首页    期刊浏览 2024年11月03日 星期日
登录注册

文章基本信息

  • 标题:Synthesis of Monoesters of Pyrroloquinoline Quinone and Imidazopyrroloquinoline, and Radical Scavenging Activities Using Electron Spin Resonance in Vitro and Pharmacological Activity in Vivo
  • 本地全文:下载
  • 作者:Teizi URAKAMI ; Chieko YOSHIDA ; Takaaki AKAIKE
  • 期刊名称:Journal of Nutritional Science and Vitaminology
  • 印刷版ISSN:0301-4800
  • 电子版ISSN:1881-7742
  • 出版年度:1997
  • 卷号:43
  • 期号:1
  • 页码:19-33
  • DOI:10.3177/jnsv.43.19
  • 出版社:Center for Academic Publications Japan
  • 摘要:Monoesters with the ester groups at C-2 of pyrroloquinol-ine quinone (PQQ) and C-9 of imidazopyrroloquinoline (IPQ) were synthesized, and radical scavenging activities of coenzyme PQQ, IPQ compounds synthesized from PQQ and various amino acids, and mono-esters of PQQ and IPQ were studied in vitro and in vivo. PQQ and PQQ monoesters had strong radical scavenging activity using ESR in in vitro experiments. The ICso value for superoxide (02-) was from 1 to 6×10-8M and that for the hydroxy radical ('OH) was from 4 to 6×10-5M. IPQ compounds and IPQ monoesters also showed radical scavenging activity. These compounds prevented injury during in vivo experiments, such as hydrocortisone-induced cataracts, endotoxin shock and CCl4-induced liver injury (isolated hepatocytes and rats). Especially, the monoesters of PQQ and IPQ prevented liver injury in rats equally by oral or intra-peritoneal administration. These results suggest that PQQ functions as a radical scavenging factor in addition to being a cofactor of quinoprotein enzymes, and monoesters with the ester groups at C-2 of PQQ and C-9 of IPQ are developed as treatment or preventive medicine for disease caused by radical compounds on the basis of strong radical scavenging activities, absorbability into cells, toxicity, safety and chemical stability.
  • 关键词:coenzyme PQQ;pyrroloquinoline quinone;imidazopyrrolo-quinoline;TPQ;radical scavenging activity;ESR;protective effect on liver injury
国家哲学社会科学文献中心版权所有