The Protease Inhibitor Darunavir Prevents Esophagitis and Impairments in Esophageal Barrier Function in a Mouse Model of GERD

. GERD induced inflammation, with significant increases in edema, MPO, KC, DIS, histological changes and HIF-2α, and disrupted barrier function, reducing ZO-1 and OCLD levels. All these alterations were significantly reversed in darunavir-treated animals. These findings demonstrate that darunavir, a clinically available drug with anti-pepsin properties, inhibits GERD-induced inflammation and HIF-2α activation, preserving tight junction proteins and mucosal integrity. Thus, darunavir could be repurposed as a novel therapeutic option for GERD.

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Publication Details

Journal
American Journal of Physiology-Gastrointestinal and Liver Physiology
Published
2026-04-21
DOI
https://doi.org/10.1152/ajpgi.00058.2025
Primary Topic
Gastroesophageal reflux and treatments
Type
article
Field-Weighted Citation Impact
0.00

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article

The Protease Inhibitor Darunavir Prevents Esophagitis and Impairments in Esophageal Barrier Function in a Mouse Model of GERD

Alexandre Havt, Álvaro Xavier Franco, Humberto Barbosa da Costa Filho, Thiago M. Sales et al.
American Journal of Physiology-Gastrointestinal and Liver Physiology
Gastroesophageal reflux and treatments
article

The Protease Inhibitor Darunavir Prevents Esophagitis and Impairments in Esophageal Barrier Function in a Mouse Model of GERD

Alexandre Havt, Álvaro Xavier Franco, Humberto Barbosa da Costa Filho, Thiago M. Sales, Stuart Jon Spechler, Antonio Carlos Pereira de Oliveira, Pedro Marcos Gomes Soares, Lara Mara Gomes Da Silva, a de Castro Lopes, Marcellus Henrique Loiola Ponte de Souza, Lucas Antônio Duarte Nicolau, CN Monteiro, Marco Antônio de Freitas Clementino, Ananda Moara Lima Daniel, Rhonda Frances Souza, Antonia Beatriz Alves Ferreira, Sarah Antonieli Carneiro Alicrim
article en

Abstract

. GERD induced inflammation, with significant increases in edema, MPO, KC, DIS, histological changes and HIF-2α, and disrupted barrier function, reducing ZO-1 and OCLD levels. All these alterations were significantly reversed in darunavir-treated animals. These findings demonstrate that darunavir, a clinically available drug with anti-pepsin properties, inhibits GERD-induced inflammation and HIF-2α activation, preserving tight junction proteins and mucosal integrity. Thus, darunavir could be repurposed as a novel therapeutic option for GERD.

American Journal of Physiology-Gastrointestinal and Liver Physiology
Universidade Federal do Ceará (BR), Baylor University Medical Center (US)
Conselho Nacional de Desenvolvimento Científico e Tecnológico
Good health and well-being
Openalex Percentile: Top 11%
Gastroesophageal reflux and treatments
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