作者
Charles N Serhan, Jane F Maddox, Nicos A Petasis, Irini Akritopoulou-Zanze, Aikaterina Papayianni, Hugh R Brady, Sean P Colgan, James L Madara
发表日期
1995/11/1
期刊
Biochemistry
卷号
34
期号
44
页码范围
14609-14615
出版商
American Chemical Society
简介
Revised Manuscript Received September 13, 1995® abstract: Lipoxins (LX) are bioactive eicosanoids that carry a tetraene structure and serve as regulators of inflammation, in part by inhibiting neutrophil migration and adhesion. Lipoxin A4 is rapidly regulated by conversion to inactive LX metabolites via local metabolism that involves dehydrogenation as the predominant route. Here, several LXA4 analogs were designed that resisted rapid conversion by both differentiated HL-60 cellsand recombinant 15-hydroxyprostaglandin dehydrogenase, systems where native LXA4 is degraded within minutes. The rank order of conversion by recombinant dehydrogenase was LXA4 methyl ester> PGE2~ PGE2 methyl ester> LXA4>>> the novel LXA4 analogs. In addition, 15 (RZS)-methyl-LXA4, 15-cyclohexyl-LXA4, and 16-phenoxy-LXA4 proved to retain LXA4 bioactivity and inhibited neutrophil transmigration across …
引用总数
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