献   

Effect of Epstein-Barr virus latent membrane protein 1 on expression of P53 protein in nasopharyngeal carcinoma cells     

ZHANG Su-zhen  HUANG Pei-chun  XU Yong  CHEN Jin  CAI Kang-rong  HUANG He 《园艺学报》2004,20(9):1646-1649

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Regulation of MMP-2 and TIMP-3 expression by uPA signal transduction system in human bone giant cell tumor     

XU Ruo-bing  WEN Jian-ming  ZHANG Meng  LV Chang-hai  XIAO Gang  ZHANG Wen-min  LIANG Hui-zhen 《园艺学报》2004,20(11):1982-1988

AIM: To study effects of urokinase-type plasminogen activator (uPA) signal transduction on expression of matrix metalloproteinase-2 (MMP-2) and tissue inhibitor of matrix metalloproteinase-3 (TIMP-3) in giant cell tumor of bone (GCT). METHODS: Expression of uPAR, MMP-2 and TIMP-3 in GCT tissue was detected by immunohistochemistry. Phosphorylation level of mitogen-activated protein kinase (p44) in uPA/uPAR signal pathway in cultured GCT cells was detected by immunoprecipitation. The expression of MMP-2 and TIMP-3 in cultured cells after treatment with uPA-ATF or anti-uPAR antibody was also detected by Western blotting. RESULTS: 1) Urokinase-type plasminogen activator receptor (uPAR) was positive on the cell membrane and in cytoplasm of some mononuclear stromal cells (MSCs) and multinucleated giant cells (MGCs); 2) MMP-2 was positive in the cytoplasm and on the cell membrane of almost all of MSCs and some of MGCs. The polar distribution of MMP-2 in the cytoplasm of MGCs was especially obvious; 3) The expression of TIMP-3 of some MSCs and MGCs in GCT was much lower than MMP-2. The positive signal also showed a prominent polarity; 4) After treatment with uPA-ATF, the phosphorylation level of p44 in GCT cultured cells was much higher than the control. Addition of anti-uPAR antibody in the cells remarkably down-regulated the phosphorylation level of p44 as compared with the control group, suggesting that uPA-ATF participates cell signal transduction and this reaction can be inhibited by anti-uPAR antibody; 5) uPA-ATF cell signal pathway up-regulated expression of MMP-2 and TIMP-3, while anti-uPAR antibody down-regulated the expression of MMP-2 and TIMP-3. CONCLUSION: These results demonstrate for the first time that uPA-ATF directly regulates the expression of MMP-2 and TIMP-3 by signal transduction pathway, and the over-expression of MMP-2 and TIMP-3 may play an important role in local osteolysis of GCT.  相似文献