Glutathione and cysteines suppress cytotoxicity of gas phase of cigarette smoke by direct reacting with unsaturated carbonyl compounds in the gas phase.
Acrolein
/ toxicity
Aldehydes
/ toxicity
Antioxidants
/ pharmacology
Chromatography, High Pressure Liquid
Cysteine
/ analogs & derivatives
Environmental Pollutants
/ toxicity
Gases
Glutathione
/ pharmacology
Ketones
/ toxicity
Mass Spectrometry
Protein Carbonylation
/ drug effects
Smoke
Tobacco Products
/ toxicity
Cigarette smoke gas phase
Cysteine
Cytotoxicity
Glutathione
Protein carbonylation
Unsaturated carbonyl compounds
Journal
Biochemical and biophysical research communications
ISSN: 1090-2104
Titre abrégé: Biochem Biophys Res Commun
Pays: United States
ID NLM: 0372516
Informations de publication
Date de publication:
19 02 2019
19 02 2019
Historique:
received:
26
12
2018
accepted:
08
01
2019
pubmed:
19
1
2019
medline:
8
11
2019
entrez:
19
1
2019
Statut:
ppublish
Résumé
Unsaturated carbonyl compounds, such as acrolein (ACR) and methyl vinyl ketone (MVK), are environmental pollutants, and are contained in smoke, automobile exhaust, and heated oil. We have previously reported that major cytotoxic factors in the gas phase of cigarette smoke are ACR and MVK. ACR and MVK induce cell damage by reactive oxygen species generation via protein kinase C and NADPH oxidases, and antioxidants, such as glutathione (GSH) and N-acetylcysteine (NAC), can effectively suppress their cytotoxic activities. In this study, we attempted to elucidate the molecular mechanism(s) for suppression of ACR- and MVK-induced cytotoxic activities by these antioxidants. GSH, NAC, L- and D-cysteines completely suppressed cell damage induced by gas phase extract of cigarette smoke. The results of HPLC and mass spectrometry showed that GSH and NAC directly reacted with ACR and MVK. Cysteines and cysteine derivatives suppressed ACR-induced GAPDH carbonylation, a representative protein for carbonylation. The current results suggest that GSH, NAC, and cysteines directly reacted with ACR and MVK, and suppressed these unsaturated carbonyl compounds-induced cell damage by inhibition of protein carbonylation.
Identifiants
pubmed: 30654934
pii: S0006-291X(19)30048-8
doi: 10.1016/j.bbrc.2019.01.040
pii:
doi:
Substances chimiques
Aldehydes
0
Antioxidants
0
Environmental Pollutants
0
Gases
0
Ketones
0
Smoke
0
Acrolein
7864XYD3JJ
Glutathione
GAN16C9B8O
Cysteine
K848JZ4886
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
988-993Informations de copyright
Copyright © 2019 Elsevier Inc. All rights reserved.