Journal
INTERNATIONAL IMMUNOPHARMACOLOGY
Volume 11, Issue 4, Pages 468-474Publisher
ELSEVIER
DOI: 10.1016/j.intimp.2010.12.017
Keywords
Sildenafil; N9 microglial cells; Pro-inflammatory mediators; Nuclear factor-kappa B; Mitogen-activated protein kinase; Reactive oxygen species
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Funding
- National Key Scientific Project for New Drug Discovery and Development, P. R. China. [2009ZX09301-012]
- Key Laboratory for New Drug Screening, Key Laboratory for Pharmacodynamics, of Liaoning Province, P. R. China
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Excessive activation of microglial cells has been implicated in various neuroinflammation. The present study showed that sildenafil, a PDE5 inhibitor, significantly suppressed NO, interleukin 1 beta (IL-1 beta) and tumor necrosis factor alpha (TNF-alpha) production induced by LPS in microglial cells through decreasing the protein and/or mRNA expressions of inducible NO synthase (iNOS), IL-1 beta and TNF-alpha in a concentration-dependent manner. Sildenafil also blocked I kappa B alpha phosphorylation and degradation, inhibited the phosphorylation of mitogen-activated protein kinases (MAPKs), extracellular signal-regulated kinases 1 and 2 (ERK1/2), p38 MAPK, and c-Jun N-terminal kinase (JNK). Moreover, the increase of the expression of gp91phox, a critical and catalytic subunit of NADPH oxidase, and the levels of intracellular reactive oxygen species (iROS) induced by LPS were markedly inhibited by sildenafil. In summary, these data suggest that sildenafil exerts its in vitro anti-inflammatory effect in LPS-activated N9 microglial cells by blocking nuclear factor-kappa B (NF-kappa B) and MAPKs activation, which may be partly due to its potent down-regulation of the NADPH-derived iROS production. Crown Copyright (C) 2010 Published by Elsevier B.V. All rights reserved.
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