邻苯二甲酸二丁酯对蚕豆胚根细胞微核形成的影响及毒理机制

研究常用增塑剂邻苯二甲酸二丁酯(di-n-butyl phthalate,DBP)对农作物生长的影响,为农用地膜及其残留物的环境安全性评估提供实验依据。以蚕豆为试材,DBP处理浓度为0(CK)、9 mmol·L-1、18 mmol·L-1、27 mmol·L-1和36 mmol·L-1,培养24 h、48 h和72 h后,观测根尖细胞染色体结构变化,测试胚根抗氧化酶活性。结果显示:DBP暴露的蚕豆胚根生长速率减缓;随着DBP暴露时间延长,根尖正在进行分裂的细胞被阻断在有丝分裂前期的比例增加,微核率升高,出现多种类型的染色体畸变;DBP暴露的胚根超氧化物歧化酶(superoxide dismutase,SOD)活性提高5.41%~29.68%,过氧化物酶(peroxidase,POD)活性随DBP浓度增加而递减,过氧化氢酶(catalase,CAT)活性显著降低14.00%~43.08%。结果表明,DBP对蚕豆胚根具有遗传毒性,且能够破坏纺锤丝的结构。     

不同粒径大气颗粒物几种重金属成分分析及其致突变性研究

采集冬季太原市一采样点不同粒径大气颗粒物,经分析,总悬浮颗粒物日均浓度为1.04mg/m~3,严重超标。其中粒径小于7.0μm的占49.6％,小于3.3μm的占33.5％。颗粒物无机提取液中5种金属元素的浓度由高到低依次为Pb、Mn、Cr、Ni和Cd。每一种元素均呈随颗粒物粒径减小浓度增高的趋势。以SOS显色法和小鼠体内骨髓细胞染色体畸变试验检测颗粒物的无机提取液和模拟肺泡液溶出液的遗传毒性,表明小粒径颗粒物遗传毒性较强;小于1.1μm的颗粒物,仅用相当于5m~3或10m~3空气量的样品液,即可诱发SOS反应或致染色体损伤。     

Genotoxicity study of high aspect ratio silver nanowires

The genotoxicity potential of silver nanowires synthesized via the solution-based polyol method has been investigated. They were found to be non-mutagenic in three Salmonella strains and were not genotoxic in a clastogenicity assay in mice. Residual surfactant was found to have an effect on the toxicological properties of the nanowires by increasing the rate of Ag⁺ release. Residual surfactant can be easily degraded via a UV treatment.     

First-trimester maternal serum human chorionic gonadotrophin as a marker for fetal chromosomal disorders

The Dutch Working Party on Prenatal Diagnosis has initiated a study on the possibilities of first-trimester screening for fetal chromosomal disorders. We report on maternal serum human chorionic gonadotrophin (MS-hCG) measurements in 1348 pregnancies with a chromosomally normal fetus and 53 pregnancies with a chromosomally abnormal fetus. The median MS-hCG concentration in 24 pregnancies with Down's syndrome was 1.19 multiples of the normal median (MoM). The MS-hCG distributions in normal and Down's syndrome pregnancies did not differ significantly (t-test: t = 1.945, p >0.05). We also found no difference between normal pregnancies and pregnancies with other chromosomal disorders (six cases of trisomy 18, MoM = 0.80; four cases of sex chromosome abnormality, MoM = 1.01; 17 cases of chromosomal mosaicism in chorionic villi, MoM = 1.11). Selecting an upper limit at the 90th centile could detect 25 per cent of pregnancies with Down's syndrome. We conclude that, in the first trimester, MS-hCG as a screening factor for Down's syndrome is of minor value. However, MS-hCG could be a useful factor in a first-trimester screening programme based on a combination of markers.     

Effects of Zn~（2＋） on root growth，cell division，and nucleoli of Allium cepa L．

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平阳霉素三种成分诱发CHO-K1细胞株染色体畸变和姐妹染色单体交换的研究

本文报道平阳霉素(Pingyangmycin,PYM)的三种成分A_2、A_5和A_6诱发CHO-K1细胞染色体畸变和姐妹染色单体交换(SCEs)。处理后第一次分裂中期染色体型畸变占优势,其中有大量的染色体碎裂(Disintegration),在含染色体碎裂的细胞中三分之一伴随出现双微体(Double minutes,DMs)。细胞畸变的频率随处理浓度升高而增加。 处理后第二次分裂中期,细胞畸变的频率仍随处理试剂浓度增加而升高,SCEs频率随处理浓度升高而递增。 上述三种成分诱发染色休畸变的类型没有质的差异。     

Maternal serum CA 125 levels in pregnancies with chromosomally-normal and -abnormal fetuses

We measured the maternal serum cancer antigen 125 (MS-CA 125) levels in 98 nonpregnant women, 765 first- and second-trimester pregnancies with chromosomally-normal fetuses, and 54 chromosomally-abnormal pregnancies. To determine the MS-CA 125 concentration, we used a new automated microparticle enzyme immunoassay with low inter-assay variability. The median MS-CA 125 level decreased from the first to the second trimester of pregnancy and was higher than that in non-pregnant women. We found no difference between normal and Down's syndrome (n = 29) pregnancies ( t-test: t = 0·57, p >0·5). The MS-CA 125 levels in pregnancies with other chromosomal abnormalities showed no difference either, compared with the normals. We conclude that MS-CA 125 is not a useful marker for fetal Down's syndrome, nor for other chromosomal disorders in pregnancy.     

High resolution chromosomes from first trimester trophoblast cultures

A simple method for obtaining prometaphase chromosomes from cultured first trimester cells involves the addition of BrdU and FdU 11 h before harvest and ethidium bromide 1.5 h before harvest. High resolution R-banding is obtained by acridine orange staining.     

Blood transferrin receptor expression in chromosomally abnormal fetuses

In a cross-sectional study of 13 chromosomally abnormal fetuses, umbilical venous blood was obtained by cordocentesis at 17–32 weeks' gestation. Fetal blood transferrin receptor (CD71) expression (mean=79·8 per cent, range=60–98 per cent) and nucleated red cell count (mean=10·4 × 10⁹ per 1, range=1·0–25·0 × 10⁹ per 1) were significantly higher than the appropriate normal mean for gestation (z=3·92, P<0·0001 and z=3·69, P<0·001, respectively). These haematological changes in chromosomally abnormal fetuses would facilitate their prenatal diagnosis by analysis of fetal nucleated red blood cells isolated from the maternal circulation on the basis of CD71 expression.     

Prenatal diagnosis of mosaicism 46, XX/46, XX, −21, +t(21q21q)

Mosaicism for a structural chromosome abnormality in amniotic cell cultures indicative of true fetal mosaicism is a rare event. In addition to the laboratory findings the clinical interpretation for counselling in such cases is based on observation of the same abnormality in liveborns as well as previous experience with prenatal diagnosis of the same or similar abnormalities. We report here the prenatal diagnos is of 46,XX/46,XX,−21,+t(21q21q) which was confirmed in fetal skin cell and amnion cell cultures.