Effects of shinbuto and ninjinto on prostaglandin E 2 production in lipopolysaccharide-treated human gingival fibroblasts
Previously, we revealed that several kampo medicines used for patients with excess and/or medium patterns (kakkonto (TJ-1), shosaikoto (TJ-9), hangeshashinto (TJ-14), and orento (TJ-120)) reduced prostaglandin (PG)E levels using LPS-treated human gingival fibroblasts (HGFs). Recently, we examined ot...
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Veröffentlicht in: | PeerJ (San Francisco, CA) CA), 2017-12, Vol.5, p.e4120, Article e4120 |
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Sprache: | eng |
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Zusammenfassung: | Previously, we revealed that several kampo medicines used for patients with excess and/or medium patterns (kakkonto (TJ-1), shosaikoto (TJ-9), hangeshashinto (TJ-14), and orento (TJ-120)) reduced prostaglandin (PG)E
levels using LPS-treated human gingival fibroblasts (HGFs). Recently, we examined other kampo medicines used for patients with the deficiency pattern [bakumondoto (TJ-29), shinbuto (TJ-30), ninjinto (TJ-32), and hochuekkito (TJ-41)] and the herbs comprising shinbuto and ninjinto using the same experimental model. Shinbuto and ninjinto concentration-dependently reduced LPS-induced PGE
production by HGFs, whereas hochuekkito weakly reduced and bakumondoto did not reduce PGE
production. Shinbuto and ninjinto did not alter cyclooxygenase (COX) activity or the expression of molecules involved in the arachidonic acid cascade. Therefore, we next examined which herbs compromising shinbuto and ninjinto reduce LPS-induced PGE
production. Among these herbs, shokyo (
) and kankyo (
) strongly and concentration-dependently decreased LPS-induced PGE
production. However, both shokyo and kankyo increased the expression of cytosolic phospholipase (cPL)A
but did not affect annexin1 or COX-2 expression. These results suggest that shokyo and kankyo suppress cPLA
activity. We demonstrated that kampo medicines suppress inflammatory responses in patients with the deficiency pattern, and in those with excess or medium patterns. Moreover, kampo medicines that contain shokyo or kankyo are considered to be effective for the treatment of inflammatory diseases. |
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ISSN: | 2167-8359 2167-8359 |
DOI: | 10.7717/peerj.4120 |