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1.
苯并(a)芘致毒的鱼的分子生态毒理学指标研究   总被引:11,自引:1,他引:10       下载免费PDF全文
通过测定典型的多环芳烃类物质苯并(a)芘(BaP)致毒后鱼体内几种重要分子生态毒理学指标的变化,来反映苯并(a)芘致毒对鱼体的影响.结果表明,肝脏ATPase活性降低,GST活性升高,DNA加合物相对标记水平(RAL)也增大,而EROD活性没有明显改变.这说明苯并(a)芘致毒对鱼体正常生命活动产生了重大影响,并具有潜在的致癌性.  相似文献   

2.
This study was designed to investigate the in vivo effects of benzo[a]pyrene (BaP) on hepatic ethoxyresorufin-O-deethylase (EROD) activity and its correlation with cytochrome P450 1A (CYP1A) protein levels in Sebastiscus marmoratus, which were exposed through a water column to BaP (10, 100, 1000 ng/L, respectively) or were treated with intraperitoneal injections of BaP (0.5, 1, 5, 10 mg/kg, respectively) every 7 d. The results showed that after 25 d of waterborne exposure to 1000 ng/L BaP, fish hepatic CYP1A levels and EROD activity were significantly induced. In contrast, EROD activity was not altered 7 d after second ip injections, whereas, CYP1A protein levels were increased. Dose-dependent increase of biliary BaP metabolites demonstrated that the catalytic activity of CYP1A was induced by treatment with BaP. The lowest observable effect concentration with regard to biliary BaP metabolites (100 ng/L) was much lower than that with reference to EROD activity (1000 ng/L). The results suggest that biliary polycyclic aromatic hydrocarbon (PAH) metabolites were shown to better reflect the contamination gradients of PAHs than EROD activity. It appeared to be necessary to measure CYP1A protein levels to complement the EROD activity in relevant toxicological assessments.  相似文献   

3.
This study was designed to investigate the in vivo effects of benzo[a]pyrene (BaP) on hepatic ethoxyresorufin-O-deethylase (EROD) activity and its correlation with cytochrome P4501A (CYP1A) protein levels in Sebastiscus marmoratus, which were exposed through a water column to BaP (10, 100, 1000 ng/L, respectively) or were treated with intraperitoneal injections of BaP (0.5, 1, 5, 10 mg/kg, respectively) every 7 d. The results showed that after 25 d of waterborne exposure to 1000 ng/L BaP, fish hepatic CYP1A levels and EROD activity were significantly induced. In contrast, EROD activity was not altered 7 d after second intraperitoneal injections, whereas, CYP1A protein levels were increased. Dose-dependent increase of biliary BaP metabolites demonstrated that the catalytic activity of CYP1A was induced by treatment with BaP. The lowest observable effect concentration with regard to biliary BaP metabolites (100 ng/L) was much lower than that with reference to EROD activity (1000 ng/L). The results suggest that biliary polycyclic aromatic hydrocarbon (PAH) metabolites were shown to better reflect the contamination gradients of PAHs than EROD activity. It appeared to be necessary to measure CYP1A protein levels to complement the EROD activity in relevant toxicological assessments.  相似文献   

4.
Several main metabolites of benzo[a]pyrene (BaP) formed by Penicillium chrysogenum, Benzo[a]pyrene-1,6-quinone (BP 1,6- quinone), trans-7,8-dihydroxy-7,8-dihydrobenzo[a]pyrene (BP 7,8-diol), 3-hydroxybenzo[a]pyrene (3-OHBP), were identified by high-performance liquid chromatography (HPLC). The three metabolites were liable to be accumulated and were hardly further metabolized because of their toxicity to microorganisms. However, their further degradation was essential for the complete degradation of BaP. To enhance their degradation, two methods, degradation by coupling Penicillium chrysogenum with KMnO4 and degradation only by Penicillium chrysogenum, were compared; Meanwhile, the parameters of degradation in the superior method were optimized. The results showed that (1) the method of coupling Penicillium chrysogenum with KMnO4 was better and was the first method to be used in the degradation of BaP and its metabolites; (2) the metabolite, BP 1,6-quinone was the most liable to be accumulated in pure cultures; (3) the effect of degradation was the best when the concentration of KMnO4 in the cultures was 0.01% (w/v), concentration of the three compounds was 5 mg/L and pH was 6.2. Based on the experimental results, a novel concept with regard to the bioremediation of BaP-contaminated environment was discussed, considering the influence on environmental toxicity of the accumulated metabolites.  相似文献   

5.
研究了脊尾白虾(Exopalaemon carinicauda)在对苯并[a]芘(benzo[a]pyrene,BaP)的富集(15 d)、释放(15 d)过程中肝脏的生物标志物(EROD、GST、SOD、CAT、GPx、MDA)的响应,结果显示:在富集阶段,第1 d低浓度实验组(0.05 g/L)和高浓度实验组(0.45 g/L)六种生物标志物即均显著受到诱导(P0.05),诱导程度与暴露浓度成正相关,而后不同种类生物标志物呈现差异性的变化趋势,EROD继续上升并在第10 d后达到稳定状态,GST继续上升并在第10 d后受到抑制下降,SOD、CAT、GPx均受到抑制逐渐下降,且均在15 d时低于对照组水平,MDA呈现持续上升的趋势,直接反映了肝脏的氧化损伤程度。在释放阶段,低浓度实验组各生物标志物的恢复速度较高浓度实验组要快,且均能恢复到接近对照组水平(P0.05),高浓度实验组各生物标志物则均未能恢复到对照组水平(P0.05)。实验结果表明,脊尾白虾肝脏具有一定恢复能力,各生物标志物对BaP暴露的敏感性具有一定差异,BaP暴露的浓度及时间是影响各生物标志物响应变化的主要因素。  相似文献   

6.
苯并[α]芘〔benzo[α]pyrene,BaP〕是环境中广泛存在的一种致癌多环芳烃,带来的健康风险受到普遍关注. 基于生理的药代动力学(physiologically based pharmacokinetic, PBPK)模型是一种预测污染物在生物体内部剂量的数学模型,近年来在健康风险评估中应用广泛. 本文介绍了BaP对生物体的健康危害,概述了BaP的PBPK模型研究进展,指出了BaP人体PBPK模型存在BaP及代谢物的代谢机理尚未完全明确、代谢参数可靠性不高、模型还需继续完善等问题,并探讨了PBPK模型在BaP健康风险评估中的应用. 一方面,PBPK模型在阐明内暴露监测结果及补充完善污染物在人体内的代谢机理方面具有明显优势,基于PBPK模型分析完善了BaP生物标志物3-羟基苯并[α]芘在肾小管重吸收的肾脏排泄机制;另一方面,PBPK模型作为外推工具,通过种间外推可以量化污染物的种间药代动力学差异,减小动物健康剂量水平外推至人体基准值的不确定性;通过体外到体内的外推可以关联内外暴露剂量,利用反剂量学推导人体健康基准值. 这两种外推方法的应用均可以提高人体健康基准值推导的科学性、准确性. 并以BaP为例剖析了PBPK模型不确定性来源,提出了提高模型精确性的方法. 最后,为了进一步推动完善BaP的人体健康风险评估方法体系,本文探讨总结了3个重点研究方向:一是探索PBPK模型应用于BaP健康风险评估的方法体系;二是探索可靠性更高的BaP健康风险评估概率模型;三是开展BaP的生物标志物用于人体健康风险评估可行性研究.   相似文献   

7.
细胞色素P450酶(CYP450)和谷胱甘肽转移酶(GST)是动物体内主要的解毒酶,在外源毒物的转化和代谢过程中具有重要作用.本文在实验条件下, 将健康性成熟黑斑蛙(Rana nigromaculata)暴露于浓度分别为0.005、0.01、0.05、0.1、0.5和1.0 mg·L-1的Cd溶液中30 d, 采用荧光分光光度法和紫外分光光度法测定精巢组织乙氧基异酚恶唑脱乙基酶(EROD)、红霉素N-脱甲基酶 (ERND)、氨基比林-N-脱甲基醇酶(APND)和谷胱甘肽转移酶(GST)活性,探讨Cd在精巢的可能代谢过程和毒性机理.结果表明, 与对照组比较, EROD和GST酶活性在0.5和1.0 mg·L-1 Cd处理组被显著抑制; ERND酶活性在0.01~1.0 mg·L-1 Cd处理组均被显著抑制;而APND酶活性在各处理组响应变化不明显.结果显示, 精巢EROD、ERND和GST对Cd胁迫的敏感性高于APND, 黑斑蛙精巢中EROD、ERND和GST酶活性的响应可用来评价环境中低水平Cd的污染效应.  相似文献   

8.
苯并[a]芘对鲫鱼生物标志物的影响研究   总被引:18,自引:2,他引:16  
研究了苯并[a]芘暴露对鲫鱼(Carassius auratus)的几种生物标志物的影响.在鲫鱼接受3个不同质量分数苯并[a]芘(BaP)的腹腔注射14 d后,分析了其肝脏7-乙氧基-3-异吩噁唑酮-脱乙基酶(EROD)活性,以及超氧化物歧化酶(SOD)、过氧化氢酶(CAT)、谷胱甘肽过氧化物酶(GPx)等抗氧化酶活性和红细胞核异常(NA)率变化.结果显示:w(BaP)为1 mg/kg处理组的EROD活性显著升高(P<0.001).w(BaP)为0.1和1 mg/kg处理组SOD活性显著低于对照组(P<0.001),在暴露结束时,w(BaP)为1 mg/h处理组CAT活性显著低于对照组(P<0.01),而w(BaP)为0.1和1 mg/kg处理组GPx活性被显著抑制(P<0.001).表明BaP对EROD活性有诱导作用,而对SOD,CAT和GPx等抗氧化酶活性的抑制作用明显.所有处理组NA率与对照组均无显著差异.因此,鲫鱼EROD,SOD,CAT和GPx等酶活性的改变适于作为生物标志物,可以用来显示暴露于多环芳烃有机污染物鱼类的生活状态.   相似文献   

9.
It has been reported that there is an interaction between Benzo[a]pyrene (BaP), a widespread carcinogenic polycyclic aromatic hydrocarbon, and tributyltin (TBT), an organometal used as an antifouling biocide. This study was therefore designed to examine the potential in vivo influence of BaP, TBT and their mixture on splenic antioxidant defense systems of Sebastiscus marmoratus. The fish were exposed to water containing environmentally relevant concentrations of BaP, TBT and their mixture. Spleens were collected for biochemical analysis after exposure for 7, 25, 50 d and after recovery for 7, 20 d. Cotreatment with BaP and TBT for 7 d potentiated the induction of glutathione peroxidase (GPx) activity by BaP or TBT alone. The cotreatment for 25 and 50 d resulted in inhibition of GPx activity, which was similar to the effect of TBT. Splenic glutathione S-transferase (GST) activities were significantly elevated in S. marmoratus exposed to BaP starting from 7 d and remained high up to 25 d. However, no further activity change was found with prolonged exposure. Cotreatment of BaP and TBT primarily inhibited the GST activity, which was similar to the effect of TBT. Cotreatment with BaP and TBT for 25 or 50 d potentiated the depletion of GSH (glutathione) by BaP or TBT alone. MDA (malondialdehyde) contents in spleen of S. marmoratus were not significantly altered compared with the control during the test period. Spleen, as an immune organ, is sensitive to exposure of BaP or TBT. It should have an effective mechanism to counteract oxidative damage. Antioxidative defense systems in spleen of S. marmoratus should be considered as potential biomarkers. Short-term exposure of BaP or TBT could result in induction of antioxidant defense system. A significant decrease of these indices, such as GSH, GST, GPx might indicate more severe contamination.  相似文献   

10.
在前期建立的苯并[a]芘(benzo[a]pyrene,BaP)诱导上调表达的蚯蚓cDNA文库中,发现一种过氧化物还原蛋白peroxiredoxin6(PRDX6)基因片段,并提交到GenBank.Blastx比对与基因进化分析结果表明,该序列与已知PRDX6的最高相似率为86%,期望值为4E-30.序列分析表明,该序列具有PRDX6基因含Cys编码的一个特征motif,表明该序列属于PRDX6基因.为进一步验证蚯蚓PRDX6基因对多环芳烃污染的响应情况,使用OECD推荐方法,进行了土壤菲、芘、荧蒽和苯并芘污染对蚯蚓的毒性响应的试验(周期28 d),并采用定量PCR方法,检测了各实验组蚯蚓PRDX6基因的表达差异.结果发现,1.0 mg·kg-1的芘和苯并[a]芘均可显著上调蚯蚓PRDX6基因的表达,表明PRDX6基因可作为土壤污染引起蚯蚓抗氧化应激检测的分子标记.  相似文献   

11.
IntroductionBeingatypicalpolycyclicaromatichydrocarbons(PAHs) ,benzo[a]pyrene(BaP)deservesseriousstudybecausePAHsarenowrecognizedasmajorenvironmentalpollutants .ExposuretoPaHsisvirtuallyunavoidableandisstronglysuspendedofbeingacausativefactorincertaintumo…  相似文献   

12.
多溴联苯醚(PBDEs)是广泛存在于环境中的一种新型持久性有机污染物.四溴联苯醚同分异构体中的BDE-47是多溴联苯醚中最重要的单体之一.试验采用人工土壤培养法,通过亚急性试验,研究了在不同暴露时间阶段下,不同BDE-47剂量对赤子爱胜蚓(Eisenia fetida)抗氧化酶(过氧化氢酶CAT)、代谢酶(谷胱甘肽转移酶GST)以及二者基因表达的影响.结果表明,在暴露14 d和28 d时,CAT活性被诱导上升并且差异显著;GST活性变化差异不显著;CAT基因表达水平在第14 d时呈现抑制效应,在后续的第28 d和第42 d基因表达水平上调;GST基因表达水平整体呈现诱导效应,并且差异显著,随着暴露时间的增加,低毒处理组(10、50 mg·kg-1)的基因表达水平逐渐下调至低于对照组的水平,高毒处理组(100、200 mg·kg-1)的基因表达量仍高于对照组水平;在BDE-47的暴露试验中,CAT与GST活性及其基因表达水平两项指标对低毒处理组较高毒处理组更为敏感.  相似文献   

13.
本研究于2018年10月4日至2019年1月30日在洛阳市高新和林校2个采样点位同步连续采集秋冬季PM2.5样品,使用气相色谱-质谱联用仪(GC-MS)对PM2.5中优先控制的16种多环芳烃(polycyclic aromatic hydrocarbons,PAHs)进行了分析测定.对优良天和污染天PM2.5中16种PAHs的质量浓度和组成分布特征进行了研究,利用特征比值法和主成分分析法对其主要来源进行了定性解析,并使用苯并[a]芘(BaP)毒性当量法和增量终生致癌风险模型评估了对人体的健康风险.结果表明在采样期内,高新和林校两个采样点的PM2.5中16种PAHs质量浓度变化范围分别为24.33~90.26 ng·m-3和23.81~76.99 ng·m-3.随着PM2.5污染程度的加重,PAHs浓度明显升高(污染天为优良天的1.3倍),不同环数PAHs贡献顺序均为:4环(43%~48%) > 5~6环(32%~35%) > 2~3环(20%~22%).大气中PAHs主要来自于燃烧源,包括燃煤、生物质燃烧以及机动车排放等,其中燃煤对PAHs污染贡献最大(优良天:49.28%~56.38%,污染天:49.44%~60.60%).BaP毒性当量浓度表明,污染天存在更高的人体健康风险;增量终生致癌风险结果表明,污染天致癌风险高于优良天,成人呼吸暴露风险高于儿童,在研究区域内不同污染水平下健康风险属于可接受水平(<1×10-6).  相似文献   

14.
苯并[a]芘(BaP)是一类兼具强致癌性和非致癌毒性的物质,可随PM_(2.5)经呼吸途径进入人体而威胁健康.本文采集2016年北京城区监测点PM_(2.5)样品并采用气相色谱质谱联用仪测定其载带BaP浓度.通过BaP的流行病学及动物毒理学数据的检索和分析,确定BaP呼吸暴露的致癌和非致癌毒效应评价终点及其剂量效应关系.运用伤残调整生命年(DALYs)指标估算了呼吸途径人群PM_(2.5)载带BaP暴露导致的疾病负担.结果显示北京市BaP导致总疾病负担为431.36 DALYs·a~(-1),每千人DALYs为0.03 a~(-1).其中非致癌效应的疾病负担为1.98 DALYs·a~(-1),致癌效应为429.39 DALYs·a~(-1).不同毒效应的疾病负担排序为:癌症(99.54%)发育毒性(0.41%)生殖毒性(0.04%).不同季节的疾病负担贡献差异较大.北京市BaP暴露导致疾病负担的主要贡献季节为冬季,疾病负担贡献的顺序为冬季(88.01%)秋季(4.91%)春季(4.34%)夏季(2.74%).  相似文献   

15.
This study analyzed the function of different glutathione S-transferase(GST) isoforms and detoxification metabolism responses in Manila clam, Ruditapes philippinarum, exposed to 4 kinds of polycyclic aromatic hydrocarbons(PAHs) single, and their mixtures for 15 days under laboratory conditions. 13 kinds of GSTs in R. philippinarum were classified, and the results of tissue distribution indicated that 12 kinds of GSTs(except GST sigma 3) expressed most in digestive glands. We detected the m RNA e...  相似文献   

16.
三氯异氰尿酸与盐酸环丙沙星对蛋白核小球藻的毒性效应   总被引:4,自引:0,他引:4  
测试了典型渔药三氯异氰尿酸(Trichloroisocyanuric acid,TCCA)、盐酸环丙沙星(Ciprofloxacin hydrochloride,CPFX)对蛋白核小球藻(Chlorella pyrenoidosa)的急性毒性及其Ⅰ相、Ⅱ相代谢酶活性的影响.结果表明,TCCA和CPFX作用小球藻96h后EC50分别为0.31 mg·L-1和20.61mg·L-1.TCCA在低浓度下对小球藻Ⅰ、Ⅱ相代谢酶GSH、GST、CAT和EROD都存在诱导作用,当TCCA浓度大于0.13 mg·L-1时,对GSH、GST和EROD的诱导减弱.GSH、GST、EROD三种酶对CPFX作用的响应较弱,当CPFX大于70.20mg·L-1时,GST受到显著抑制,而EROD则明显升高,与对照组差异显著,GSH没有明显变化.CAT对CPFX作用的响应较敏感,表现为典型适应性诱导现象"钟形曲线",适合作为CPFX暴露的生物标记物.  相似文献   

17.
麦穗鱼物种敏感性评价   总被引:13,自引:4,他引:9  
分别进行了Cd、Cu对麦穗鱼和Cu对大型溞的急性毒性试验,结合麦穗鱼、大型溞的室内毒性试验数据和文献毒性数据,使用物种敏感性分布法对麦穗鱼的6种典型污染物的敏感性进行了对比分析.结果表明:①麦穗鱼对各类污染物的敏感性较高,尤其对有机污染物反应灵敏,其中对农药类相对最为敏感,表明麦穗鱼可以作为潜在的有机污染监测的指示生物和水质基准的代表性受试生物.②在鱼类敏感性排序中,鲤科鱼类对各类污染物的敏感性较强,而我国的鱼类以鲤科为主,因此在水质基准制定和环境监测中应充分考虑鲤科鱼类的作用及其毒性数据;③麦穗鱼在鱼类敏感性排序中位置稳定,并且具有体型小、易获得等特性,表明麦穗鱼是环境监测中较为理想的指示生物,同时也是潜在的水质基准受试生物.  相似文献   

18.
应用基于生理的药代动力学(PBPK)模型预测苯并(α)芘(BaP)暴露的人体内部剂量,基于贝叶斯的马尔科夫链蒙特卡洛模拟(MCMC)方法对模型参数进行校准和优化,最后运用已优化的模型对BaP内暴露基准值进行推导.研究发现,基于贝叶斯的MCMC方法对模型后验参数校准后,模型精度明显提高,两个数据集验证结果显示残差平方和分别降低了72%和94%.PBPK模型以BaP和子代谢物3-羟基苯并(α)芘(3-OHBaP)的体内动力学过程为结构基础,模拟BaP体内浓度分布大小为脂肪>肾脏>皮肤>缓慢灌注组织>快速灌注组织>静脉血>肝脏;3-OHBaP体内浓度分布大小为肾脏>快速灌注组织>脂肪>肺>静脉血>缓慢灌注组织>肝脏>皮肤.敏感性分析显示,快速灌注组织-血分配系数对模型输出影响最大,灵敏度系数超过了200%;排泄系数影响最小,只有肾小球过滤率KBR的灵敏度系数超过了1%.以美国国家环境保护局推荐的参考浓度2.0×10-6mg/m3为外暴露安全基准值,基于PBPK模型推导了职业暴露的BaP生物监测当量(BE),结果显示BE值为0.405pmol/mol肌酐(尿液3-OHBaP平均浓度),为基于人体内暴露剂量水平进行定量健康风险评估奠定了基础.  相似文献   

19.
Tributyltin(TBT), an organometal used as an antifouling biocide, has been reported to induce masculinization of fish. Benzo [a]pyrene (BaP), a widespread carcinogenic polycyclic aromatic hydrocarbon, has been reported that its microsomal metabolites can produce an estrogenic response when tested in vitro. This study was therefore designed to examine the potential in vivo influence of TBT, BaP and their mixture on sex hormone levels in serum of Sebastiscus marmoratus, which were given 2 separate intraperitoneally (ip) injections(a single injection every 7 d) of TBT(0.5, 1, 5 and 10 mg/kg), BaP(0.5, 1, 5 and 10 mg/kg), or both in combination(0.5, 1, 5 and 10 mg/kg); control fish received olive oil vehicle only. Six days after the 2nd injection, serum samples were collected and analyzed for sex hormone levels and alkali labile protein phosphorus (ALPP), which is related to the yolk precursor protein vitellogenin. The pollutants at all doses significantly reduced serum testosterone, estradiol and ALPP content after 2 injections compared with the corresponding controls. The reduction of the estradiol levels should be response for the decrease of the vitellogenin levels. The results in the present study suggested that aromatase seems not the major target acted by TBT and BaP in fish. This study demonstrated that TBT or BaP exposure both inhibit the reproductive potential in female Sebastiscus marmoratus. Combined effect of TBT and BaP on the serum testosterone, estradiol and ALPP was not antagonism from the anticipation.  相似文献   

20.
选择0#柴油和平湖原油乳化液对缢蛏(Sinonovacula constricta)进行氧化胁迫实验,选取典型的抗氧化酶-超氧化物歧化酶(SOD)、过氧化氢酶(CAT)、谷光甘肽硫转移酶(GST)及过氧化物酶(POD)用于衡量油类污染物对生物体造成的氧化压力大小.此外,结合综合生物标志物响应(Integrated Biomarker Responses,IBR)指标,对2种石油污染物对缢蛏的毒性响应进行定量化评价.结果表明,不同浓度的0#柴油和平湖原油对缢蛏消化腺中的4种酶表现出不同程度的诱导效应,各试验组在暴露前期均表现出诱导或抑制,但对4种酶的影响存在时间顺序性,SOD、CAT和GST的酶活性表现为升高-降低的过程,POD表现为降低-升高的过程,活性达到峰值的时间SOD和CAT要早于GST和POD.结合计算出的IBR数值来看,高浓度0#柴油能够引起最为显著的生物效应变化,显示该石油污染物高毒性的特征,0#柴油生物毒性大于平湖原油生物毒性.  相似文献   

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