4.7 Article

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

Journal

JOURNAL OF NATURAL PRODUCTS
Volume 81, Issue 5, Pages 1173-1182

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.jnatprod.7b00826

Keywords

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Funding

  1. National Research Foundation of Korea - Korean Government [NRF-2015R1A2A1A15 055871, NRF-2016R1A6A3A11933576, NRF-2015M3A9D9067478]
  2. Bio and Medical Technology Development Program of the National Research Foundation (NRF) - Ministry of Science and ICT [2017M3A9G8083382]
  3. Korea Health Technology R and D Project through the Korea Health Industry Development Institute (KHIDI) - Ministry of Health and Welfare, Republic of Korea [HI1SC0001]
  4. National Research Foundation of Korea [2015M3A9D9067478] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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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.

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