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    Histamine 2 receptor agonism and histamine 4 receptor antagonism ameliorate inflammation in a model of psoriasis (2020)

    Art
    Zeitschriftenartikel / wissenschaftlicher Beitrag
    Autoren
    Rossbach, Kristine
    Wahle, Katharina
    Bruer, Gustav
    Brehm, Ralph
    Langeheine, Marion
    Rode, Kristina
    Schaper-Gerhardt, Katrin
    Gutzmer, Ralf
    Werfel, Thomas
    Kietzmann, Manfred
    Bäumer, Wolfgang (WE 14)
    Quelle
    Acta dermato-venereologica
    Bandzählung: 100
    Heftzählung: 19
    Seiten: adv00342
    ISSN: 1651-2057
    Sprache
    Englisch
    Verweise
    URL (Volltext): https://www.medicaljournals.se/acta/content/abstract/10.2340/00015555-3674
    DOI: 10.2340/00015555-3674
    Pubmed: 33104231
    Kontakt
    Institut für Pharmakologie und Toxikologie

    Koserstr. 20
    14195 Berlin
    +49 30 838 53221
    pharmakologie@vetmed.fu-berlin.de

    Abstract / Zusammenfassung

    Psoriasis is a chronic inflammatory skin disorder characterized by hyperproliferative keratinocytes and immune cell infiltration into the skin, often accompanied by itch. Histamine, acting via histamine 1-4 receptors, is known to modulate immune responses in the skin and to induce itch. The aim of this study was to test the role of histamine 2 receptors and histamine 4 receptors in the imiquimod-induced psoriasis-like skin inflammation model. BALB/c mice were treated intraperitoneally with amthamine (histamine 2 receptor agonist), JNJ-39758979 (histamine 4 receptor antagonist), a combination of both, or vehicle twice daily in a preventive manner. Imiquimod was applied once daily onto the back skin for 10 consecutive days. Stimulation of histamine 2 receptors and blockade of histamine 4 receptors ameliorated imiquimod-induced skin inflammation. The combination of amthamine and JNJ-39758979 reduced skin inflammation even more pronounced, diminished epidermal hyperproliferation, and inhibited spontaneous scratching behaviour. A combination of histamine 2 receptor agonist and histamine 4 receptor antagonists could represent a new strategy for the treatment of psoriasis.