2023
DOI: 10.1016/j.heliyon.2023.e21004
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A2BR facilitates the pathogenesis of H. pylori-associated GU by inducing oxidative stress through p38 MAPK phosphorylation

Weihong Tang,
Minchang Guan,
Ze Li
et al.
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“…Treatment with BAY60-6583 (an A2BR agonist) exacerbates gastric ulceration in rats, while PSB1115 (an A2BR antagonist) has the opposite effect. Incubation of GES-1 cells with agonists increased apoptosis, migration, and oxidative stress, effects that are reversed by inhibitors of the p38MAPK pathway ( Tang et al, 2023 ). In summary, combating H. pylori infection can be approached from various angles, and agents such as A2BR antagonists, TLR6 agonists, and SHP1 agonists hold promise as novel therapeutic strategies against H. pylori infection in the future.…”
Section: New Approachesmentioning
confidence: 99%
“…Treatment with BAY60-6583 (an A2BR agonist) exacerbates gastric ulceration in rats, while PSB1115 (an A2BR antagonist) has the opposite effect. Incubation of GES-1 cells with agonists increased apoptosis, migration, and oxidative stress, effects that are reversed by inhibitors of the p38MAPK pathway ( Tang et al, 2023 ). In summary, combating H. pylori infection can be approached from various angles, and agents such as A2BR antagonists, TLR6 agonists, and SHP1 agonists hold promise as novel therapeutic strategies against H. pylori infection in the future.…”
Section: New Approachesmentioning
confidence: 99%