Journal
ACTA OBSTETRICIA ET GYNECOLOGICA SCANDINAVICA
Volume 93, Issue 10, Pages 991-996Publisher
WILEY
DOI: 10.1111/aogs.12462
Keywords
Oxytocin; pelvic organ prolapse; relaxin-2; relaxin receptor; uterosacral ligament
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Funding
- German Phlebological Society (Deutsche Gesellschaft fur Phlebologie)
- AKF program of the University Clinic Tubingen
- University of Heidelberg
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ObjectivePelvic organ prolapse (POP) is a major health concern for women. Its pathophysiology is yet not fully understood. We reported an impaired functional state of the smooth muscle compartment in uterosacral ligaments from patients with POP, which was cholinergic, stimulated by oxytocin and modulated by relaxin-2. The current study investigated the presence of oxytocin and relaxin-2 and their receptors in the uterosacral ligament from POP/non-POP patients. DesignTranslational investigation on clinical samples. SettingUniversity hospital departments. Population and samplesFourty-three samples of uterosacral ligament from pre-menopausal patients with (n=20) and without POP (n=23). MethodsPresence of relaxin-2, its receptors RXFP1 and RXFP2, and of oxytocin and its receptor were analysed by immunohistochemistry and classified using a staining score. Additionally, Western blot analysis was performed. Main outcome measuresPresence patterns with respect to POP and non-POP uterosacral ligament samples for pathophysiological understanding of POP. ResultsRelaxin-2, oxytocin and their receptors were expressed in endothelial cells, the smooth muscle compartment and vasa vasorum in the arteries and veins of the uterosacral ligament, in the smooth muscle compartment present in the ground reticulum and in nerves running through the uterosacral ligament. The presence level of relaxin-2 was higher in the uterosacral ligament of the POP cohort (p<0.001). ConclusionsWe demonstrated that relaxin-2 had an increased presence in uterosacral ligaments from patients with POP, suggesting a role of the relaxin system in the pathogenesis of POP and identifying the relaxin system as a potential therapeutic target for the pharmacological treatment of POP.
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