The ginger component 6-shogaol prevents TNF-α-induced barrier loss via inhibition of PI3K/Akt and NF-κB signaling
Autor: | Jörg D. Schulzke, Julia Luettig, Susanne M. Krug, Rita Rosenthal, In-Fah M. Lee |
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Rok vydání: | 2016 |
Předmět: |
0301 basic medicine
Anti-Inflammatory Agents Catechols Ginger Biology Tight Junctions Phosphatidylinositol 3-Kinases 03 medical and health sciences Downregulation and upregulation Claudin-1 Humans Protein kinase B PI3K/AKT/mTOR pathway B-Lymphocytes Tight junction Tumor Necrosis Factor-alpha NF-kappa B NFKB1 Up-Regulation Cell biology Intestines 030104 developmental biology Biochemistry Claudins Phosphorylation Tumor necrosis factor alpha Caco-2 Cells Signal transduction HT29 Cells Signal Transduction Food Science Biotechnology |
Zdroj: | Molecular Nutrition & Food Research. 60:2576-2586 |
ISSN: | 1613-4125 |
DOI: | 10.1002/mnfr.201600274 |
Popis: | cope Anti-inflammatory properties of the ginger-derived pungent component 6-shogaol (6-SG) have been studied intensively in recent years. Purpose of this study was to characterize the influence of 6-SG on inflammation-related intestinal barrier dysfunction, especially its paracellular component. Methods and results The effect of 6-SG was studied in the human intestinal cell models HT-29/B6 and Caco-2 either under control conditions or challenged by the pro-inflammatory cytokine tumor necrosis factor α (TNF-α). Electrophysiological measurements, freeze-fracture electron microscopy, and protein analyses were performed. 6-SG partially prevented both, the TNF-α-induced decrease in transepithelial resistance and the rise in fluorescein permeability. By inhibiting phosphatidylinositol-3-kinase/Akt signaling 6-SG prevented the TNF-α-induced increase in protein expression of claudin-2, a channel-forming tight junction protein. In addition, the TNF-α-induced disassembly of the sealing tight junction protein claudin-1 was attenuated, the latter of which was due to TNF-α-triggered phosphorylation of nuclear factor kappa light chain enhancer of activated B cells (NF-κB). Conclusion 6-SG has barrier-protective effects by affecting TNF-α-induced claudin-2 upregulation and claudin-1 disassembly via inhibition of phoshatidylinositol-3-kinase/Akt and nuclear factor kappa light chain enhancer of activated B-cell signaling. Therefore, 6-SG-containing food might be beneficial for barrier preservation during intestinal inflammation. |
Databáze: | OpenAIRE |
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