• Title of article

    Nonylphenol induces apoptosis via mitochondria- and Fas-l-mediated pathways in the liver of adult male rat

  • Author/Authors

    Jubendradass، نويسنده , , R. and D’Cruz، نويسنده , , Shereen Cynthia and Judith Amala Rani، نويسنده , , S. and Mathur، نويسنده , , P.P.، نويسنده ,

  • Issue Information
    روزنامه با شماره پیاپی سال 2012
  • Pages
    7
  • From page
    405
  • To page
    411
  • Abstract
    Nonylphenol (NP) is an environmental contaminant known to possess estrogenic properties. Humans are constantly exposed to NP by contaminated water and food products. In the present study we sought to investigate whether treatment with low doses of NP induces apoptosis in the liver of adult rats. Rats were administered with NP by oral gavage at the doses of 15,150 and 1500 μg/kg body weight per day for 45 days. Plasma aspartate aminotransferase (AST) and alanine aminotransferase (ALT) were assayed. Apoptosis-related proteins namely cytochrome c, caspase-3, caspase-8, caspase-9, Fas and Fas-l, and expression of bcl-2 mRNA and bax mRNA were examined in the liver. Levels of AST and ALT were increased in the treated rats. Western blot analysis revealed elevation in the levels of cytochrome c, caspase-3, caspase-8, caspase-9, Fas and Fas-l in the liver of NP-treated rats. Decreased expression of bcl-2 mRNA (anti-apoptotic) and increased expression of bax mRNA (apoptotic) were observed in the liver of treated rats. Increased localization of caspase-3 in the hepatocytes and DNA damage were observed in the liver of treated rat. It is concluded that NP induces apoptosis in liver involving both mitochondria-dependent and Fas–Fas-l pathways and thereby, leading to hepatic damage in rats.
  • Keywords
    caspase-3 , DNA fragmentation , Fas , Fas-L , Caspase-9 , oxidative stress , Liver , Hepatic damage , Nonylphenol , apoptosis
  • Journal title
    Regulatory Toxicology and Pharmacology
  • Serial Year
    2012
  • Journal title
    Regulatory Toxicology and Pharmacology
  • Record number

    1489596