In Vitro Formation of 8-hydroxy-2-deoxyguanosine (8-OHdG) in Calf Thymus DNA upon Treatment of 2-deoxyguanosine with Propyl Gallate and 2,6-di-tert-butyl-p-benzoquinone

Oxidative DNA damage caused by propyl gallate (PG) and 2,6-di-tert-butyl-p-benzoquinone (BHT-quinone, a metabolite of butylated hydroxytoluene (BHT)) was analyzed from the 8-hydroxy-2¢-deoxyguanosine (8-OHdG) formation in calf thymus DNA and DNA base, 2¢-deoxyguanosine (dG). PG in the presence of Cu...

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Main Authors: Budiawan Budiawan, Dwi Retno Widiastuti
Format: Article
Language:English
Published: Universitas Indonesia 2015-12-01
Series:Makara Journal of Science
Subjects:
Online Access:http://journal.ui.ac.id/index.php/science/article/view/5171/3481
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author Budiawan Budiawan
Dwi Retno Widiastuti
author_facet Budiawan Budiawan
Dwi Retno Widiastuti
author_sort Budiawan Budiawan
collection DOAJ
description Oxidative DNA damage caused by propyl gallate (PG) and 2,6-di-tert-butyl-p-benzoquinone (BHT-quinone, a metabolite of butylated hydroxytoluene (BHT)) was analyzed from the 8-hydroxy-2¢-deoxyguanosine (8-OHdG) formation in calf thymus DNA and DNA base, 2¢-deoxyguanosine (dG). PG in the presence of CuCl2 increased the 8-OHdG formation in calf thymus DNA by around 9.17 times as compared to the control (untreated DNA). In the presence of CuCl2 at 1.28×10-5 M, the 8-OHdG per dG ratio resulting from the reaction of dG with PG at various concentrations (20–150 ppm) ranged from 75.50 to 312.06 8-OHdG per 105 dG. The 8-OHdG formation increased when the PG concentration was increased from 20 ppm to 80 ppm, and then, it began to plateau around 80 ppm. On the other hand, BHT-quinone increased the formation of 8-OHdG in the presence of CuCl2 by 0.05 times as compared to the control (untreated DNA). LC-MS/MS analysis was used to identify the molecular structure of 8-OHdG, which had a base peak (M+. + 1) at m/z = 284 and two main fragments at m/z = 167.9 and m/z = 139.9.
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spelling doaj.art-191acfc4a0e54292ac77a4d4733a46ff2022-12-22T02:54:53ZengUniversitas IndonesiaMakara Journal of Science2339-19952356-08512015-12-0119416717610.7454/mss.v19i4.5171In Vitro Formation of 8-hydroxy-2-deoxyguanosine (8-OHdG) in Calf Thymus DNA upon Treatment of 2-deoxyguanosine with Propyl Gallate and 2,6-di-tert-butyl-p-benzoquinoneBudiawan Budiawan0Dwi Retno Widiastuti1Department of Chemistry, Faculty of Mathematics and Natural Sciences, Universitas Indonesia, Depok 16424, IndonesiaDepartment of Chemistry, Faculty of Mathematics and Natural Sciences, Universitas Indonesia, Depok 16424, IndonesiaOxidative DNA damage caused by propyl gallate (PG) and 2,6-di-tert-butyl-p-benzoquinone (BHT-quinone, a metabolite of butylated hydroxytoluene (BHT)) was analyzed from the 8-hydroxy-2¢-deoxyguanosine (8-OHdG) formation in calf thymus DNA and DNA base, 2¢-deoxyguanosine (dG). PG in the presence of CuCl2 increased the 8-OHdG formation in calf thymus DNA by around 9.17 times as compared to the control (untreated DNA). In the presence of CuCl2 at 1.28×10-5 M, the 8-OHdG per dG ratio resulting from the reaction of dG with PG at various concentrations (20–150 ppm) ranged from 75.50 to 312.06 8-OHdG per 105 dG. The 8-OHdG formation increased when the PG concentration was increased from 20 ppm to 80 ppm, and then, it began to plateau around 80 ppm. On the other hand, BHT-quinone increased the formation of 8-OHdG in the presence of CuCl2 by 0.05 times as compared to the control (untreated DNA). LC-MS/MS analysis was used to identify the molecular structure of 8-OHdG, which had a base peak (M+. + 1) at m/z = 284 and two main fragments at m/z = 167.9 and m/z = 139.9.http://journal.ui.ac.id/index.php/science/article/view/5171/348126-di-tert-butil-p-benzoquinoneDNA adduct8-hydroxy-2¢-deoxyguanosinepropyl gallate
spellingShingle Budiawan Budiawan
Dwi Retno Widiastuti
In Vitro Formation of 8-hydroxy-2-deoxyguanosine (8-OHdG) in Calf Thymus DNA upon Treatment of 2-deoxyguanosine with Propyl Gallate and 2,6-di-tert-butyl-p-benzoquinone
Makara Journal of Science
2
6-di-tert-butil-p-benzoquinone
DNA adduct
8-hydroxy-2¢-deoxyguanosine
propyl gallate
title In Vitro Formation of 8-hydroxy-2-deoxyguanosine (8-OHdG) in Calf Thymus DNA upon Treatment of 2-deoxyguanosine with Propyl Gallate and 2,6-di-tert-butyl-p-benzoquinone
title_full In Vitro Formation of 8-hydroxy-2-deoxyguanosine (8-OHdG) in Calf Thymus DNA upon Treatment of 2-deoxyguanosine with Propyl Gallate and 2,6-di-tert-butyl-p-benzoquinone
title_fullStr In Vitro Formation of 8-hydroxy-2-deoxyguanosine (8-OHdG) in Calf Thymus DNA upon Treatment of 2-deoxyguanosine with Propyl Gallate and 2,6-di-tert-butyl-p-benzoquinone
title_full_unstemmed In Vitro Formation of 8-hydroxy-2-deoxyguanosine (8-OHdG) in Calf Thymus DNA upon Treatment of 2-deoxyguanosine with Propyl Gallate and 2,6-di-tert-butyl-p-benzoquinone
title_short In Vitro Formation of 8-hydroxy-2-deoxyguanosine (8-OHdG) in Calf Thymus DNA upon Treatment of 2-deoxyguanosine with Propyl Gallate and 2,6-di-tert-butyl-p-benzoquinone
title_sort in vitro formation of 8 hydroxy 2 deoxyguanosine 8 ohdg in calf thymus dna upon treatment of 2 deoxyguanosine with propyl gallate and 2 6 di tert butyl p benzoquinone
topic 2
6-di-tert-butil-p-benzoquinone
DNA adduct
8-hydroxy-2¢-deoxyguanosine
propyl gallate
url http://journal.ui.ac.id/index.php/science/article/view/5171/3481
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