Key result
NOP ligands offer a new option for the treatment of acute and chronic pain with the potential for a decreased side effect profile, particularly when designed as multi-target agents.
NOP ligands represent a promising novel therapeutic target for pain management with a potentially favorable side effect profile.
NOP ligands merit preclinical pursuit for pain with potentially fewer side effects; leaves open clinical translation absent randomized trials.
IMPORTANCE OF THE FIELD: The interactions of nociceptin/orphanin FQ (N/OFQ) and the opioid receptor-like receptor 1 (nociceptin opioid peptide--NOP) have been implicated in a variety of systems including cardiovascular, respiratory, immune, and the central and peripheral nervous systems. AREAS COVERED IN THIS REVIEW: To elucidate the endogenous role of the N/OFQ-NOP system through the use of knockout and knockdown animal preparations, though most advances have been made using a host of synthetic agonists and antagonists. This review gives a brief history of the receptor-ligand discovery, the development of these agonists and antagonists within the last 10 years as published, and the therapeutic indications thereof focusing on pain. WHAT THE READER WILL GAIN: The use of NOP ligands in pain has been controversial at best; however, there are indications that both agonists and antagonists have a place in the clinical setting for acute and chronic pain. NOP ligands have potential as novel therapeutics, interestingly, when incorporated into a rationally-designed multi-target agent. TAKE HOME MESSAGE: The discovery of N/OFQ and NOP opened a new option for the treatment of pain with the potential for a decreased side effect profile. Numerous compounds have been designed to target this system, the most promising of which have mixed profiles.
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Largent‐Milnes et al. (2010) conducted a review in Pain. NOP ligands was evaluated. NOP ligands offer a new option for the treatment of acute and chronic pain with the potential for a decreased side effect profile, particularly when designed as multi-target agents.
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