江苏沿江优先控制有机毒物污染预警体系的探讨

长江（江苏段）的有机毒物污染控制对于保障饮用水安全具有十分重要的意义，通过对长江（江苏段）有机毒物污染和沿岸污染源现状的分析，提出并举例说明筛选优先控制有机毒物的方法，并对建设江苏沿江优先控制有机毒物污染的预警体系提出了建议。     

细胞色素P450酶系作为生物标志物在毒理学上的应用

细胞色素P450酶系是一种血红素-硫铁蛋白(heme-thiolate protein)，它是由结构和功能相关的超家族(superfamily)基因编码的含铁血红素同工酶组成。对许多内源性和外源性的化学物质尤其是对环境有害化合物存在有氧氧化代谢作用以实现机体的解毒作用，但在某些情况下，外来物质可能被转化为具细胞毒性、致突变性或致癌作用更强的物质，起毒性活化作用。本文对细胞色素P450的研究简史及其作为生物标志物在毒理学上的应用作了简要的综述。提出细胞色素P450酶系在毒理学上的意义是可作为污染物潜在影响的早期预警信号系统对环境污染上物进行监测和预报，且对于制定预防性的管理措施，及时避免或减轻环境污染的损害都具有重要意义。     

湖南早前寒武纪变质结晶基底的Sm-Nd同位素年龄

出露在湘东北益阳一浏阳，呈近东西向断续分布，经角闪岩相一绿片岩相变质结晶片岩、层状、似层状超镁铁质岩的sm—Nd全岩等时线年龄为2．6—3．028Ga、2．2—1．9Ga，应属湖南早前寒纪结晶基底岩片。     

Early prenatal diagnosis of A lethal syndrome of multiple congenital contractures

An ultrasonic diagnosis of a lethal, autosomally recessive syndrome of multiple congenital contractures was made in seven high-risk pregnancies on the 13rd to 17th gestational weeks. The diagnostic findings were the development of progressive subcutaneous oedema from the 13th gestational week on and the decrease of fetal limb movements.     

First trimester amniocentesis between the seventh and 13th weeks: Evaluation of the earliest possible genetic diagnosis

Amniocentesis performed at the 12th week and later gives reliable results. The procedure can be performed using regimens developed for mid-trimester amniotic fluid (AF) cells. Extension to the 10th–11th week is, in principle, feasible. However, the high cytogenetic failure rate is a difficulty and despite a high clone count, the culture time is prolonged. The problem of the relatively high loss of AF could be overcome by cell filtration techniques and replacement of the fluid. Because of the short turnover rate of the AF, this may be unnecessary or replacement with an isotonic solution may be sufficient. (Pseudo)mosaicism appears to occur more frequently in early than in late amniocentesis. As yet, data are too sparse to allow a comparison with chorionic villus sampling. There are no reliable follow-up data from which to estimate the abortion rate and the number of embryonic malformations.     

Genetic amniocentesis at 7–14 weeks of gestation

Genetic amniocentesis performed at 7–14 weeks of gestation was studied in a series of 138 patients of whom 50 wanted termination of pregnancy (⩽ 12 weeks). The material for analysis consisted of 132 samples due to two sampling failures and four samples being handled incorrectly. Forty-eight samples (36 per cent) were taken at 7–12 weeks of gestation, mainly transvaginally (36/48:75 per cent). The success rate of culture and karyotyping increased with the duration of pregnancy, but was only satisfactory from week 11 onwards. The time until harvest was then 14–15 days. The transvaginal approach is easy to perform and was accepted by the women, but we experienced bacterial or fungal overgrowth in 17 per cent of these samples, whereas no infection occurred in the samples taken transabdominally (n = 96). We conclude that genetic amniocentesis is feasible from week 11, but further studies concerning side effects, especially focusing on the procedure-related abortion risk, should be carried out before early amniocentesis is routinely applied.     

细胞色素P450酶系及其在毒理学上的应用

综述了细胞色素P450酶系在生物有机体中催化代谢外来化合物的 影响因素。作为生物体内的混合功能氧化酶系统的重要组成部分。P ytP450酶系（Cytochrome P450）在毒理学上的意义是作为早期预警系统来监测和预报环境污染状况的。在实际应用中，常以动物（多以鱼作为实验材料）肝脏中P450酶系的诱导作为评价多环芳烃、多氯联苯、二恶英、石油烃类环境污染状况的最灵敏的生物学反应之一。对P450作为生化指标的优点和局限性也进行了探讨。     

内蒙古赤峰红花沟金矿田矿床成因

基于野外调研 ,对赤峰红花沟金矿田的控矿构造及其矿体、岩体与地层之间的地质关系进行深入研究 ,提出金矿化发生在燕山早期 ,对燕山早期岩石化学与矿石氢氧同位素进行系统分析 ,得出本区矿床成因为重熔型成因 ,其成矿热液为原生岩浆水 ,后期有少量的大气降水加入。     

Comparative study of 15 lysosomal enzymes in chorionic villi and cultured amniotic fluid cells. Early prenatal diagnosis in seven pregnancies at risk for lysosomal storage diseases

A large number of chorionic villi samples obtained from women undergoing elective first trimester termination of pregnancy was analysed by enzyme assays similar to those applied to cultured amniotic cells. The levels of 15 lysosomal enzymes were compared to those observed in tissue cultures of amniotic cells obtained through amniocentesis at 16-18 weeks of pregnancy and the results were discussed in order to assess the usefulness of trophoblast biopsy for first trimester diagnosis of hereditary lysosomal diseases. The data suggest the applicability of this source of fetal cells for prenatal diagnosis of fifteen respective genetically determined enzyme deficiencies with the probable exception of α-L -iduronidase deficiency. Enzyme determinations were performed on chorionic villi samples of two pregnancies at risk for Tay-Sachs disease, three pregnancies for GM₁ gangliosidosis type 1, one for mucopolysaccharidosis type VI and one for Wolman's disease.     

Chorion biopsy in early pregnancy: A method of early prenatal diagnosis for inherited disorders

Chorion biopsy was performed in 165 cases at 6–12 weeks of pregnancy, following an ultrasonic or embryo-fetoscopic chorion frondosum localization. One hundred patients had their biopsies taken immediately before induced abortion. In 39 cases abortion was carried out 5–10 days after biopsy. In 26 pregnant patients biopsy was performed for genetic reasons. Fetal sex was determined in ‘native’ smears from biopsy specimens for cytological investigation, using X- and Y-chromatin assays. Fetal sex diagnosis proved correct in all the cases. In 40 observations, the origin of the biopsy specimen was histologically checked. In 16 biopsy specimens, a number of enzymes were simultaneously assayed: β-D-ghcosidase, β-D-galacto-sidase, β-D-hexosaminidase, β-D-glucuronidase, α-L-fucosidase, β-D-mannosidase, sphingo-myelinase and arylsulphatase A. The levels of the above enzymes were compared to those observed in tissue cultures of amniotic cells obtained through amniocentesis at 16–18 weeks of pregnancy. The amniotic sac remained intact in all cases of chorion biopsy. If the pregnancy was maintained after the biopsy, no spontaneous abortions were recorded, and pregnancies resulted in the timely delivery of full-term healthy infants. Therefore, the method described is a valuable means of diagnosing inherited disorders, with promising applications in prenatal medicine.