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偏头痛发作和胃复安对托芬那酸吸收的影响。

Effects of migraine attack and metoclopramide on the absorption of tolfenamic acid.

作者信息

Tokola R A, Neuvonen P J

出版信息

Br J Clin Pharmacol. 1984 Jan;17(1):67-75. doi: 10.1111/j.1365-2125.1984.tb05001.x.

Abstract

The effect of acute migraine attack and rectally given metoclopramide on the absorption of orally given tolfenamic acid (300 mg) was investigated in seven female patients in a crossover study consisting of four phases, two without migraine and two during migraine. Metoclopramide hydrochloride (20 mg) or placebo was given double-blind. Migraine attacks delayed the absorption of tolfenamic acid. Serum concentrations of tolfenamic acid 1.5 and 2 h after drug administration remained smaller, the peak serum concentration (tmax) occurred later and the area under the serum concentration-time curve between zero and 2 h (AUC0-2 h) remained decreased during migraine. Metoclopramide pretreatment in migraine attacks increased the serum concentration of tolfenamic acid at 1.5 h, but its peak concentration, time to peak concentration and the AUC0-5 h remained unchanged as compared with the values obtained with tolfenamic acid alone. Between the absorption of tolfenamic acid without migraine and after metoclopramide pretreatment during migraine no significant differences existed. When the patients were studied without migraine the serum concentrations of tolfenamic acid 45 min and 60 min after its administration were higher after metoclopramide than after placebo pretreatment. During migraine attacks the serum concentrations and the AUC0-5.5 h of metoclopramide were slightly lowered. The impairment of drug absorption by migraine was not related to the duration or severity of the attack. The observed changes in drug absorption during migraine attacks are obviously due to the delay in gastric emptying. Rectally administered metoclopramide accelerates the absorption of orally given tolfenamic acid.

摘要

在一项由四个阶段组成的交叉研究中,对7名女性患者进行了急性偏头痛发作和直肠给予甲氧氯普胺对口服托芬那酸(300毫克)吸收影响的研究,该研究包括两个无偏头痛阶段和两个偏头痛阶段。采用双盲法给予盐酸甲氧氯普胺(20毫克)或安慰剂。偏头痛发作延迟了托芬那酸的吸收。给药后1.5小时和2小时托芬那酸的血清浓度仍然较低,血清峰值浓度(tmax)出现较晚,在偏头痛期间,零至2小时血清浓度-时间曲线下面积(AUC0-2h)仍然降低。偏头痛发作时进行甲氧氯普胺预处理可使1.5小时时托芬那酸的血清浓度升高,但其峰值浓度、达峰时间和AUC0-5h与单独使用托芬那酸时相比保持不变。在无偏头痛时托芬那酸的吸收与偏头痛期间甲氧氯普胺预处理后的吸收之间无显著差异。在无偏头痛情况下研究患者时,托芬那酸给药后45分钟和60分钟的血清浓度在甲氧氯普胺预处理后高于安慰剂预处理后。在偏头痛发作期间,甲氧氯普胺的血清浓度和AUC0-5.5h略有降低。偏头痛对药物吸收的损害与发作的持续时间或严重程度无关。在偏头痛发作期间观察到的药物吸收变化显然是由于胃排空延迟所致。直肠给予甲氧氯普胺可加速口服托芬那酸的吸收。

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本文引用的文献

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Cephalalgia. 1981 Jun;1(2):83-9. doi: 10.1111/j.1468-2982.1981.tb00014.x.

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