Apocynin inhibits NADPH oxidase in phagocytes but stimulates ROS production in non-phagocytic cells
Jazyk angličtina Země Nizozemsko Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
15716123
DOI
10.1016/j.bbagen.2004.12.008
PII: S0304-4165(04)00307-1
Knihovny.cz E-zdroje
- MeSH
- acetofenony farmakologie MeSH
- antioxidancia farmakologie MeSH
- aorta účinky léků metabolismus MeSH
- fagocyty enzymologie MeSH
- fibroblasty účinky léků metabolismus MeSH
- inhibitory enzymů farmakologie MeSH
- krysa rodu Rattus MeSH
- kultivované buňky MeSH
- NADPH-oxidasy antagonisté a inhibitory MeSH
- potkani Wistar MeSH
- reaktivní formy kyslíku metabolismus MeSH
- zvířata MeSH
- Check Tag
- krysa rodu Rattus MeSH
- mužské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- acetofenony MeSH
- acetovanillone MeSH Prohlížeč
- antioxidancia MeSH
- inhibitory enzymů MeSH
- NADPH-oxidasy MeSH
- reaktivní formy kyslíku MeSH
Apocynin is a naturally occurring methoxy-substituted catechol, experimentally used as an inhibitor of NADPH oxidase. Since it acts as a potent inhibitor in studies with neutrophils and macrophages, no inhibitory effect can often be found in non-phagocyte cells. In our experiments, apocynin even stimulated reactive oxygen species (ROS) production by vascular fibroblasts. Even when added to macrophages, apocynin initially caused an increase in ROS production. The inhibition of ROS formation followed, suggesting that in the presence of leukocyte myeloperoxidase and hydrogen peroxide, apocynin is converted to another compound. Apocynin pre-activated with H2O2 and horseradish peroxidase (HRP) inhibited ROS production immediately. In non-phagocytes, apocynin stimulated ROS production and no inhibition was observed even after 60 min. Apocynin treated with H2O2 and HRP, however, decreased ROS production in the same manner as in macrophages. The stimulatory effect on ROS production can be abolished by tiron and superoxide dismutase (SOD), suggesting that superoxide was the produced species. The effect of apocynin was inhibited by diphenylene iodinium (DPI), a non-scavenging NADPH oxidase inhibitor. It can be summarized that apocynin stimulates cell superoxide production. In the presence of peroxidase and hydrogen peroxide, however, it is converted into another compound that acts as an inhibitor of superoxide production. It strongly suggests that under conditions in vivo, apocynin can have opposite effects on phagocytes and non-phagocyte cells. It acts as an inhibitor of phagocyte NADPH oxidase but also as a ROS production stimulator in non-phagocyte cells.
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