奥美拉唑膏对马胃酸分泌的影响。

C P Daurio, J E Holste, F M Andrews, A M Merritt, J T Blackford, F Dolz, D R Thompson
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引用次数: 74

摘要

在一项多中心试验中,在2期交叉设计中,13匹空心马每天口服1次,膏体中含有剂量为4和5 mg/kg体重的奥美拉唑,以评估稳态胃酸抑制。在每个时间段,分别在5次给药后5-8小时、10次给药后13-16小时和15次给药后21-24小时评估基础(未刺激)胃输出量和pentagastrin刺激胃输出量。在开始奥美拉唑治疗前的一个月内,每匹马收集一次胃酸分泌的基线数据。计算奥美拉唑治疗后胃酸分泌相对于基线值的抑制作用,并以百分比表示。本试验还收集了药代动力学数据。在4 mg/kg体重下,奥美拉唑口服膏状制剂在治疗后5-8小时抑制基础胃酸和pentagastra刺激的胃酸分泌99%,在21-24小时抑制83%(基础胃酸)和90% (pentagastra刺激的胃酸)。奥美拉唑以5 mg/kg体重给药后的抑制作用并不明显大于4 mg/kg体重给药时。这项研究的结果可能会导致一种有效和实用的抗分泌性治疗马溃疡疾病的发展。
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Effect of omeprazole paste on gastric acid secretion in horses.

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.

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