DNA damage in a solution containing copper(II) ions and ascorbic acid: Effect of the presence of sulfite
Some antioxidant compounds have a pro-oxidant effect in the presence of transition metal ions, due to the reduction of Mn+ to M(n-1)+ with simultaneous formation of free radicals, which then promote DNA damage. In the present study, we evaluated the pUC19 DNA damage in a solution containing Cu(II) a...
| Authors: | , , |
|---|---|
| Format: | article |
| Status: | Published version |
| Publication Date: | 2022 |
| Country: | Brasil |
| Institution: | Universidade de São Paulo (USP) |
| Repository: | Brazilian Journal of Pharmaceutical Sciences |
| Language: | English |
| OAI Identifier: | oai:revistas.usp.br:article/204110 |
| Online Access: | https://www.revistas.usp.br/bjps/article/view/204110 |
| Access Level: | Open access |
| Keyword: | Gel electrophoresis. DNA damage. copper. ascorbic acid. sulfite. |
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DNA damage in a solution containing copper(II) ions and ascorbic acid: Effect of the presence of sulfiteGel electrophoresis. DNA damage. copper. ascorbic acid. sulfite.Some antioxidant compounds have a pro-oxidant effect in the presence of transition metal ions, due to the reduction of Mn+ to M(n-1)+ with simultaneous formation of free radicals, which then promote DNA damage. In the present study, we evaluated the pUC19 DNA damage in a solution containing Cu(II) and ascorbic acid (AA) or S(IV) saturated with air by agarose gel electrophoresis. Our results showed that this damage decreases if AA and S(IV) are simultaneously added. This study also illustrates the importance of Cu(II) in this process, as no DNA damage was observed when AA or S(IV) were present in the absence of this metallic ion. Our data showed that DNA preservation depends on the concentration of AA and S(IV) and occurs when the [S(IV)]:[AA] ratio ranges from 1:1 to 20:1. Absorbance measurements and thermodynamic data show that no reaction occurs between AA and S(IV) when this mixture (pH 5.5) is added to pUC-19 DNA. The presence of dissolved oxygen may be the cause of AA consumption in the mixture of these two antioxidants, which subsequently decreases DNA damage.Universidade de São Paulo. Faculdade de Ciências Farmacêuticas2022-11-09info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttps://www.revistas.usp.br/bjps/article/view/20411010.1590/s2175-979020200004181084Brazilian Journal of Pharmaceutical Sciences; Vol. 57 (2021)Brazilian Journal of Pharmaceutical Sciences; v. 57 (2021)Brazilian Journal of Pharmaceutical Sciences; Vol. 57 (2021)2175-97901984-8250reponame:Brazilian Journal of Pharmaceutical Sciencesinstname:Universidade de São Paulo (USP)instacron:USPenghttps://www.revistas.usp.br/bjps/article/view/204110/187726Copyright (c) 2022 Brazilian Journal of Pharmaceutical Scienceshttps://creativecommons.org/licenses/by/4.0info:eu-repo/semantics/openAccessBoscolo Requeijo, ThaisPires Serrano, Silvia HelenaDorigan Moya, Horacio2022-11-09T19:19:51Zoai:revistas.usp.br:article/204110Revistahttps://www.revistas.usp.br/bjps/indexPUBhttps://old.scielo.br/oai/scielo-oai.phpbjps@usp.br||elizabeth.igne@gmail.com2175-97901984-8250opendoar:2022-11-09T19:19:51Brazilian Journal of Pharmaceutical Sciences - Universidade de São Paulo (USP)false |
| dc.title.none.fl_str_mv |
DNA damage in a solution containing copper(II) ions and ascorbic acid: Effect of the presence of sulfite |
| title |
DNA damage in a solution containing copper(II) ions and ascorbic acid: Effect of the presence of sulfite |
| spellingShingle |
DNA damage in a solution containing copper(II) ions and ascorbic acid: Effect of the presence of sulfite Boscolo Requeijo, Thais Gel electrophoresis. DNA damage. copper. ascorbic acid. sulfite. |
| title_short |
DNA damage in a solution containing copper(II) ions and ascorbic acid: Effect of the presence of sulfite |
| title_full |
DNA damage in a solution containing copper(II) ions and ascorbic acid: Effect of the presence of sulfite |
| title_fullStr |
DNA damage in a solution containing copper(II) ions and ascorbic acid: Effect of the presence of sulfite |
| title_full_unstemmed |
DNA damage in a solution containing copper(II) ions and ascorbic acid: Effect of the presence of sulfite |
| title_sort |
DNA damage in a solution containing copper(II) ions and ascorbic acid: Effect of the presence of sulfite |
| dc.creator.none.fl_str_mv |
Boscolo Requeijo, Thais Pires Serrano, Silvia Helena Dorigan Moya, Horacio |
| author |
Boscolo Requeijo, Thais |
| author_facet |
Boscolo Requeijo, Thais Pires Serrano, Silvia Helena Dorigan Moya, Horacio |
| author_role |
author |
| author2 |
Pires Serrano, Silvia Helena Dorigan Moya, Horacio |
| author2_role |
author author |
| dc.subject.por.fl_str_mv |
Gel electrophoresis. DNA damage. copper. ascorbic acid. sulfite. |
| topic |
Gel electrophoresis. DNA damage. copper. ascorbic acid. sulfite. |
| description |
Some antioxidant compounds have a pro-oxidant effect in the presence of transition metal ions, due to the reduction of Mn+ to M(n-1)+ with simultaneous formation of free radicals, which then promote DNA damage. In the present study, we evaluated the pUC19 DNA damage in a solution containing Cu(II) and ascorbic acid (AA) or S(IV) saturated with air by agarose gel electrophoresis. Our results showed that this damage decreases if AA and S(IV) are simultaneously added. This study also illustrates the importance of Cu(II) in this process, as no DNA damage was observed when AA or S(IV) were present in the absence of this metallic ion. Our data showed that DNA preservation depends on the concentration of AA and S(IV) and occurs when the [S(IV)]:[AA] ratio ranges from 1:1 to 20:1. Absorbance measurements and thermodynamic data show that no reaction occurs between AA and S(IV) when this mixture (pH 5.5) is added to pUC-19 DNA. The presence of dissolved oxygen may be the cause of AA consumption in the mixture of these two antioxidants, which subsequently decreases DNA damage. |
| publishDate |
2022 |
| dc.date.none.fl_str_mv |
2022-11-09 |
| dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion |
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article |
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publishedVersion |
| dc.identifier.uri.fl_str_mv |
https://www.revistas.usp.br/bjps/article/view/204110 10.1590/s2175-979020200004181084 |
| url |
https://www.revistas.usp.br/bjps/article/view/204110 |
| identifier_str_mv |
10.1590/s2175-979020200004181084 |
| dc.language.iso.fl_str_mv |
eng |
| language |
eng |
| dc.relation.none.fl_str_mv |
https://www.revistas.usp.br/bjps/article/view/204110/187726 |
| dc.rights.driver.fl_str_mv |
Copyright (c) 2022 Brazilian Journal of Pharmaceutical Sciences https://creativecommons.org/licenses/by/4.0 info:eu-repo/semantics/openAccess |
| rights_invalid_str_mv |
Copyright (c) 2022 Brazilian Journal of Pharmaceutical Sciences https://creativecommons.org/licenses/by/4.0 |
| eu_rights_str_mv |
openAccess |
| dc.publisher.none.fl_str_mv |
Universidade de São Paulo. Faculdade de Ciências Farmacêuticas |
| publisher.none.fl_str_mv |
Universidade de São Paulo. Faculdade de Ciências Farmacêuticas |
| dc.source.none.fl_str_mv |
Brazilian Journal of Pharmaceutical Sciences; Vol. 57 (2021) Brazilian Journal of Pharmaceutical Sciences; v. 57 (2021) Brazilian Journal of Pharmaceutical Sciences; Vol. 57 (2021) 2175-9790 1984-8250 reponame:Brazilian Journal of Pharmaceutical Sciences instname:Universidade de São Paulo (USP) instacron:USP |
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Universidade de São Paulo (USP) |
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USP |
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USP |
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Brazilian Journal of Pharmaceutical Sciences |
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Brazilian Journal of Pharmaceutical Sciences |
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Brazilian Journal of Pharmaceutical Sciences - Universidade de São Paulo (USP) |
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bjps@usp.br||elizabeth.igne@gmail.com |
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