室内常见气传真菌孢子的细胞毒性研究

分别以MTT比色法和细胞克隆形成率实验，观察了室内常见气传真菌孢子对中国仓鼠（CHL）肺上皮细胞的存活和增殖能力的影响，并通过检测细胞培养液中乳酸脱氢酶（LDH）活力，胞内Ca^2 ,K^ 含量，观察真菌孢子对细胞膜通透性的影响，结果表明，室内常见气传真菌孢子能显影响CHL细胞的活性，并可使细胞膜通透性发生改变，引起胞内LDH外渗，细胞内外离子发生交换，细胞内K^ 浓度降低，而细胞外的Ca^2 有内流的趋势。     

Prenatal diagnosis of medium-chain acyl-CoA dehydrogenase (MCAD) deficiency in a family with a previous fatal case of sudden unexpected death in childhood

Medium-chain acyl-CoA dehydrogenase (MCAD) deficiency is a potentially fatal inherited disease with a carrier frequency of approximately 1:100 in most Caucasian populations. The disease is implicated in sudden unexpected death in childhood. A prevalent disease-causing point mutation (A985G) in the MCAD gene has been characterized, thus rendering diagnosis easy in the majority of cases. Since the clinical spectrum of MCAD deficiency ranges from death in the first days of life to an asymptomatic life, there are probably other genetic factors—in addition to MCAD mutations—involved in the expression of the disease. Thus, families who have experienced the death of a child from MCAD deficiency might have an increased risk of a seriously affected subsequent child. In such a family we have therefore performed a prenatal diagnosis on a chorionic villus sample by a highly specific and sensitive polymerase chain reaction (PCR) assay for the G985 mutation. The analysis was positive and resulted in abortion. We verified the diagnosis by direct analysis on blood spots and other tissue material from the aborted fetus and from family members.     

生物硝化池污水中硝化细菌的快速定量研究

实验采用聚合酶链式反应（PCR）技术与最大几率数法（MPN）相结合的MPN－PCR法对生物硝化池污水中的硝化细菌进行快速定量。所用的一对PCR引物是在对硝化细菌的16SrRNA基因进行系统比较的基础上设计合成的，可以扩增出大小为388bp的DNA片段。以从生物硝化池污水中抽提的含硝化细菌DNA的混合DNA为模板，进行PCR扩增并确定合适的扩增条件。运用MPN－PCR法进行定量检测的整个过程可在几小时之内完成。     

Determination of alkali-labile phosphoprotein phosphorus from fish plasma using the Tb^3＋-tiron complex as a fluorescence probe

A sensitive method based on the fluorescence quenching effect of the Tb^3＋-Tiron complex is proposed for the determination of alkali-labile phosphoprotein phosphorus （ALP） released from fish plasma. The detection limit was 5.4 ng/ml （S/N=2）, and the relative standard deviation of the quenching effect （6 replicates） was 4.6%. The results obtained by the proposed method were in good agreement with those obtained by the colorimetric assay. The advantages of the present method are its relatively simple detection procedure, the lack of toxic organic solvents, and high sensitivity.     

Immunotoxicity of bisphenol a to Carassius auratus Lymphocytes and macrophages following in vitro exposure

Bisphenol A （BPA） is the monomer component of polycarbonate plastics and classified as an endocrine disrupting chemical （EDC）. The reproductive toxicity of BPA has been extensively studied in mammals; however, relatively little information is available on the immunotoxic responses of fish to BPA. In this study, we investigated the effects of BPA on the immune functions of lymphocytes and macrophages in Carassius auratus. The effects of BPA were compared with those of two natural steroid hormones, estradiol and hydrocortisone. Proliferation of the two types of cells in response to PHA was measured using colorimetric MTT assay. Macrophage respiratory burst stimulated by Con A was measured using chemiluminescence assay. Results showed that BPA （0.054-5.4 mg/L）, estradiol （0.0002-2.0 mg/L） and hydrocortisone （5-50 mg/L） significantly induced Carassius auratus lymphocyte proliferation while higher doses of hydrocortisone （500-5000 mg/L） appeared to be inhibitory. BPA （0.005-50 mg/L）, estradiol （0.005-800 mg/L） and hydrocortisone （0.005-500 mg/L） markedly enhanced macrophage proliferation, whereas higher doses of BPA （500-1000 mg/L） appeared to inhibit cell proliferation. Furthermore, higher dosage of BPA （50 mg/L） and hydrocortisone （50 and 500 mg/L） suppressed the macrophages respiratory burst while estradiol is stimulative all the doses tested （0.05-500 mg/L）. In conclusion, BPA could have immunotoxicity to Carassius auratus and functional changes of lymphocyte and macrophage in Carassius auratus may be different between low and high dosages.     

二氧化氯消毒前后污水毒性的变化及消毒条件的影响

采用发光细菌试验和umu试验,分别考察了二氧化氯投加量和反应时间对污水二氧化氯消毒后急性毒性和遗传毒性变化的影响.结果表明,随着二氧化氯消毒剂投加量的增加,消毒后水样的急性毒性不断增大,但遗传毒性逐渐减小后趋于稳定.随着反应时间的延长,二氧化氯的消耗量不断增大,消毒后水样的急性毒性先增大后减小,遗传毒性逐渐减小后趋于稳定.由于消毒条件对污水急性毒性和遗传毒性有着不同的影响,说明污水中产生急性毒性和产生遗传毒性的物质不同,对于某一种污水,通过控制消毒条件可以使消毒后污水的急性毒性和遗传毒性都较低.     

上海市若干环境污染物的诱变性

用中国仓鼠肺成纤维细胞(V_(79)),进行次黄嘌呤—鸟嘌呤磷酸核糖转移酶位点(HGPRT Locus)试验,检测了上海市若干环境污染物的诱变性。结果发现,污染物量与诱变性之间呈剂量—反应关系。所有样品经代谢活化后(加S_9),其诱变性均有增高的趋势。卷烟焦油、油烟冷凝物的T/C值均>3,而不加S_9的黄浦江水和自来水样,则对V_(79)细胞可能具有间接的诱变作用(T/C值<3)。     

发光细菌法监测废水综合毒性研究

运用发光细菌法对 2 6个污染源废水样的毒性进行测定。并以毒性较为稳定的 Hg Cl2 作参比毒物 ,使此法所测得的毒性定量化。据水质毒性分级标准 ,对水样毒性的测定结果进行评价 ,属 级低毒的 1 1个 , 级中毒 4个 , 级重毒1个 , 级高毒 3个 , 级剧毒 7个。另从辽阳化纤厂五个废水样可以看出距离污染源越近毒性越强。这一结果既与实际情况相符又与鱼的毒性试验结果一致 ,证明发光菌监测工业废水是可行的。     

东亚钳蝎抑制型神经毒素基因在昆虫细胞中的表达及活性鉴定

基因BmKIT3R 是根据东亚钳蝎 (ButhusmartensiiKarsch)抑制型神经毒素基因BmKIT3 优化而得的 .将优化过的蝎毒素基因BmKIT3R 通过Bac to Bac操作技术 ,使重组杆状病毒基因组DNA转染到草地粘虫sf2 1细胞中对IT3R 基因进行表达 ,经SDS PAGE检测在 8.7× 10 3 处有一表达条带 .表达产物经生物鉴定 ,证明具有很高的活性 ,它对昆虫具有非常明显的致死作用 .图 3参 5     

酚类化合物对不同组织细胞DNA损伤的研究

应用单细胞凝胶电泳技术 ,研究了酚类化合物对不同组织细胞DNA的损伤 .试验结果表明 ,酚类化合物均能引起不同组织细胞不同程度的DNA损伤 ,并呈现剂量效应关系 .其高剂量组与对照组相比 ,均有极显著性差异 (P <0 0 1 ) .不同组织细胞对同一种药物呈现出不同的敏感性 .酚类化合物遗传毒性效应与其结构密切相关