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十溴二苯乙烷对部分血糖内分泌干扰的计算机辅助理论研究

Computer-aided Theoretical Study of Endocrine Disrupting of Some Blood Glucose by DBDPE
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摘要 随着十溴二苯乙烷(decabromodiphenyl ethane,DBDPE)的大量应用,它已经广泛存在于各种环境介质中,具有潜在的生物毒性。为了探究DBDPE影响血糖代谢水平的具体作用机制,应用DS3.5软件将其与部分血糖内分泌蛋白受体进行分子对接,并利用DBDPE类似物来构建三维定量构效关系(3D-QSAR)模型,预测出DBDPE的半最大效应浓度的负对数值(-logEC 50)为5.86。结果表明,DBDPE是通过与部分血糖内分泌受体(雌激素受体、甲状腺激素受体和孕激素受体)结合而影响血糖代谢水平的。另外,根据构建模型,可以预测类似DBDPE的未知内分泌干扰物的活性数据。这些为认识DBDPE在机体内的作用机制、全面评价它的生态风险提供了理论依据。 With decabromodiphenyl ethane(DBDPE)being widely used in the world,it has been detected in various environmental media and has potential biological toxicity.In order to explore the specific mechanism of DBDPE affecting the metabolism of blood glucose,the molecular dockings between DBDPE and glucose endocrine protein receptor were carried out by DS3.5 software and the three-dimensional quantitative structure-activity relationship(3D-QSAR)model was constructed on the basis of DBDPE analogs.The forecasting negative logarithm of the concentration for 50%of maximum effect(-logEC 50)of DBDPE is 5.86.The results showed that DBDPE affected blood glucose by binding to certain endocrine receptors(estrogen receptor,thyroid hormone receptor and progesterone receptor).In addition,based on the model,we are able to predict the activity of DBDPE analogs which are potential unknown endocrine disruptors.Taken together,our results provide the theoretical basis for understanding the mechanism of DBDPE in vivo and evaluating its ecological risk comprehensively.
作者 张天庆 杨秀榕 曾凡刚 张严 Zhang Tianqing;Yang Xiurong;Zeng Fangang;Zhang Yan(College of Life and Environmental Science,Minzu University of China,Beijing 100081,China;School of Environment and Natural Resources,Renmin University of China,Beijing 100872,China)
出处 《生态毒理学报》 CAS CSCD 北大核心 2019年第4期92-103,共12页 Asian Journal of Ecotoxicology
基金 北京市大学生科学研究与创业行动计划(2017110018)
关键词 十溴二苯乙烷(DBDPE) 分子对接 3D-QSAR模型 干扰血糖内分泌 DBDPE molecular docking 3D-QSAR model interference glucose endocrine
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  • 1汝绍刚.国内十溴二苯乙烷的研究进展[J].山东化工,2006,35(3):16-18. 被引量:12
  • 2Allen J R, Barsotti D A, Lambrecht L K, et al. Reproductive effects of halogenated aromatic hydrocarbons on nonhuman primates [ J ]. Ann N Y Acad S, 1979,320 : 419 - 425. 被引量:1
  • 3Arisawa K, Tureda H, Mikasa H. Background exposure to PCDDs/PCDFs/PCDBs and its potential health effects: a review of epidemiolosic studies [ J ]. J Med Inves, 2005, 52(1 -2) :10-21. 被引量:1
  • 4Barnes D G, Daston G P, Evans J S, et al. Benchmark Dose Workshop: criteria for use of a benchmark dose to estimate a reference dose [ J]. Regul Toxicol Pharmacol, 1995,21 (2) : 296 - 306. 被引量:1
  • 5Barsotti D A, Abrahamson L J, Allen J R. Hormonal alterations in female rhesus monkeys fed a diet containing 2,3,7,8 - tetrachlorodibenzo - P - dioxin [ J ] . Bull Environ Contam Toxicol, 1979. 21 (4 - 5 ) :463 - 469. 被引量:1
  • 6Bertazzi P A, Bemucci I, Brambilla G, et al. The Seveso studies on early and long - term effects of dioxin exposure : a review [ J ]. Environ Health Perspect, 1998, 106(Suppl 2) :625 -633. 被引量:1
  • 7Bertazzi P A, Consonni D, Bachetti S, et al. Health effects of dioxin exposure : a 20 year mortality study [ J ].Am J Epidemiol,2001,153(11) :1031 - 1044. 被引量:1
  • 8Subhash C. Basak, Denise Mills, Brian D. Gute. Predicting pharmacological and toxicological activity of heteroeyclic compounds using QSAR and molecular modeling [J]. TOP Heterocycl Chem, 2006 3:39-80. 被引量:1
  • 9Bimbaum L S, Tuomisto J. Non - carcinogenic effects of TCDD in animals[J]. Food Addit Contain,2000,17(4) : 275 - 288. 被引量:1
  • 10Blankenship A, Matsumura F. 2, 3, 7, 8 Tetrachlorodibenzo - P - dioxin - induced activation of a protein tyrosine kinase, pp60src, in routine hepatic eytosol using a cell - free system [J]. Mol Pharmacol, 1997,52(4) :667--675. 被引量:1

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