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Antioxidant and antiinflammatory activities of xanthorrhizol in hippocampal neurons and primary cultured microglia
Author(s) -
Lim Chol Seung,
Jin DaQing,
Mok Hyejung,
Oh Sang Jin,
Lee Jung Uk,
Hwang Jae Kwan,
Ha Ilho,
Han JungSoo
Publication year - 2005
Publication title -
journal of neuroscience research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.72
H-Index - 160
eISSN - 1097-4547
pISSN - 0360-4012
DOI - 10.1002/jnr.20692
Subject(s) - pharmacology , microglia , neurotoxicity , neuroprotection , antioxidant , nitric oxide synthase , chemistry , lipid peroxidation , proinflammatory cytokine , nitric oxide , reactive oxygen species , biochemistry , inflammation , medicine , immunology , toxicity , organic chemistry
Xanthorrhizol, a natural sesquiterpenoid isolated from the rhizome of Curcuma xanthorrhiza Roxb (Zingiberaceae), has antibacterial activities and protective effects against cisplatin‐induced hepatotoxicity. In this study, we investigated the activities of xanthorrhizol as an antioxidant or antiinflammatory agent using neuronal and microglial cells. Xanthorrhizol had potent neuroprotective effects on glutamate‐induced neurotoxicity and reactive oxygen species (ROS) generation in the murine hippocampal HT22 cell line. Also, xanthorrhizol inhibited H 2 O 2 ‐induced lipid peroxidation in rat brain homogenates. The properties of xanthorrhizol as an antiinflammatory agent were investigated in microglial activation by lipopolysaccharide. It reduced the expression of cyclooxygenase‐2 and the inducible nitric oxide synthase, which consequently resulted in the reduction of nitric oxide. The production of proinflammatory cytokines, such as interleukin‐6 and tumor necrosis factor‐α in activated microglial cells, was reduced by xanthorrhizol. These results suggest that xanthorrhizol could be an effective candidate for the treatment of Alzheimer's disease‐ and other neurological disease‐related ROS and inflammation. © 2005 Wiley‐Liss, Inc.