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亚慢性2,3,7,8四氯二苯并二噁英暴露对大鼠肝脏的毒性 被引量:3

Liver Toxicity of Subchronic 2,3,7,8-tetrachlorodibenzo-p-dioxin Exposure in Rats
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摘要 目的:了解亚慢性2,3,7,8四氯二苯并二噁英(TCDD)暴露对大鼠肝脏的毒性作用。方法:1月龄SD大鼠随机分为阴性对照组(予玉米油)和3个TCDD(2、10和50 ng.kg-1.d-1)实验组,每组30只,雌雄各半,连续暴露13周后测定血清丙氨酸氨基转移酶(ALT)和天门冬氨酸氨基转移酶(AST)活性,观察肝脏病理组织学变化。结果:亚慢性TCDD暴露对大鼠体质量和主要脏器相对重量无明显影响;血清AST和ALT活性在实验组升高:雌鼠AST和ALT在10和50 ng.kg-1.d-1组高于对照组和2 ng.kg-1.d-1组(P<0.05);雄鼠AST在50 ng.kg-1.d-1组高于其它3组(P<0.05),ALT在各组间差异无统计学意义;病理观察发现实验组肝组织坏死,肝血窦瘀血和肝细胞空泡样变。结论:亚慢性TCDD暴露对大鼠肝脏具有毒性作用,且雌鼠比雄鼠的肝脏对TCDD的毒性更敏感。 Objective:To study the liver toxicity of subchronic 2,3,7,8-tetrachlorodibenzo-p-dioxin(TCDD)exposure in rats.Method:One hundred and twenty one-month-old rats were allocated randomly into control group(given corn oil)and three doses of TCDD(2,10 and 50 ng·kg-1·d-1)groups,30 rats in each group,in half respectively male and female.The exposure lasted for 13 weeks.Thirteen weeks later,the serum levels of alanine transaminase(ALT)and aspartate amino transferase(AST)were tested,the hepatic histopathology observation was also performed.Results: Subchronic TCDD exposure had no obvious effects on the body weight and the relative weight of main organs in rats.In females,AST and ALT in the 10 and 50 ng·kg-1·d-1 groups were higher than control and 2 ng·kg-1·d-1 groups(P0.05).In males,the AST level in the 50 ng·kg-1·d-1 group was higher than other three groups(P0.05),no significant differences were found in ALT among groups.The pathological changes were found in TCDD treated liver,such as necrosis,gore in hepatic sinusoid and vacuolization of hepatocytes.Conclusion: Subchronic TCDD exposure has toxic effects on rat liver,the female rats are more sensitive to TCDD liver toxicity than males.
出处 《汕头大学医学院学报》 2010年第4期205-208,F0002,共5页 Journal of Shantou University Medical College
基金 广东省自然科学基金资助项目(05301076) 教育部留学回国人员科研启动基金资助项目(2005)
关键词 2 3 7 8四氯二苯并二噁英 亚慢性暴露 肝脏 丙氨酸氨基转移酶 天冬氨酸氨基转移酶 2 3 7 8-tetrachlorodibenzo-p-dioxin subchronic exposure liver alanine tansaminase aspartate amino transferase
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参考文献11

  • 1BOCK K W,KOHLE C.The mammalian aryl hydrocarbon (Ah)receptor:from mediator of dioxin toxicity toward physiological functions in skin and liver[J].Biol Chem,2009,390(12):1225-1235.
  • 2CZEPIEL J,BIESIADA G,GAJDA M,et al.The effect of TCDD dioxin on the rat liver in biochemical and histological assessment[J].Folia Biol(Krakow),2010,58(1-2):85-90.
  • 3BOVERHOF D R,BURGOON L D,TASHIRO C.Temporal and dose-dependent hepatic gene expression patterns in mice provide new insights into TCDD-Mediated hepatotoxicity[J].Toxicology Science,2005,85(2):1048-1063.
  • 4董丽,汤乃军.四氯并二口恶口英的肝脏毒性[J].中华劳动卫生职业病杂志,2005,23(1):60-62. 被引量:7
  • 5汤乃军,刘云儒,任大林.2,3,7,8-四氯二苯并二恶英对SD大鼠肝脏SOD、GST、MDA影响的实验研究[J].中国工业医学杂志,2003,16(6):335-337. 被引量:18
  • 6BELL D R,CIODE S,FAN M Q.Toxicity of 2,3,7,8-tetrachlorodibenzo-p-dioxin in the developing male wistar(Han) rat.Ⅱ:chronic dosing causes developmental delay[J].Toxicological Sciences,2007,99(1):224-233.
  • 7SEEFELD M D,ALBRECHT R M,PETERSON R E.Effects of 2,3,7,8-tetrachlorodibenzo-p-dioxin on indocyanine green blood clearance in rhesus monkeys[J].Toxicology,1979,14(3):263-272.
  • 8MOCARELLI P,MAROCCHI A,BRAMBILLA P,et al.Clinical laboratory manifestations of exposure to dioxin in children.A six-year study of the effects of an environmental disaster near Scveso,Italy[J].JAMA,1986,256(19):2687-2695.
  • 9TEN T G W,GUCHELAAR H J,KOCH J,et al.Perinatal dioxin exposure,cytochrome P-450 activity,liver functions and thyroid hormones at follow-up after 7-12 years[J].Chernosphere,2008,70(10):1865-1872.
  • 10IISEN A,BRIEF J M,KOPPE J G,et al.Signs of enhanced neuromotor maturation in children due to porinatal load with background levels of dioxins.Follow-up until age 2 years and 7 months[J].Chemosphere,1996,33(7):1317-1326.

二级参考文献40

  • 1[1]Jakoby WB,Ketterer B,Mannervik B.Glutathione transferases:nomenclature[J].Biochem-Pharmacol,1984,33(16):2539-2540.
  • 2[2]Maier A,Dalton TP,Puga A.Disruption of dioxin-inducible phase Ⅰ and phase Ⅱ gene expression patterns by cadmium,chromium,and arsenic[J].Mol-Carcinog,2000,28(4):225-235.
  • 3[3]Hassoun EA,Bagchi D,Stohs SJ.Evidence of 2,3,7,8-tetrachlorodibenzo-p-dioxin(TCDD)induced tissue damage in fetal and placental tissues and changes in amniotic fluid lipid metabolites of pregnant CF1 mice[J].Toxicol Lett,1995,76(3):245-250.
  • 4[4]Bestervelt LL,Piper DW,Pitt JA,et al.Lipid peroxidation in the adrenal glands of male rats exposed to 2,3,7,8-tetrachlorodibenzo-p-dioxin(TCDD)[J].Toxicol Lett,1994,70(2):139-145.
  • 5[5]Nohl H,de-Silva D,Summer KH.2,3,7,8-tetrachlorodibenzo-p-dioxin induces oxygen activation associated with cell respiration[J].Free Radic Biol Med,1989,6(4):369-374.
  • 6[6]Stohs SJ,Al-Bayati ZF,Hassan MQ,et al.Glutathione peroxidase and reactive oxygen species in TCDD-induced Iipid peroxidation[J].Adv Exp Med Biol,1986,197357-197365.
  • 7[7]Hermansky SJ,Mohammadpour HA,Murray WJ,et al.Effect of thyroidectomy on 2,3,7,8-tetrachlorodibenzo-p-dioxin-induced lipid peroxidation[J].Pharmacology,1987,35(6):301-307.
  • 8[8]al-Turk WA,Shara MA,Mohammadpour H,et al.Dietary iron and 2,3,7,8-tetrachlorodibenzo-p-dioxin induced alterations in hepatic lipid peroxidation,glutathione content and body weight[J].Drug Chem Toxicol,1988,11(1):55-70.
  • 9[9]Stohs SJ,Al-Bayati ZF,Hassan MQ,et al.Glutathione peroxidase and reactive oxygen species in TCDD-induced lipid peroxidation[J].Adv Exp Med Biol,1986,197:357-365.
  • 10[10]Latchoumycandane C,Chitra KC,Mathur PP.The effect of 2,3,7,8-tetrachlorodibenzo-p-dioxin on the antioxidant system in mitochondrial and microsomal fractions of rat testis[J].Toxicology,2002,171(2-3):127-135.

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  • 1TSYDENOVA O, BENGTSSON M. Chemical hazards associated with treatment of waste electrical and electronic equipment [ J ]. Waste Manag, 2011, 31( 1 ): 45-58.
  • 2国家质量监督检验检疫总局.GB/321603-2008化学品急性经口毒性实验方法[S].北京:中国标准出版社,2008.
  • 3国家质量监督检验检疫总局.GB5085.2-2007危险废物鉴别标准急性毒性初筛[S].北京:中国标准出版社,2007.
  • 4国家质量监督检验检疫总局.GB/T21763-2008化学品啮齿类动物亚慢性经口毒性实验方法[S].北京:中国标准出版社,2008.
  • 5SONG Y, WU N, TAO H, et al. Thyroid endocrine dysregulation and erythrocyte DNA damage associated with PBDE exposure in juvenile crucian carp collected from an e-waste dismantling site in Zhejiang Province, China[ J ]. Environ Toxicol Chem, 2012, 31 ( 9 ): 2047-2051.
  • 6LAI IK, CHAI Y, SIMMONS D, et al. Dietary selenium as a modulator of PCB 126-induced hepatotoxicity in male Sprague-Dawley rats [ J ]. Toxicol Sci, 2011, 124( 1 ): 202-214.
  • 7VAGULA M C, KUBELDIS N, NELATURY C F. Effects of BDE-85 on the oxidative status and nerve conduction in rodents [ J ]. Int J Toxicol, 2011, 30(4 ): 428-434.
  • 8HEREDIA L, TORRENTE M, COLOMINA M T, et al. Behavioral effects of oral subacute exposure to BDE-209 in young adult mice : a preliminary study[ J ]. Food Chem Toxicol, 2012, 50( 3/4 ): 707-712.
  • 9FISCHER C, FREDRIKSSON A, ERIKSSON P. Coexposure of neonatal mice to a flame retardant PBDE 99 ( 2, 2', 4, 4', 5-pentabromodiphenyl ether )and methyl mercury enhances developmental neurotoxic defects [ J ]. Toxicol Sci, 2008, 101 ( 2 ): 275-285.
  • 10卞建春,王林,陈大伟,刘学忠,顾建红,卓丽玲,刘宗平.铅镉联合暴露对大鼠肾脏的氧化损伤[J].中国兽医学报,2009,29(12):1617-1619. 被引量:16

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