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Effect of omeprazole paste on gastric acid secretion in horses
Author(s) -
DAURIO C. P.,
HOLSTE J. E.,
ANDREWS F. M.,
MERRITT A. M.,
BLACKFORD J. T.,
DOLZ F.,
THOMPSON D. R.
Publication year - 1999
Publication title -
equine veterinary journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.82
H-Index - 87
eISSN - 2042-3306
pISSN - 0425-1644
DOI - 10.1111/j.2042-3306.1999.tb05171.x
Subject(s) - omeprazole , pentagastrin , gastric acid , crossover study , basal (medicine) , horse , medicine , secretion , pharmacokinetics , gastroenterology , pharmacology , endocrinology , chemistry , biology , placebo , paleontology , alternative medicine , pathology , insulin
Summary In a multicentre trial, 13 cannulated horses were treated orally once daily with a paste that delivered omeprazole at a dose of 4 and 5 mg/kg bwt in a 2‐period crossover design to evaluate steady state gastric acid suppression. In each period, basal (unstimulated) and pentagastrin‐stimulated gastric output were evaluated at 5–8 h after 5 doses, at 13–16 h after 10 doses, and at 21–24 h after 15 doses. Baseline data for gastric acid secretion were collected once for each horse in the month prior to initiation of omeprazole treatment. The inhibition of gastric acid secretion relative to baseline values, following treatment with omeprazole, were calculated and expressed as per cent. Pharmacokinetic data were also collected in this trial. At 4 mg/kg bwt, the oral paste formulation of omeprazole inhibited both basal and pentagastrin‐stimulated gastric acid secretion by 99% at 5–8 h after treatment and by 83% (basal) and 90% (pentagastrin‐stimulated) at 21–24 h. Inhibition following the administration of omeprazole at a dose of 5 mg/kg bwt was not significantly greater than when given at 4 mg/kg bwt. The results from this study could possibly lead to the development of an effective and practical antisecretory treatment of ulcer disease in horses.