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dc.contributor.authorStefani, Luciana Cadoreen_US
dc.contributor.authorMuller, Suzanaen_US
dc.contributor.authorTorres, Iraci L. S.en_US
dc.contributor.authorRazzolini, Brunaen_US
dc.contributor.authorRozisky, Joanna R.en_US
dc.contributor.authorFregni, Felipeen_US
dc.contributor.authorMarkus, Reginaen_US
dc.contributor.authorCaumo, Wolneien_US
dc.date.accessioned2014-03-10T20:34:28Z
dc.date.issued2013en_US
dc.identifier.citationStefani, Luciana Cadore, Suzana Muller, Iraci L. S. Torres, Bruna Razzolini, Joanna R. Rozisky, Felipe Fregni, Regina Markus, and Wolnei Caumo. 2013. “A Phase II, Randomized, Double-Blind, Placebo Controlled, Dose-Response Trial of the Melatonin Effect on the Pain Threshold of Healthy Subjects.” PLoS ONE 8 (10): e74107. doi:10.1371/journal.pone.0074107. http://dx.doi.org/10.1371/journal.pone.0074107.en
dc.identifier.issn1932-6203en
dc.identifier.urihttp://nrs.harvard.edu/urn-3:HUL.InstRepos:11878959
dc.description.abstractBackground: Previous studies have suggested that melatonin may produce antinociception through peripheral and central mechanisms. Based on the preliminary encouraging results of studies of the effects of melatonin on pain modulation, the important question has been raised of whether there is a dose relationship in humans of melatonin on pain modulation. Objective: The objective was to evaluate the analgesic dose response of the effects of melatonin on pressure and heat pain threshold and tolerance and the sedative effects. Methods: Sixty-one healthy subjects aged 19 to 47 y were randomized into one of four groups: placebo, 0.05 mg/kg sublingual melatonin, 0.15 mg/kg sublingual melatonin or 0.25 mg/kg sublingual melatonin. We determine the pressure pain threshold (PPT) and the pressure pain tolerance (PPTo). Quantitative sensory testing (QST) was used to measure the heat pain threshold (HPT) and the heat pain tolerance (HPTo). Sedation was assessed with a visual analogue scale and bispectral analysis. Results: Serum plasma melatonin levels were directly proportional to the melatonin doses given to each subject. We observed a significant effect associated with dose group. Post hoc analysis indicated significant differences between the placebo vs. the intermediate (0.15 mg/kg) and the highest (0.25 mg/kg) melatonin doses for all pain threshold and sedation level tests. A linear regression model indicated a significant association between the serum melatonin concentrations and changes in pain threshold and pain tolerance (R2 = 0.492 for HPT, R2 = 0.538 for PPT, R2 = 0.558 for HPTo and R2 = 0.584 for PPTo). Conclusions: The present data indicate that sublingual melatonin exerts well-defined dose-dependent antinociceptive activity. There is a correlation between the plasma melatonin drug concentration and acute changes in the pain threshold. These results provide additional support for the investigation of melatonin as an analgesic agent. Brazilian Clinical Trials Registry (ReBec): (U1111-1123-5109). IRB: Research Ethics Committee at the Hospital de Clínicas de Porto Alegre.en
dc.language.isoen_USen
dc.publisherPublic Library of Scienceen
dc.relation.isversionofdoi:10.1371/journal.pone.0074107en
dc.relation.hasversionhttp://www.ncbi.nlm.nih.gov/pmc/articles/PMC3788771/pdf/en
dash.licenseLAAen_US
dc.titleA Phase II, Randomized, Double-Blind, Placebo Controlled, Dose-Response Trial of the Melatonin Effect on the Pain Threshold of Healthy Subjectsen
dc.typeJournal Articleen_US
dc.description.versionVersion of Recorden
dc.relation.journalPLoS ONEen
dash.depositing.authorFregni, Felipeen_US
dc.date.available2014-03-10T20:34:28Z
dc.identifier.doi10.1371/journal.pone.0074107*
dash.contributor.affiliatedFregni, Felipe


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