{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,2]],"date-time":"2026-10-02T20:17:06Z","timestamp":1790972226846,"version":"4.1.0"},"reference-count":22,"publisher":"Wiley","issue":"3","license":[{"start":{"date-parts":[[2000,5,1]],"date-time":"2000-05-01T00:00:00Z","timestamp":957139200000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["J Parenter Enteral Nutr"],"published-print":{"date-parts":[[2000,5]]},"abstract":"<jats:p><jats:italic>Background:<\/jats:italic> Mitogen\u2010activated protein kinase (MAPK) cascades represent a major signal system to transduce extracellular signals into cellular responses. Overactivity of MAPK has been implicated in the development of many diseases, including cancer and sepsis. This study investigated the hypothesis that fish oil altered the membrane phospholipid composition and modulated MAPK activity. <jats:italic>Methods:<\/jats:italic> RAW 264.7 cells, a mouse macrophage (M(\u03d5) cell line, were grown in eicosapentaenoic acid (EPA)\u2010rich media (114 \u03bcmol\/L) for 48 hours. M\u03d5 were washed and exposed to <jats:italic>Escherichia coli<\/jats:italic> lipopolysaccharide (LPS; 1 \u03bcg\/mL) for 10 minutes. Both total and activated (phosphorylated) portions of MAPK (P44 and P42) were determined by Western blot assays. AP\u20101 transcription factor activity was determined by electrophoretic mobility gel shift assays (EMSA). M\u03d5 tumor necrosis factor (TNF) mRNA expression was measured by Northern blot assays. <jats:italic>Results:<\/jats:italic> LPS stimulation induced RAW cell phosphorylation of P44\/P42. In contrast, RAW cells grown in EPA\u2010rich media had less P44\/P42 activation in the presence of LPS. Total P44\/P42 were not affected by EPA or LPS. Similarly, EPA also inhibited AP\u20101 activity. Inhibition of P44\/P42 activity with PD98059 reduced both AP\u20101 activity and TNF mRNA expression of LPS\u2010stimulated M\u03d5. <jats:italic>Conclu<\/jats:italic>sions: Our data suggest that fish oil regulates macrophage proinflammatory gene activation, at least in part, by modulating the MAPK activity. <jats:italic>(Journal of Parenteral and Enteral Nutrition<\/jats:italic> <jats:bold>24:159\u2013163,<\/jats:bold> 2000)<\/jats:p>","DOI":"10.1177\/0148607100024003159","type":"journal-article","created":{"date-parts":[[2008,5,14]],"date-time":"2008-05-14T19:51:26Z","timestamp":1210794686000},"page":"159-163","source":"Crossref","is-referenced-by-count":60,"title":["Fish Oil Modulates Macrophage P44\/P42 Mitogen\u2010Activated Protein Kinase Activity Induced By Lipopolysaccharide"],"prefix":"10.1002","volume":"24","author":[{"given":"Chong\u2010Jeh","family":"Lo","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Ken 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