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Metabolites of Latilactobacillus curvatus BYB3 and Indole Activate Aryl Hydrocarbon Receptor to Attenuate Lipopolysaccharide-Induced Intestinal Barrier Dysfunction
This study aimed to investigate the effects of the metabolites of Latilactobacillus curvatus BYB3 and indole-activated aryl hydrocarbon receptor (AhR) to increase the tight junction (TJ) proteins in an in vitro model of intestinal inflammation. In a Western blot assay, the metabolites of L. curvatus...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Korean Society for Food Science of Animal Resources
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9647186/ https://www.ncbi.nlm.nih.gov/pubmed/36415578 http://dx.doi.org/10.5851/kosfa.2022.e51 |
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author | Wang, Xing Yong, Cheng Chung Oh, Sejong |
author_facet | Wang, Xing Yong, Cheng Chung Oh, Sejong |
author_sort | Wang, Xing |
collection | PubMed |
description | This study aimed to investigate the effects of the metabolites of Latilactobacillus curvatus BYB3 and indole-activated aryl hydrocarbon receptor (AhR) to increase the tight junction (TJ) proteins in an in vitro model of intestinal inflammation. In a Western blot assay, the metabolites of L. curvatus BYB3 reduced the TJ demage in lipoploysaccharide (LPS) stimulated-Caco-2 cells. This reduction was a result of upregulating the expression of TJ-associated proteins and suppressing the nuclear factor-κB signaling. Immunofluorescence images consistently revealed that LPS disrupted and reduced the expression of TJ proteins, while the metabolites of L. curvatus BYB3 and indole reversed these alterations. The protective effects of L. curvatus BYB3 were observed on the intestinal barrier function when measuring transepithelial electrical resistance. Using high-performance liquid chromatography analysis the metabolites, the indole-3-latic acid and indole-3-acetamide concentrations were found to be 1.73±0.27 mg/L and 0.51±0.39 mg/L, respectively. These findings indicate that the metabolites of L. curvatus BYB3 have increasing mRNA expressions of cytochrome P450 1A1 (CYP1A1) and AhR, and may thus be applicable for therapy of various inflammatory gut diseases as postbiotics. |
format | Online Article Text |
id | pubmed-9647186 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Korean Society for Food Science of Animal Resources |
record_format | MEDLINE/PubMed |
spelling | pubmed-96471862022-11-21 Metabolites of Latilactobacillus curvatus BYB3 and Indole Activate Aryl Hydrocarbon Receptor to Attenuate Lipopolysaccharide-Induced Intestinal Barrier Dysfunction Wang, Xing Yong, Cheng Chung Oh, Sejong Food Sci Anim Resour SPECIAL SECTION ARTICLE: New concept of probiotics for human and animal health This study aimed to investigate the effects of the metabolites of Latilactobacillus curvatus BYB3 and indole-activated aryl hydrocarbon receptor (AhR) to increase the tight junction (TJ) proteins in an in vitro model of intestinal inflammation. In a Western blot assay, the metabolites of L. curvatus BYB3 reduced the TJ demage in lipoploysaccharide (LPS) stimulated-Caco-2 cells. This reduction was a result of upregulating the expression of TJ-associated proteins and suppressing the nuclear factor-κB signaling. Immunofluorescence images consistently revealed that LPS disrupted and reduced the expression of TJ proteins, while the metabolites of L. curvatus BYB3 and indole reversed these alterations. The protective effects of L. curvatus BYB3 were observed on the intestinal barrier function when measuring transepithelial electrical resistance. Using high-performance liquid chromatography analysis the metabolites, the indole-3-latic acid and indole-3-acetamide concentrations were found to be 1.73±0.27 mg/L and 0.51±0.39 mg/L, respectively. These findings indicate that the metabolites of L. curvatus BYB3 have increasing mRNA expressions of cytochrome P450 1A1 (CYP1A1) and AhR, and may thus be applicable for therapy of various inflammatory gut diseases as postbiotics. Korean Society for Food Science of Animal Resources 2022-11 2022-11-01 /pmc/articles/PMC9647186/ /pubmed/36415578 http://dx.doi.org/10.5851/kosfa.2022.e51 Text en © Korean Society for Food Science of Animal Resources https://creativecommons.org/licenses/by-nc/3.0/This is an Open-Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | SPECIAL SECTION ARTICLE: New concept of probiotics for human and animal health Wang, Xing Yong, Cheng Chung Oh, Sejong Metabolites of Latilactobacillus curvatus BYB3 and Indole Activate Aryl Hydrocarbon Receptor to Attenuate Lipopolysaccharide-Induced Intestinal Barrier Dysfunction |
title | Metabolites of Latilactobacillus curvatus BYB3 and
Indole Activate Aryl Hydrocarbon Receptor to Attenuate
Lipopolysaccharide-Induced Intestinal Barrier Dysfunction |
title_full | Metabolites of Latilactobacillus curvatus BYB3 and
Indole Activate Aryl Hydrocarbon Receptor to Attenuate
Lipopolysaccharide-Induced Intestinal Barrier Dysfunction |
title_fullStr | Metabolites of Latilactobacillus curvatus BYB3 and
Indole Activate Aryl Hydrocarbon Receptor to Attenuate
Lipopolysaccharide-Induced Intestinal Barrier Dysfunction |
title_full_unstemmed | Metabolites of Latilactobacillus curvatus BYB3 and
Indole Activate Aryl Hydrocarbon Receptor to Attenuate
Lipopolysaccharide-Induced Intestinal Barrier Dysfunction |
title_short | Metabolites of Latilactobacillus curvatus BYB3 and
Indole Activate Aryl Hydrocarbon Receptor to Attenuate
Lipopolysaccharide-Induced Intestinal Barrier Dysfunction |
title_sort | metabolites of latilactobacillus curvatus byb3 and
indole activate aryl hydrocarbon receptor to attenuate
lipopolysaccharide-induced intestinal barrier dysfunction |
topic | SPECIAL SECTION ARTICLE: New concept of probiotics for human and animal health |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9647186/ https://www.ncbi.nlm.nih.gov/pubmed/36415578 http://dx.doi.org/10.5851/kosfa.2022.e51 |
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