Sulfide (Na₂S) and Polysulfide (Na₂S₂) Interacting with Doxycycline Produce/Scavenge Superoxide and Hydroxyl Radicals and Induce/Inhibit DNA Cleavage.

DNA cleavage EPR spectroscopy doxycycline hydrogen sulfide hydroxyl radical oxytetracycline polysulfides superoxide tetracycline •cPTIO radical

Journal

Molecules (Basel, Switzerland)
ISSN: 1420-3049
Titre abrégé: Molecules
Pays: Switzerland
ID NLM: 100964009

Informations de publication

Date de publication:
22 Mar 2019
Historique:
received: 22 02 2019
revised: 15 03 2019
accepted: 19 03 2019
entrez: 27 3 2019
pubmed: 27 3 2019
medline: 16 7 2019
Statut: epublish

Résumé

Doxycycline (DOXY) is an antibiotic routinely prescribed in human and veterinary medicine for antibacterial treatment, but it has also numerous side effects that include oxidative stress, inflammation, cancer or hypoxia-induced injury. Endogenously produced hydrogen sulfide (H₂S) and polysulfides affect similar biological processes, in which reactive oxygen species (ROS) play a role. Herein, we have studied the interaction of DOXY with H₂S (Na₂S) or polysulfides (Na₂S₂, Na₂S₃ and Na₂S₄) to gain insights into the biological effects of intermediates/products that they generate. To achieve this, UV-VIS, EPR spectroscopy and plasmid DNA (pDNA) cleavage assay were employed. Na₂S or Na₂S₂ in a mixture with DOXY, depending on ratio, concentration and time, displayed bell-shape kinetics in terms of producing/scavenging superoxide and hydroxyl radicals and decomposing hydrogen peroxide. In contrast, the effects of individual compounds (except for Na₂S₂) were hardly observable. In addition, DOXY, as well as oxytetracycline and tetracycline, interacting with Na₂S or other studied polysulfides reduced the

Identifiants

pubmed: 30909480
pii: molecules24061148
doi: 10.3390/molecules24061148
pmc: PMC6470963
pii:
doi:

Substances chimiques

Sulfides 0
Superoxides 11062-77-4
Hydroxyl Radical 3352-57-6
polysulfide 9080-49-3
Doxycycline N12000U13O
sodium sulfide YGR27ZW0Y7

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : Agentúra na Podporu Výskumu a Vývoja
ID : 15-0371; 17-0384; 15-0565
Organisme : Vedecká Grantová Agentúra MŠVVaŠ SR a SAV
ID : 2/0079/19; 1/0041/15; 2/0053/19; 2/0014/17

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Auteurs

Anton Misak (A)

Institute of Clinical and Translational Research, Biomedical Research Center, University Science Park for Biomedicine, Slovak Academy of Sciences, 845 05 Bratislava, Slovakia. anton.misak@savba.sk.

Lucia Kurakova (L)

Department of Pharmacology and Toxicology, Faculty of Pharmacy, Comenius University, 832 32 Bratislava, Slovakia. lucia.k@protonmail.ch.

Eduard Goffa (E)

Cancer Research Institute, Biomedical Research Center, University Science Park for Biomedicine, Slovak Academy of Sciences, 845 05 Bratislava, Slovakia. eduard.goffa@savba.sk.

Vlasta Brezova (V)

Faculty of Chemical and Food Technology, Slovak University of Technology in Bratislava, 812 37 Bratislava, Slovakia. vlasta.brezova@stuba.sk.

Marian Grman (M)

Institute of Clinical and Translational Research, Biomedical Research Center, University Science Park for Biomedicine, Slovak Academy of Sciences, 845 05 Bratislava, Slovakia. marian.grman@savba.sk.

Elena Ondriasova (E)

Department of Pharmacology and Toxicology, Faculty of Pharmacy, Comenius University, 832 32 Bratislava, Slovakia. ondriasova@fpharm.uniba.sk.

Miroslav Chovanec (M)

Cancer Research Institute, Biomedical Research Center, University Science Park for Biomedicine, Slovak Academy of Sciences, 845 05 Bratislava, Slovakia. miroslav.chovanec@savba.sk.

Karol Ondrias (K)

Institute of Clinical and Translational Research, Biomedical Research Center, University Science Park for Biomedicine, Slovak Academy of Sciences, 845 05 Bratislava, Slovakia. karol.ondrias@savba.sk.

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