Nociceptin/Orphanin FQ Opioid Peptide-Receptor Expression in the Endometriosis-Associated Nerve Fibers-Possible Treatment Option?
Qihui GuanRenata Voltolini VelhoAlice JordanSabrina PommerIrene RaddeJalid SehouliSylvia MechsnerPublished in: Cells (2023)
Endometriosis (EM) is a chronic inflammatory disease affecting millions of women worldwide. Chronic pelvic pain is one of the main problems of this condition, leading to quality-of-life impairment. Currently, available treatment options are not able to treat these women accurately. A better understanding of the pain mechanisms would be beneficial to integrate additional therapeutic management strategies, especially specific analgesic options. To understand pain in more detail, nociceptin/orphanin FQ peptide (NOP) receptor expression was analyzed in EM-associated nerve fibers (NFs) for the first time. Laparoscopically excised peritoneal samples from 94 symptomatic women (73 with EM and 21 controls) were immunohistochemically stained for NOP, protein gene product 9.5 (PGP9.5), substance P (SP), calcitonin gene-related peptide (CGRP), tyrosine hydroxylase (TH), and vasoactive intestinal peptide (VIP). Peritoneal NFs of EM patients and healthy controls were positive for NOP and often colocalized with SP-, CGRP-, TH-, and VIP-positive nerve fibers, suggesting that NOP is expressed in sensory and autonomic nerve fibers. In addition, NOP expression was increased in EM associate NF. Our findings highlight the potential of NOP agonists, particularly in chronic EM-associated pain syndromes and deserve further study, as the efficacy of NOP-selective agonists in clinical trials.
Keyphrases
- chronic pain
- pain management
- neuropathic pain
- clinical trial
- polycystic ovary syndrome
- peripheral nerve
- end stage renal disease
- mental health
- signaling pathway
- genome wide
- oxidative stress
- randomized controlled trial
- newly diagnosed
- poor prognosis
- spinal cord injury
- ejection fraction
- spinal cord
- blood pressure
- heart rate
- drug induced
- rectal cancer
- pregnant women
- metabolic syndrome
- type diabetes
- long non coding rna
- patient reported outcomes
- immune response
- binding protein
- combination therapy
- lps induced
- breast cancer risk
- double blind