Inhibition of Lipopolysaccharide-Induced Inflammatory Signaling by Soft Coral-Derived Prostaglandin A 2 in RAW264.7 Cells.
Osamu OhnoEika MizunoJunichiro MiyamotoTomoyuki HoshinaTakuya SanoKenji MatsunoPublished in: Marine drugs (2022)
Lipopolysaccharide (LPS) is a component of the outer membrane of Gram-negative bacteria and causes inflammatory diseases. We searched MeOH extracts of collected marine organisms for inhibitors of LPS-induced nitric oxide (NO) production in RAW264.7 cells and identified prostaglandin A 2 (PGA 2 ) as an active compound from the MeOH extract of the soft coral Lobophytum sp. PGA 2 inhibited the production of NO and reduced the expression of inducible NO synthase (iNOS) in LPS-stimulated RAW264.7 cells. Although short preincubation with PGA 2 did not inhibit LPS-induced degradation and resynthesis of IκBα, the suppressive effect of PGA 2 was observed only after a prolonged incubation period prior to LPS treatment. In addition, PGA 2 -inhibited NO production was negated by the addition of the EP4 antagonist L161982. Thus, PGA 2 was identified as an inhibitor of LPS-induced inflammatory signaling in RAW264.7 cells.
Keyphrases
- lps induced
- inflammatory response
- lipopolysaccharide induced
- induced apoptosis
- cell cycle arrest
- oxidative stress
- nitric oxide
- toll like receptor
- endoplasmic reticulum stress
- poor prognosis
- cell death
- anti inflammatory
- hydrogen peroxide
- signaling pathway
- cell proliferation
- replacement therapy
- nitric oxide synthase
- pi k akt
- multidrug resistant