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腺苷 A2A 受体有助于固定草药复方 STW 5(Iberogast®)在大鼠小肠制剂中的抗炎作用。

Adenosine A2A receptor contributes to the anti-inflammatory effect of the fixed herbal combination STW 5 (Iberogast®) in rat small intestinal preparations.

机构信息

Löwen-Apotheke, Waldheim, Germany.

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 2012 Apr;385(4):411-21. doi: 10.1007/s00210-011-0714-y. Epub 2011 Dec 10.

Abstract

STW 5 (Iberogast®), an established herbal combination, was effective in randomized, double blind clinical studies in functional dyspepsia and irritable bowel syndrome. Since STW 5 was found to influence intestinal motility and has anti-inflammatory properties, this study investigated the expression of adenosine receptors and characterized their role in the control of the anti-inflammatory action of STW 5 and its fresh plant component STW 6 in inflammation-disturbed rat small intestinal preparations. The inflammation was induced by intraluminal instillation of 2,4,6-trinitrobenzene sulfonic acid (TNBS, 0.01 M). The effects of coincubation with selective receptor agonists and antagonists, STW 5, STW 6, or combinations of these compounds on acetylcholine (ACh)-evoked contraction of ileum/jejunum preparations were tested. Adenosine receptor mRNA expression was examined by reverse transcription-polymerase chain reaction (RT-PCR). In untreated preparations, RT-PCR revealed the presence of all adenosine receptor subtypes. Suppressed expression was detected for all subtypes in inflamed tissues, except for A(2B)R mRNA, which was unaffected. STW 5 reversed these effects and enhanced A(2A)R expression above control levels. Radioligand binding assays confirm the affinity of STW 5 to the A(2A)R, and the A(2A)R antagonist was able to prevent the effect of STW 5 on TNBS-induced attenuation of the ACh contraction. Our findings provide evidence that STW 5, but not STW 6 interacts with A(2A)R, which is involved in the anti-inflammatory action of STW 5. STW 6 did not contribute to adenosine A(2A)R-mediated anti-inflammatory effect of STW 5. Other signaling pathways could be involved in the mechanism of action of STW 6.

摘要

STW 5(Iberogast®)是一种已被证实的草药混合物,在功能性消化不良和肠易激综合征的随机、双盲临床研究中具有疗效。由于 STW 5 被发现可影响肠道蠕动并具有抗炎特性,因此本研究调查了腺苷受体的表达,并描述了它们在控制 STW 5 及其新鲜植物成分 STW 6 的抗炎作用中的作用,在炎症紊乱的大鼠小肠制剂中。炎症是通过腔内滴注 2,4,6-三硝基苯磺酸(TNBS,0.01 M)诱导的。通过共孵育选择性受体激动剂和拮抗剂、STW 5、STW 6 或这些化合物的组合,测试它们对乙酰胆碱(ACh)引起的回肠/空肠制剂收缩的影响。通过逆转录-聚合酶链反应(RT-PCR)检查腺苷受体 mRNA 的表达。在未处理的制剂中,RT-PCR 显示存在所有腺苷受体亚型。除 A(2B)R mRNA 不受影响外,在炎症组织中检测到所有亚型的表达受到抑制。STW 5 逆转了这些作用,并使 A(2A)R 的表达增强到对照水平以上。放射性配体结合测定法证实 STW 5 对 A(2A)R 的亲和力,并且 A(2A)R 拮抗剂能够阻止 STW 5 对 TNBS 诱导的 ACh 收缩减弱的作用。我们的研究结果提供了证据,表明 STW 5 而不是 STW 6 与 A(2A)R 相互作用,这涉及 STW 5 的抗炎作用。STW 6 没有促进 STW 5 对腺苷 A(2A)R 介导的抗炎作用。其他信号通路可能参与 STW 6 的作用机制。

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