六价铬致小鼠DNA损伤及肝肾氧化应激的实验研究

为研究六价铬(Cr(Ⅵ))摄入后对机体造成的损伤,将重铬酸钾(K2Cr2O7)以25、50、100 mg·kg-1对小鼠进行灌胃,染毒时间为1 d、3 d和5 d.检测外周血淋巴细胞DNA损伤及肝肾组织活性氧自由基(ROS)水平、脂质过氧化产物丙二醛(MDA)含量,以及超氧化物歧化酶(SOD)和过氧化氢酶(CAT)活性.实验结果表明,经Cr(Ⅵ)染毒1 d、3 d和5 d后小鼠外周血淋巴细胞DNA损伤及肝ROS水平与对照组相比均有明显升高,肝脏抗氧化酶活性也有显著改变,但MDA含量差异不显著,而肾组织中各指标均未见有明显改变.由此认为,经口摄入Cr(Ⅵ)后能导致DNA损伤并且对肝脏造成氧化应激.     

Histopathological impact of industrial wastewater on the vital organs of Oreochromis mossambicus

The acute toxicity of paper mill wastewater to Oreochromis mossambicus was investigated with the lethal concentration (LC50) value 6.5% for 96?h exposure. This concentration was used as a baseline to study the effects of paper mill effluent on histopathological changes in gills, liver, kidney, and brain of fish. In the gills, filament cell proliferation, cellular infiltration, hemorrhage, and epithelial lifting were observed. In the liver, vacuolation of hepatocytes and necrosis were noted. In kidney, exfoliation and swollen with pyknotic nuclei were identified. Similarly, the brain also showed enlarged pyramidal cells, binucleated nuclei, vacoulation, and necrosis. These changes occurred predominantly in 21days following exposure of fish to the industrial waste water. Paper mill wastewater was found to be highly toxic to fish.     

Per- and polyfluoroalkyl substances and obesity,type 2 diabetes and non-alcoholic fatty liver disease: a review of epidemiologic findings

Abstract

Per- and polyfluoroalkyl substances, a group of fluoro-surfactants widely detected in the environment, wildlife, and humans, have been linked to adverse health effects. A growing body of literature has addressed their effects on obesity, diabetes and non-alcoholic fatty liver disease/non-alcoholic steatohepatitis. This review summarizes the brief historical use and chemistry of per- and polyfluoroalkyl substances, routes of human exposure, as well as the epidemiologic evidence for associations between exposure to per- and polyfluoroalkyl substances and the development of obesity, diabetes and non-alcoholic fatty liver disease/non-alcoholic steatohepatitis. We identified 22 studies on obesity and 32 studies on diabetes, while only 1 study was found for non-alcoholic fatty liver disease/non-alcoholic steatohepatitis by searching PubMed for human studies. Approximately two-third of studies reported positive associations between per- and polyfluoroalkyl substances exposure and the prevalence of obesity and/or type 2 diabetes. Causal links between per- and polyfluoroalkyl substances and obesity, diabetes and non-alcoholic fatty liver disease/non-alcoholic steatohepatitis, however, require further large-scale prospective cohort studies combined with mechanistic laboratory studies to better assess these associations.     

挥发性甲基硅氧烷的体外代谢行为

挥发性甲基硅氧烷(volatile methyl siloxanes,VMSs)的高产量、环境广泛存在性和毒性使其成为备受关注的新型环境污染物.VMSs在生物体中的代谢速率是决定其生物富集性的关键因子,但是目前还没有此类物质代谢速率的测试和报道.利用了鲈鱼和鹌鹑肝微粒体的体外代谢体系,测定了16种常见VMSs(D3~D6和L3~L14)的固有清除率.VMSs在鲈鱼肝微粒体中的固有清除率为0~0.031 m L·(h·mg)-1.D5在鲈鱼肝微粒体中难以代谢,与其在水生食物网中呈现显著生物放大性相一致;L4~L14均难以代谢,表明链状VMSs可能具有较高的生物富集性.VMSs在鹌鹑肝微粒体中的固有清除率[0.25~1.7m L·(h·mg)-1]显著高于鲈鱼,较快的代谢速率表明D3~D6和L3~L14在鸟类中可能不存在明显的生物放大现象;应用B[a]P作为基准物质校正代谢速率的测定误差,分析VMSs代谢速率的构效关系,发现影响VMSs在鸟类肝微粒体中代谢速率的主要因素为疏水性和电性参数.     

BIOLOGICAL INDICATORS AND BIOLOGICAL EFFECTS OF ESTUARINE/COASTAL POLLUTION1

ABSTRACT: Sustained interest in and concern about the health status of the aquatic environment has resulted in extensive research focused on (1) effects of pollution on survival, growth, and reproduction of resource species at all life stages; (2) diseases of fish and shellfish, as they may be related to pollution and as they may serve as indicators of environmental stress; and (3) contaminant body burdens in fish and shellfish - their effects on the aquatic animals and their potential effects on humans. Effects, lethal and sublethal, of pollutants on life history stages of fish and shellfish have been documented, as have impacts on local stocks in badly degraded habitats, but as yet there has been no adequate quantitative demonstration of effects on entire aquatic species - probably because of the difficulty in sorting out relative effects of the many environmental factors that influence abundance. Sublethal effects, especially those that result in disease, have been examined intensively, and some diseases and disease syndromes have been associated statistically with pollution. Other pollution indicators (biochemical, physiological, genetic, behavioral, and ecological) have also received some attention, as have body burdens of contaminants in aquatic species. Research, especially that conducted during the past decade, has done much to clarify the many pathways and toxic effects of contaminants on aquatic animals, and has also helped to identify mechanisms for survival of fish and shellfish in the presence of environmental changes caused by human activities.     

镉对中华蟾蜍蝌蚪生长、变态和Dios、TRs表达以及肝脏的影响

镉(cadmium,Cd)是一种典型的工业毒素和环境污染物,对两栖类生物具有强烈的毒性作用。为了探讨镉对两栖类生物的毒害作用,选择中华蟾蜍蝌蚪作为受试生物,研究了不同浓度Cd对中华蟾蜍蝌蚪生长、变态和Dios、TRs表达以及肝脏的的影响,结果表明,500μg·L~(~(-1))Cd可以极显著降低蝌蚪的变态率、全长、尾长和体重(P0.01);Real-time PCR结果显示,在变态高峰期,500μg·L~(~(-1))Cd可以显著下调Dio2、TRα和TRβ mRNA的相对表达量(P0.05),显著上调Dio3 mRNA的相对表达量(P0.05);透射电镜试验结果显示Cd可以破坏中华蟾蜍蝌蚪肝脏细胞胞浆中的细胞器和胆管中的微绒毛。综合以上结果,可知,高浓度的Cd可以紊乱甲状腺的内分泌和导致肝脏的病变,进而影响中华蟾蜍蝌蚪的生长和变态。     

苯并\[a\]芘对马氏珠母贝肝组织抗氧化酶活性的影响

为揭示不同浓度苯并[a]芘(B[a]P)对海洋贝类的生态毒理效应,将马氏珠母贝(Pinctada martensi)暴露于不同浓度(1、4和8μg.L-1)B[a]P中,检测暴露3、7和10d后,B[a]P对马氏珠母贝肝组织抗氧化酶(超氧化物歧化酶SOD、谷胱甘肽硫转移酶GST和过氧化氢酶CAT)活性的影响。结果表明:暴露时间3d时,随着B[a]P浓度的增加,SOD活性无明显变化,GST的活性被激活,在7d和10d受到抑制,GST活性表现为抑制,并表现出一定的剂量-效应关系,而CAT的活性在染毒后第7天受到激活;暴露时间10d时,SOD活性增加,GST活性和CAT活性均受到抑制。B[a]P暴露时间相同,GST活性和CAT活性变化趋势基本相似。B[a]P浓度相同(1和4μg.L-1)时,随着暴露时间的延长,SOD活性无明显变化,GST的活性受到抑制,CAT的活性表现为先激活后抑制的趋势。另外,相对于SOD活性,GST和CAT的活性变化可以更好地反映B[a]P对马氏珠母贝胁迫的毒性效应。     

SO2衍生物对C57BL/6小鼠肝脏T细胞亚群CD4+/CD8+的影响

为探讨二氧化硫(SO2)的肝脏免疫毒理效应,利用流式细胞仪(FACS)检测技术,分析了SO2体内代谢衍生物——亚硫酸钠(Na2SO3)与亚硫酸氢钠(NaHSO3)混合液(两者摩尔比为3:1)腹腔注射染毒对C57BL/6小鼠肝脏淋巴细胞T细胞亚群CD4+和CD8+的百分数以及CD4+/CD8+细胞比值的影响.实验组剂量分别为25、100、400mg·kg-1(body weight),染毒一周后,制备肝脏淋巴细胞悬液,经特异性荧光标记的CD4(FITC)、CD8(PE)单克隆抗体染色后,采用FACS流式细胞仪检测T淋巴细胞亚群百分数.研究发现:1)染毒后所有处理组肝脏CD4+T细胞所占的百分数显著升高(p<0.05);2)CD8+T细胞所占的百分数在100mg·kg-1、400mg·kg-1染毒组显著降低(p<0.05);3)CD4+/CD8+的比值在100mg·kg-1、400mg·kg-1染毒组显著升高(p<0.01).研究结果显示:SO2体内衍生物亚硫酸钠和亚硫酸氢钠可使肝脏CD4+/CD8+T细胞的比值显著升高,即SO2衍生物可使肝脏CD4和CD8淋巴细胞比例严重失调而使机体产生免疫紊乱.     

胚胎期和哺乳早期全氟辛烷磺酸盐(PFOS)暴露对大鼠肝脏脂肪酸代谢影响的microRNA组学研究

研究低剂量全氟辛烷磺酸(perfluorooctane sulfonate,PFOS)对大鼠幼仔肝脏中microRNA的表达及脂肪酸代谢的影响,并且从microRNA分子角度探讨PFOS对肝脏相关功能影响的分子毒性机制及预测其他一些潜在的毒性效应。PFOS染毒剂量为3.2mg·kg-1,对照组给予同等体积的含2%的聚氧乙烯山梨糖醇酐单月桂酸酯乳化剂(Tween 20),利用高通量miRNA芯片技术观察了胚胎期和哺乳早期经PFOS染毒后出生第1和7天(PND1和PND7)大鼠肝脏组织miRNA的表达情况。结果显示,PFOS能够引起仔鼠肝脏microRNA表达量的变化,PND1和PND7时显著变化的microRNA个数分别为46和9个。miR-125a-3p、miR-23a*、miR-25及miR-494同时在PND1和PND7显著性表达,PND1呈现下调性变化,PND7呈现上调性变化。通过生物信息学和统计学分析发现:PFOS具有大鼠肝脏早期发育毒性,而且胚胎期的毒性效应强于哺乳早期;大鼠幼仔肝脏早期发育中,PFOS对其糖脂代谢及细胞凋亡过程具有毒性效应;胚胎期和哺乳早期,在低剂量PFOS暴露下,β和ω氧化代谢是肝脏脂肪酸代谢的主要方式;脂酰COA合成酶、脂酰COA脱氢酶及烯酰COA水合酶等脂肪酸代谢过程的关键酶,是PFOS暴露下microRNA潜在的靶分子。研究表明,PFOS具有多种肝脏早期发育毒性,低剂量PFOS暴露下,microRNA能够调节肝脏脂肪酸代谢相关靶基因的表达,进而调控脂肪酸代谢过程。