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Kinin B1 receptors as a therapeutic target for inflammation
Authors:Fatimunnisa Qadri  Michael Bader
Affiliation:1. Max-Delbrück Center for Molecular Medicine (MDC), Berlin, Germany;2. Berlin Institute of Health (BIH), Berlin, Germany;3. Charité University Medicine Berlin, Germany;4. German Center for Cardiovascular Research (DZHK) site Berlin, Berlin, Germany;5. Institute for Biology, University of Lübeck, Lübeck, Germany
Abstract:Introduction: Kinins are peptide mediators exerting their pro-inflammatory actions by the selective stimulation of two distinct G-protein coupled receptors, termed BKB1R and BKB2R. While BKB2R is constitutively expressed in a multitude of tissues, BKB1R is hardly expressed at baseline but highly inducible by inflammatory mediators. In particular, BKB1R was shown to be involved in the pathogenesis of numerous inflammatory diseases.

Areas covered: This review intends to evaluate the therapeutic potential of substances interacting with the BKB1R. To this purpose we summarize the published literature on animal studies with antagonists and knockout mice for this receptor.

Expert Opinion: In most cases the pharmacological inhibition of BKB1R or its genetic deletion was beneficial for the outcome of the disease in animal models. Therefore, several companies have developed BKB1R antagonists and tested them in phase I and II clinical trials. However, none of the developed BKB1R antagonists was further developed for clinical use. We discuss possible reasons for this failure of translation of preclinical findings on BKB1R antagonists into the clinic.

Keywords:B1 receptor  B2 receptor  bradykinin  carboxypeptidase M  des-Arg9-bradykinin  des-Arg10-kallidin  inflammatory diseases  kallidin  kallikrein-kinin system  kinins  kininogen  plasma kallikrein  tissue kallikrein
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