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Research ArticleExperimental Studies

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

KEIKO YOKOYAMA, KANA HASHIBA, HIDETSUGU WAKABAYASHI, KEN HASHIMOTO, KAZUE SATOH, TERUO KURIHARA, NOBORU MOTOHASHI and HIROSHI SAKAGAMI
Anticancer Research November 2004, 24 (6) 3917-3922;
KEIKO YOKOYAMA
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KANA HASHIBA
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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 27 tropolones on nitric oxide (NO) production by mouse macrophage-like Raw 264.7 cells. All of these compounds failed to stimulate the Raw 264.7 cells to produce detectable amounts of NO, but inhibited NO production by lipopolysaccharide (LPS)-activated Raw 264.7 cells to various extents. Generally, the ability of tropolones to inhibit LPS-stimulated NO production was inversely related to their cytotoxic activity. Western blot and RT-PCR analyses demonstrated that the most active compound, 2,4-dibromo-7-methoxytropone [21], significantly reduced both the intracellular concentration of iNOS protein and the expression of iNOS mRNA. ESR spectroscopy showed that [21] did not produce radicals under alkaline condition, nor scavenged NO, produced by NOC-7. These data suggested that the inhibitory effect of [21] on NO production might be generated via the inhibition of iNOS expression, rather than a radical-mediated mechanism.

Footnotes

  • Received March 30, 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 Tropolones
KEIKO YOKOYAMA, KANA HASHIBA, HIDETSUGU WAKABAYASHI, KEN HASHIMOTO, KAZUE SATOH, TERUO KURIHARA, NOBORU MOTOHASHI, HIROSHI SAKAGAMI
Anticancer Research Nov 2004, 24 (6) 3917-3922;

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Inhibition of LPS-stimulated NO Production in Mouse Macrophage-like Cells by Tropolones
KEIKO YOKOYAMA, KANA HASHIBA, HIDETSUGU WAKABAYASHI, KEN HASHIMOTO, KAZUE SATOH, TERUO KURIHARA, NOBORU MOTOHASHI, HIROSHI SAKAGAMI
Anticancer Research Nov 2004, 24 (6) 3917-3922;
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