Analysis of the anti-allodynic effects of combination of a synthetic cannabinoid and a selective noradrenaline re-uptake inhibitor in nerve injury-induced neuropathic mice
dc.authorid | Ulugol, Ahmet/0000-0003-4643-1124 | |
dc.authorid | Gunduz, Ozgur/0000-0002-2470-3021 | |
dc.authorid | Karadag, Cetin Hakan/0000-0002-4763-986X | |
dc.authorwosid | GÜNDÜZ, Özgür/AAH-8717-2019 | |
dc.authorwosid | Ulugol, Ahmet/V-9665-2019 | |
dc.authorwosid | Gunduz, Ozgur/A-2351-2016 | |
dc.authorwosid | Karadag, Cetin Hakan/H-4899-2013 | |
dc.contributor.author | Gunduz, O. | |
dc.contributor.author | Topuz, R. D. | |
dc.contributor.author | Karadag, C. H. | |
dc.contributor.author | Ulugol, A. | |
dc.date.accessioned | 2024-06-12T11:19:46Z | |
dc.date.available | 2024-06-12T11:19:46Z | |
dc.date.issued | 2016 | |
dc.department | Trakya Üniversitesi | en_US |
dc.description.abstract | BackgroundCombining drugs not only reduces specific adverse effects of each of the drug at a higher dose but also may lead to enhanced efficacy. Tapentadol is a recently discovered analgesic possessing -opioid receptor agonism and noradrenaline re-uptake inhibition in a single molecule. Taking into consideration, the pharmacological similarities between opioids and cannabinoids, we assumed that combination of cannabinoids with noradrenaline re-uptake inhibitors might also be effective. We therefore aimed to determine whether combining 1:1, 1:3 and 3:1 fixed ratios of the synthetic cannabinoid WIN 55,212-2 and the selective noradrenaline re-uptake inhibitor maprotiline exert anti-allodynic synergy on nerve-injured neuropathic mice. MethodsPartial tight ligation of the sciatic nerve was made in mice; on pre-operative and post-operative 15 days basal mechanical allodynia, cold allodynia and motor function were assessed using von Frey filaments, hot/cold plate and rota rod apparatus. ResultsMechanical and cold allodynia developed in all groups on post-operative 15 days. Development of cold allodynia was statistically significant in all groups (p<0.05); therefore, cold allodynia was used in combination studies. As shown by isobolographic analysis, interactions of 1:1 and 3:1 ratios of WIN 55,212-2:maprotiline combinations were supra-additive, whereas 1:3 ratio was sub-additive. ConclusionsOverall, our data suggest that combination of a cannabinoid with a selective noradrenaline re-uptake inhibitor may offer a beneficial treatment option for neuropathic pain. | en_US |
dc.description.sponsorship | TUBITAK [113S162] | en_US |
dc.description.sponsorship | This work was supported by a grant from TUBITAK (113S162). | en_US |
dc.identifier.doi | 10.1002/ejp.752 | |
dc.identifier.endpage | 471 | en_US |
dc.identifier.issn | 1090-3801 | |
dc.identifier.issn | 1532-2149 | |
dc.identifier.issue | 3 | en_US |
dc.identifier.pmid | 26206340 | en_US |
dc.identifier.scopus | 2-s2.0-84958839704 | en_US |
dc.identifier.scopusquality | Q1 | en_US |
dc.identifier.startpage | 465 | en_US |
dc.identifier.uri | https://doi.org/10.1002/ejp.752 | |
dc.identifier.uri | https://hdl.handle.net/20.500.14551/25338 | |
dc.identifier.volume | 20 | en_US |
dc.identifier.wos | WOS:000370446500014 | en_US |
dc.identifier.wosquality | Q2 | en_US |
dc.indekslendigikaynak | Web of Science | en_US |
dc.indekslendigikaynak | Scopus | en_US |
dc.indekslendigikaynak | PubMed | en_US |
dc.language.iso | en | en_US |
dc.publisher | Wiley-Blackwell | en_US |
dc.relation.ispartof | European Journal Of Pain | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | Rat Formalin Test | en_US |
dc.subject | Chronic Pain | en_US |
dc.subject | Tactile Allodynia | en_US |
dc.subject | Receptor Agonist | en_US |
dc.subject | Win 55,212-2 | en_US |
dc.subject | Tapentadol | en_US |
dc.subject | Tolerance | en_US |
dc.subject | Antinociception | en_US |
dc.subject | Win-55,212-2 | en_US |
dc.subject | Analgesics | en_US |
dc.title | Analysis of the anti-allodynic effects of combination of a synthetic cannabinoid and a selective noradrenaline re-uptake inhibitor in nerve injury-induced neuropathic mice | en_US |
dc.type | Article | en_US |