2011
DOI: 10.1007/s11418-011-0552-8
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Phellinus baumii ethyl acetate extract inhibits lipopolysaccharide-induced iNOS, COX-2, and proinflammatory cytokine expression in RAW264.7 cells

Abstract: Mushrooms are valuable sources of biologically active compounds possessing anticancer, antiplatelet, and anti-inflammatory properties. Phellinus baumii is a mushroom used in folk medicine for a variety of human diseases. However, its potential anti-inflammatory effect has remained unclear. Therefore, we studied the effect of P. baumii ethyl acetate extract (PBEAE) on inflammatory mediator and proinflammatory cytokine protein and/or mRNA expression levels using the nitric oxide (NO) assay, enzyme immunoassay (E… Show more

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Cited by 30 publications
(17 citation statements)
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“…In addition, macrophages express iNOS that signals for production of NO encouraging a highly microbicidal environment [69]. The overproduction of NO further stimulates synthesis of COX-2 that functions in conversion of arachidonic acid to prostaglandins [71, 72]. …”
Section: Resultsmentioning
confidence: 99%
“…In addition, macrophages express iNOS that signals for production of NO encouraging a highly microbicidal environment [69]. The overproduction of NO further stimulates synthesis of COX-2 that functions in conversion of arachidonic acid to prostaglandins [71, 72]. …”
Section: Resultsmentioning
confidence: 99%
“…12,13 Among them, the extracts of P. baumii and P. linteus have recently found to have anti-inflammatory effects in LPS-induced RAW264.7 cells. 14,15 Hispidin is the basic styrylpyrone-type polyphenol pigment in Phellinus and Inonotus species. Mushroom-derived styrylpyrone pigments may function similarly to plant flavonoids due to their structural similarity.…”
Section: Discussionmentioning
confidence: 99%
“…NO and cell viability assays were performed as described during our previous work [18]. Briefly, RAW264.7 cells (1×10 6 cells/mL) were pre-incubated with RGSF (25, 50, 100, and 200 μg/mL) or vehicle for 30 min and then stimulated with LPS (100 ng/mL) for 18 h. One-hundred microliter of cell supernatant from each well were transferred into 96-well microplates and mixed with an equal volume of Griess reagent at room temperature.…”
Section: Methodsmentioning
confidence: 99%