总N—亚硝基化合物接触量与胃癌死亡率的生态学相关性

在胃癌高发区福建省长乐县和低发区山东省崂山县和随机选择近６０名３５－６４岁男性一，以份饭法收集２４ｈ膳食和１２ｈ尿液，测定总Ｎ－亚硝基人合物（ＴＮＯＣ）含量，计算膳食摄入量和尿中排出量人群日均膳食摄往我为７．０７４．３１μｍｏｌ，低发区为４．０７±３．６７μｍｏｌ，Ｐ〈０．００１；１２ｈ尿中排出量高发区为１１３±０．６１μｍｏｌ，低发区为０．３４±０．２７μｍｏｌ，Ｐ〈０．００１；尿中排出量与膳食     

江西省食管癌与岩石类型

利用江西省大量岩石类型和食管癌死亡调查资料，对食管癌死亡率与人群生存区岩石类型的相关性进行了研究。结果表明，江西省食管癌死亡率与岩石类型密切相关。食管癌死亡率与变质岩、碳酸盐岩、第四系松散岩、红色碎屑岩呈正相关，与岩浆岩呈负相关，与碎屑岩相关不显著。     

吸烟烟气对鼠肺细胞膜的损伤和茶多酚的保护作用

本文以香烟气相物质作用鼠肺细胞膜为模型,用脂肪酸自旋标记物5-DOXYL和16DOXYL分别研究膜浅层和深层的动态性质受气相烟的影响,并用紫外可见分光光度法研究气相烟对膜脂的作用。结果发现,在实验的气相烟流量下,香烟气相物质能引发鼠肺细胞膜的脂质过氧化,并且使膜浅层的流动性增大。但对膜深层的动态性质没有明显的改变,如果在鼠肺细胞中预先加入粗晶态或粉态茶多酚。则肺细胞的过氧化和膜的动态性质改变受到抑制,而且这种抑制作用与茶多酚浓度呈量效关系,而茶多酚本身对膜浅层无明显作用,但对膜深层的流动性有一定影响,而且两种茶多酚的作用相似。     

Assessing the human health effects of PCBs

Toxic effects can be induced in experimental animals by high doses of pure PCBs, and in man by PCDF-contaminated PCB. In order to assess the effects of ordinary, uncontaminated PCB on man, a group of capacitor workers who had direct occupational exposure to Aroclors 1254, 1242, and 1016 during the period 1946 to 1977 has been under medical surveillance since 1976. This group presented some indications of non-AhR-mediated microsomal enzyme induction during the period of direct exposure, but no chloracne or increased cancer mortality. Multiple regression studies revealed no significant associations between lipid PCB levels and clinical indicators of hepatotoxicity, hypertension, or pulmonary impairment.     

The Nile delta-Alexandria coast: vulnerability to sea-level rise,consequences and adaptation

Like many delta systems, the coastal zoneof the Nile delta has been designated as avulnerable zone to a rising sea level as aconsequence of expected climate changescombined with geological and human factors.In view of the understanding of thesefactors, a degree of vulnerabilityanalysis has been carried out to betterlocate which sectors need to be assessedand adapted to possible sea level rise(SLR) for the Nile delta-Alexandria region of Egypt.Results reveal that not all of the coastalzones of the Nile delta are vulnerable toaccelerated sea-level rise at the samelevel. Based on multiple criteria the Niledelta-Alexandria coast can be categorizedinto vulnerable (30%), invulnerable (55%)and artificially protected coastalstretches (15%). These criteria include:local subsidence or uplifting, relativesea-level rise (RSLR), land topography,width of lagoon barriers, beach-face slope,high-elevated features such as dunes andridges, eroding and accreting coastlinesand protection works.Moreover, this study evaluates thelong-term relative sea-level rise andsubsidence rates along the Nile delta andAlexandria coasts. Statistical analysis oflong-term tide gauge data recorded atAlexandria, Burullus and Port Said yieldsvalues of 1.6, 1.0 and 2.2 mm/yr,respectively. These values of relativesea-level rise and long-term subsidencerate obtained from age-dated sediment coresections are inconsistent: long-termsubsidence appears to be larger (maximum of7 mm/ yr). This discrepancy might beexplained if the subsidence is episodic,and occurs rather abruptly during majorearthquakes that occur every few hundredyears associated with fault trend lines.Rising sea levels could have significantlongterm impacts on the Nile delta,including the distribution of ground watersalinity and erosion of the narrow andlow-lying barriers of the Burullus andManzala lagoons. Adaptive measures alongthe study area particularly those relatedto coastal protective structures are alsoevaluated.     

中国沿海常见棘毒鱼类的毒性研究：日本鬼背鳍棘中Ⅰ型毒腺细？…

皮光、电镜方法研究了日本鬼Ｙｏｕ背鳍棘中Ⅰ型毒腺细胞的形成过程。结果表明：位于背鳍棘两侧纵沟内的毒腺组织周围有较致密的结缔组织的鞘膜包绕，该鞘膜钝性剥离后可见内面光滑，有Ⅰ型和Ⅱ型型毒腺细胞的痕迹。而毒腺组织内下侧与毒棘的骨组织相连处结缔组织疏松，有许多小的梭形细胞；在梭形细胞之间及周围有新形成的幼稚腺细胞，其组织结构类似Ⅰ型毒腺细胞。透射电镜下可见该区域的结缔组织中除结缔组织的细胞及成分以外，有     

Molecular evidence of fetal-derived chromosome 21 markers (STRs) in transcervical samples

Transcervical cells (TCCs), collected by flushing or aspiration at 8–13 weeks of gestation, were analysed for the presence of fetal-derived DNA sequences. DNA extracted from maternal peripheral blood, TCC samples, and placental tissue was amplified by the polymerase chain reaction (PCR) to detect small tandem repeat (STR) markers specific to chromosome 21. STR products of fetal origin could be clearly observed in four TCC samples. TCC samples collected by flushing or aspiration were also analysed by fluorescent in situ hybridization (FISH) using X and Y probes simultaneously: 46,XY cells could be detected in all TCC samples obtained from mothers with male fetuses.     

Isolating fetal nucleated red blood cells from maternal blood: The baylor experience—1995

In our previous work we have isolated fetal cells from maternal blood and used fluorescent in situ hybridization (FISH) for chromosome-specific probes to detect aneuploidy. Current efforts in the Baylor College of Medicine programme are focusing on obtaining consistency in flow-sorting methodology and on determining sensitivity and specificity. To this end, systematic evaluation of five glycophorin A (gly A) antibodies all produced agglutination, leading us to abandon the use of gly A antibodies for positive selection of fetal cells. Conversely, we have found LDS-751 to be useful for nuclear selection. CD45 negative selection can best be accomplished by the use of flasks coated with goat antibodies against mouse antibodies. Positive selection by flow sorting for either CD71⁺ cells or gamma-globin-positive cells seems to be successful. Using these two approaches, we have recently detected male (fetal) cells in pregnancies in which the fetus was 46, XY in 10 of 18 and in 12 of 14 cases, respectively.     

The characterization of hCG regulation in cultured human amniotic fluid cells

The media from primary cultures and subcultures of second trimester human amniotic fluid (AF) cells were assayed by radioimmunoassay to quantitate production of human chorionic gonadotropin (hCG). Primary AF cultures produce more hCG per cell than do the corresponding subcultures. Sodium butyrate (2 mM) stimulates AF subcultures to produce 5-13 times more hCG per cell or per mg of cellular protein than do untreated subcultures. This stimulatory effect of sodium butyrate is dose dependent between 0 and 5 mM. Addition of sodium butyrate 24 hours after subculture, while stimulating production of hCG during the subsequent 3 days, also results in fewer cells and less protein per culture. This effect on cell growth is also dose-dependent. Previous investigators have proposed that the stimulation of hCG by sodium butyrate in other types of cell cultures is due to an effect of that agent on culture growth. Therefore, in these studies AF cells are allowed to grow to confluency before sodium butyrate was added. Production of hCG was stimulated by sodium butyrate about four-fold during the next 5 days although no significant changes were observed either in number of cells or amount of cellular protein per culture. These results suggest that stimulation of hCG by sodium butyrate is not dependent on its effect on growth of the cultures.     

Isolating fetal cells in maternal circulation for prenatal diagnosis

Fetal cells unequivocally exist in and can be isolated from maternal blood. Erythroblasts, trophoblasts, granulocytes and lymphocytes have all been isolated by various density gradient and flow sorting techniques. Chromosomal abnormalities detected on isolated fetal cells include trisomy 21, trisomy 18, Klinefelter syndrome (47,XXY) and 47,XYY. Polymerase chain reaction (PCR) technology has enabled the detection of fetal sex, Mendelian disorders (e.g. β-globin mutations), HLA polymorphisms, and fetal Rhesus (D) blood type. The fetal cell type that has generated the most success is the nucleated erythrocyte; however, trophoblasts, lymphocytes and granulocytes are also considered to be present in maternal blood. Fetal cells circulate in maternal blood during the first and second trimesters, and their detection is probably not affected by Rh or ABO maternal-fetal incompatibilities. Emphasis is now directed toward determining the most practical and efficacious manner for this technique to be applied to prenatal genetic diagnosis. Only upon completion of clinical evaluations could it be considered appropriate to offer this technology as an alternative to conventional invasive and non-invasive methods of prenatal cytogenetic diagnosis.