We have recently shown that apocynin elicits an oxidative stress in N11 mouse glial cells and other cell types. Here we report that apocynin increased the accumulation of nitrite, the stable derivative of nitric oxide (NO), in the extracellular medium of N11 cell cultures, and the NO synthase (NOS) activity in cell lysates. The increased synthesis of NO was associated with increased expression of inducible NOS (iNOS) mRNA, increased nuclear translocation of the redox-sensitive transcription factor NF-kappa B and decreased intracellular level of its inhibitor IkB alpha. These effects, accompanied by increased production of H2O2, were very similar to those observed after incubation with bacterial lipopolysaccharide (LPS) and were inhibited by catalase. These results suggest that apocynin, similarly to LPS, induces increased NO synthesis by eliciting a generation of reactive oxygen species (ROS), which in turn causes NF-kappa B activation and increased expression of iNOS. Therefore, the increased bioavailability of NO reported in the literature after in vivo or in vitro treatments with apocynin might depend, at least partly, on the drug-elicited induction of iNOS, and not only on the inhibition of NADPH oxidase and the subsequent decreased scavenging of NO by oxidase-derived ROS, as it is often supposed.

The NADPH oxidase inhibitor apocynin induces nitric oxide synthesis via oxidative stress

RIGANTI, Chiara;COSTAMAGNA, Costanzo;DOUBLIER, Sophie Michelle;MIRAGLIA, ERICA;POLIMENI, Manuela;BOSIA, Amalia;GHIGO, Dario Antonio
2008-01-01

Abstract

We have recently shown that apocynin elicits an oxidative stress in N11 mouse glial cells and other cell types. Here we report that apocynin increased the accumulation of nitrite, the stable derivative of nitric oxide (NO), in the extracellular medium of N11 cell cultures, and the NO synthase (NOS) activity in cell lysates. The increased synthesis of NO was associated with increased expression of inducible NOS (iNOS) mRNA, increased nuclear translocation of the redox-sensitive transcription factor NF-kappa B and decreased intracellular level of its inhibitor IkB alpha. These effects, accompanied by increased production of H2O2, were very similar to those observed after incubation with bacterial lipopolysaccharide (LPS) and were inhibited by catalase. These results suggest that apocynin, similarly to LPS, induces increased NO synthesis by eliciting a generation of reactive oxygen species (ROS), which in turn causes NF-kappa B activation and increased expression of iNOS. Therefore, the increased bioavailability of NO reported in the literature after in vivo or in vitro treatments with apocynin might depend, at least partly, on the drug-elicited induction of iNOS, and not only on the inhibition of NADPH oxidase and the subsequent decreased scavenging of NO by oxidase-derived ROS, as it is often supposed.
2008
228(3)
277
285
http://www.sciencedirect.com/science?_ob=MImg&_imagekey=B6WXH-4RDR181-1-W&_cdi=7159&_user=525216&_pii=S0041008X07005650&_orig=search&_coverDate=05%2F01%2F2008&_sk=997719996&view=c&wchp=dGLzVlz-zSkWz&md5=b758c046b93899b8e97c4e2d53429a5f&ie=/sdarticle.pdf
apocynin; glial cells; nitric oxide; nuclear factor-kB; oxidative stress; catalase; lipopolysaccharide; NADPH oxidase
RIGANTI C; COSTAMAGNA C; DOUBLIER S; MIRAGLIA E; POLIMENI M; BOSIA A; GHIGO D
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2318/27577
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