Nociceptin/orphanin FQ receptor system blockade as an innovative strategy for increasing resilience to stress

Peptides. 2021 Jul:141:170548. doi: 10.1016/j.peptides.2021.170548. Epub 2021 Apr 20.

Abstract

The ability to successfully cope with stress is known as 'resilience', and resilient individuals are less prone to develop psychopathologies. Understanding the neurobiological mechanisms of resilience may be instrumental to improve current therapies and benefit high-risk subjects. This review summarizes the complex interplay that exists between physiological and pathological responses to stressful events and the nociceptin/orphanin FQ (N/OFQ) - N/OFQ receptor (NOP) system, including: the effects of stress in regulating N/OFQ release and NOP expression; the ability of the N/OFQ-NOP system to modulate the hypothalamic-pituitary-adrenal axis; behavioral studies; and evidence in humans correlating this peptidergic system with psychopathologies. Available findings support the view that N/OFQ signaling stimulates the hypothalamic-pituitary-adrenal axis, thus increasing stress circulating hormones and corticotropin-releasing factor signaling. Additionally, activation of the NOP receptor inhibits monoamine transmission, including 5-HT, and this may contribute to maladaptive outcomes of stress. Ultimately, the N/OFQ system seems to have an important role in stress vulnerability, and blockade of NOP signaling may provide an innovative strategy for the treatment of stress related psychopathologies.

Keywords: Hypothalamic-pituitary-adrenal axis; NOP receptor; Nociceptin/orphanin FQ; Psychopathology; Resilience; Stress.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • Humans
  • Hypothalamo-Hypophyseal System / physiology
  • Narcotic Antagonists / pharmacology
  • Nociceptin
  • Nociceptin Receptor
  • Opioid Peptides / physiology*
  • Pituitary-Adrenal System / physiology
  • Receptors, Opioid / physiology*
  • Stress, Psychological / drug therapy
  • Stress, Psychological / etiology*

Substances

  • Narcotic Antagonists
  • Opioid Peptides
  • Receptors, Opioid
  • Nociceptin Receptor
  • OPRL1 protein, human