Chloroform fraction of Solanum tuberosum L. cv Jayoung epidermis suppresses LPS-induced inflammatory responses in macrophages and DSS-induced colitis in mice
[Display omitted] •CFPJ is chloroform fraction isolated from peel of ‘Jayoung’, a color-fleshed potato.•CFPJ inhibited the LPS-induced iNOS, COX-2, and cytokine expressions in macrophages.•CFPJ suppressed the LPS-induced activation of NF-κB/IκB-α and p38/MKK signaling.•CFPJ attenuated the DSS-induce...
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Veröffentlicht in: | Food and chemical toxicology 2014-01, Vol.63, p.53-61 |
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Hauptverfasser: | , , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
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•CFPJ is chloroform fraction isolated from peel of ‘Jayoung’, a color-fleshed potato.•CFPJ inhibited the LPS-induced iNOS, COX-2, and cytokine expressions in macrophages.•CFPJ suppressed the LPS-induced activation of NF-κB/IκB-α and p38/MKK signaling.•CFPJ attenuated the DSS-induced colitis severity assessed by DAI and colon length.•CFPJ suppressed the production of pro-inflammatory mediators in DSS-induced colitis.
In this study, the authors investigated the molecular mechanism underlying the antiinflammatory effects of the chloroform fraction of the peel of ‘Jayoung’ (CFPJ), a color-fleshed potato, on lipopolysaccharide (LPS)-induced RAW 264.7 macrophages and in mice with dextran sulfate sodium (DSS)-induced colitis. CFPJ inhibited the expressions of inducible nitric oxide synthase (iNOS) and cyclooxygenase-2 (COX-2) at the transcription level, and attenuated the transcriptional activity of nuclear factor-κB (NF-κB) by reducing the translocation of NF-κB depending on degradation of inhibitory κB-α (IκB-α). Furthermore, CFPJ attenuated the phosphorylations of mitogen-activated protein kinase kinases3/6 (MKK3/6) and of p38. In colitis model, CFPJ significantly reduced the severity of colitis and the productions and protein levels of pro-inflammatory mediators in colonic tissue. These results suggest that the anti-inflammatory effects of CFPJ are associated with the suppression of NF-κB and p38 activation in macrophages, and support its possible therapeutic role for the treatment of colitis. |
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ISSN: | 0278-6915 1873-6351 |
DOI: | 10.1016/j.fct.2013.10.040 |