Nociceptin/Orphanin FQ Opioid Peptide-Receptor Expression in the Endometriosis-Associated Nerve Fibers-Possible Treatment Option?

被引:3
|
作者
Guan, Qihui [1 ]
Velho, Renata Voltolini [1 ]
Jordan, Alice [1 ]
Pommer, Sabrina [1 ]
Radde, Irene [1 ]
Sehouli, Jalid [1 ]
Mechsner, Sylvia [1 ]
机构
[1] Charite, Dept Gynecol Charite, Endometriosis Res Ctr, Ctr Oncol Surg, Campus Virchow Klinikum,Augustenburger Pl 1, D-13353 Berlin, Germany
关键词
chronic inflammation; endometriosis; nerve fibers; NOP; opioid receptors; pelvic pain; INTRATHECALLY ADMINISTERED NOCICEPTIN; ORL1; RECEPTOR; PELVIC PAIN; AGONIST; LIGANDS; DISORDERS; POTENT; WOMEN;
D O I
10.3390/cells12101395
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
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.
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页数:10
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