Pharmacokinetics of cimetidine in dogs after oral administration of cimetidine tablets

Long-term oral treatment with cimetidine is recommended to reduce vomiting in dogs with chronic gastritis. Despite this, few studies have specifically examined the plasma disposition and pharmacokinetics of cimetidine in dogs, particularly following repeated oral administration. The pharmacokinetics...

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Veröffentlicht in:Journal of veterinary pharmacology and therapeutics 2009-06, Vol.32 (3), p.213-218
Hauptverfasser: LE TRAON, G, BURGAUD, S, HORSPOOL, L.J.I
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container_title Journal of veterinary pharmacology and therapeutics
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creator LE TRAON, G
BURGAUD, S
HORSPOOL, L.J.I
description Long-term oral treatment with cimetidine is recommended to reduce vomiting in dogs with chronic gastritis. Despite this, few studies have specifically examined the plasma disposition and pharmacokinetics of cimetidine in dogs, particularly following repeated oral administration. The pharmacokinetics of cimetidine following oral administration as tablets was investigated in healthy dogs. Cimetidine was absorbed rapidly post-treatment (tmax = 0.5 h). A mean absolute bioavailability of 75% was calculated following a single oral administration of 5 mg cimetidine/kg body weight. After intravenous administration, a plasma half-life of 1.6 h was calculated. Repeated oral administration at the recommended dose rate and regime (5 mg/kg body weight three times daily) for 30 consecutive days did not lead to any accumulation of cimetidine in plasma. Food intake concomitant with oral administration of cimetidine delayed (tmax = 2.25 h) and decreased the rate and extent of absorption (AUC) by about 40%. Cimetidine was well absorbed in fasted dogs. Administration of food decreased the bioavailability of cimetidine by 40%. Cimetidine does not accumulate over time in plasma when administered long term to dogs.
doi_str_mv 10.1111/j.1365-2885.2008.01026.x
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Despite this, few studies have specifically examined the plasma disposition and pharmacokinetics of cimetidine in dogs, particularly following repeated oral administration. The pharmacokinetics of cimetidine following oral administration as tablets was investigated in healthy dogs. Cimetidine was absorbed rapidly post-treatment (tmax = 0.5 h). A mean absolute bioavailability of 75% was calculated following a single oral administration of 5 mg cimetidine/kg body weight. After intravenous administration, a plasma half-life of 1.6 h was calculated. Repeated oral administration at the recommended dose rate and regime (5 mg/kg body weight three times daily) for 30 consecutive days did not lead to any accumulation of cimetidine in plasma. Food intake concomitant with oral administration of cimetidine delayed (tmax = 2.25 h) and decreased the rate and extent of absorption (AUC) by about 40%. Cimetidine was well absorbed in fasted dogs. 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source Wiley Online Library - AutoHoldings Journals; MEDLINE
subjects Administration, Oral
Animal Feed
Animals
Anti-Ulcer Agents - administration & dosage
Anti-Ulcer Agents - blood
Anti-Ulcer Agents - pharmacokinetics
bioavailability
Biological Availability
Chromatography, High Pressure Liquid - veterinary
cimetidine
Cimetidine - administration & dosage
Cimetidine - blood
Cimetidine - pharmacokinetics
Cross-Over Studies
dog diseases
dogs
Dogs - blood
Dogs - metabolism
dosage
drug formulations
Female
gastritis
Gastritis - drug therapy
Gastritis - veterinary
Injections, Intravenous - veterinary
intravenous injection
Male
oral administration
pharmacokinetics
stomach
Tablets
vomiting
title Pharmacokinetics of cimetidine in dogs after oral administration of cimetidine tablets
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