{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"omics_type":["Unknown"],"volume":["36(5)"],"submitter":["Roche-Catholy M"],"funding":["Vetoquinol"],"pubmed_abstract":["<h4>Background</h4>In people and dogs, torasemide has higher bioavailability, longer half-life, and longer duration of action than equivalent doses of furosemide but data regarding pharmacological properties of torasemide in cats are limited.<h4>Objective</h4>To assess pharmacokinetic and pharmacodynamic parameters of torasemide in healthy cats, and to investigate the effects of a single administration of torasemide on indicators of diuresis, plasma creatinine concentration, blood pressure, electrolyte concentrations and markers of the renin-angiotensin-aldosterone system (RAAS).<h4>Animals</h4>Six clinically healthy adult European shorthair cats.<h4>Methods</h4>Randomized 4-period crossover design with 3 groups and 4 treatments. Pharmacokinetic parameters were obtained using a noncompartmental analysis, and the clinically effective dose was assessed using a Hill model.<h4>Results</h4>Mean absolute bioavailability was estimated at 88.1%. Mean total body clearance was 3.64 mL/h/kg and mean terminal half-life was 12.9 hours. Urine output significantly increased after torasemide administration (P < .001). The urine sodium : potassium ratio (uNa : uK) paralleled and was statistically correlated to urine output (P < .001). Administration of a single torasemide dose led to a significant dose-dependent increase in urine aldosterone : creatinine ratio (uAldo : C; P < .001) and a transient decrease in plasma potassium concentration (P < .001) but did not affect blood pressure or plasma creatinine concentration.<h4>Conclusions and clinical importance</h4>A single torasemide dose leads to a significant increase in diuresis and renin-angiotensin-aldosterone system (RAAS) activation in healthy cats, with high absolute bioavailability, and without clinically relevant adverse effects. Pharmacokinetic parameters indicate that once daily dosing of 0.27 mg/kg may be appropriate in a clinical setting."],"journal":["Journal of veterinary internal medicine"],"pagination":["1782-1791"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC9511087"],"repository":["biostudies-literature"],"pubmed_title":["Pharmacokinetic and pharmacodynamic properties of orally administered torasemide in healthy cats."],"pmcid":["PMC9511087"],"pubmed_authors":["de Salazar Alcala AG","Paepe D","Smets P","Schneider M","Hellemans A","Roche-Catholy M","Woehrle F","Devreese M","Broeckx BJG"],"additional_accession":[]},"is_claimable":false,"name":"Pharmacokinetic and pharmacodynamic properties of orally administered torasemide in healthy cats.","description":"<h4>Background</h4>In people and dogs, torasemide has higher bioavailability, longer half-life, and longer duration of action than equivalent doses of furosemide but data regarding pharmacological properties of torasemide in cats are limited.<h4>Objective</h4>To assess pharmacokinetic and pharmacodynamic parameters of torasemide in healthy cats, and to investigate the effects of a single administration of torasemide on indicators of diuresis, plasma creatinine concentration, blood pressure, electrolyte concentrations and markers of the renin-angiotensin-aldosterone system (RAAS).<h4>Animals</h4>Six clinically healthy adult European shorthair cats.<h4>Methods</h4>Randomized 4-period crossover design with 3 groups and 4 treatments. Pharmacokinetic parameters were obtained using a noncompartmental analysis, and the clinically effective dose was assessed using a Hill model.<h4>Results</h4>Mean absolute bioavailability was estimated at 88.1%. Mean total body clearance was 3.64 mL/h/kg and mean terminal half-life was 12.9 hours. Urine output significantly increased after torasemide administration (P < .001). The urine sodium : potassium ratio (uNa : uK) paralleled and was statistically correlated to urine output (P < .001). Administration of a single torasemide dose led to a significant dose-dependent increase in urine aldosterone : creatinine ratio (uAldo : C; P < .001) and a transient decrease in plasma potassium concentration (P < .001) but did not affect blood pressure or plasma creatinine concentration.<h4>Conclusions and clinical importance</h4>A single torasemide dose leads to a significant increase in diuresis and renin-angiotensin-aldosterone system (RAAS) activation in healthy cats, with high absolute bioavailability, and without clinically relevant adverse effects. Pharmacokinetic parameters indicate that once daily dosing of 0.27 mg/kg may be appropriate in a clinical setting.","dates":{"release":"2022-01-01T00:00:00Z","publication":"2022 Sep","modification":"2026-06-20T03:25:16.377Z","creation":"2025-04-04T12:04:50.128Z"},"accession":"S-EPMC9511087","cross_references":{"pubmed":["35906901"],"doi":["10.1111/jvim.16500"]}}