Journal
JOURNAL OF PARENTERAL AND ENTERAL NUTRITION
Volume 27, Issue 3, Pages 176-180Publisher
WILEY
DOI: 10.1177/0148607103027003176
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Funding
- NIDDK NIH HHS [K08 DK60778-01] Funding Source: Medline
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Background: Lipopolysaccharide (LPS)-stimulated macrophages (MPhi) produce excess tumor necrosis factor (TNF), and the direct inhibition of IKB phosphorylation and its subsequent separation from the nuclear factor kappaB (NFkappaB)-IkappaB complex has been experimentally supported as a mechanism for omega-3 fatty acid (FA) inhibition of this TNF response. However, TNF production is a late event in the LPS-induced MPhi inflammatory cascade, and in addition to NFkappaB-associated pathways, a separate transcription factor, activator protein-1 (A-P-1) is an important pathway for MPhi proinflammatory cytokine production. The mitogen-activated protein kinase (MAPK) cascade regulates both NFkappaB-IkappaB and AP-1-associated gene transcription through several cross-amplifying phosphorylation kinases, specifically p44/42 [ie, extracellular signal-regulated kinase (ERK) 1/2], p38, and c/jun N-terminal kinase (JNK)/stress-activated protein kinase (SAPK). The activation of these kinases occurs in the proximal MAPK cascade and activation modulates AP-1 activation. In this set of experiments, it was hypothesized that inhibition of ALA-PK signaling phosphorylation kinases by omega-3 fatty acids in a model of LPS-stimulated MPhis would alter the activation of the proinflammatory cytokine transcription factor AP-1. Methods: RAW 264.7 cells were pretreated with a sterile, commercially available, pharmaceutical grade omega-3 FA emulsion, equivalent grade omega-6 FA emulsion, or Dulbecco's modified eagles medium (media alone) for 4 hours. Cells were washed twice and exposed to LPS for 15 minutes. Total cell lysates were collected, and both total and phosphorylated portions of the p44/42, p38, and JNK/SAPK proteins were determined by Western blotting. AP-1 nuclear translocation was determined by electromobility shift assay. Results: Phosphorylation of p44/42 and JNK/SAPK proteins of the MAPK pathways in LPS-stimulated MPhis was significantly reduced by omega-3 FA treatment compared with MPhi treated with omega-6 FA or media alone. In contrast, phosphorylation of p38 was not inhibited in the presence of omega-3 or omega-6 FA treatment compared with media alone. omega-3 FA pretreatment inhibited A-P-1 activation. Conclusions: omega-3 FA inhibited p44/42 and JNK/SAPK phosphorylation; however, p38 remained unchanged. Phosphorylation of p44/42 and JNK/SAPK are the immediate prior steps in AP-1 activation. Attenuated AP-1 activation and subsequent attenuated gene-level proinflammatory cytokine elaboration is anticipated after inhibition of these MAPK intermediates and is confirmed by the reduction in A-P-1 activity. These results provide further evidence for the transcriptional level regulation in. the elaboration of proinflammatory cytokines by omega-3 FA in this MPhi model.
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