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Cyclosporine A and palmitic acid treatment synergistically induce cytotoxicity in HepG2 cells.

Abstract

Immunosuppressant cyclosporine A (CsA) treatment can cause severe side effects. Patients taking immunosuppressant after organ transplantation often display hyperlipidemia and obesity. Elevated levels of free fatty acids have been linked to the etiology of metabolic syndromes, nonalcoholic fatty liver and steatohepatitis. The contribution of free fatty acids to CsA-induced toxicity is not known. In this study we explored the effect of palmitic acid on CsA-induced toxicity in HepG2 cells. CsA by itself at therapeutic exposure levels did not induce detectible cytotoxicity in HepG2 cells. Co-treatment of palmitic acid and CsA resulted in a dose dependent increase in cytotoxicity, suggesting that fatty acid could sensitize cells to CsA-induced cytotoxicity at the therapeutic doses of CsA. A synergized induction of caspase-3/7 activity was also observed, indicating that apoptosis may contribute to the cytotoxicity. We demonstrated that CsA reduced cellular oxygen consumption which was further exacerbated by palmitic acid, implicating that impaired mitochondrial respiration might be an underlying mechanism for the enhanced toxicity. Inhibition of c-Jun N-terminal kinase (JNK) attenuated palmitic acid and CsA induced toxicity, suggesting that JNK activation plays an important role in mediating the enhanced palmitic acid/CsA-induced toxicity. Our data suggest that elevated FFA levels, especially saturated FFA such as palmitic acid, may be predisposing factors for CsA toxicity, and patients with underlying diseases that would elevate free fatty acids may be susceptible to CsA-induced toxicity. Furthermore, hyperlipidemia/obesity resulting from immunosuppressive therapy may aggravate CsA-induced toxicity and worsen the outcome in transplant patients.

Links

  • Publisher Full Text
  • Authors

    Luo Y, Rana P, Will Y

    Institution

    Compound Safety Prediction Group, Pfizer Global Research & Development, Groton, CT 06340, USA. yi.luo@pfizer.com

    Source

    Toxicology and applied pharmacology 261:2 2012 Jun 1 pg 172-80

    MeSH

    Cell Survival
    Cyclosporine
    Dose-Response Relationship, Drug
    Drug Synergism
    Hep G2 Cells
    Humans
    Immunosuppressive Agents
    JNK Mitogen-Activated Protein Kinases
    Mitochondria
    Oxidative Stress
    Palmitic Acid

    Pub Type(s)

    Journal Article

    Language

    eng

    PubMed ID

    22521608