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

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.

MeSH terms

  • Animals
  • Anti-Inflammatory Agents / therapeutic use*
  • Enteritis / chemically induced
  • Enteritis / drug therapy*
  • Enteritis / physiopathology
  • Ileum / drug effects
  • Ileum / physiopathology
  • Jejunal Diseases / chemically induced
  • Jejunal Diseases / drug therapy*
  • Jejunal Diseases / physiopathology
  • Jejunum / drug effects
  • Jejunum / physiopathology
  • Male
  • Plant Extracts / therapeutic use*
  • RNA, Messenger / metabolism
  • Rats
  • Rats, Wistar
  • Receptor, Adenosine A2A / genetics
  • Receptor, Adenosine A2A / physiology*
  • Trinitrobenzenesulfonic Acid

Substances

  • Anti-Inflammatory Agents
  • Plant Extracts
  • RNA, Messenger
  • Receptor, Adenosine A2A
  • iberogast
  • Trinitrobenzenesulfonic Acid