Pattern recognition receptors in chronic pain: Mechanisms and therapeutic implications

Jungo Kato, Nilesh M. Agalave, Camilla I. Svensson

Research output: Contribution to journalReview article

20 Citations (Scopus)

Abstract

For the individual, it is vital to promptly detect and recognize a danger that threatens the integrity of the body. Pattern recognition receptors (PRRs) are several classes of protein families originally classified as receptors detecting exogenous pathogens. PRRs are also capable of recognizing molecules released from damaged tissues (damage-associated molecular pattern molecules; DAMPs) and thereby contribute to danger recognition. Importantly, it is now evident that PRRs, such as toll-like receptors (TLRs) and receptors for advanced glycation end products (RAGE), are not only expressed in peripheral immune cells but also present in neurons and glial cells in the nervous system. These PRR-expressing cells work in concert, enabling highly sensitive danger recognition. However, this sensitiveness can act as a double-edged sword. Accumulated evidence has led to the hypothesis that aberrant activation of PRRs may play a crucial role in the pathogenesis of pathological pain. Indeed, numerous studies employing gene deletion or pharmacological inhibition of PRRs successfully reversed or prevented pathological pain in experimental animal models. Furthermore, a number of preclinical studies have shown the therapeutic potential of targeting PRRs for chronic pain. Here, we review the current knowledge regarding the role of PRRs in chronic pain and discuss the promise and challenges of targeting PRRs as a novel therapeutic approach for chronic pain.

Original languageEnglish
Pages (from-to)261-273
Number of pages13
JournalEuropean Journal of Pharmacology
Volume788
DOIs
Publication statusPublished - 2016
Externally publishedYes

Keywords

  • Chronic pain
  • DAMPs
  • PRRs
  • RAGE
  • TLR

ASJC Scopus subject areas

  • Pharmacology

Fingerprint Dive into the research topics of 'Pattern recognition receptors in chronic pain: Mechanisms and therapeutic implications'. Together they form a unique fingerprint.

Cite this