1. Academic Validation
  2. Zingiberene attenuates hydrogen peroxide-induced toxicity in neuronal cells

Zingiberene attenuates hydrogen peroxide-induced toxicity in neuronal cells

  • Hum Exp Toxicol. 2015 Feb;34(2):135-44. doi: 10.1177/0960327114538987.
B Togar 1 H Türkez 2 A D Stefano 3 A Tatar 4 D Cetin 5
Affiliations

Affiliations

  • 1 Department of Biology, Faculty of Science, Atatürk University, Erzurum, Turkey [email protected].
  • 2 Department of Molecular Biology and Genetics, Faculty of Science, Erzurum Technical University, Erzurum, Turkey.
  • 3 Department of Pharmacology, G. D'Annunzio University, Chieti, Italy.
  • 4 Department of Medical Genetics, Faculty of Medicine, Atatürk University, Erzurum, Turkey.
  • 5 Department of Medical Pharmacology, Faculty of Medicine, Atatürk University, Erzurum, Turkey.
Abstract

In this experimental design, we explored the neuroprotective potential of zingiberene (ZGB), a monocyclic sesquiterpene, in hydrogen peroxide (H2O2)-induced toxicity in newborn rat cerebral cortex cell cultures for the first time. The rats were exposed to H2O2 for 6 h to determine the oxidative stress levels. To evaluate cell viability, both 3-(4,5-dimethylthiazole-2-yl)-2,5-diphenyltetrazolium bromide and Lactate Dehydrogenase assays were carried out. Total antioxidant capacity (TAC) and total oxidative stress (TOS) parameters were used to evaluate oxidative changes. Besides determining 8-hydroxy-2-deoxyguanosine (8-OH-dG) levels in vitro, single-cell gel electrophoresis was also performed to measure the resistance of neuronal DNA to H2O2- exposed rats. Our results showed that survival and TAC levels of the cells decreased, while TOS, 8-OH-dG levels and the mean values of the total scores of cells showing DNA damage increased in the H2O2 alone-treated cultures. But pretreatment of ZGB suppressed the cytotoxicity, genotoxicity and oxidative stress that were increased by H2O2. Based on these observations, it is suggested that the sesquiterpene ZGB can be used as a novel and natural potential therapeutic in counteracting oxidative damages in the field of neurodegenerative disorders.

Keywords

DNA damage; H2O2; Zingiberene; cultured neuron; neuroprotective action; oxidative stress.

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