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[Melatonin influences the release of endogenous opioid peptides in rat periaqueductal gray].
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2000
Year
Pain MedicineCentral MechanismsMolecular PharmacologyEndogenous Opioid PeptidesPain ManagementPush-pull PerfusionAnesthetic PharmacologyHealth SciencesBehavioral NeuroscienceBehavioural PharmacologyBehavioral PharmacologyNeuropharmacologyNervous SystemPharmacologyMelatoninPain ResearchPush-pull Perfusion TechniqueNeurophysiologyPhysiologyNeuropeptide ReceptorNeuroscienceAnesthesiaMedicineNeuropeptides
The present study was undertaken to explore central mechanisms underlying the analgesic effect of melatonin. Push-pull perfusion technique and radioimmunoassay were used to observe the changes in the contents of beta-endorphin (beta-Ep) and leucine-enkephalin (L-EK) in the perfusate from the rat periaqueductal gray (PAG) after administration of melatonin. 30 50 min after an intraperitoneal injection of melatonin (110 mg/kg), the beta-Ep content in the perfusate was increased significantly, while the L-EK content was not changed. Pain threshold was measured using the warm water tail-flick test during the push-pull perfusion of the PAG. It was found that the rat pain threshold was increased significantly 40 min after the intraperitoneal injection of melatonin (110 mg/kg). The results suggest that melatonin may promote the release of beta-Ep in the PAG, which may be one of the mechanisms of the analgesic effect of melatonin.