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Elucidation of Plasma-induced Chemical Modifications on Glutathione and Glutathione Disulphide.
Klinkhammer, Christina; Verlackt, Christof; Smilowicz, Dariusz; Kogelheide, Friederike; Bogaerts, Annemie; Metzler-Nolte, Nils; Stapelmann, Katharina; Havenith, Martina; Lackmann, Jan-Wilm.
Afiliação
  • Klinkhammer C; Physical Chemistry II, Ruhr University Bochum, 44780, Bochum, Germany.
  • Verlackt C; PLASMANT, University of Antwerp, 2610 Wilrijk, Antwerp, Belgium.
  • Smilowicz D; Inorganic Chemistry I-Bioinorganic Chemistry, Ruhr University Bochum, 44780, Bochum, Germany.
  • Kogelheide F; Biomedical Applications of Plasma Technology, Ruhr University Bochum, 44780, Bochum, Germany.
  • Bogaerts A; PLASMANT, University of Antwerp, 2610 Wilrijk, Antwerp, Belgium.
  • Metzler-Nolte N; Inorganic Chemistry I-Bioinorganic Chemistry, Ruhr University Bochum, 44780, Bochum, Germany.
  • Stapelmann K; Biomedical Applications of Plasma Technology, Ruhr University Bochum, 44780, Bochum, Germany.
  • Havenith M; Plasma for Life Sciences, Department of Nuclear Engineering, North Carolina State University, Raleigh, NC, 27695, USA.
  • Lackmann JW; Physical Chemistry II, Ruhr University Bochum, 44780, Bochum, Germany.
Sci Rep ; 7(1): 13828, 2017 10 23.
Article em En | MEDLINE | ID: mdl-29062059
ABSTRACT
Cold atmospheric pressure plasmas are gaining increased interest in the medical sector and clinical trials to treat skin diseases are underway. Plasmas are capable of producing several reactive oxygen and nitrogen species (RONS). However, there are open questions how plasma-generated RONS interact on a molecular level in a biological environment, e.g. cells or cell components. The redox pair glutathione (GSH) and glutathione disulphide (GSSG) forms the most important redox buffer in organisms responsible for detoxification of intracellular reactive species. We apply Raman spectroscopy, mass spectrometry, and molecular dynamics simulations to identify the time-dependent chemical modifications on GSH and GSSG that are caused by dielectric barrier discharge under ambient conditions. We find GSSG, S-oxidised glutathione species, and S-nitrosoglutathione as oxidation products with the latter two being the final products, while glutathione sulphenic acid, glutathione sulphinic acid, and GSSG are rather reaction intermediates. Experiments using stabilized pH conditions revealed the same main oxidation products as were found in unbuffered solution, indicating that the dominant oxidative or nitrosative reactions are not influenced by acidic pH. For more complex systems these results indicate that too long treatment times can cause difficult-to-handle modifications to the cellular redox buffer which can impair proper cellular function.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Dissulfeto de Glutationa / Gases em Plasma / Glutationa Limite: Humans Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Dissulfeto de Glutationa / Gases em Plasma / Glutationa Limite: Humans Idioma: En Ano de publicação: 2017 Tipo de documento: Article