Neuroprotective Effects of the Extract of Zingiberis Rhizoma

건강 추출물의 뇌세포 보호 작용

  • 정길생 (원광대학교 인수공통감염병연구센터) ;
  • 리빈 (원광대학교 약학대학) ;
  • 이동성 (원광대학교 약학대학) ;
  • 최현규 (원광대학교 약학대학) ;
  • 김윤철 (원광대학교 약학대학)
  • Received : 2010.07.23
  • Accepted : 2010.08.18
  • Published : 2010.09.30

Abstract

Glutamate-induced oxidative injury contributes to neuronal degeneration in many central nervous system (CNS) diseases, such as Parkinson's disease, Alzheimer's disease, epilepsy and ischemia. Inducible heme oxygenase (HO)-1 acts against oxidants that are thought to play a role in the pathogenesis of these diseases. NNMBS098, a composition comprising the water insoluble of the 70% EtOH extract of Zingiberis Rhizoma, showed the potent neuroprotective effects on glutamateinduced neurotoxicity by induced the expression of heme oxygenase (HO)-1 and increased HO activity in the mouse hippocampal HT22 cells. Furthermore, NNMBS098 caused the nuclear accumulation of nuclear factor E2-related factor 2 (Nrf2) in mouse hippocampal HT22 cells. In addition, we found that treatment with c-Jun N-terminal kinase (JNK) inhibitor (SP600125) reduced NNMBS098-induced HO-1 expression and NNMBS098 also increased JNK phosphorylation. Therefore, these results suggest that NNMBS098 increases cellular resistance to glutamate-induced oxidative injury in mouse hippocampal HT22 cells, presumably through JNK pathway-Nrf2-dependent HO-1 expression.

Keywords

References

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