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本文引用的文献

1
In vitro antiinflammatory activity of a new sesquiterpene lactone isolated from Siegesbeckia glabrescens.从一枝黄花中分离得到的一种新的倍半萜内酯的体外抗炎活性。
Phytother Res. 2011 Sep;25(9):1323-7. doi: 10.1002/ptr.3420. Epub 2011 Feb 10.
2
Garlic (Allium sativum L.) and cardiovascular diseases.大蒜(葱属植物大蒜)与心血管疾病。
Bratisl Lek Listy. 2010;111(8):452-6.
3
Protective effects of Allium sativum against defects of hypercholesterolemia on pregnant rats and their offspring.大蒜对高胆固醇血症孕鼠及其后代缺陷的保护作用。
Int J Clin Exp Med. 2010 Jun 10;3(2):152-63.
4
Garlic-derived anticancer agents: structure and biological activity of ajoene.大蒜来源的抗癌剂:大蒜素的结构和生物活性。
Biofactors. 2010 Jan-Feb;36(1):78-85. doi: 10.1002/biof.76.
5
Carabrol suppresses LPS-induced nitric oxide synthase expression by inactivation of p38 and JNK via inhibition of I-kappaBalpha degradation in RAW 264.7 cells.Carabrol 通过抑制 I-kappaBalpha 的降解来抑制 LPS 诱导的 RAW 264.7 细胞中一氧化氮合酶的表达,从而使 p38 和 JNK 失活。
Biochem Biophys Res Commun. 2010 Jan 15;391(3):1400-4. doi: 10.1016/j.bbrc.2009.12.073. Epub 2009 Dec 22.
6
Substituted ajoenes as novel anti-cancer agents.取代阿霍烯作为新型抗癌剂。
Bioorg Med Chem Lett. 2008 Oct 1;18(19):5277-9. doi: 10.1016/j.bmcl.2008.08.056. Epub 2008 Aug 22.
7
Garlic (Allium sativum) extract inhibits lipopolysaccharide-induced Toll-like receptor 4 dimerization.大蒜(蒜)提取物可抑制脂多糖诱导的Toll样受体4二聚化。
Biosci Biotechnol Biochem. 2008 Feb;72(2):368-75. doi: 10.1271/bbb.70434. Epub 2008 Feb 7.
8
Does garlic have a role as an antidiabetic agent?大蒜是否具有抗糖尿病药物的作用?
Mol Nutr Food Res. 2007 Nov;51(11):1353-64. doi: 10.1002/mnfr.200700082.
9
A cytokine-mediated link between innate immunity, inflammation, and cancer.先天性免疫、炎症和癌症之间由细胞因子介导的联系。
J Clin Invest. 2007 May;117(5):1175-83. doi: 10.1172/JCI31537.
10
A scent of therapy: pharmacological implications of natural products containing redox-active sulfur atoms.一种治疗的气息:含氧化还原活性硫原子的天然产物的药理学意义。
Nat Prod Rep. 2006 Dec;23(6):851-63. doi: 10.1039/b609523m. Epub 2006 Sep 28.

大蒜中含硫化合物的抗炎活性。

Anti-inflammatory activity of sulfur-containing compounds from garlic.

机构信息

Research Center for Cell Fate Control, College of Pharmacy, Sookmyung Women's University, Seoul, Korea.

出版信息

J Med Food. 2012 Nov;15(11):992-9. doi: 10.1089/jmf.2012.2275. Epub 2012 Oct 11.

DOI:10.1089/jmf.2012.2275
PMID:23057778
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3491620/
Abstract

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.

摘要

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。