Cryptotanshinone Suppressed Inflammatory Cytokines Secretion in RAW264.7 Macrophages through Inhibition of the NF-κB and MAPK Signaling Pathways

被引:111
作者
Tang, Shu [1 ]
Shen, Xiao-Yan [1 ]
Huang, He-Qing [1 ]
Xu, Suo-Wen [1 ]
Yu, Yang [1 ]
Zhou, Chang-Hua [1 ]
Chen, Shao-Rui [1 ]
Le, Kang [1 ]
Wang, Yu-Hua [1 ]
Liu, Pei-Qing [1 ]
机构
[1] Sun Yat Sen Univ, Higher Educ Mega Ctr, Lab Pharmacol & Toxicol, Sch Pharmaceut Sci, Guangzhou 510006, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
cryptotanshinone; lipopolysaccharides; cytokines; NF-kappa B; MAPKs; SALVIA-MILTIORRHIZA BUNGE; TANSHINONE-I; CELL-LINE; ACTIVATION; EXPRESSION; MEDIATORS; PROTEINS; EXTRACT; TLR4;
D O I
10.1007/s10753-010-9214-3
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Cryptotanshinone (CTS), a major constituent extracted from the medicinal herb Salvia miltiorrhiza Bunge, has well-documented antioxidative and anti-inflammatory effects. In the present study, the pharmacological effects and underlying molecular mechanisms of CTS on lipopolysaccharide (LPS)-induced inflammatory responses were investigated. By enzyme-linked immunosorbent assay, we observed that CTS reduced significantly the production of proinflammatory mediators (tumor necrosis factor-alpha and interleukin-6) induced by LPS in murine macrophage-like RAW264.7 cells. Mechanistically, CTS inhibited markedly the phosphorylation of mitogen-activated protein kinases (MAPKs), including ERK1/2, p38MAPK, and JNK, which are crucially involved in regulation of proinflammatory mediator secretion. Moreover, immunofluorescence and western blot analysis indicated that CTS abolished completely LPS-triggered nuclear factor-kappa B (NF-kappa B) activation. Taken together, these data implied that NF-kappa B and MAPKs might be the potential molecular targets for clarifying the protective effects of CTS on LPS-induced inflammatory cytokine production in macrophages.
引用
收藏
页码:111 / 118
页数:8
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