Author
Listed:
- Rajbir Singh
(University of Louisville)
- Sandeep Chandrashekharappa
(Institute for Stem Cell Biology and Regenerative Medicine (inStem), GKVK campus)
- Sobha R. Bodduluri
(University of Louisville)
- Becca V. Baby
(University of Louisville)
- Bindu Hegde
(University of Louisville)
- Niranjan G. Kotla
(Institute for Stem Cell Biology and Regenerative Medicine (inStem), GKVK campus)
- Ankita A. Hiwale
(Institute for Stem Cell Biology and Regenerative Medicine (inStem), GKVK campus)
- Taslimarif Saiyed
(Centre for Cellular and Molecular Platforms (C-CAMP), GKVK campus)
- Paresh Patel
(Centre for Cellular and Molecular Platforms (C-CAMP), GKVK campus)
- Matam Vijay-Kumar
(University of Toledo College of Medicine and Life Sciences)
- Morgan G. I. Langille
(Dalhousie University)
- Gavin M. Douglas
(Dalhousie University)
- Xi Cheng
(University of Toledo College of Medicine and Life Sciences)
- Eric C. Rouchka
(University of Louisville)
- Sabine J. Waigel
(University of Louisville)
- Gerald W. Dryden
(University of Louisville)
- Houda Alatassi
(University of Louisville)
- Huang-Ge Zhang
(University of Louisville)
- Bodduluri Haribabu
(University of Louisville)
- Praveen K. Vemula
(Institute for Stem Cell Biology and Regenerative Medicine (inStem), GKVK campus)
- Venkatakrishna R. Jala
(University of Louisville)
Abstract
The importance of gut microbiota in human health and pathophysiology is undisputable. Despite the abundance of metagenomics data, the functional dynamics of gut microbiota in human health and disease remain elusive. Urolithin A (UroA), a major microbial metabolite derived from polyphenolics of berries and pomegranate fruits displays anti-inflammatory, anti-oxidative, and anti-ageing activities. Here, we show that UroA and its potent synthetic analogue (UAS03) significantly enhance gut barrier function and inhibit unwarranted inflammation. We demonstrate that UroA and UAS03 exert their barrier functions through activation of aryl hydrocarbon receptor (AhR)- nuclear factor erythroid 2–related factor 2 (Nrf2)-dependent pathways to upregulate epithelial tight junction proteins. Importantly, treatment with these compounds attenuated colitis in pre-clinical models by remedying barrier dysfunction in addition to anti-inflammatory activities. Cumulatively, the results highlight how microbial metabolites provide two-pronged beneficial activities at gut epithelium by enhancing barrier functions and reducing inflammation to protect from colonic diseases.
Suggested Citation
Rajbir Singh & Sandeep Chandrashekharappa & Sobha R. Bodduluri & Becca V. Baby & Bindu Hegde & Niranjan G. Kotla & Ankita A. Hiwale & Taslimarif Saiyed & Paresh Patel & Matam Vijay-Kumar & Morgan G. I, 2019.
"Enhancement of the gut barrier integrity by a microbial metabolite through the Nrf2 pathway,"
Nature Communications, Nature, vol. 10(1), pages 1-18, December.
Handle:
RePEc:nat:natcom:v:10:y:2019:i:1:d:10.1038_s41467-018-07859-7
DOI: 10.1038/s41467-018-07859-7
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