Adenosine and Its Receptors in the Pathogenesis and Treatment of Inflammatory Skin Diseases.

Int J Mol Sci

Department of Dermatology, University Hospital Heidelberg, Im Neuenheimer Feld 440, 69120 Heidelberg, Germany.

Published: May 2024

AI Article Synopsis

  • Inflammatory skin diseases are caused by inflammation, which involves many different cells and chemicals in the body.
  • Adenosine is an important helper in our immune system that helps control inflammation and works through specific receptors in our cells.
  • Research shows that focusing on adenosine receptors can help reduce inflammation in skin diseases and could work well with regular treatments, showing good results in animal studies and ongoing trials.

Article Abstract

Inflammatory skin diseases highlight inflammation as a central driver of skin pathologies, involving a multiplicity of mediators and cell types, including immune and non-immune cells. Adenosine, a ubiquitous endogenous immune modulator, generated from adenosine triphosphate (ATP), acts via four G protein-coupled receptors (A, A, A, and A). Given the widespread expression of those receptors and their regulatory effects on multiple immune signaling pathways, targeting adenosine receptors emerges as a compelling strategy for anti-inflammatory intervention. Animal models of psoriasis, contact hypersensitivity (CHS), and other dermatitis have elucidated the involvement of adenosine receptors in the pathogenesis of these conditions. Targeting adenosine receptors is effective in attenuating inflammation and remodeling the epidermal structure, potentially showing synergistic effects with fewer adverse effects when combined with conventional therapies. What is noteworthy are the promising outcomes observed with A agonists in animal models and ongoing clinical trials investigating A agonists, underscoring a potential therapeutic approach for the management of inflammatory skin disorders.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11172165PMC
http://dx.doi.org/10.3390/ijms25115810DOI Listing

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