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Tea extracts protect normal lymphocytes but not leukemia cells from UV radiation-induced ROS production: An EPR spin trap study

  • Semra Tepe Çam
  • , Mustafa Polat
  • , Meriç Arda Esmekaya
  • , Ayşe G. Canseven
  • , Nesrin Seyhan

Research output: Contribution to journalArticlepeer-review

5 Citations (Scopus)

Abstract

Purpose: An ex vivo method for detection of free radicals and their neutralization by aqueous tea in human normal lymphocytes and MEC-1 leukemia cells under ultraviolet (UV) irradiation was investigated.Materials and methods: This method is based on the electron paramagnetic resonance (EPR) spectroscopy spin-trapping technique. 5-tert-butoxycarbonyl 5-methyl-1-pyrroline N-oxide (BMPO) was used as the spin trap. Normal human lymphocytes and leukemia cells were exposed to UVB radiation (290-315 nm) at 47.7 and 159 mJ/cm2 and to UVA radiation (315-400 nm) at 53.7 J/cm2.Results: No significant radical production at 47.7 mJ/cm2 UVB dose in both cell lines was observed. In normal cells, free radical production was observed at 159 mJ/cm2 UVB and 53.7 J/cm2 UVA doses. However, both UV sources did not significantly produce free radicals in leukemia cells. A radical scavenging property of tea extracts (black, green, sage, rosehip) was observed in normal lymphocytes after both UVB and UVA exposure. In leukemia cells, the intensities of EPR signals produced in BMPO with tea extracts were found to be increased substantially after UVA exposure.Conclusion: These results showed that UV radiation induced free radical formation in normal human lymphocytes and indicated that tea extracts may be useful as photoprotective agents for them. On the other hand, tea extracts facilitated free radical production in leukemia cells.

Original languageEnglish
Pages (from-to)673-680
Number of pages8
JournalInternational Journal of Radiation Biology
Volume91
Issue number8
DOIs
Publication statusPublished - 3 Aug 2015

Keywords

  • EPR spin trap
  • Lymphocyte
  • UV
  • antioxidants
  • leukemia
  • radicals
  • tea extract

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