Macelignan protects HepG2 cells against tert-butylhydroperoxide-induced oxidative damage

Biofactors. 2007;29(1):1-10. doi: 10.1002/biof.5520290101.

Abstract

In this study, we investigated the protective effect of macelignan, isolated from Myristica fragrans Houtt. (nutmeg) against tert-butylhydroperoxide (t-BHP)-induced cytotoxicity in a human hepatoma cell line, HepG2. The tetrazolium dye colorimetric test (MTT test) and lactate dehydrogenase (LDH) assay were used to monitor cell viability and necrosis, respectively. Lipid peroxidation [malondialdehyde (MDA) formation] was estimated by the fluorometric method. Intracellular reactive oxygen species (ROS) formation was measured using a fluorescent probe 2',7'-dichlorofluorescein diacetate (DCFH-DA), and DNA damage was detected using single cell gel electrophoresis (comet assay). The results showed that macelignan significantly reduced the cell growth inhibition and necrosis caused by t-BHP. Furthermore, macelignan ameliorated lipid peroxidation as demonstrated by a reduction in MDA formation in a dose-dependent manner. It was also found that macelignan reduced intracellular ROS formation and DNA damaging effect caused by t-BHP. These results strongly suggest that macelignan has significant protective ability against oxidative damage caused by reactive intermediates.

MeSH terms

  • Cell Line, Tumor
  • Cell Proliferation / drug effects
  • Cell Survival / drug effects
  • Comet Assay
  • DNA Damage / drug effects*
  • Dose-Response Relationship, Drug
  • Humans
  • L-Lactate Dehydrogenase / metabolism
  • Lignans / chemistry
  • Lignans / pharmacology*
  • Lipid Peroxidation / drug effects
  • Malondialdehyde / metabolism
  • Molecular Structure
  • Myristica
  • Oxidation-Reduction / drug effects
  • Oxidative Stress / drug effects*
  • Reactive Oxygen Species / metabolism
  • Time Factors
  • tert-Butylhydroperoxide / pharmacology*

Substances

  • Lignans
  • Reactive Oxygen Species
  • Malondialdehyde
  • macelignan
  • tert-Butylhydroperoxide
  • L-Lactate Dehydrogenase