Abstract
Pro-inflammatory mediators, such as nitric oxide (NO), prostaglandin E2 (PGE2), and several cytokines (tumor necrosis factor (TNF)-α, interleukin (IL)-1β, and IL-6) are responsible for central nervous system (CNS) injuries that include ischemia, Alzheimer’s disease, and neural death. Inhibition of these pro-inflammatory mediators would be an effective therapy to reduce the progression of neurodegenerative diseases. In this study, we examined the anti-inflammatory effects of a human prothrombin fragment-2-derived peptide, NSA9 (NSAVQLVEN), on the production of pro-inflammatory mediators in lipopolysaccharide (LPS)-activated brain microglia. NSA9 significantly inhibited the release of NO, PGE2, and pro-inflammatory cytokines in a dose-dependent manner. Furthermore, NSA9 reduced the expression of inducible NO synthase (iNOS) and cyclooxygenase (COX)-2 mRNA and protein, which control the production of NO and PGE2, respectively. Moreover, NSA9 suppressed the LPS-induced nuclear translocation and activation of nuclear factor-κB (NF-κB). These results suggest that NSA9 strongly inhibits the pro-inflammatory responses of microglia through the modulation of NF-κB activity.
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