4.7 Review

Opioidergic Signaling-A Neglected, Yet Potentially Important Player in Atopic Dermatitis

Journal

Publisher

MDPI
DOI: 10.3390/ijms23084140

Keywords

atopic dermatitis (AD); cutaneous barrier; delta-opioid receptor (DOR); inflammation; itch; kappa-opioid receptor (KOR); keratinocyte; mast cell; mu-opioid receptor (MOR); nociceptin/orphanin FQ (NOP) receptor; opioid; skin

Funding

  1. National Research, Development and Innovation Office [134235, 134725, 134993, 120187 GINOP-2.3.2-15-2016-00026, EFOP3.6.3-VEKOP-16-2017-00009]
  2. Janos Bolyai Research Scholarship of the Hungarian Academy of Sciences [BO/00660/21/5, BO/00905/19/5]
  3. New National Excellence Programof theMinistry for Innovation and Technology from the source of the National Research, Development and Innovation Fund [UNKP-21-5-DE-465, UNKP-21-5-DE-491]

Ask authors/readers for more resources

Atopic dermatitis is a common skin disease, especially prevalent among children. Although there have been advancements in understanding its pathogenesis, curative treatments are still lacking. Therefore, it is important to further investigate the mechanisms and explore new therapeutic approaches.
Atopic dermatitis (AD) is one of the most common skin diseases, the prevalence of which is especially high among children. Although our understanding about its pathogenesis has substantially grown in recent years, and hence, several novel therapeutic targets have been successfully exploited in the management of the disease, we still lack curative treatments for it. Thus, there is an unmet societal demand to identify further details of its pathogenesis to thereby pave the way for novel therapeutic approaches with favorable side effect profiles. It is commonly accepted that dysfunction of the complex cutaneous barrier plays a central role in the development of AD; therefore, the signaling pathways involved in the regulation of this quite complex process are likely to be involved in the pathogenesis of the disease and can provide novel, promising, yet unexplored therapeutic targets. Thus, in the current review, we aim to summarize the available potentially AD-relevant data regarding one such signaling pathway, namely cutaneous opioidergic signaling.

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