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

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.
AuthorsJong Hee Sohn, Kyu Lee Han, Jeong Han Choo, Jae-Kwan Hwang
JournalBioFactors (Oxford, England) (Biofactors) Vol. 29 Issue 1 Pg. 1-10 ( 2007) ISSN: 0951-6433 [Print] Netherlands
PMID17611289 (Publication Type: Journal Article)
Chemical References
  • Lignans
  • Reactive Oxygen Species
  • Malondialdehyde
  • macelignan
  • tert-Butylhydroperoxide
  • L-Lactate Dehydrogenase
Topics
  • 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, 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)

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