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从矮柳珊瑚细胞培养物中分离得到的 C-甲基香豆素色酮的分离、合成及抑菌效果。

Isolation, Synthesis, and Antisepsis Effects of a C-Methylcoumarinochromone Isolated from Abronia nana Cell Culture.

机构信息

College of Pharmacy, CMRI, Research Institute of Pharmaceutical Sciences, BK21 Plus KNU Multi-Omics Based Creative Drug Research Team , Kyungpook National University , Daegu 41566 , Republic of Korea.

Aging Research Center , Korea Research Institute of Bioscience and Biotechnology , Daejeon 34141 , Republic of Korea.

出版信息

J Nat Prod. 2018 May 25;81(5):1173-1182. doi: 10.1021/acs.jnatprod.7b00826. Epub 2018 May 15.

Abstract

Only a few isoflavones have been isolated from plants of the genus Abronia. The biological properties of compounds isolated from Abronia species have not been well established, and their antisepsis effects have not been reported yet. In the present study, a new C-methylcoumarinochromone, was isolated from Abronia nana suspension cultures. Its structure was deduced as 9,11-dihydroxy-10-methylcoumarinochromone (boeravinone Y, 1) by spectroscopic data analysis and verified by chemical synthesis. The potential inhibitory effects of 1 against high mobility group box 1 (HMGB1)-mediated septic responses were investigated. Results showed that 1 effectively inhibited lipopolysaccharide-induced release of HMGB1 and suppressed HMGB1-mediated septic responses, in terms of reduction of hyperpermeability, leukocyte adhesion and migration, and cell adhesion molecule expression. In addition, 1 increased the phagocytic activity of macrophages and exhibited bacterial clearance effects in the peritoneal fluid and blood of mice with cecal ligation and puncture-induced sepsis. Collectively, these results suggested that 1 might have potential therapeutic activity against various severe vascular inflammatory diseases via inhibition of the HMGB1 signaling pathway.

摘要

从 Abronia 属植物中仅分离得到少数几种异黄酮。从 Abronia 属植物中分离得到的化合物的生物学特性尚未得到很好的确定,其防腐作用尚未报道。在本研究中,从 Abronia nana 悬浮培养物中分离得到了一种新的 C-甲基香豆素色酮。通过光谱数据分析推断其结构为 9,11-二羟基-10-甲基香豆素色酮(boeravinone Y,1),并通过化学合成得到验证。研究了 1 对高迁移率族蛋白 1(HMGB1)介导的败血症反应的潜在抑制作用。结果表明,1 可有效抑制脂多糖诱导的 HMGB1 释放,并抑制 HMGB1 介导的败血症反应,表现为降低通透性、白细胞黏附和迁移以及细胞黏附分子表达。此外,1 可增加巨噬细胞的吞噬活性,并在盲肠结扎和穿刺诱导败血症小鼠的腹腔液和血液中显示出清除细菌的作用。总之,这些结果表明,1 可能通过抑制 HMGB1 信号通路对各种严重血管炎症性疾病具有潜在的治疗活性。

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