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Research ArticleExperimental Studies

Inhibition of LPS-stimulated NO Production in Mouse Macrophage-like Cells by Azulenes

KANA HASHIBA, KEIKO YOKOYAMA, HIDETSUGU WAKABAYASHI, KEN HASHIMOTO, KAZUE SATOH, TERUO KURIHARA, NOBORU MOTOHASHI and HIROSHI SAKAGAMI
Anticancer Research November 2004, 24 (6) 3939-3944;
KANA HASHIBA
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KEIKO YOKOYAMA
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HIDETSUGU WAKABAYASHI
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KEN HASHIMOTO
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KAZUE SATOH
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TERUO KURIHARA
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NOBORU MOTOHASHI
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HIROSHI SAKAGAMI
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Abstract

We investigated the effect of twenty-seven azulenes on nitric oxide (NO) production by mouse macrophage-like Raw 264.7 cells. No azulene derivative alone induced NO production by the Raw 264.7 cells, but inhibited lipopolysaccharide (LPS)-stimulated NO production to various extents. The ability of azulenes to inhibit NO generation by activated macrophages was generally increased when their cytotoxic activity declined. Western blot and RT-PCR analyses demonstrated that the most potent compound, 1,3-difluoroazulene [11], slightly inhibited the expression of inducible NO synthase (iNOS), but only at extremely high concentrations. ESR spectroscopy showed that [11] did not produce radical under alkaline condition, nor scavenged O -2 (generated by HX-XOD reaction) or NO (generated by NOC-7). These data suggest that the inhibitory effect of [11] may be produced via a mechanism other than iNOS induction and a radical-mediated mechanism.

Footnotes

  • Received March 3, 2004.
  • Accepted September 22, 2004.
  • Copyright© 2004 International Institute of Anticancer Research (Dr. John G. Delinassios), All rights reserved
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Anticancer Research
Vol. 24, Issue 6
Novemeber-December 2004
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Inhibition of LPS-stimulated NO Production in Mouse Macrophage-like Cells by Azulenes
KANA HASHIBA, KEIKO YOKOYAMA, HIDETSUGU WAKABAYASHI, KEN HASHIMOTO, KAZUE SATOH, TERUO KURIHARA, NOBORU MOTOHASHI, HIROSHI SAKAGAMI
Anticancer Research Nov 2004, 24 (6) 3939-3944;

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Inhibition of LPS-stimulated NO Production in Mouse Macrophage-like Cells by Azulenes
KANA HASHIBA, KEIKO YOKOYAMA, HIDETSUGU WAKABAYASHI, KEN HASHIMOTO, KAZUE SATOH, TERUO KURIHARA, NOBORU MOTOHASHI, HIROSHI SAKAGAMI
Anticancer Research Nov 2004, 24 (6) 3939-3944;
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