| Autor: |
Miyazawa, Shinano, Sakai, Misa, Omae, Yuma, Ogawa, Yusuke, Shigemori, Hideyuki, Miyamae, Yusaku |
| Předmět: |
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| Zdroj: |
Bioscience, Biotechnology & Biochemistry; Oct2024, Vol. 88 Issue 10, p1136-1143, 8p |
| Abstrakt: |
Peroxisome proliferator-activated receptor γ (PPARγ) belongs to the nuclear receptor superfamily and is involved in the inflammatory process. Previously, we synthesized the ligands of PPARγ that possess the hybrid structure of a food-derived cinnamic acid derivative (CA) and GW9662, an irreversible PPARγ antagonist. These ligands activate the transcription of PPARγ through the covalent bond formation with the Cys285 residue of PPARγ, whereas their anti-inflammatory effect has not been examined yet. Here, we show the anti-inflammatory effect of the covalent PPARγ ligands in RAW264 cells, murine macrophage-like cells. GW9662 suppressed the production of nitric oxide (NO) stimulated by lipopolysaccharide and exerted a synergistic effect in combination with CA. The compounds bearing their hybrid structure dramatically inhibited NO production and transcription of proinflammatory cytokines. A comparison study suggested that the 2-chloro-5-nitrobenzoyl group of the ligands is important for anti-inflammation. Furthermore, we synthesized an alkyne-tagged analogue that becomes an activity-based probe for future mechanistic study. [ABSTRACT FROM AUTHOR] |
| Databáze: |
Supplemental Index |
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