Research Center for Cell Fate Control, College of Pharmacy, Sookmyung Women's University, Seoul, Korea.
J Med Food. 2012 Nov;15(11):992-9. doi: 10.1089/jmf.2012.2275. Epub 2012 Oct 11.
We identified four anti-inflammatory sulfur-containing compounds from garlic, and their chemical structures were identified as Z- and E-ajoene and oxidized sulfonyl derivatives of ajoene. The sulfur compounds inhibited the production of nitric oxide (NO) and prostaglandin E(2) (PGE(2)) and the expression of the pro-inflammatory cytokines tumor necrosis factor-α, interleukin-1β, and interleukin-6 in lipopolysaccharide (LPS)-activated macrophages. Western blotting and reverse transcription-polymerase chain reaction analysis demonstrated that these sulfur compounds attenuated the LPS-induced expression of the inducible NO synthase (iNOS) and cyclooxygenase-2 (COX-2) proteins and mRNA. Moreover, these sulfur-containing compounds suppressed the nuclear factor-κB (NF-κB) transcriptional activity and the degradation of inhibitory-κBα in LPS-activated macrophages. Furthermore, we observed that they markedly inhibited the LPS-induced phosphorylations of p38 mitogen-activated protein kinases and extracellular signal-regulated kinases (ERK) at 20 μM. These data demonstrate that the sulfur compounds from garlic, (Z, E)-ajoene and their sulfonyl analogs, can suppress the LPS-induced production of NO/PGE(2) and the expression of iNOS/COX-2 genes by inhibiting the NF-κB activation and the phosphorylations of p38 and ERK. Taken together, these data show that Z- and E-ajoene and their sulfonyl analogs from garlic might have anti-inflammatory therapeutic potential.
我们从大蒜中鉴定出四种具有抗炎作用的含硫化合物,它们的化学结构分别为 Z-和 E-丙烯基硫醚以及丙烯基硫醚的氧化磺酰衍生物。这些含硫化合物抑制了脂多糖(LPS)激活的巨噬细胞中一氧化氮(NO)和前列腺素 E2(PGE2)的产生以及促炎细胞因子肿瘤坏死因子-α、白细胞介素-1β和白细胞介素-6 的表达。Western blot 和逆转录-聚合酶链反应分析表明,这些含硫化合物减弱了 LPS 诱导的诱导型一氧化氮合酶(iNOS)和环氧化酶-2(COX-2)蛋白和 mRNA 的表达。此外,这些含硫化合物抑制了 LPS 激活的巨噬细胞中核因子-κB(NF-κB)转录活性和抑制性-κBα的降解。此外,我们观察到它们在 20μM 时显著抑制了 LPS 诱导的 p38 丝裂原激活蛋白激酶和细胞外信号调节激酶(ERK)的磷酸化。这些数据表明,大蒜中的含硫化合物(Z,E)-丙烯基硫醚及其磺酰类似物可以通过抑制 NF-κB 激活和 p38 和 ERK 的磷酸化来抑制 LPS 诱导的 NO/PGE2 产生和 iNOS/COX-2 基因的表达。综上所述,这些数据表明,大蒜中的 Z-和 E-丙烯基硫醚及其磺酰类似物可能具有抗炎治疗潜力。