Thymol improves barrier function and attenuates inflammatory responses in porcine intestinal epithelial cells during lipopolysaccharide (LPS)-induced inflammation
dc.contributor.author | Omonijo, Faith | |
dc.contributor.author | Liu, Shangxi | |
dc.contributor.author | Hui, Qianru | |
dc.contributor.author | Zhang, Hua | |
dc.contributor.author | Lahaye, Ludovic | |
dc.contributor.author | Bodin, Jean-Christophe | |
dc.contributor.author | Nyachoti, Martin | |
dc.contributor.author | Yang, Chengbo | |
dc.date.accessioned | 2019-02-28T16:06:25Z | |
dc.date.available | 2019-02-28T16:06:25Z | |
dc.date.issued | 2018-12-19 | |
dc.date.submitted | 2019-02-26T23:28:33Z | en |
dc.description.abstract | It is well known that essential oil thymol exhibits anti-bacterial activity. The protective effects of thymol on pig intestine during inflammation is yet to be investigated. In this study, an in vitro (LPS)-induced inflammation model using IPEC-J2 cells was established. Cells were pre-treated with thymol for 1 h and then exposed to LPS for various assays. Interleukin 8 (IL-8) secretion, the mRNA abundance of cytokines, ROS, nutrient transporters, and tight junction proteins was measured. The results showed that LPS stimulation increased IL-8 secretion, reactive oxygen species (ROS) production, and tumor necrosis factor alpha (TNF-α) mRNA abundance (P < 0.05), but the mRNA abundance of sodium-dependent glucose transporter 1 (SGLT1), excitatory amino acid transporter 1 (EAAC1) and H+/peptide cotransporter 1 (PepT1) were decreased (P < 0.05). Thymol blocked ROS production (P < 0.05) and tended to decrease the production of LPS-induced IL-8 secretion (P = 0.0766). The mRNA abundance of IL-8 and TNF-α was reduced by thymol pre-treatment (P < 0.05), but thymol was unable to improve the gene expression of nutrient transporters (P > 0.05). The transepithelial electrical resistance (TEER) was reduced and cell permeability increased by LPS treatment (P < 0.05), but these effects were attenuated by thymol (P < 0.05). Moreover, thymol increased zonula occludens-1 (ZO-1) and actin staining in the cells. However, the mRNA abundance of ZO-1 and occludin-3 was not affected by either LPS or thymol treatments. These results indicated that thymol can enhance barrier function and reduce ROS production and pro-inflammatory cytokine gene expression in the epithelial cells during inflammation. The regulation of barrier function by thymol and LPS may be at post-transcriptional or post-translational levels. | en_US |
dc.identifier.uri | http://hdl.handle.net/1993/33767 | |
dc.language.iso | eng | en_US |
dc.rights | open access | en_US |
dc.subject | Research Subject Categories::FORESTRY, AGRICULTURAL SCIENCES and LANDSCAPE PLANNING | en_US |
dc.subject | Animal Science | en_US |
dc.title | Thymol improves barrier function and attenuates inflammatory responses in porcine intestinal epithelial cells during lipopolysaccharide (LPS)-induced inflammation | en_US |
dc.type | Article | en_US |