THE EFFECT OF LAUREL LEAF EXTRACT AGAINST TOXICITY INDUCED BY 2,3,7,8-TETRACHLORODIBENZO-P-DIOXIN IN CULTURED RAT HEPATOCYTES

被引:9
作者
Turkez, Hasan [2 ]
Geyikoglu, Fatime [1 ]
机构
[1] Ataturk Univ, Dept Biol, Fac Sci, TR-25240 Erzurum, Turkey
[2] Erzurum Tech Univ, Fac Sci, Dept Mol Biol & Genet, Erzurum, Turkey
来源
ARHIV ZA HIGIJENU RADA I TOKSIKOLOGIJU-ARCHIVES OF INDUSTRIAL HYGIENE AND TOXICOLOGY | 2011年 / 62卷 / 04期
关键词
antioxidant capacity; cell viability; genotoxicity; hepatoprotectivity; NOBILIS L. LEAVES; OXIDATIVE STRESS; ANTIOXIDANT ACTIVITIES; PHENOLIC-COMPOUNDS; HEPATITIS-C; IN-VITRO; LIVER; TCDD; VULGARE; ASSAY;
D O I
10.2478/10004-1254-62-2011-2118
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) is a very toxic environmental pollutant that raises great public concern about its impact on human health. Recent studies indicate that laurel leaf extract exhibits antioxidant properties that can counter the toxic effects of certain compounds in the liver. The aim of this study was to assess how effective LE is against the toxicity of TCDD in a primary culture of rat hepatocytes. The extract (50 mg L-1, 100 mg L-1, and 200 mg L-1) was added to cultures alone or with TCDD (1.61 mg L-1 and 3.22 mg L-1) for 48 hours. Cell viability was measured using the [3-(4,5-dimethyl-thiazol-2-yl) 2,5-diphenyltetrazolium bromide] (MTT) assay and the lactate dehydrogenase (LDH) cytotoxicity assay, while oxidative damage was assessed by measuring total antioxidant capacity (TAC) and total oxidative stress (TOS). DNA damage was also analysed using the micronucleus (MN) assay of the cultured hepatocytes. TCDD alone lowered, and laurel extract had no effect on cell viability. TCDD also increased TOS and significantly decreased TAG. It significantly increased the frequency of micronucleated hepatocytes in a dose-dependent manner. In cultures exposed to LE alone, TOS did not change and TAG significantly increased in a dose-dependent manner. Added to TCDD, laurel countered its toxic effects and showed protective effects against TCDD-mediated DNA damage. This points to the therapeutic potential of laurel against TCDD toxicity in the liver.
引用
收藏
页码:309 / 315
页数:7
相关论文
共 44 条
  • [11] Modulation of cell proliferation and polyamine metabolism in rat liver cell cultures by the iron chelator O-trensox
    Gaboriau, Francois
    Laupen-Chassay, Cindy
    Pasdeloup, Nicole
    Pierre, Jean-Louis
    Brissot, Pierre
    Lescoat, Gerard
    [J]. BIOMETALS, 2006, 19 (06) : 623 - 632
  • [12] Ganguly C, 2010, ASIAN PAC J CANCER P, V11, P25
  • [13] Animal models of human response to dioxins
    Grassman, JA
    Masten, SA
    Walker, NJ
    Lucier, GW
    [J]. ENVIRONMENTAL HEALTH PERSPECTIVES, 1998, 106 : 761 - 775
  • [14] HALLIWELL B, 1990, METHOD ENZYMOL, V186, P1
  • [15] The relative abilities of TCDD and its congeners to induce oxidative stress in the hepatic and brain tissues of rats after subchronic exposure
    Hassoun, EA
    Li, F
    Abushaban, A
    Stohs, SJ
    [J]. TOXICOLOGY, 2000, 145 (2-3) : 103 - 113
  • [16] Hibasami H, 2003, INT J MOL MED, V12, P147
  • [17] HUFF J, 1994, ANNU REV PHARMACOL, V34, P343
  • [18] Protective effects of tea melanin against 2,3,7,8-tetrachlorodibenzo-p-dioxin-induced toxicity:: Antioxidant activity and aryl hydrocarbon receptor suppressive effect
    Hung, Yao-Ching
    Huang, Guewha Steven
    Sava, Vasyl Mykhailovych
    Blagodarsky, Vyacheslav Andreevych
    Hong, Meng-Yen
    [J]. BIOLOGICAL & PHARMACEUTICAL BULLETIN, 2006, 29 (11) : 2284 - 2291
  • [19] Oxidative stress in chronic hepatitis C: not just a feature of late stage disease
    Jain, SK
    Pemberton, PW
    Smith, A
    McMahon, RFT
    Burrows, PC
    Aboutwerat, A
    Warnes, TW
    [J]. JOURNAL OF HEPATOLOGY, 2002, 36 (06) : 805 - 811
  • [20] Enhanced TGF-β1 is involved in 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) induced oxidative stress in C57BL/6 mouse testis
    Jin, Mei Hua
    Hong, Chang Hee
    Lee, Hye Young
    Kang, Hyo Jin
    Han, Sang Won
    [J]. TOXICOLOGY LETTERS, 2008, 178 (03) : 202 - 209