纳米二氧化钛致日本青鳉鱼胚胎毒性效应特征

采用青鳉鱼胚胎暴露的方法,研究不同浓度纳米TiO_2对胚胎的毒性效应.结果表明,纳米TiO_224 h的半数致死率LD50为115.17 mg·L~(-1),但不同浓度组引起致死效应差别很大,不存在剂量—效应关系.随着处理浓度从高到低的变化,青鳉鱼胚胎孵化率呈现V字型降低.孵化率最低的为0.1 mg·L~(-1)纳米TiO_2处理组,其孵化率低于10%.高浓度组纳米TiO_2(1 mg·L~(-1)试验组和10 mg·L~(-1)试验组)导致青鳉鱼胚胎孵化时间延迟1—2周.高浓度组(1 mg·L~(-1)和10 mg·L~(-1)处理组)和低浓度组(0.1 mg·L~(-1)和0.01 mg·L~(-1)处理组)的纳米TiO_2对青鳉鱼胚胎和幼鱼造成的畸形毒性特征不同.高浓度组主要造成卵黄囊水肿,低浓度组的毒性特征主要是卵膜破损和胚胎急性致死.对纳米TiO_2的致毒机理,尤其是低于0.1mg·L~(-1)的毒性效应和致毒机理需要进一步研究.     

2,3,7,8-TCDD的短期暴露对HepG2肝癌细胞内小分子代谢产物的影响

为了研究二恶英对细胞的代谢毒性,探究其肝毒性的作用机制,以二恶英中毒性最强的2,3,7,8-四氯代二苯并-对-二恶英(TCDD)为代表污染物,以HepG2肝癌细胞为受试对象,采用四甲基偶氮唑蓝(MTT)法和高效液相色谱/串联质谱法考察了TC-DD的24h暴露对HepG2细胞的增殖活性以及细胞的葡萄糖、氨基酸、尿素和甘油等小分子代谢物的影响。结果显示,短暂的TCDD暴露对HepG2细胞的增殖活性无显著影响。24h的TCDD暴露对细胞的葡萄糖消耗量无显著影响,但当TCDD浓度增至1nmol·L-1时,葡萄糖的消耗量表现出一定的降低趋势。0.01nmol·L-1TCDD就会使细胞脯氨酸和谷氨酸的合成能力下降,且谷氨酸的变化表现出明显的剂量-效应关系;TCDD可刺激细胞对缬氨酸、苏氨酸、酪氨酸、甲硫氨酸以及亮氨酸与异亮氨酸的吸收,并具有明显的浓度依赖性。随着TCDD浓度的增加,甘油和尿素产生量的降低趋势逐渐明显,1nmol·L-1TCDD处理24h后,甘油和尿素的产生量仅为对照组的1%和18%。研究表明,TCDD在短时间内使HepG2细胞内的一系列小分子代谢产物发生了不同程度的改变,且呈现出一定的剂量-效应关系。可见,TCDD可通过干扰HepG2肝癌细胞的代谢过程产生毒性。     

水体低氧的早期暴露对青鳉(Oryzias latipes)后期的生长、性别比和繁殖能力的影响

水体低氧已是全球性生态问题,常以季节性、偶发性和昼夜间等不同形式存在于不同的水体中。长期低氧可影响鱼类正常的生长和繁殖,但鱼类早期生活阶段暴露于不同形式的低氧后,后期的生长和繁殖是否会受到不利影响,目前研究甚少。本研究在实验室模拟了连续低氧(2.8 mg·L~(-1)DO)(H1)、昼夜低氧(H2)和发生在胚胎器官形成时期的偶发性低氧(H3)等3种情景对青鳉胚胎的发育影响,评估了这一早期暴露对青鳉后期的生长、存活和繁殖的影响。我们发现,3种低氧方式都可以显著延长青鳉胚胎的孵化周期,引起胚胎卵黄囊吸收和鱼鳔发育异常;暴露结束120 d后,H1组青鳉成鱼的畸形率显著升高、存活率和生长速度都显著下降;H1、H2和H3组中成鱼的雌雄比都发生了改变,鱼群中以雄鱼为主,且产卵量和受精率都显著下降。结果表明,鱼类早期胚胎发育阶段所受到的低氧暴露可对后期生长和繁殖产生不利影响,对子代补充和种群稳定产生重要影响;鱼类关键发育期所经历的低氧事件,以及昼夜低氧事件所产生的生态后果不容忽视。     

运动对2,3,7,8-四氯二苯并二恶英急性暴露大鼠肝脏抗氧化能力的影响

观察8周中等强度游泳运动对2,3,7,8-四氯二苯并二恶英(2,3,7,8-tetrachlorodibenzo-p-dioxin,2,3,7,8-TCDD)急性暴露大鼠肝脏氧化应激的影响。以8周龄雄性Sprague Dawley大鼠为研究对象,将大鼠随机分为玉米油静养组(NC组)、玉米油运动组(EC组)、TCDD静养组(NT)和TCDD运动组(ET组)。将TCDD溶于玉米油中,NT和ET组大鼠按照10μg·kg-1(以单位体重计)腹腔注射TCDD,NC和EC组大鼠注射等量玉米油。正式实验开始后,EC和ET组大鼠进行运动(尾部负重5%游泳30min),每周运动5 d,共8周,NC和NT组大鼠不进行任何运动干预。8周后,称重并宰杀大鼠,收集血清和肝组织样本,待测血清天门冬氨酸氨基转移酶(AST)、丙氨酸氨基转移酶(ALT)的活性;肝组织丙二醛(MDA)含量,超氧化物歧化酶(SOD)、过氧化氢酶(CAT)以及谷胱甘肽过氧化物酶(GSH-Px)的活性。将数据进行多因素方差分析,结果表明,染毒可升高大鼠血清AST的活性,增加肝脏MDA的含量,降低肝脏SOD、CAT和GSH-Px的活性;运动可降低大鼠肝脏GSH-Px的活性;染毒后运动可减少肝脏MDA的含量,升高肝脏SOD、CAT和GSH-Px的活性。研究表明,TCDD急性暴露可导致大鼠肝细胞功能受损,导致大鼠肝脏发生氧化应激。8周有氧运动改善TCDD急性暴露诱导的肝细胞损伤,改善肝脏氧化应激,这可能是运动改善TCDD肝毒性的机制之一。     

二恶英类毒理学研究新进展

二恶英类的毒理学研究已有30多年的历史,在一系列二恶英类污染事件和国际公约的推动下,近年来二恶英类毒理学研究成为备受关注的热点.综述了近年来二恶英类毒理学研究的一些新的观点和发现,涵盖了分子毒性机理、致癌毒性、非致癌毒性和非致癌剂量-效应风险度评价方法等诸多领域,其中TCDD毒性效应的负反馈调节机制研究和对人体健康非致癌效应的影响引起了国内外广大毒理学研究工作者的关注.在总结前人研究的基础上对二恶英类毒理学研究今后的发展进行了展望.     

Cu2+和Cd2+对日本青鳉（Oryzias latipes）早期发育阶段的急性毒性效应研究

为探究并比较淡水鱼种日本青鳉早期发育阶段对Cu2和Cd2等重金属胁迫的响应,在实验室通过半静态方式,对日本青鳉受精卵和仔稚鱼分别进行了48 h和96 h急性毒性实验.结果表明:Cu2对日本青鳉胚胎24、48 h-LC50分别为8.164 mg·L-1和6.965 mg·L-1;Cd2+对日本青鳝胚胎24、48 h-LC50分别为63.084 mg· L-1和53.093 mg ·L-1;较低浓度组Cu2+(≤1.97 mg ·L-1)时日本青鳉胚胎的发育速率快于对照组,而较高浓度组(≥3.87 mg·L-1)胚胎的发育速率则慢于对照组;与Cu2略有不同,无论浓度高低Cd2对胚胎的孵化速率均产生抑制作用;Cu2+和Cd2质量浓度分别高于1.97 mg·Lq和19.68 mg· L-1时,两种重金属离子均显著降低胚胎的孵化率(P＜0.05).Cu2对日本青鳉初孵仔鱼24、48、72和96 h-LC50分别为5361 mg·L-1、2.844 mg·L-1、2.020 mg·L-1和1352 mg·L-1;Cd2+对日本青鳉初孵仔鱼24、48、72和96 h-LC50分别为15.907 mg·L-1、10550 mg·L-1、7.986 mg· L-1和6346 mg·L-1;Cu2+对日本青鳉稚鱼24、48、72和96 h-LC50分别为5.732 mg·L-1、4.037 mg· L-1、2A98 mg·L-1和1.955 mg·L-1;Cd2+对日本青鳉稚鱼的24、48、72和96 h-LC50分别为16A19 mg·L、11.745 mg· L-1、8516 mg·L-1和6.776 mg· L-1.与其它淡水水生生物相比,日本青鳉仔稚鱼对铜和镉离子较为敏感.     

城镇污水处理厂进出水对日本青鱂早期阶段亚慢性毒性效应

采用日本青鳉胚胎及幼鱼暴露评估污水处理厂进出水的综合毒性效应。水样采自广州市3个污水处理厂的进水口和出水口。96 h青鳉幼鱼急性毒性试验表明:6个水样均没有对青鳉幼鱼产生急性毒性效应。14 d胚胎暴露试验结果:3个污水处理厂的进水及1号和3号污水处理厂的出水均引起胚胎死亡,胚胎孵化率均低于70%且均与对照组产生了显著性差异(p0.05)。3个厂的进水和1号、2号厂出水的鱼苗畸形率与对照组也有显著差异(p0.05),其中3号厂进水鱼苗畸形率高达(33.73±8.94)%。而6个水样的胚胎孵化时间均与对照组无显著差异(p0.05),均在9 d左右。7 d鱼苗暴露试验结果:1、2、3号3个水厂进水的鱼苗死亡率分别是(30.16±2.75)%,(24.07±1.60)%,(37.90±4.77)%,与对照组产生明显差异(p0.05)。出水对鱼苗的致死效应明显低于进水,但出水对鱼苗的致死效应相对于对照组仍有显著差异(p0.05)。     

城镇污水处理厂进出水对日本青鳉早期阶段亚慢性毒性效应

采用日本青鳉胚胎及幼鱼暴露评估污水处理厂进出水的综合毒性效应。水样采自广州市3个污水处理厂的进水口和出水口。96 h青鳉幼鱼急性毒性试验表明:6个水样均没有对青鳉幼鱼产生急性毒性效应。14 d胚胎暴露试验结果:3个污水处理厂的进水及1号和3号污水处理厂的出水均引起胚胎死亡,胚胎孵化率均低于70%且均与对照组产生了显著性差异(p0.05)。3个厂的进水和1号、2号厂出水的鱼苗畸形率与对照组也有显著差异(p0.05),其中3号厂进水鱼苗畸形率高达(33.73±8.94)%。而6个水样的胚胎孵化时间均与对照组无显著差异(p0.05),均在9 d左右。7 d鱼苗暴露试验结果:1、2、3号3个水厂进水的鱼苗死亡率分别是(30.16±2.75)%,(24.07±1.60)%,(37.90±4.77)%,与对照组产生明显差异(p0.05)。出水对鱼苗的致死效应明显低于进水,但出水对鱼苗的致死效应相对于对照组仍有显著差异(p0.05)。     

2,3,7,8-四氯苯并二噁英（TCDD）短期染毒可造成着床前胚胎丢失并伴随雌性生殖器官中毒物相关蛋白的诱导表达（Short Time Exposure of TCDD Causing Loss of Implantation Failure of Embryos and Its Associated with Induced Expression of Relevant Proteins）

为探明妊娠早期胚胎的丢失是否与卵巢、输卵管、子宫组织受到2,3,7,8-四氯苯并二噁英(TCDD)直接毒害有关,检测了NIH小鼠胚胎着床前期和后期TCDD暴露对胚胎毒性影响的敏感性,并利用免疫组化方法分析了模型动物肝脏、子宫、输卵管和卵巢组织中TCDD所引起的AhR、ARNT以及Cyp1a2分子标记物的变化.检测发现:妊娠第9d,100ng·kg-1·d-1剂量TCDD经口染毒,造成胚胎着床数量减少,且着床前期暴露的影响大于着床后期;子宫蜕膜反应受到明显抑制;胚胎迁移率没有明显变化,但胚胎数量减少.免疫组织化学分析发现正常组小鼠的肝脏、子宫、输卵管和卵巢组织中有AhR和Cyp1a2弱阳性信号表达,ARNT有细胞核的强阳性信号表达;妊娠第1～8d、第1～3d和第4～8d处理组小鼠肝脏、子宫、输卵管和卵巢组织中的AhR、Cyp1a2的阳性面积和光密度值均高于正常组;随处理时间和组织蓄积量的增加,ARNT在组织中的变化由胞核(妊娠第1～3d组)表达到胞浆(妊娠第4～8d组)表达,然后完全无表达(妊娠第1～8d组).以上研究结果表明:TCDD对早期妊娠小鼠子宫、输卵管和卵巢组织中的AhR、ARNT和Cyp1a2的激活和代谢方式与肝脏相同,说明雌性生殖系统中的组织有TCDD蓄积和代谢活性,这可能是导致早期胚胎迁移、着床等过程改变,造成胚胎丢失的重要原因.     

邻苯二甲酸二(2-乙基己)酯和邻苯二甲酸单乙基己基酯对幼年期及青年期海洋青鳉(Oryzias melastigma)的内分泌干扰效应

本研究从邻苯二甲酸二(2-乙基己)酯(DEHP)和邻苯二甲酸单乙基己酯(MEHP)对幼鱼期及青年期海洋青鳉(Oryzias melastigma)的生殖发育毒性效应出发,从雌激素受体(ER)、过氧化物增殖激活受体(PPAR)及芳香烃受体(AhR)通路探讨DEHP和MEHP致毒机制.本实验将孵化后1周的幼鱼分别暴露于溶剂对照、低浓度DEHP(0.1 mg·L-1)、高浓度DEHP(0.5 mg·L-1)、低浓度MEHP(0.1 mg·L-1)和高浓度MEHP(0.5 mg·L-1)23 d、53 d,组织病理学结果显示,DEHP和MEHP导致雌性青鳉肝损伤,表现为肝糖原降低,肝细胞质水肿变性;DEHP和MEHP促进了性成熟,表现为促进雌性青鳉卵巢中卵细胞的发育.荧光定量PCR结果显示,DEHP和MEHP显著影响了ER、PPAR及AhR通路,并且对青年期的影响强于幼鱼期,DEHP对ER、PPAR及AhR通路的影响较MEHP强.所以DEHP及MEHP可能通过ER、PPAR和AhR通路影响了肝脏发育,造成了肝损伤,促进雌性青鳉卵巢发育,对ER、PPAR和AhR通路影响显示出发育阶段特异性.     

Temperature and developmental plasticity during embryogenesis in the Atlantic cod<Emphasis Type="Italic"> Gadus morhua</Emphasis> L.

Atlantic cod (Gadus morhua L.) embryos were reared at 4 °C, 7 °C, and 10 °C, and the relative timing of developmental events was characterized, with particular reference to myotomal muscle. Embryos started to feed at an apparently equivalent stage of development, so comparisons were made between temperature groups on the basis of percentage of time to first feeding and somite stage. No differences were found in the time of hatching or timing of appearance of the otic placode, unpaired median fin fold, gut lumen, otic vesicle, lens of the eye, otoliths, first muscular contractions, swim bladder, and hindgut, or in the rate of development of somites, myotubes, myofibrils, and acetylcholinesterase activity over the temperature range studied. In contrast, closure of the blastopore occurred late with respect to segmentation at higher temperatures, at the 3-somite, 10-somite, and 12-somite stages at 4 °C, 7 °C, and 10 °C respectively. Muscle cellularity was also markedly altered in the 10 °C group relative to the 4 °C and 7 °C groups. Larvae reared at 10 °C had significantly more (+14%) deep white fibers at hatch (P <0.001), whereas numbers of superficial red fibers remained unchanged. It is suggested that differences in muscle cellularity might be related to changes in the relative timing of epiboly, through differential proliferation of presomitic myogenic cells and/or their relative exposure to inductive signals.     

五氯酚暴露诱导斑马鱼胚胎细胞凋亡相关基因的变化及caspase-2基因克隆和系统进化分析

应用基因芯片技术研究发现,暴露于五氯酚的斑马鱼胚胎中有14个涉及细胞凋亡行为的基因表达发生了显著改变.利用生物信息学方法构建这些功能基因系统进化树,分析与环境毒物诱导的细胞凋亡行为密切相关的caspase-2基因和其他基因之间的同源关系.斑马鱼caspase-2基因由10个外显子和9个内含子组成,cDNA长1308bp,含一个开放阅读框(ORF),编码435个氨基酸.6种脊椎动物Caspase-2氨基酸序列的保守性及系统进化分析结果表明,在特定功能区结构域中氨基酸序列表现出较高的同源性,Caspase-2在进化上高度保守.利用RT-PCR技术,斑马鱼caspase-2基因cDNA被克隆并确认.研究结果表明斑马鱼caspase-2基因是一个研究细胞凋亡行为的模型分子,可为环境化合物的分子毒性评价及其机制研究提供一种分子标记。     

六溴环十二烷(HBCD)对斑马鱼发育早期能量代谢及软骨、肌肉和鱼鳍发育的影响

六溴环十二烷(hexabromocyclododecane, HBCDs)是一种添加型阻燃剂，在环境中广泛存在。由于具有持久性、生物蓄积性和毒性等特征，HBCD很可能在水生生物体内富集并对其生长发育产生影响。将斑马鱼胚胎暴露于不同浓度的HBCD(0.1、0.5和1 mg·L^-1)，通过油红O和阿尔新蓝染色观察幼鱼发育状况，并通过能量代谢及发育相关基因探讨可能的作用机制。结果表明，HBCD暴露影响了幼鱼对卵黄囊内生脂肪的吸收，并对幼鱼躯干骨骼肌、头部软骨和鱼鳍的发育产生损害。进一步研究发现，暴露组幼鱼体内ATP含量降低，ATP合成酶及电子呼吸链中还原性辅酶Ⅰ(NOX)和细胞色素C氧化酶(COX)等的活性显著降低；同时，早期发育相关基因如骨形成蛋白bmp、肌肉决定因子myod以及sox9a和wnt等基因的转录水平均受到显著抑制(P<0.05)。上述结果表明，HBCD会影响早期发育阶段的斑马鱼对卵黄囊营养物质的吸收，干扰体内能量代谢，导致能量供应不足，并通过bmp-sox9和wnt-myod等信号通路影响软骨组织、鱼鳍和骨骼肌的正常发育。     

Spontaneous Interspecific Hybridization and Patterns of Pollen Dispersal in Ex Situ Populations of a Tree Species (Sinojackia xylocarpa) that is Extinct in the Wild

Abstract:  For endangered plants interspecific hybridization occurring in ex situ collections may lead to failure of reintroduction actions. We used Sinojackia xylocarpa , a well documented Chinese endemic species that is extinct in the wild, as a model case to address this concern. We used paternity analyses to assess the spontaneous hybridization and patterns of pollen flow between S. xylocarpa and its congener species, S. rehderiana , in conserved populations in Wuhan Botanic Garden. Interspecific hybridization events were detected in seven out of eight maternal trees of S. xylocarpa , and an average of 32.7% seeds collected from maternal trees of S. xylocarpa were hybrids. The paternity of 93 out of 249 seedlings from S. xylocarpa assigned to S. rehderiana provided convincing evidence that spontaneous interspecific hybridization occurred extensively in the living garden collection we studied. Different patterns of pollen dispersal (predominantly short-distance vs. long-distance pollination) were observed between intra- and interspecific hybridization events in the garden. Pollen dispersal within the ex situ populations was not restricted by distance, as evidenced by a lack of significant correlations between the average effective pollen dispersal distance (δ) and the geographic distances (d1 and d2) between maternal and paternal trees. The interspecific pollen-dispersal distance ranged from 10 to 620.1 m (mean 294.4 m). Such extensive hybridization in ex situ collections could jeopardize the genetic integrity of endangered species and irrevocably contaminate the gene pool if such hybrids are used for reintroduction and restoration. We recommend strongly that measures be taken to minimize the genetic risks of this kind of hybridization, including establishing buffer zones in ex situ collections, manipulating flowering phenology, testing seed lots before use in reintroduction programs, and controlling pollination for seed purity.     

Relationships between exposure to polyhalogenated aromatic hydrocarbons and organochlorine pesticides and the risk for developing type 2 diabetes: a systematic review and a meta-analysis of exposures to 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD)

A systematic review was performed to evaluate the association between environmental exposures to polyhalogenated aromatic hydrocarbons (PHAHs) and organochlorine (OC) pesticides and the risk for type 2 diabetes (T2D). Searches of EMbase, Google Scholar, Medline, and Scopus were performed. Reports were included if they were original human studies whose design included a control group and if the sample size was larger than 10 participants per group. The articles were excluded if the type of diabetes was unknown or Type 1. Odds ratios (OR), 95% confidence intervals (CI), and modified Naranjo scores for the effects of environmental contaminants were determined for each study. Of the 35 eligible studies, six were included in the meta-analysis; these focused specifically on 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD). Meta-analysis of these studies showed no significant increased OR for the development of T2D from exposure to TCDD. However, subgroup analysis showed significant elevated OR for the development of T2D if exposure is repeated and accompanied by exposure to other persistent pesticides (OR?=?1.48; 1.10–1.90) but a decreased odds for T2D with exposure resulting from accidental exposure (OR?=?0.46; 0.39–0.52). Our results suggest that there are significant risks of developing T2D in populations with recurring exposures to TCDD in concert with other persistent chlorinated pesticides. A mean Naranjo score of 2.0 was determined for all 35 articles; this score was 2.5 when examining only TCDD studies and 2.1 when examining studies that looked only at T2D. Each of these Naranjo scores suggests a possible association between the prevalence of T2D and exposure to PHAHs or OC pesticides.     

纳米银和银离子对斑马鱼胚胎早期生长发育的影响及作用机制

为探究纳米银对水生生物的毒性作用,选取斑马鱼胚胎为受试生物,考察了纳米银对斑马鱼胚胎早期生长发育的影响,同时比较了纳米银与银离子对斑马鱼胚胎的毒性作用和机理。实验将受精后4小时(4 hpf)的斑马鱼胚胎分别暴露于不同浓度的纳米银和银离子溶液中至96 hpf,观察并记录了胚胎的死亡、孵化和畸形等指标。应用吖啶橙(AO)染色实验研究了胚胎暴露之后的细胞凋亡情况,并且应用荧光定量PCR技术分析了相关基因的表达水平。研究结果表明,随着暴露浓度的增加,纳米银和银离子均能导致斑马鱼胚胎的死亡率增加和孵化率降低,并且引起孵化延迟。纳米银和银离子的96 h半数致死浓度(96 h-LC50)分别为11.75 mg·L-1和0.054 mg·L-1。银离子毒性远大于纳米银毒性。暴露的斑马鱼胚胎均表现出体长变短和卵黄囊肿大的畸形。AO染色结果表明,纳米银和银离子处理组胚胎的躯干和卵黄囊部位存在细胞凋亡信号。基因表达分析结果显示,1.93 mg·L-1纳米银显著提高了斑马鱼胚胎caspase9的表达(P0.05),而0.006 mg·L-1的银离子就能显著上调COX-2a(P0.01)和COX-17(P0.05)基因的表达,同时0.036 mg·L-1银离子增加了斑马鱼体内p53基因的表达(P0.05)。以上研究结果说明,纳米银可能通过caspase通路诱导细胞凋亡进而影响斑马鱼胚胎的生长发育;而银离子不但影响氧化系统基因通路,还能通过p53诱导凋亡进而阻滞斑马鱼胚胎的生长发育。     

Protein expression profile in the testis of rats chronically exposed to low-dose 2, 3, 7, 8-tetrachlorodibenzo-p-dioxin

The chronic effects low-dose 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) were examined on protein expression profiles in rat testis, sperm, and serum gonadal hormones. A total of 32 male rats were randomly divided into three TCDD-exposed groups, administered either 140, 350, or 875 ng TCDD/kg/week for 29 weeks, respectively, and one control group receiving only corn oil. The proteins from rat testis were separated and analyzed by two-dimensional gel electrophoresis and mass spectrometry. TCDD induced significant decreases in sperm counts and serum gonadal hormone levels compared with controls. TCDD altered testicular protein expression levels. Several interesting volume-altered proteins that were related to the reproductive toxicities or other toxicities of TCDD were identified. Among these proteins, PERF15 was the only down-regulated protein; sperm protein SSP411, ubiquitin carboxyl-terminal hydrolase L-3, and eukaryotic translation elongation factor 1 gamma were up-regulated by TCDD. The differentially expressed proteins and other data provide further insight into the mechanisms of reproductive toxicity mediated by low-dose TCDD exposure.     

Photodegradation of TCDD in soil containing organic solvents

Studies were conducted to understand 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) behaviour in the near surface zone in relation to the operating conditions: UV-intensity, temperature and exposure modes. Comparisons have been made between Oriel lamp exposure tests and sunlight exposure tests. Under Oriel lamp exposure, the convective transport of TCDD, which depends on operating temperature, was the limiting factor in the cleanup process. The product differences between Oriel exposure tests and sunlight exposure tests probably result from the difference of UV-intensities.     

AzaC预处理增加TCDD对特殊细胞P450基因的诱导

利用RT-PCR检测不同物质诱导细胞的CYP基因 mRNA的表达水平.在HepG2细胞,TCDD能诱导CYP1A1、CYP1B1及CYP1A2基因表达,CYP1A1、CYP1B1基因比CYP1A2基因更容易被诱导,用AzaC处理后CYP1B1基因表达无改变;在A549细胞和SPC-A1细胞,Azac预处理后增加了TCDD对CYP1家族的诱导.也就是AzaC增加了CYP1A1、CYP1A2和CYP1B1基因表达水平.图1表1参10