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Formyl peptide receptor type 2 agonists to kick-start resolution pharmacology

期刊

BRITISH JOURNAL OF PHARMACOLOGY
卷 177, 期 20, 页码 4595-4600

出版社

WILEY
DOI: 10.1111/bph.15212

关键词

annexin A1; GPCRs; lipoxins; small molecule agonists; therapeutic innovation

资金

  1. Juvenile Diabetes Research Foundation United Kingdom
  2. Science Foundation Ireland [15/US/B3130, 15/IA/3152]
  3. Horizon 2020 Framework Programme [675111]
  4. William Harvey Research Foundation
  5. Wellcome Trust [086867/Z/08/Z]
  6. Wellcome Trust [086867/Z/08/Z] Funding Source: Wellcome Trust
  7. Science Foundation Ireland (SFI) [15/US/B3130, 15/IA/3152] Funding Source: Science Foundation Ireland (SFI)

向作者/读者索取更多资源

One way to develop innovative approaches for the treatment of chronic diseases is to exploit the biology of the resolution of inflammation. With this terminology, we identify the integrated and complex network of mediators and pathways that ensure a timely and spatially regulated inflammatory response. Pro-resolving mediators act on specific receptors. This provides an opportunity for developing a new arm of pharmacology we have termed resolution pharmacology. Here we present the reasoning behind the need to develop new medicines based on resolution and use a prototype GPCR as an example. Understanding how the formyl peptide receptor type 2 (FPR2) operates in a cell-specific manner can guide the development of agonists as new therapeutics that could be of benefit as a therapy or co-therapy for several diseases that affect our society. FPR2 agonists would be among the first drugs to establish resolution pharmacology as the pharmacological approach for the third decade of the millennium.

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