Anti-inflammatory Activity of Salvianolic Acid B in Microglia Contributes to its Neuroprotective Effect

被引:122
作者
Wang, Shao-Xia [1 ,2 ]
Hu, Li-Min [1 ]
Gao, Xiu-Mei [2 ]
Guo, Hong [1 ,2 ]
Fan, Guan-Wei [1 ,2 ]
机构
[1] Tianjin Univ Tradit Chinese Med, Tianjin Key Lab Tradit Chinese Med Pharmacol, Tianjin 300193, Peoples R China
[2] Tianjin Univ Tradit Chinese Med, Minist Educ, Key Lab Pharmacol Tradit Chinese Med Formulae, Tianjin 300193, Peoples R China
基金
中国国家自然科学基金;
关键词
Salvianolic acid B; Microglial activation; Neuroprotective drugs; Inflammation; CENTRAL-NERVOUS-SYSTEM; SMOOTH-MUSCLE-CELLS; NF-KAPPA-B; DEFICIENT MOUSE AORTA; NECROSIS-FACTOR-ALPHA; ENDOTHELIAL-CELLS; PC12; CELLS; INDUCED NEUROTOXICITY; PLATELET-AGGREGATION; DOPAMINERGIC-NEURONS;
D O I
10.1007/s11064-010-0151-1
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
This study examined whether Salvianolic acid B (Sal B), a major active component of Chinese herb Radix Salviae Miltiorrhizae, may exert an anti-inflammatory effect in microglia and may be neuroprotective by regulating microglial activation. Our results showed that Sal B significantly reduced the production of nitric oxide (NO), tumor necrosis factor-alpha (TNF-alpha), interleukin-1 beta (IL-1 beta) and reactive oxygen species (ROS) induced by lipopolysaccharide (LPS) treatment in rat primary microglia in a dose-dependent manner. Sal B had no effects on ATP-dependent IL-1 beta release and interferon (IFN)-gamma-induced NO production. Sal B also suppressed LPS-induced inducible nitric oxide synthase (iNOS), TNF-alpha, and IL-1 beta mRNA expression, which was accompanied by inhibiting transcription factor NF-kappa B activation. Sal B could protect neurons through inhibition of microglial activation in a microglia-neuron coculture system. In conclusion, these data demonstrate that anti-inflammatory activity of Sal B in microglia contributes to its neuroprotective effect and suggest that it may be useful for preventing microglia-mediated neuroinflammation.
引用
收藏
页码:1029 / 1037
页数:9
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