Pharmacological evidence for the possible involvement of the NMDA receptor pathway in the anticonvulsant effect of tramadol in mice

Background: Previous studies have shown controversial results regarding the pro- or anticonvulsant effects of tramadol. Additionally, the underlying mechanism of seizure induction or alleviation by tramadol has not been fully understood. In the current study, the effects of tramadol on pentylenetet...

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Main Authors: Mazyar Zahir, Amir Rashidian, Mohsen Hoseini, Reyhaneh Akbarian, Mohsen Chamanara
Format: Article
Language:English
Published: AIMS Press 2022-11-01
Series:AIMS Neuroscience
Subjects:
Online Access:https://www.aimspress.com/article/doi/10.3934/Neuroscience.2022024?viewType=HTML
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author Mazyar Zahir
Amir Rashidian
Mohsen Hoseini
Reyhaneh Akbarian
Mohsen Chamanara
author_facet Mazyar Zahir
Amir Rashidian
Mohsen Hoseini
Reyhaneh Akbarian
Mohsen Chamanara
author_sort Mazyar Zahir
collection DOAJ
description Background: Previous studies have shown controversial results regarding the pro- or anticonvulsant effects of tramadol. Additionally, the underlying mechanism of seizure induction or alleviation by tramadol has not been fully understood. In the current study, the effects of tramadol on pentylenetetrazole (PTZ)-induced seizure and the possible involvement of the N-methyl-D-aspartate (NMDA) pathway were assessed in mice. Methods: Male Naval Medical Research Institute (NMRI) mice were treated with intravenous infusion of PTZ in order to induce clonic seizures and determine seizure threshold. Tramadol was injected intraperitoneally (0.1–150 mg/kg) 30 minutes prior to elicitation of seizures. The possible effects of intraperitoneal injections of NMDA receptor antagonists, ketamine (0.5 mg/kg) and MK-801 (0.5 mg/kg) on the anticonvulsant property of tramadol were investigated subsequently. Results: Tramadol (1–100 mg/kg) increased PTZ-induced seizure threshold in a dose-dependent, time-independent manner, with optimal anticonvulsant effect at a dose of 100 mg/kg. Acute administration of either ketamine (0.5 mg/kg) or MK-801 (0.5 mg/kg) potentiated the anticonvulsant effect of a subeffective dose of tramadol (0.3 mg/kg). Conclusion: These results suggest a possible role of the NMDA pathway in the anticonvulsant effect of tramadol.
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spelling doaj.art-a03c33a7c01345e697986c887a23547b2023-01-10T01:45:54ZengAIMS PressAIMS Neuroscience2373-79722022-11-019444445310.3934/Neuroscience.2022024Pharmacological evidence for the possible involvement of the NMDA receptor pathway in the anticonvulsant effect of tramadol in miceMazyar Zahir 0Amir Rashidian 1Mohsen Hoseini 2Reyhaneh Akbarian3Mohsen Chamanara41. Department of Pharmacology, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran1. Department of Pharmacology, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran 2. Experimental Medicine Research Center, Tehran University of Medical Sciences, Tehran, Iran1. Department of Pharmacology, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran 2. Experimental Medicine Research Center, Tehran University of Medical Sciences, Tehran, Iran1. Department of Pharmacology, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran3. Department of Pharmacology, School of Medicine, Aja University of Medical Sciences, P.O. Box 1411718541, Tehran, IranBackground: Previous studies have shown controversial results regarding the pro- or anticonvulsant effects of tramadol. Additionally, the underlying mechanism of seizure induction or alleviation by tramadol has not been fully understood. In the current study, the effects of tramadol on pentylenetetrazole (PTZ)-induced seizure and the possible involvement of the N-methyl-D-aspartate (NMDA) pathway were assessed in mice. Methods: Male Naval Medical Research Institute (NMRI) mice were treated with intravenous infusion of PTZ in order to induce clonic seizures and determine seizure threshold. Tramadol was injected intraperitoneally (0.1–150 mg/kg) 30 minutes prior to elicitation of seizures. The possible effects of intraperitoneal injections of NMDA receptor antagonists, ketamine (0.5 mg/kg) and MK-801 (0.5 mg/kg) on the anticonvulsant property of tramadol were investigated subsequently. Results: Tramadol (1–100 mg/kg) increased PTZ-induced seizure threshold in a dose-dependent, time-independent manner, with optimal anticonvulsant effect at a dose of 100 mg/kg. Acute administration of either ketamine (0.5 mg/kg) or MK-801 (0.5 mg/kg) potentiated the anticonvulsant effect of a subeffective dose of tramadol (0.3 mg/kg). Conclusion: These results suggest a possible role of the NMDA pathway in the anticonvulsant effect of tramadol.https://www.aimspress.com/article/doi/10.3934/Neuroscience.2022024?viewType=HTMLanticonvulsantsmicen-methylaspartateseizurestramadol
spellingShingle Mazyar Zahir
Amir Rashidian
Mohsen Hoseini
Reyhaneh Akbarian
Mohsen Chamanara
Pharmacological evidence for the possible involvement of the NMDA receptor pathway in the anticonvulsant effect of tramadol in mice
AIMS Neuroscience
anticonvulsants
mice
n-methylaspartate
seizures
tramadol
title Pharmacological evidence for the possible involvement of the NMDA receptor pathway in the anticonvulsant effect of tramadol in mice
title_full Pharmacological evidence for the possible involvement of the NMDA receptor pathway in the anticonvulsant effect of tramadol in mice
title_fullStr Pharmacological evidence for the possible involvement of the NMDA receptor pathway in the anticonvulsant effect of tramadol in mice
title_full_unstemmed Pharmacological evidence for the possible involvement of the NMDA receptor pathway in the anticonvulsant effect of tramadol in mice
title_short Pharmacological evidence for the possible involvement of the NMDA receptor pathway in the anticonvulsant effect of tramadol in mice
title_sort pharmacological evidence for the possible involvement of the nmda receptor pathway in the anticonvulsant effect of tramadol in mice
topic anticonvulsants
mice
n-methylaspartate
seizures
tramadol
url https://www.aimspress.com/article/doi/10.3934/Neuroscience.2022024?viewType=HTML
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