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薄荷油对大鼠小肠吸收和分泌过程的影响。

Influence of peppermint oil on absorptive and secretory processes in rat small intestine.

作者信息

Beesley A, Hardcastle J, Hardcastle P T, Taylor C J

机构信息

Department of Biomedical Science, Sheffield University.

出版信息

Gut. 1996 Aug;39(2):214-9. doi: 10.1136/gut.39.2.214.

Abstract

BACKGROUND

Peppermint oil is used to relieve the symptoms of irritable bowel syndrome, relaxing intestinal smooth muscle by reducing the availability of calcium, but its effects on intestinal transport are unknown.

AIMS

To determine the effect of peppermint oil on intestinal transport processes.

METHODS

The influence of peppermint oil on intestinal transport was investigated in rat jejunum using both intestinal sheets mounted in Ussing chambers and brush border membrane vesicles.

RESULTS

Mucosal peppermint oil (1 and 5 mg/ml) had no significant effect on basal short circuit current, but inhibited the increase associated with sodium dependent glucose absorption. The increased short circuit current induced by serosal acetylcholine, a reflection of calcium mediated electrogenic chloride secretion, was unaffected by mucosal peppermint oil (5 mg/ml). In contrast, serosal peppermint oil (1 mg/ml) inhibited the response to acetylcholine without reducing the effect of mucosal glucose. In brush border membrane vesicles active glucose uptake was inhibited by extravesicular peppermint oil at concentrations of 0.5 and 1 mg/ml.

CONCLUSIONS

Peppermint oil in the intestinal lumen inhibits enterocyte glucose uptake via a direct action at the brush border membrane. Inhibition of secretion by serosal peppermint oil is consistent with a reduced availability of calcium.

摘要

背景

薄荷油用于缓解肠易激综合征的症状,通过减少钙的可利用性来松弛肠道平滑肌,但其对肠道转运的影响尚不清楚。

目的

确定薄荷油对肠道转运过程的影响。

方法

使用安装在尤斯灌流小室中的肠片和刷状缘膜囊泡,在大鼠空肠中研究薄荷油对肠道转运的影响。

结果

黏膜薄荷油(1和5毫克/毫升)对基础短路电流无显著影响,但抑制了与钠依赖性葡萄糖吸收相关的增加。由浆膜乙酰胆碱诱导的短路电流增加,反映了钙介导的电致氯分泌,不受黏膜薄荷油(5毫克/毫升)影响。相比之下,浆膜薄荷油(1毫克/毫升)抑制了对乙酰胆碱的反应,而不降低黏膜葡萄糖的作用。在刷状缘膜囊泡中,浓度为0.5和1毫克/毫升的细胞外薄荷油抑制了活性葡萄糖摄取。

结论

肠腔内的薄荷油通过对刷状缘膜的直接作用抑制肠上皮细胞葡萄糖摄取。浆膜薄荷油对分泌的抑制与钙的可利用性降低一致。

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