Loss of 5-lipoxygenase activity protects mice against paracetamol-induced liver toxicity

Br J Pharmacol. 2016 Jan;173(1):66-76. doi: 10.1111/bph.13336. Epub 2015 Nov 16.

Abstract

Background and purpose: Paracetamol (acetaminophen) is the most widely used over-the-counter analgesic and overdosing with paracetamol is the leading cause of hospital admission for acute liver failure. 5-Lipoxygenase (5-LO) catalyses arachidonic acid to form LTs, which lead to inflammation and oxidative stress. In this study, we examined whether deletion or pharmacological inhibition of 5-LO could protect mice against paracetamol-induced hepatic toxicity.

Experimental approach: Both genetic deletion and pharmacological inhibition of 5-LO in C57BL/6J mice were used to study the role of this enzyme in paracetamol induced liver toxicity. Serum and tissue biochemistry, H&E staining, and real-time PCR were used to assess liver toxicity.

Key results: Deletion or pharmacological inhibition of 5-LO in mice markedly ameliorated paracetamol-induced hepatic injury, as shown by decreased serum alanine transaminase and aspartate aminotransferase levels and hepatic centrilobular necrosis. The hepatoprotective effect of 5-LO inhibition was associated with induction of the antitoxic phase II conjugating enzyme, sulfotransferase2a1, suppression of the pro-toxic phase I CYP3A11 and reduction of the hepatic transporter MRP3. In 5-LO(-/-) mice, levels of GSH were increased, and oxidative stress decreased. In addition, PPAR α, a nuclear receptor that confers resistance to paracetamol toxicity, was activated in 5-LO(-/-) mice.

Conclusions and implications: The activity of 5-LO may play a critical role in paracetamol-induced hepatic toxicity by regulating paracetamol metabolism and oxidative stress.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetaminophen / adverse effects*
  • Acetaminophen / metabolism
  • Alanine Transaminase / blood
  • Angiogenic Proteins / metabolism
  • Animals
  • Aspartate Aminotransferases / blood
  • Chemical and Drug Induced Liver Injury / enzymology
  • Chemical and Drug Induced Liver Injury / genetics*
  • Chemical and Drug Induced Liver Injury / pathology
  • Chemical and Drug Induced Liver Injury / prevention & control*
  • Cytochrome P-450 CYP3A / metabolism
  • Glutathione / metabolism
  • Hydrogen Peroxide / metabolism
  • Lipoxygenase / deficiency*
  • Lipoxygenase / genetics
  • Lipoxygenase / metabolism
  • Liver / metabolism
  • Male
  • Membrane Proteins / metabolism
  • Mice
  • Mice, Knockout
  • Necrosis
  • Oxidative Stress / drug effects
  • PPAR alpha / metabolism
  • Protective Agents / pharmacology
  • Sulfotransferases / metabolism
  • Thiobarbituric Acid Reactive Substances / metabolism

Substances

  • Angiogenic Proteins
  • Membrane Proteins
  • PPAR alpha
  • Protective Agents
  • Thiobarbituric Acid Reactive Substances
  • mitogen-regulated protein 3, mouse
  • Acetaminophen
  • Hydrogen Peroxide
  • Lipoxygenase
  • Cyp3a11 protein, mouse
  • Cytochrome P-450 CYP3A
  • Aspartate Aminotransferases
  • Alanine Transaminase
  • Sulfotransferases
  • Glutathione