Abstract
Exclusive enteral nutrition using polymeric formula (PF) is a well-established therapeutic option for active Crohn's disease; however, its mechanisms of action are unknown. We investigated the anti-inflammatory effects of PF in an in vitro model of epithelial cell inflammation. PF did not affect cell viability over a range of dilutions, but when PF was added to the culture medium the interleukin (IL)-8 response to proinflammatory stimuli was significantly reduced. This effect was due to PF acting directly on the cells as the IL-8 response was still reduced when PF was separated from the proinflammatory stimuli in a 2-compartment system. In the presence of PF, nuclear factor (NF)-kappaB nuclear migration was not inhibited; however, IkappaBalpha degradation was delayed. PF has direct anti-inflammatory effects upon immortalized colonic enterocytes. Therefore PF may, in part, modulate gut inflammation by directly reducing the inflammatory response of the intestinal epithelium.
MeSH terms
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Blotting, Western
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Cell Survival / drug effects
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Cells, Cultured
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Culture Media
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Drug Combinations
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Enterocytes / drug effects
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Enterocytes / metabolism
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Enterocytes / pathology
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Enzyme-Linked Immunosorbent Assay
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HT29 Cells / drug effects
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HT29 Cells / metabolism
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HT29 Cells / pathology
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Humans
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Immunoglobulin G / therapeutic use*
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Inflammatory Bowel Diseases / drug therapy*
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Inflammatory Bowel Diseases / metabolism
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Inflammatory Bowel Diseases / pathology
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Interleukin-1alpha / therapeutic use*
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Interleukin-8 / metabolism
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Lipopolysaccharides / therapeutic use*
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NF-kappa B / drug effects
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NF-kappa B / metabolism
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Transcription Factor RelA / therapeutic use*
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Transforming Growth Factor beta / therapeutic use*
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Tumor Necrosis Factor-alpha / therapeutic use*
Substances
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Culture Media
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Drug Combinations
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Immunoglobulin G
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Interleukin-1alpha
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Interleukin-8
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Lipopolysaccharides
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NF-kappa B
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TONSL protein, human
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Transcription Factor RelA
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Transforming Growth Factor beta
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Tumor Necrosis Factor-alpha