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多潘立酮、甲氧氯普胺、氯波必利和曲美布汀对豚鼠胃十二指肠制剂作用的比较研究

A comparative study on the effects of domperidone, metoclopramide, clebopride and trimebutine on the gastro-duodenal preparation of the guinea pig.

作者信息

Schuurkes J A, Helsen L F, Van Nueten J M

出版信息

Jpn J Pharmacol. 1985 Oct;39(2):123-30. doi: 10.1254/jjp.39.123.

Abstract

UNLABELLED

Domperidone (dopamine antagonist), metoclopramide and clebopride (both dopamine antagonists and stimulators of the intramural cholinergic system), and trimebutine (spasmolytic) are used in the treatment of digestive disorders such as dyspepsia or gastritis. Our aim was to compare the effects of these compounds on the isolated intact gastroduodenal preparation of the guinea pig. Domperidone (IC50 = 10(-6) M), clebopride (10(-5) M) and metoclopramide (2 X 10(-5) M) antagonized gastric relaxations induced by dopamine. In contrast with clebopride, domperidone and metoclopramide enhanced the amplitude of gastric contractions, moderately reduced contractile frequency, and enhanced antroduodenal coordination in a dose-dependent manner (EC50 for domperidone 3 X 10(-7) M, for metoclopramide 2 X 10(-5) M). Trimebutine reduced gastric spontaneous activity and antroduodenal coordination. Trimebutine had a direct relaxatory effect on gastric tone (EC50 = 4 X 10(-6) M). The mechanism of this inhibitory effect remains unknown but our data indicate that it is not mediated via dopamine or opiate receptor subtypes.

CONCLUSION

domperidone, clebopride, metoclopramide and trimebutine exert distinct and diverse effects on the motility parameters of the gastroduodenal preparation of the guinea pig. These diverging actions may help explain the differences in patients' responsiveness to the treatment of digestive disorders such as dyspepsia or gastritis.

摘要

未标记

多潘立酮(多巴胺拮抗剂)、甲氧氯普胺和氯波必利(均为多巴胺拮抗剂及肠壁内胆碱能系统刺激剂)以及曲美布汀(解痉药)用于治疗消化不良或胃炎等消化系统疾病。我们的目的是比较这些化合物对豚鼠离体完整胃十二指肠标本的作用。多潘立酮(IC50 = 10^(-6) M)、氯波必利(10^(-5) M)和甲氧氯普胺(2×10^(-5) M)可拮抗多巴胺诱导的胃舒张。与氯波必利不同,多潘立酮和甲氧氯普胺可增强胃收缩幅度,适度降低收缩频率,并以剂量依赖方式增强胃十二指肠协调性(多潘立酮的EC50为3×10^(-7) M,甲氧氯普胺为2×10^(-5) M)。曲美布汀可降低胃自发活动及胃十二指肠协调性。曲美布汀对胃张力有直接舒张作用(EC50 = 4×10^(-6) M)。这种抑制作用的机制尚不清楚,但我们的数据表明其并非通过多巴胺或阿片受体亚型介导。

结论

多潘立酮、氯波必利、甲氧氯普胺和曲美布汀对豚鼠胃十二指肠标本的运动参数具有不同且多样的作用。这些不同的作用可能有助于解释患者对消化不良或胃炎等消化系统疾病治疗反应的差异。

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