Sulforaphane suppressed LPS-induced inflammation in mouse peritoneal macrophages through Nrf2 dependent pathway

被引:276
作者
Lin, Wen [2 ]
Wu, Rachel T. [2 ]
Wu, Tienyuan [2 ]
Khor, Tin-Oo [2 ]
Wang, Hu [2 ]
Kong, Ah-Ng [1 ]
机构
[1] Rutgers State Univ, Ctr Canc Prevent Res, Dept Pharmaceut, Ernest Mario Sch Pharm, Piscataway, NJ 08854 USA
[2] Rutgers State Univ, Grad Program Pharmaceut Sci, Piscataway, NJ 08854 USA
关键词
Sulforaphane; Nuclear E2-factor related factor 2; Inflammation; Peritoneal macrophage; Tumor necrosis factor-alpha; Interleukin-1 beta Cyclooxygenase-2; Inducible nitric oxide synthase;
D O I
10.1016/j.bcp.2008.07.036
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Sulforaphane (SFN) is a natural isothiocyanate that is present in cruciferous vegetables such as broccoli and cabbage. Previous studies have shown that SFN is effective in preventing carcinogenesis induced by carcinogens in rodents, which is related in part to its potent anti-inflammation properties. In the present study, we compared the anti-inflammatory effect of SFN on LPS-stimulated inflammation in primary peritoneal macrophages derived from Nrf2 (+/+) and Nrf2 (-/-) mice. Pretreatment of SFN in Nrf2 (+/+) primary peritoneal macrophages potently inhibited LPS-stimulated mRNA expression, protein expression and production of TNF-alpha, IL-1 beta, COX-2 and iNOS. HO-1 expression was significantly augmented in LPS-stimulated Nrf2 (+/+) primary peritoneal macrophages by SFN. Interestingly, the anti-inflammatory effect was attenuated in Nrf2 (-/-) primary peritoneal macrophages. We concluded that SFN exerts its anti-inflammatory activity mainly via activation of Nrf2 in mouse peritoneal macrophages. (C) 2008 Elsevier Inc. All rights reserved.
引用
收藏
页码:967 / 973
页数:7
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