dc.contributor.author | Tosyali H.K. | |
dc.contributor.author | Bora E.S. | |
dc.contributor.author | Çinaroğlu O.S. | |
dc.contributor.author | Erbaş O. | |
dc.date.accessioned | 2024-02-04T13:30:18Z | |
dc.date.available | 2024-02-04T13:30:18Z | |
dc.date.issued | 2023 | |
dc.identifier.issn | 11283602 | |
dc.identifier.uri | https://doi.org/10.26355/eurrev_202312_34573 | |
dc.identifier.uri | http://hdl.handle.net/11446/4889 | |
dc.description.abstract | OBJECTIVE: Peripheral nerve injuries present challenges in achieving full functional restoration, necessitating effective therapeutic strategies. Oxytocin, known for its neuroprotective and anti-inflammatory properties, has shown potential in nerve recovery. This study aims to elucidate the role of oxytocin in nerve recovery via the nuclear factor erythroid 2-related factor 2 (Nrf2) and irisin pathways. MATERIALS AND METHODS: Adult male Wistar rats (n=30) were subjected to surgical dissection of sciatic nerves and divided into Control, Surgery and Saline Group, and Surgery and Oxytocin (OT) group. Electromyographic (EMG) recordings, inclined plane tests, and histological assessments were conducted to evaluate nerve function, and Nerve growth factor (NGF) immunoexpression and axonal parameters were measured. Plasma irisin levels, nerve NGF, and Nrf2 levels were quantified. RESULTS: The Surgery and Saline Group exhibited impaired EMG latency, amplitude, and inclined plane score compared to Controls, while the Surgery and OT Group demonstrated improved outcomes. Histomorphometric analysis revealed increased NGF immunoexpression, axon number, diameter, and reduced fibrosis in the Surgery and OT Group. Plasma irisin levels were higher following oxytocin administration. Additionally, nerve NGF and Nrf2 levels were elevated in the Surgery and OT Group. CONCLUSIONS: OT administration mitigated nerve injury effects, promoting functional and histological improvements. Elevated NGF and Nrf2 levels, along with increased irisin, indicated the potential interplay of these pathways in enhancing nerve recovery. The results align with OT’s neuroprotective and anti-inflammatory roles, suggesting its potential as a therapeutic intervention for nerve injuries. OT’s positive impact on nerve recovery is associated with its modulation of Nrf2 and irisin pathways, which collectively enhance antioxidant defense and neurotrophic support and mitigate inflammation. These findings underline OT’s potential as a therapeutic agent to enhance nerve regeneration and recovery. Further research is needed to elucidate the intricate molecular mechanisms and potential clinical applications of OT in nerve injury management. © 2023 Verduci Editore s.r.l. All rights reserved. | en_US |
dc.language.iso | eng | en_US |
dc.publisher | Verduci Editore s.r.l | en_US |
dc.relation.ispartof | European Review for Medical and Pharmacological Sciences | en_US |
dc.identifier.doi | 10.26355/eurrev_202312_34573 | |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | Nerve recovery | en_US |
dc.subject | Oxytocin | en_US |
dc.subject | Peripheral nerve damage | en_US |
dc.subject | irisin | en_US |
dc.subject | nerve growth factor | en_US |
dc.subject | oxytocin | en_US |
dc.subject | sodium chloride | en_US |
dc.subject | synpitan forte | en_US |
dc.subject | transcription factor Nrf2 | en_US |
dc.subject | antiinflammatory agent | en_US |
dc.subject | fibronectin | en_US |
dc.subject | nerve growth factor | en_US |
dc.subject | oxytocin | en_US |
dc.subject | transcription factor Nrf2 | en_US |
dc.subject | adult | en_US |
dc.subject | animal experiment | en_US |
dc.subject | animal model | en_US |
dc.subject | animal tissue | en_US |
dc.subject | Article | en_US |
dc.subject | axon | en_US |
dc.subject | axon diameter | en_US |
dc.subject | cohort analysis | en_US |
dc.subject | drug activity | en_US |
dc.subject | electromyography | en_US |
dc.subject | experimental sciatic nerve injury | en_US |
dc.subject | fibrosis | en_US |
dc.subject | histochemistry | en_US |
dc.subject | histopathology | en_US |
dc.subject | inclined plane test | en_US |
dc.subject | male | en_US |
dc.subject | motor function test | en_US |
dc.subject | nerve function | en_US |
dc.subject | nerve regeneration | en_US |
dc.subject | nonhuman | en_US |
dc.subject | peripheral nerve injury | en_US |
dc.subject | protein blood level | en_US |
dc.subject | protein expression | en_US |
dc.subject | rat | en_US |
dc.subject | rat model | en_US |
dc.subject | Wistar rat | en_US |
dc.subject | animal | en_US |
dc.subject | pathology | en_US |
dc.subject | sciatic nerve | en_US |
dc.subject | Animals | en_US |
dc.subject | Anti-Inflammatory Agents | en_US |
dc.subject | Fibronectins | en_US |
dc.subject | Male | en_US |
dc.subject | Nerve Growth Factor | en_US |
dc.subject | NF-E2-Related Factor 2 | en_US |
dc.subject | Oxytocin | en_US |
dc.subject | Peripheral Nerve Injuries | en_US |
dc.subject | Rats | en_US |
dc.subject | Rats, Wistar | en_US |
dc.subject | Sciatic Nerve | en_US |
dc.title | Oxytocin mitigates peripheral nerve damage via Nrf2 and irisin pathway | en_US |
dc.type | article | en_US |
dc.department | DBÜ | en_US |
dc.identifier.issue | 24 | en_US |
dc.identifier.volume | 27 | en_US |
dc.identifier.startpage | 11340 | en_US |
dc.identifier.endpage | 11350 | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.department-temp | Tosyali, H.K., Department of Orthopedics and Traumatology, Faculty of Medicine, Celal Bayar University, Manisa, Turkey; Bora, E.S., Department of Emergency Medicine, Izmir Ataturk Research and Training Hospital, Izmir, Turkey; Çinaroğlu, O.S., Department of Emergency Medicine, Faculty of Medicine, Izmir Katip Çelebi University, Izmir, Turkey; Erbaş, O., Department of Physiology, Faculty of Medicine, Demiroğlu Bilim University, Istanbul, Turkey | en_US |
dc.identifier.pmid | 38095383 | en_US |
dc.identifier.scopus | 2-s2.0-85179766276 | en_US |
dc.authorscopusid | 57189620270 | |
dc.authorscopusid | 55672440000 | |
dc.authorscopusid | 58317792500 | |
dc.authorscopusid | 55469991100 | |