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DOI 10.1016/j.bbrc.2009.08.103

Медицинская библиотека · Biochemical and biophysical research communications · 2009

MK615 attenuates Porphyromonas gingivalis lipopolysaccharide-induced pro-inflammatory cytokine release via MAPK inactivation in murine macrophage-like RAW264.7 cells.

Morimoto Yoko, Kikuchi Kiyoshi, Ito Takashi, Tokuda Masayuki, Matsuyama Takashi, Noma Satoshi, Hashiguchi Teruto, Torii Mitsuo, Maruyama Ikuro, Kawahara Ko-Ichi

СтатьяПоддержка исследования: вне правительства СШАПеревод пока не подготовлен

Аннотация

The Japanese apricot, known as Ume in Japanese, has been a traditional Japanese medicine for centuries, and is a familiar and commonly consumed food. The health benefits of Ume are now being widely recognized and have been strengthened by recent studies showing that MK615, an extract of compounds from Ume, has strong anticancer and anti-inflammatory effects. However, the potential role of MK615 in the periodontal field remains unknown. Here, we found that MK615 significantly reduced the production of pro-inflammatory mediators (tumor necrosis factor-alpha and interleukin-6) induced by Porphyromonas gingivalis lipopolysaccharide (LPS), a major etiological agent in localized chronic periodontitis, in murine macrophage-like RAW264.7 cells. MK615 markedly inhibited the phosphorylation of ERK1/2, p38MAPK, and JNK, which is associated with pro-inflammatory mediator release pathways. Moreover, MK615 completely blocked LPS-triggered NF-kappaB activation. The present results suggest that MK615 has potential as a therapeutic agent for treating inflammatory diseases such as periodontitis.

Для цитирования: Morimoto Yoko, Kikuchi Kiyoshi, Ito Takashi, Tokuda Masayuki, Matsuyama Takashi, Noma Satoshi, Hashiguchi Teruto, Torii Mitsuo, Maruyama Ikuro, Kawahara Ko-Ichi. MK615 attenuates Porphyromonas gingivalis lipopolysaccharide-induced pro-inflammatory cytokine release via MAPK inactivation in murine macrophage-like RAW264.7 cells.. Biochemical and biophysical research communications. 2009. DOI: 10.1016/j.bbrc.2009.08.103.

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