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

被引:0
|
作者
Sebastian Michael
Heba Abdel-Aziz
Dieter Weiser
Christa E. Müller
Olaf Kelber
Karen Nieber
机构
[1] Löwen-Apotheke,Scientific Department
[2] Steigerwald Arzneimittelwerk GmbH,PharmaCenter Bonn, Pharmaceutical Institute, Pharmaceutical Chemistry I
[3] University of Bonn,Institute of Pharmacy, Pharmacology for Natural Sciences
[4] University of Leipzig,undefined
关键词
Iberogast; Inflammation; Adenosine receptors; TNFα; Isometric contraction; TNBS;
D O I
暂无
中图分类号
学科分类号
摘要
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 A2BR mRNA, which was unaffected. STW 5 reversed these effects and enhanced A2AR expression above control levels. Radioligand binding assays confirm the affinity of STW 5 to the A2AR, and the A2AR 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 A2AR, which is involved in the anti-inflammatory action of STW 5. STW 6 did not contribute to adenosine A2AR-mediated anti-inflammatory effect of STW 5. Other signaling pathways could be involved in the mechanism of action of STW 6.
引用
收藏
页码:411 / 421
页数:10
相关论文
共 45 条
  • [41] Bicyclol promotes toll-like 2 receptor recruiting inosine 5-monophosphate dehydrogenase II to exert its anti-inflammatory effect
    Zhang, You-Wen
    Guo, Yan-Shen
    Bao, Xiu-Qi
    Sun, Hua
    Zhang, Dan
    JOURNAL OF ASIAN NATURAL PRODUCTS RESEARCH, 2016, 18 (05) : 475 - 485
  • [42] In search of secreted protein biomarkers for the anti-inflammatory effect of β2-adrenergic receptor agonists:: Application of DIGE technology in combination with multivariate and univariate data analysis tools
    Verhoeckx, KCM
    Gaspari, M
    Bijlsma, S
    van der Greef, J
    Witkamp, RF
    Doornbos, RP
    Rodenburg, RJT
    JOURNAL OF PROTEOME RESEARCH, 2005, 4 (06) : 2015 - 2023
  • [43] The Protective Effect of 5-Aminosalicylic Acid against Non-Steroidal Anti-Inflammatory Drug-Induced Injury through Free Radical Scavenging in Small Intestinal Epithelial Cells
    Jung, Eun Suk
    Jang, Hyun Joo
    Hong, Eun Mi
    Lim, Hye Li
    Lee, Sang Pyo
    Kae, Sea Hyub
    Lee, Jin
    MEDICINA-LITHUANIA, 2020, 56 (10): : 1 - 10
  • [44] STUDIES ON ANTI-INFLAMMATORY AGENTS .17. EFFECTS OF 2-AMINO-3-ETHOYXYCARBONYL-6-BENZYL-4,5,6,7-TETRAHYDROTHIENO[2,3-C]PYRIDINE (Y-3642) HYDROCHLORIDE ON OXIDATIVE PHOSPHORYLATION, SWELLING AND ADENOSINE TRIPHOSPHATASE OF RAT LIVER MITOCHONDRIA
    NAKANISHI, M
    IMAMURA, H
    IKEGAMI, K
    YAKUGAKU ZASSHI, 1971, 91 (07): : 702 - +
  • [45] ABT-702 (4-amino-5-(3-bromophenyl)-7-(6-morpholino-pyridin-3-yl)pyrido[2,3-d]pyrimidine), a novel orally effective adenosine kinase inhibitor with analgesic and anti-inflammatory properties.: II.: In vivo characterization in the rat
    Kowaluk, EA
    Mikusa, J
    Wismer, CT
    Zhu, CZ
    Schweitzer, E
    Lynch, JJ
    Lee, CH
    Jiang, MQ
    Bhagwat, SS
    Gomtsyan, A
    McKie, J
    Cox, BF
    Polakowski, J
    Reinhart, G
    Williams, M
    Jarvis, MF
    JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS, 2000, 295 (03): : 1165 - 1174