Gut microbiome drives glycodeoxycholic acid-mediated attenuation of hypertension

Gut microbiota and bile acids are increasingly recognized to regulate blood pressure, but the mechanisms remain unclear. Takeda G-protein coupled receptor 5 (TGR5) is a major receptor for secondary bile acids. We hypothesized that loss of TGR5 function remodels gut microbiota and influences blood pressure. Using CRISPR/Cas9, TGR5 knockout (Tgr5KO) rats on the Dahl Salt-Sensitive (S) background were generated and characterized. Compared to the control S rats, Tgr5KO rats demonstrated significantly lower blood pressure, a distinct shift in gut microbiota composition, and an increase in the secondary bile acid, particularly, glycodeoxycholic acid. Supplementation of glycodeoxycholic acid to the control S rats produced a similar gut microbial shift and lowered blood pressure. Furthermore, cecal microbiota transplantation from Tgr5KO to control S rats lowered blood pressure in the recipient rats. This first loss-of-function study demonstrates that deletion of TGR5 remodels gut microbiota, increases glycodeoxycholic acid, and lowers blood pressure regardless of TGR5 signaling status, identifying a promising gut–liver axis target for lowering hypertension.

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Publication Details

Journal
Gut Microbes
Published
2026-06-24
DOI
https://doi.org/10.1080/19490976.2026.2691346
Primary Topic
Gut microbiota and health
Type
article
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article

Gut microbiome drives glycodeoxycholic acid-mediated attenuation of hypertension

Pritam Bardhan, Ishan Manandhar, Wisdom Ahlidja, Tao Yang et al.
Gut Microbes
Gut microbiota and health
article

Gut microbiome drives glycodeoxycholic acid-mediated attenuation of hypertension

Pritam Bardhan, Ishan Manandhar, Wisdom Ahlidja, Tao Yang, Sanjana Kumariya, Sareh Zeydabadinejad, Sachin Aryal, Matam Vijay–Kumar, Lavanya Reddivari, Sudhan Pachhain, Beng San Yeoh, Piu Saha, Oluwatosin Mautin Akinola, Islam Osman, Charles Thodeti, Narendra Kondapalli, Ramakumar Tummala, Blair Mell, Bina Joe
article en

Abstract

Gut microbiota and bile acids are increasingly recognized to regulate blood pressure, but the mechanisms remain unclear. Takeda G-protein coupled receptor 5 (TGR5) is a major receptor for secondary bile acids. We hypothesized that loss of TGR5 function remodels gut microbiota and influences blood pressure. Using CRISPR/Cas9, TGR5 knockout (Tgr5KO) rats on the Dahl Salt-Sensitive (S) background were generated and characterized. Compared to the control S rats, Tgr5KO rats demonstrated significantly lower blood pressure, a distinct shift in gut microbiota composition, and an increase in the secondary bile acid, particularly, glycodeoxycholic acid. Supplementation of glycodeoxycholic acid to the control S rats produced a similar gut microbial shift and lowered blood pressure. Furthermore, cecal microbiota transplantation from Tgr5KO to control S rats lowered blood pressure in the recipient rats. This first loss-of-function study demonstrates that deletion of TGR5 remodels gut microbiota, increases glycodeoxycholic acid, and lowers blood pressure regardless of TGR5 signaling status, identifying a promising gut–liver axis target for lowering hypertension.

Gut MicrobesVol. 18(1)
University of Toledo (US)
Good health and well-being
Openalex Percentile: Top 10%
Gut microbiota and health
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