Excessive production of inflammatory mediators such as nitric oxide(NO), prostaglandin E2(PGE2), and proinflammatory cytokines, including tumor necrosis factor-alpha(TNF-α) and interleukin-1beta(IL-1β) from activated microglia contributes to uncontr...
Excessive production of inflammatory mediators such as nitric oxide(NO), prostaglandin E2(PGE2), and proinflammatory cytokines, including tumor necrosis factor-alpha(TNF-α) and interleukin-1beta(IL-1β) from activated microglia contributes to uncontrolled inflammation in neurodegenerative diseases. It seems possible that treatment with anti-inflammatory agents, including plants used in Oriental medicine, might delay the progression of neurodegeneration through the inhibition of microglial activation. The present study is focused on the inhibitory effect of the rhizome hexane fraction extract of Zingiberis Rhizoma Crudus(Ginger Hexan Extract; GHE) on the production of inflammatory mediators such as NO, PGE2, and proinflammatory cytokines in lipopolysaccharide (LPS)-stimulated BV2 cells, a mouse microglial cell line. GHE significantly inhibited the excessive production of NO, PGE2, TNF-α, and IL-1β in LPS-stimulated BV2 cells. In addition, GHE attenuated the mRNA expressions and protein levels of inducible nitric oxide synthase(iNOS), cyclooxygenase-2(COX-2), and proinflammatory cytokines. The anti-inflammatory properties of GHE may make it useful as a therapeutic candidate for the treatment of human neurodegenerative diseases.