Potential anticancer activity of carvone in N2a neuroblastoma cell line


Aydin E., TÜRKEZ H., KELEŞ M. S.

TOXICOLOGY AND INDUSTRIAL HEALTH, cilt.31, sa.8, ss.764-772, 2015 (SCI-Expanded) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 31 Sayı: 8
  • Basım Tarihi: 2015
  • Doi Numarası: 10.1177/0748233713484660
  • Dergi Adı: TOXICOLOGY AND INDUSTRIAL HEALTH
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.764-772
  • Anahtar Kelimeler: Carvone, neurotoxicity, cell viability, N2a neuroblastoma cell line, comet assay, oxidative status, MTT assay, OXIDATIVE STRESS, ANTIOXIDANT ACTIVITY, ESSENTIAL OILS, COMET ASSAY, DNA-DAMAGE, IN-VITRO, APOPTOSIS, INHIBITION, FLAVONOIDS, ACID
  • Atatürk Üniversitesi Adresli: Evet

Özet

Carvone (CVN) is a monocyclic monoterpene found in the essential oils of Mentha spicata var. crispa (Lamiaceae) and Carum carvi L. (Apiaceae) plants and has been reported to have antioxidant, antimicrobial, anticonvulsant, and antitumor activities. The beneficial health properties of CVN have encouraged us to look into its anticancer activity. To the best of our knowledge, reports are not available on the anticancer activity of CVN in cultured primary rat neuron and N2a neuroblastoma (NB) cells. Therefore, the present study is an attempt toward exploring the potential anticancer activity of CVN, if any, in cultured primary rat neuron and N2a NB cells. Our results indicated that CVN (only at 25mg/L) treatment led to an increase in the total antioxidant capacity levels in cultured primary rat neuron cells compared with control cells. Also, CVN (at concentrations higher than 100mg/L) treatment led to an increase in the total oxidative stress levels in both cell types. The mean values of the total scores of cells showing DNA damage (for comet assay) were not found to be significantly different from the control values in both cells (p>0.05). On the other hand, after 24h treatment with CVN, 3-(4,5-dimethylthiazol-2-yl)-2,5 diphenyltetrazolium bromide assay showed that CVN application significantly reduced the cell viability rates in both cell types at concentrations higher than 100mg/L. Summarizing, our data suggest that CVN represents little potential for promising anticancer agent to improve brain tumors therapy.