Please use this identifier to cite or link to this item: http://hdl.handle.net/11455/40253
標題: Taxifolin ameliorates cerebral ischemia-reperfusion injury in rats through its anti-oxidative effect and modulation of NF-kappa B activation
作者: Wang, Y.H.
張嘉哲
Wang, W.Y.
Chang, C.C.
Liou, K.T.
Sung, Y.J.
Liao, J.F.
Chen, C.F.
Chang, S.
Hou, Y.C.
Chou, Y.C.
Shen, Y.C.
關鍵字: cerebral ischemic-reperfusion
COX-2
ICAM-1 (CD54)
iNOS
Mac-1
(CD11b/CD18)
nuclear factor kappa B (NF-kappa B)
reactive oxygen
species
taxifolin
oxygen species production
intercellular-adhesion molecule-1
oxidative
stress
infarct volume
neutrophil infiltration
icam-1 expression
human-leukocytes
focal ischemia
brain
mechanisms
期刊/報告no:: Journal of Biomedical Science, Volume 13, Issue 1, Page(s) 127-141.
摘要: Infarction in adult rat brain was induced by middle cerebral arterial occlusion (MCAO) followed by reperfusion to examine whether taxifolin could reduce cerebral ischemic reperfusion (CI/R) injury. Taxifolin administration (0.1 and 1.0 mu g/kg, i.v.) 60 min after MCAO ameliorated infarction (by 42%+/- 7% and 62%+/- 6%, respectively), which was accompanied by a dramatic reduction in malondialdehyde and nitrotyrosine adduct formation, two markers for oxidative tissue damage. Overproduction of reactive oxygen species (ROS) and nitric oxide (NO) via oxidative enzymes (e.g., COX-2 and iNOS) was responsible for this oxidative damage. Taxifolin inhibited leukocyte infiltration, and COX-2 and iNOS expressions in CI/R-injured brain. Taxifolin also prevented Mac-1 and ICAM-1 expression, two key counter-receptors involved in firm adhesion/transmigration of leukocytes to the endothelium, which partially accounted for the limited leukocyte infiltration. ROS, generated by leukocytes and microglial cells, activated nuclear factor-kappa B (NF-kappa B) that in turn signaled up-regulation of inflammatory proteins. NF-kappa B activity in CI/R was enhanced 2.5-fold over that of sham group and was inhibited by taxifolin. Production of both ROS and NO by leukocytes and microglial cells was significantly antagonized by taxifolin. These data suggest that amelioration of CI/R injury by taxifolin may be attributed to its anti-oxidative effect, which in turn modulates NF-kappa B activation that mediates CI/R injury.
URI: http://hdl.handle.net/11455/40253
ISSN: 1021-7770
文章連結: http://dx.doi.org/10.1007/s11373-005-9031-0
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