A Role for High Mobility Group Box 1 (<scp>HMGB1</scp>) Release in the Pathogenesis of Gastroesophageal Reflux Disease

Release of HMGB1 from esophageal epithelial cells by weakly acidic bile salts, inhibited by curcumin, and increased expression of TLR4 and RAGE in ERD mucosa suggest this pathway has a role in GORD. Modulating HMGB1 activity may be a strategy for treating recurrent symptoms.

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Publication Details

Journal
Neurogastroenterology & Motility
Published
2025-05-20
DOI
https://doi.org/10.1111/nmo.70083
Citations
1
Primary Topic
Gastroesophageal reflux and treatments
Type
article
Field-Weighted Citation Impact
1.81

Funders

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article

A Role for High Mobility Group Box 1 (HMGB1) Release in the Pathogenesis of Gastroesophageal Reflux Disease

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1 citations
Neurogastroenterology & Motility
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article

A Role for High Mobility Group Box 1 (HMGB1) Release in the Pathogenesis of Gastroesophageal Reflux Disease

Madusha Peiris, Philip Woodland, Diana C. Blaydon, Tom Leech, David P. Kelsell
article en
1 citations

Abstract

Release of HMGB1 from esophageal epithelial cells by weakly acidic bile salts, inhibited by curcumin, and increased expression of TLR4 and RAGE in ERD mucosa suggest this pathway has a role in GORD. Modulating HMGB1 activity may be a strategy for treating recurrent symptoms.

Neurogastroenterology & MotilityVol. 37(11)
Queen Mary University of London (GB)
Reckitt Benckiser Pharmaceuticals
Good health and well-being
Openalex Percentile: Top 17%
Gastroesophageal reflux and treatments
1.81
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