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- Publisher Website: 10.1179/1351000213Y.0000000051
- Scopus: eid_2-s2.0-84880395062
- PMID: 23849339
- WOS: WOS:000322077700004
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Article: Genoprotection and genotoxicity of green tea (Camellia sinensis): Are they two sides of the same redox coin?
Title | Genoprotection and genotoxicity of green tea (Camellia sinensis): Are they two sides of the same redox coin? |
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Authors | |
Keywords | DNA damage ARE Green tea Pro-oxidant HO-1 Hydrogen peroxide Oxidative stress Redox tone Genoprotection |
Issue Date | 2013 |
Citation | Redox Report, 2013, v. 18, n. 4, p. 150-154 How to Cite? |
Abstract | Objectives: Regular intake of green tea associates with lower DNA damage and increased resistance of DNA to oxidant challenge. However, in vitro pro-oxidant effects of green tea have been reported. Both effects could be mediated by hydrogen peroxide (H 2 O 2 ) which is generated by autoxidation of tea catechins. In large amounts, H 2 O 2 is genotoxic, but low concentrations could activate the redox-sensitive antioxidant response element (ARE) via the Keap-1/Nrf2 redox switch, inducing genoprotective adaptations. Our objective was to test this hypothesis. Methods: Peripheral lymphocytes from healthy volunteers were incubated for 30 minutes at 37°C in freshly prepared tea solutions (0.005, 0.01, 0.05%w/v (7, 14, 71 μmol/l total catechins) in phosphate buffered saline (PBS), with PBS as control) in the presence and absence of catalase (CAT). H 2 O 2 in tea was measured colorimetrically. Oxidation-induced DNA lesions were measured by the Fpg-assisted comet assay. Results: H 2 O 2 concentrations in 0.005, 0.01, and 0.05% green tea after 30 minutes at 37°C were, respectively, ~3, ~7, and ~52 μmol/l. Cells incubated in 0.005 and 0.01% tea showed less (P < 0.001) DNA damage compared to control cells. Cells treated with 0.05% green tea showed ~50% (P < 0.001) more DNA damage. The presence of CAT prevented this damage, but did not remove the genoprotective effects of low-dose tea. No significant changes in expression of ARE-associated genes (HMOX1, NRF2, KEAP1, BACH1, and hOGG1) were seen in cells treated with tea or tea + CAT. Conclusion: Genoprotection by low-dose green tea could be due to direct antioxidant protection by green tea polyphenols, or to H 2 O 2 -independent signalling pathways. © W. S. Maney & Son Ltd 2013. |
Persistent Identifier | http://hdl.handle.net/10722/244149 |
ISSN | 2023 Impact Factor: 5.2 2023 SCImago Journal Rankings: 0.955 |
ISI Accession Number ID |
DC Field | Value | Language |
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dc.contributor.author | Ho, Cyrus K. | - |
dc.contributor.author | Choi, Siu-Wai | - |
dc.contributor.author | Siu, Parco M. | - |
dc.contributor.author | Benzie, Iris F. | - |
dc.date.accessioned | 2017-08-31T08:56:11Z | - |
dc.date.available | 2017-08-31T08:56:11Z | - |
dc.date.issued | 2013 | - |
dc.identifier.citation | Redox Report, 2013, v. 18, n. 4, p. 150-154 | - |
dc.identifier.issn | 1351-0002 | - |
dc.identifier.uri | http://hdl.handle.net/10722/244149 | - |
dc.description.abstract | Objectives: Regular intake of green tea associates with lower DNA damage and increased resistance of DNA to oxidant challenge. However, in vitro pro-oxidant effects of green tea have been reported. Both effects could be mediated by hydrogen peroxide (H 2 O 2 ) which is generated by autoxidation of tea catechins. In large amounts, H 2 O 2 is genotoxic, but low concentrations could activate the redox-sensitive antioxidant response element (ARE) via the Keap-1/Nrf2 redox switch, inducing genoprotective adaptations. Our objective was to test this hypothesis. Methods: Peripheral lymphocytes from healthy volunteers were incubated for 30 minutes at 37°C in freshly prepared tea solutions (0.005, 0.01, 0.05%w/v (7, 14, 71 μmol/l total catechins) in phosphate buffered saline (PBS), with PBS as control) in the presence and absence of catalase (CAT). H 2 O 2 in tea was measured colorimetrically. Oxidation-induced DNA lesions were measured by the Fpg-assisted comet assay. Results: H 2 O 2 concentrations in 0.005, 0.01, and 0.05% green tea after 30 minutes at 37°C were, respectively, ~3, ~7, and ~52 μmol/l. Cells incubated in 0.005 and 0.01% tea showed less (P < 0.001) DNA damage compared to control cells. Cells treated with 0.05% green tea showed ~50% (P < 0.001) more DNA damage. The presence of CAT prevented this damage, but did not remove the genoprotective effects of low-dose tea. No significant changes in expression of ARE-associated genes (HMOX1, NRF2, KEAP1, BACH1, and hOGG1) were seen in cells treated with tea or tea + CAT. Conclusion: Genoprotection by low-dose green tea could be due to direct antioxidant protection by green tea polyphenols, or to H 2 O 2 -independent signalling pathways. © W. S. Maney & Son Ltd 2013. | - |
dc.language | eng | - |
dc.relation.ispartof | Redox Report | - |
dc.subject | DNA damage | - |
dc.subject | ARE | - |
dc.subject | Green tea | - |
dc.subject | Pro-oxidant | - |
dc.subject | HO-1 | - |
dc.subject | Hydrogen peroxide | - |
dc.subject | Oxidative stress | - |
dc.subject | Redox tone | - |
dc.subject | Genoprotection | - |
dc.title | Genoprotection and genotoxicity of green tea (Camellia sinensis): Are they two sides of the same redox coin? | - |
dc.type | Article | - |
dc.description.nature | link_to_OA_fulltext | - |
dc.identifier.doi | 10.1179/1351000213Y.0000000051 | - |
dc.identifier.pmid | 23849339 | - |
dc.identifier.scopus | eid_2-s2.0-84880395062 | - |
dc.identifier.volume | 18 | - |
dc.identifier.issue | 4 | - |
dc.identifier.spage | 150 | - |
dc.identifier.epage | 154 | - |
dc.identifier.eissn | 1743-2928 | - |
dc.identifier.isi | WOS:000322077700004 | - |
dc.identifier.issnl | 1351-0002 | - |