Results 1 to 10 of about 34,491 (205)

Molecular Pathways Driving Omeprazole Nephrotoxicity [PDF]

open access: yesRedox Biology, 2020
Omeprazole, a proton pump inhibitor used to treat peptic ulcer and gastroesophageal reflux disease, has been associated to chronic kidney disease and acute interstitial nephritis. However, whether omeprazole is toxic to renal cells is unknown. Omeprazole
Maria Dolores Sanchez-niño   +2 more
exaly   +4 more sources

Omeprazole-Domperidone Fixed Dose Combination vs Omeprazole Monotherapy: A Phase 4, Open-Label, Comparative, Parallel Randomized Controlled Study in Mild to Moderate Gastroesophageal Reflux Disease

open access: yesClinical Medicine Insights: Gastroenterology, 2017
Aim: To compare the efficacy and safety of omeprazole-domperidone combination vs omeprazole monotherapy in gastroesophageal reflux disease (GERD). Methods: In a comparative, randomized controlled, phase 4 study, outpatients with GERD were randomly ...
KY Marakhouski   +3 more
doaj   +3 more sources

Acid-Neutralizing Omeprazole Formulation for Rapid Release and Absorption

open access: yesPharmaceutics
Background/Objectives: Omeprazole undergoes degradation in acidic conditions, which makes it unstable in low pHs found in the gastric environment. The vast majority of already marketed omeprazole formulations use enteric polymer coatings to protect the ...
Sreela Ramesh   +6 more
doaj   +2 more sources

Impact of obesity and roux‐en‐Y gastric bypass on the pharmacokinetics of (R)‐ and (S)‐omeprazole and intragastric pH [PDF]

open access: yesCPT: Pharmacometrics & Systems Pharmacology
This study employed physiologically‐based pharmacokinetic–pharmacodynamics (PBPK/PD) modeling to predict the effect of obesity and gastric bypass surgery on the pharmacokinetics and intragastric pH following omeprazole treatment.
Leandro F. Pippa   +7 more
doaj   +2 more sources

Binding of omeprazole to protein targets identified by monoclonal antibodies.

open access: yesPLoS ONE, 2020
Omeprazole is the most commonly used proton pump inhibitor (PPI), a class of medications whose therapeutic mechanism of action involves formation of a disulfide linkage to cysteine residues in the H+/K+ ATPase pump on gastric secretory cells.
Naw May Pearl Cartee, Michael M Wang
doaj   +3 more sources

Omeprazole inhibits proliferation and modulates autophagy in pancreatic cancer cells.

open access: yesPLoS ONE, 2011
BackgroundOmeprazole has recently been described as a modulator of tumour chemoresistance, although its underlying molecular mechanisms remain controversial.
Andrej Udelnow   +9 more
doaj   +2 more sources

Omeprazole as a Novel Treatment Option for Giardiasis in Cats [PDF]

open access: yesVeterinary Medicine and Science
Background Giardiasis is a common protozoal infection in cats, often treated with nitroimidazole derivatives such as metronidazole and secnidazole. However, there are concerns about resistance to nitroimidazoles and their adverse effects. Recent in vitro
Murat Kaan Durgut   +6 more
doaj   +2 more sources

Reprocessing Mass Spectra from Therapeutic Drug Monitoring to Unveil Proton Pump Inhibitor Use and Quantify Phenoconversion of Escitalopram Metabolism in CYP2C19-Genotyped Patients. [PDF]

open access: yesClin Pharmacol Ther
Escitalopram is a frequently prescribed antidepressant drug. CYP2C19 genotype is a major determinant of escitalopram metabolism and treatment outcome. However, real‐life studies show a high degree of genotype–phenotype mismatch in escitalopram metabolism.
Hole K   +3 more
europepmc   +2 more sources

Effects of elagolix on the pharmacokinetics of omeprazole and its metabolites in healthy premenopausal women

open access: yesClinical and Translational Science, 2022
This study evaluated the effect of repeated doses of elagolix on the pharmacokinetics (PK) of omeprazole and its metabolites in healthy premenopausal female subjects. Adult premenopausal female subjects (N = 20) received a single oral dose of omeprazole (
Ahmed Nader   +3 more
doaj   +1 more source

Omeprazole and lansoprazole enantiomers induce CYP3A4 in human hepatocytes and cell lines via glucocorticoid receptor and pregnane X receptor axis. [PDF]

open access: yesPLoS ONE, 2014
Benzimidazole drugs lansoprazole and omeprazole are used for treatment of various gastrointestinal pathologies. Both compounds cause drug-drug interactions because they activate aryl hydrocarbon receptor and induce CYP1A genes.
Aneta Novotna, Zdenek Dvorak
doaj   +1 more source

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