Abstract
The flavanol (-)-epicatechin has been found to protect against damage inflicted by peroxynitrite, an inflammatory intermediate. Here, epicatechin was tested in systems of increasing complexity. The compound efficiently protected against nitration of protein tyrosine residues by peroxynitrite (IC50 ≈ 0.02 mol epicatechin/mol peroxynitrite). However, at epicatechin concentrations completely preventing nitration of tyrosine by peroxynitrite, protection against the oxidative inactivation of glyceraldehyde-3-phosphate dehydrogenase or soybean lipoxygenase-1 was marginal (IC50 > 1 mol epicatechin/mol peroxynitrite), approximately two orders of magnitude less. Likewise, epicatechin was relatively ineffective against oxidation of thiols in cell lysates, and against the oxidation of 2′,7′-dichlorodihydrofluorescein in cultured cells. The activation of the kinases Akt/protein kinase B, ERK1/2 and p38-MAPK by peroxynitrite in murine aorta endothelial cells was not altered by epicatechin, suggesting that activation of these kinases is due to processes other than tyrosine nitration.
| Originalsprache | Englisch |
|---|---|
| Zeitschrift | Biochemical and Biophysical Research Communications |
| Jahrgang | 285 |
| Ausgabenummer | 3 |
| Seiten (von - bis) | 782-787 |
| Seitenumfang | 6 |
| ISSN | 0006-291X |
| DOIs | |
| Publikationsstatus | Veröffentlicht - 01.01.2001 |
Fördermittel
Supported by Deutsche Forschungsgemeinschaft, SFB 503/B1. H.S. is a Fellow of the National Foundation for Cancer Research (NFCR) (Bethesda, MD). We thank Dr. Gavin E. Arteel for stimulating discussion.
UN SDGs
Dieser Output leistet einen Beitrag zu folgendem(n) Ziel(en) für nachhaltige Entwicklung
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SDG 3 – Gesundheit und Wohlergehen
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