Flavonoids with iNOS inhibitory activity from Pogonatherum crinitum

Guei Jane Wang, Yi-Min Chen, Teng Mao Wang, Ching Kuo Lee, Ke Jun Chen, Tzong Huei Lee

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47 Citations (Scopus)


Pogonatherum crinitum has long been used as a folk remedy for the treatment of many inflammatory diseases in Taiwan, and till now there is still no report concerning its active principles as well as their pharmacological studies. That prompted us to investigate the bioactive constituents of Pogonatherum crinitum. Two novel chemical entities, luteolin 6-C-β-boivinopyranoside (1) and 6-trans-(2″-O-α-rhamnopyranosyl)ethenyl-5,7,3′,4′-tetrahydroxyflavone (2), along with luteolin (3), kaempferol (4), luteolin 6-C-β-fucopyranoside (5), kaempferol 3-O-α-l-rhamnopyranoside (6), luteolin 6-C-β-glucopyranoside (7), rutin (8) and kaempferol 3-O-rutinoside (9) were isolated from this plant, and identified by spectroscopic analysis. The effect of these compounds on the inhibition of NO production in LPS-activated macrophages was further evaluated. All these compounds inhibited NO production in activated RAW 264.7 cells to various degrees without affecting the cellular viability. Among the compounds examined, both compounds 1 and 2 suppressed LPS-induced NO production, with Emax values of 99.51 ± 0.23% and 92.41 ± 3.22%, respectively. The most potent compounds, 3 and 4, inhibited NO production with IC50 values of 10.41 ± 0.02 μM and 10.61 ± 0.44 μM, respectively. These effects were attributed to suppression of mRNA expression of inducible NO synthase (iNOS). Our results clearly demonstrated that these naturally occurring iNOS inhibitors may be beneficial to the treatment of inflammatory diseases associated with overproduction of NO, which provides an explanation, at least a part, for the anti-inflammatory property of Pogonatherum crinitum.

Original languageEnglish
Pages (from-to)71-78
Number of pages8
JournalJournal of Ethnopharmacology
Issue number1
Publication statusPublished - 2008 Jun 19

All Science Journal Classification (ASJC) codes

  • Pharmacology
  • Drug Discovery


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