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Dihydroavenanthramide D inhibits mast cell degranulation and exhibits anti‐inflammatory effects through the activation of neurokinin‐1 receptor
Authors:Tobias Lotts  Konstantin Agelopoulos  Ngoc Q Phan  Karin Loser  Gerhard Schmaus  Thomas A Luger  Sonja Ständer
Institution:1. Department of Dermatology, University of Münster, Münster, Germany;2. Department of Dermatology, Center for Chronic Pruritus, University Hospital Münster, Münster, Germany;3. Department of Dermatology, Experimental Dermatology and Immunobiology of the Skin, University Hospital Münster, Münster, Germany;4. Symrise AG, Holzminden, Germany
Abstract:Chronic pruritus is difficult to treat. Current treatment options are frequently ineffective and new therapeutic approaches are urgently needed. Avenanthramides are active substances in oats that exhibit anti‐inflammatory effects. Their potential to interrupt pruritus mechanisms was investigated in this study. It was found that the synthetic analog dihydroavenanthramide D (DHAvD) can interact with the neurokinin‐1 receptor (NK1R) and inhibit mast cell degranulation. DHAvD also affects inflammatory processes and reduces secretion of the cytokine interleukin‐6. Our findings indicate that DHAvD may act as a NK1R inhibitor and could be a promising candidate for topical treatments of chronic pruritus.
Keywords:chronic pruritus  interleukin‐6  neurokinin‐1 receptor antagonist  substance P
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