4-n-Nonylphenol and 17-β estradiol may induce common DNA effects in developing barnacle larvae

There is a growing concern over the potential effects of environmental endocrine disrupters on both human and wildlife populations. However, to date, minimal research has been conducted to determine the effect of estrogens and xenoestrogens at the DNA level. In this study, we used the random amplified polymorphic DNA (RAPD) assay to evaluate the effects on the genomic DNA of barnacle larvae that had been exposed to 17β-estradiol (E₂) and low concentrations of 4-n-nonylphenol (NP). DNA effects include DNA damage as well as mutations and possibly other effects at the DNA level that can be induced by chemical or physical agents that directly and/or indirectly interact with genomic DNA. Not only did exposure to NP and E₂ induce changes in RAPD profiles in the exposed barnacle larvae when compared to control patterns, but also, and more importantly, there were similarities in the RAPD modifications in the exposed populations that had been treated to either chemical. We propose that NP and E₂ induced some common DNA effects in barnacle larvae and that these specific modifications in RAPD patterns may arise as a consequence of hot spot DNA damage (e.g. DNA adducts) and/or mutations (point mutations or genomic rearrangements). This could help to explain how xenoestrogens mimic the effects produced by natural estrogens. In conclusion, in the field of endocrine disruption, the study of DNA effects induced by estrogens and/or xenoestrogens warrants further investigation. Indeed, changes at the DNA level may be the precursors of some of the numerous effects reported at higher levels of biological organisation such as the feminization of males, developmental abnormalities, and infertility.     

水传病原微生物PCR-纳米金显色快速检测方法

水传病原微生物是腹泻等肠胃疾病发病的主要原因,而发展快速、有效的检测方法对于控制和减少该类微生物的传播风险十分重要.因此,本文研究了PCR反应结合不修饰的纳米金颗粒(Gold nano-particles,AuNPs)显色检测方法的最佳盐浓度、探针含量、PCR反应条件等,并从纳米金制备、病原菌种类、检测特异性等方面进行考核,确定了最优检测条件为:10μL PCR扩增产物混合20 pmol探针,95℃反应5 min,55.5℃反应3 min后,40℃杂交10 min;此时,先后加入90μL实验用纳米金和一定浓度的PBS溶液,室温观察颜色变化.结果发现,纳米金溶液由红色变为紫色或近于无色为阳性结果,对应的吸光度值迁移出530 nm,以此可达到快速检测病原微生物的目的.     

镇江老城区古运河沉积物氮及有机质垂向分布及污染评价

为揭示镇江老城区古运河沉积物中氮及有机质的垂向分布特征及污染状况,分别采集古运河老城区上游电力路桥(D)和下游南水桥(B)两个沉积物柱状样,分析其总氮(TN)、有机氮(Org-N)、氨氮(NH+4-N)、硝氮(NO-3-N)及有机质(O.M)含量、C/N比的垂向分布特征,并通过富集系数及污染物的综合评价,揭示古运河沉积物中污染物的演化规律和污染状况.结果表明:①D点TN、Org-N、NH+4-N、NO-3-N以及O.M的平均值分别为366.33 mg·kg-1、348.02 mg·kg-1、89.47 mg·kg-1、13.51 mg·kg-1、0.43%,B点则分别为940.23 mg·kg-1、893.22 mg·kg-1、169.48 mg·kg-1、15.19 mg·kg-1、0.76%,以上指标均表现为D0.05),表明以上两个采样点沉积物对营养元素的富集过程相似;④D和B两点沉积物TN与O.M均无显著性相关,判断以上两点沉积物TN可能主要来自于外源污染;⑤有机指数评价结果显示,D和B两点有机污染呈现出清洁状态,有机氮则在较清洁、尚清洁范围.     

苯并[a]芘对马氏珠母贝血淋巴细胞DNA损伤的研究

通过单细胞凝胶电泳技术(彗星试验)研究了苯并[a]芘(B[a]P)对马氏珠母贝(Pinctada martensi)血淋巴细胞DNA的损伤。结果显示,在相同暴露时间内,不同质量浓度的B[a]P均能引起马氏珠母贝血淋巴细胞DNA损伤。4μg.L-1 B[a]P处理组DNA含量、彗尾长度和Olive尾矩均最大,分别为34.39%、281.73和60.31μm。随着暴露时间的延长,彗星尾长明显增加,表现出明显的时间-效应关系,而DNA含量和Olive尾矩没有呈现出规律性变化。此外,在不同的染毒时间内,对照组和各处理组之间均存在显著差异(P<0.05),3个指标具有很好的一致性。研究表明,彗星试验是检测B[a]P对马氏珠母贝血淋巴细胞DNA损伤的一种有效手段,马氏珠母贝血淋巴细胞DNA损伤可作为指示B[a]P污染的一种有效生物标志物用于早期预警监测。     

大田软海绵酸对黑鲷胚胎发育及仔鱼的急性毒性

为了研究大田软海绵酸(okadaic acid,OA)对生物胚胎组织发育过程的毒性作用机制,采用静水和半静水实验法,用OA毒素与过滤海水按等对数间距分设5个浓度组,同时以过滤海水为对照组,对人工养殖的黑鲷鱼卵和仔鱼进行了毒性实验。实验结果表明:一定浓度的OA使鱼卵的死亡率和孵出仔鱼的畸形率升高,但对孵化率的影响较弱。OA对黑鲷仔鱼的24、48、72和96h的LC50分别为51.63、45.58、37.97和25.72nmol·L-1,仔鱼体内毒性蓄积程度也随时间逐渐减弱。OA毒素对仔鱼的谷胱甘肽过氧化物酶(GSH-PX)和酸性磷酸酶(ACP)的活性均有诱导作用,与对ACP的影响相比,OA毒素对GSH-PX活性的诱导作用更为突出。此外,OA毒素还会对黑鲷仔鱼的肝脏细胞的核酸代谢及DNA合成有一定的影响,使得RNA和DNA的含量比值发生显著变化。