核桃楸果中微量元素的分析

用火焰原子吸收分光光度法（ＡＡＳ）测定核桃楸果中的１１种微量元素。结果Ｃｄ、Ｃｏ元素未检出,Ｚｎ、Ｃｕ、Ｍｎ、Ｓｅ等人体必需元素较丰富。酒提取液中Ｚｎ、Ｃｕ、Ｆｅ、Ｍｎ、Ｓｅ的溶出率在４％～２４％之间,Ｐｂ未检出     

某些酶活性变化对评价生长发育期大鼠锌营养的意义

雄性断乳大鼠随机分为低锌组、高锌组、正常锌组和低锌组的高锌饲料对饲组。喂相应饲料２０天后,低锌组的部分大鼠改喂高锌饲料（低 高锌组）,高锌组的部分大鼠改喂低锌饲料（高 低锌组）。分别于实验期０、２０、５０和７０天时处死。测定血浆碱性磷酸酶、５′ 核苷酸酶和铜 锌型超氧化物歧化酶活性、血浆锌及肾脏锌含量变化,以考核它们对评价锌营养状况的意义。结果表明：碱性磷酸酶、５′ 核苷酸酶以及血浆锌浓度变化对缺锌或／和补锌反应敏感。短期缺锌时（２０天）碱性磷酸酶活性就显著降低,并随缺锌时间延长该酶活性持续降低,而短期补锌（３０天）后又能显著增加其活性。受锌营养状况影响,血浆５′ 核苷酸酶活性也有类似的变化趋势。但这些酶活性又受增龄因素的影响,即随实验期增加,正常锌组碱性磷酸酶活性呈降低趋势,而５′ 核苷酸酶活性则呈增加趋势。长期严重缺锌可以影响铜 锌型超氧化物歧化酶活性;补锌后在实验期内未见到它的活性显著增加。随实验期增加,低锌组血浆锌持续降低,５０天时,显著低于高锌组;７０天时,低锌组和高 低锌组的血浆锌也显著低于高锌和低 高锌组。这些结果提示,碱性磷酸酶和５′ 核苷酸酶的活性及血浆锌变化对评价大鼠锌营养状况有一定的意?     

开郁清胃颗粒对2型糖尿病胰岛素敏感性的影响

目的：通过临床观察初步探讨开郁清胃颗粒对2型糖尿病患者胰岛素敏感性的影响。方法：以二甲双胍为对照，观察60例2型糖尿病患者治疗前后体重及腰臀围、症状积分、血糖、胰岛素、胰岛素敏感指数、血脂、焦虑及抑郁积分等指标的变化。结果：开郁清胃颗粒对2型糖尿病患者的血糖、血脂紊乱有明显的改善作用，并能减轻体重，提高胰岛素敏感性，改善焦虑及抑郁状态。结论：开郁清胃颗粒增加2型糖尿病患者的胰岛素敏感性可能与改善血脂紊乱，改善焦虑、抑郁状态及减轻体重等有关。     

抗补体蛋白对大鼠局灶脑缺血损伤的作用

0　引言　近年来脑缺血损伤的早期炎症受到重视 .有学者观察到在人脑梗塞部位白细胞集聚 ,临床预后与梗塞部位的白细胞数量有关 ,白细胞多者预后差 [1 ] .还有文献描述了大鼠持续性脑缺血损伤中的多形核中性细胞反应的时间过程 ,收稿日期 :1999-0 3 -2 6;　修回日期 :1999-0 5 -13基金项目 :国家自然科学基金资助项目 ( 3 9170 3 15 ) ;全军医药卫生科研基金资助项目 ( 92 5 0 5 2 )作者简介 :刘　立 ( 195 8-) ,男 (汉族 ) ,江苏省无锡市人 .副教授 ,博士 .Tel.( 0 2 9) 3 3 74819缺血 30 min就可以观察到多形核中性细胞于缺血部位的微血…     

亚硒酸钠和硒蛋氨酸的毒性比较

目的　比较亚硒酸钠和硒蛋氨酸毒性差异以及探讨硒中毒的指标。方法　将断乳Wistar大鼠随机分为 7组 ,每组 14只 ,雌雄各半。其中一组为对照组 ,另外六组分别给予含硒 3、6、10mg kg的亚硒酸钠或硒蛋氨酸饲料 ,于第 12周将其处死。结果　当饲料硒水平达到 3mg kg时 ,动物肝脏出现病理变化 ,在Se6mg kg时 ,体重才出现下降。饲料硒水平为 6、10mg kg时 ,同一饲料硒水平的亚硒酸钠组大鼠体重小于硒蛋氨酸组。饲料硒水平为 3、6mg kg时 ,硒蛋氨酸组大鼠的肝脏病理改变轻于亚硒酸钠组 ,雄性大鼠轻于雌性。亚硒酸钠组较硒蛋氨酸组或雌性大鼠较雄性大鼠在肝脏体重比方面变化更为明显。除雌性大鼠肝脏谷胱甘肽过氧化物酶 (GPX)活性随硒水平升高而降低外 ,其它补硒各组肝、红细胞、血浆GPX活性具有随硒水平的升高而升高的趋势。结论　大鼠硒中毒的剂量为Se 3mg kg,硒蛋氨酸的毒性小于亚硒酸钠 ,雌性大鼠对硒毒性更为敏感     

Xa21转基因大米对大鼠致畸作用的实验研究

目的　观察Xa2 1转基因大米对大鼠胚胎生长、发育的影响。方法　将初断乳Wistar大鼠按雌雄分别随机分为 4组 :转基因大米组、非转基因大米组、AIN93G对照组和敌枯双阳性对照组。单笼喂养 ,饲相应鼠料 ,喂满 90天 ,雌雄合笼。观察母鼠和胎鼠的生长发育情况。结果　转基因大米组孕鼠增重、活胎体重、身长、尾长均显著高于阳性对照组 ,而死胎数、吸收胎数、畸形率 (外观、内脏、骨骼 )均显著低于阳性对照组。转基因大米组与非转基因大米组、AIN93G对照组相比 ,所有观察指标均无统计学差异。结论　转Xa2 1基因大米与非转基因大米相比 ,对大鼠受孕率、胚胎生长发育无显著性差异。     

水中微量甲胺磷农药的检验

目的选择检出水中微量甲胺磷农药的最佳方案。方法分别使用液-液萃取法、固相萃取法、活性炭富集法提取甲胺磷含量极低的液体检材，提取液经MS／GC检验。结果液-液萃取法为阴性结果，固相萃取法、活性炭富集法为阳性结果。结论实验表明对于常规液-液萃取方法效果欠佳的甲胺磷含量极低的液体检材，采取固相萃取法或活性炭富集法进行萃取，可提高检出率。     

Expression and characterization of Gag protein of HIV-1（CN） in Pichia pastoris

To express the core protein of HIV-1 of Chinese prevalent strain （HIV-1 （CN）） in Pichia pastoris, the fulllength gag gene was inserted into the secretory expression vector pHILS1. Linearized recombinant plasmid pHILGAG by Sail was electrotransformed into the yeast strain GS115, and the yeast transformants were identified by PCR. To induce the interest protein to be expressed, the PCR positive transformants were inoculated in the medium of BMGY and BMMY, mRNA of the strain was detected by RT-PCR, and the expressed protein was analyzed by SDS-PAGE, Western blotting and thin layer scanning. mRNA （1.3 kb） was amplified by RT-PCR. SDS-PAGE and Western blotting analysis showed that the molecular mass of the expressed protein was 55 kD, which was similar to the expected value, and the expressed protein could react with McAb to HIV-1 p24. Thin layer scanning analysis demonstrated that the whole amount of the expressed protein was approximately 13 % of the soluble protein in the supernatant. The recombinant yeast had good genetic stability. The optimal expression conditions of the engineering yeast were as follows： BMMY medium, 80-90% of dissolved oxygen, 1% methanol, and 3-day-cultivation course. Gag proteins were expressed under the optimal expression condition and purified via gel filtration chromatography. The purity of the interest protein was up to 85 %. After the purified proteins were inoculated into BALB/c mice, the anti-HIV-1 antibodies in the immunized mice could be detected by Western blotting.     

DNA vaccination using bacillus Calmette-Guerin-DNA as an adjuvant to enhance immune response to three kinds of swine diseases

In order to enhance the immune efficacy of DNA vaccination, experiments were conducted to investigate the regulating effects of Bacillus Calmette-Guerin （BCG）-DNA as an adjuvant on immune responses of mice against foot-and-mouth disease （FMD）, Aujeszky＇s disease （AID） and classical swine fever （CSF）. BCG-DNA was purified from BCG by ion-exchange chromatography. Three DNA vaccines （pVSG, pVgD and pVE2） against the respective infection were constructed, and BCGDNA was coimmunized to mice by muscle injection. The results showed that titres of specific immunoglobulin （Ig）G to the vaccines mounted remarkably in the sera of the adjuvant covaccinated mice （P〈0.01）. Antibody isotype IgG2a and IgG1 also increased, respectively, in mice coimmunized with BCG-DNA compared with those of the control groups （P〈0.01）. Cellular immune cytokine interferon-gamma and cytotoxic T lymphocytes were detected in coimmunized BCG-DNA groups （P〈0. 05）. Whereas interleukin-4, humoral immune cytokine, was not significant （P〉 0. 05）. These results suggest that codelivery of BCG-DNA with DNA vaccines against FMD, AjD and CSF can enhance the induction of antigen-specific, especially, cell-mediated immunity.