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Modulatory Effect of Serotonergic System in Pentylenetetrazole-Induced Seizures and Associated Memory Deficit: Role of 5-HT(1A) and 5-HT(2A/2C)

BACKGROUND AND PURPOSE: Recent studies have recognised the memory deficit as one of the most common psychiatric issues in the patients with epilepsy, which severely affects the quality of life. Our previous studies have demonstrated the possible involvement of serotonergic system in the pathogenesis...

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Autores principales: Mishra, Awanish, Goel, Rajesh Kumar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Epilepsy Society 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7251343/
https://www.ncbi.nlm.nih.gov/pubmed/32509547
http://dx.doi.org/10.14581/jer.19012
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author Mishra, Awanish
Goel, Rajesh Kumar
author_facet Mishra, Awanish
Goel, Rajesh Kumar
author_sort Mishra, Awanish
collection PubMed
description BACKGROUND AND PURPOSE: Recent studies have recognised the memory deficit as one of the most common psychiatric issues in the patients with epilepsy, which severely affects the quality of life. Our previous studies have demonstrated the possible involvement of serotonergic system in the pathogenesis of epilepsy and associated memory deficit. The possible involvement of 5-HT(1A) and 5-HT(2A/2C) receptor has not been explored yet. Therefore, this study has been envisaged to explore the effect of 5-HT(1A) and 5-HT(2A/2C) receptor modulation on epilepsy and memory deficit in pentylenetetrazole-kindled mice. METHODS: In the present experimental approach, we examined the efficacy of modulation of 5-HT(1A) and 5-HT(2A/2C) receptor in pentylenetetrazole-induced kindling in male Swiss mice (n=75). Mice were kindled by sub-convulsive dose of pentylenetetrazole (35 mg/kg, intraperitoneal injection), at the interval of 48±2 hours). Successfully kindled animals were treated with 5-HT(1A) and 5-HT(2A/2C) receptor modulators. The effect of different treatments on seizure severity score and memory impairment was analysed. RESULTS: 5-HT(1A) receptor agonist improved the memory functions while seizure severity was not improved, and the opposite effect was observed with 5-HT(1A) receptor antagonist. On the other hand, 5-HT(2A/2C) receptor agonist significantly improved memory deficit as well as seizure severity in the kindled animals. CONCLUSIONS: The outcome of the study indicates the possible involvement of 5-HT(2A/2C) receptor in the pathogenesis of epilepsy and associated memory deficit, which can be further explored for its management.
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spelling pubmed-72513432020-06-05 Modulatory Effect of Serotonergic System in Pentylenetetrazole-Induced Seizures and Associated Memory Deficit: Role of 5-HT(1A) and 5-HT(2A/2C) Mishra, Awanish Goel, Rajesh Kumar J Epilepsy Res Original Article BACKGROUND AND PURPOSE: Recent studies have recognised the memory deficit as one of the most common psychiatric issues in the patients with epilepsy, which severely affects the quality of life. Our previous studies have demonstrated the possible involvement of serotonergic system in the pathogenesis of epilepsy and associated memory deficit. The possible involvement of 5-HT(1A) and 5-HT(2A/2C) receptor has not been explored yet. Therefore, this study has been envisaged to explore the effect of 5-HT(1A) and 5-HT(2A/2C) receptor modulation on epilepsy and memory deficit in pentylenetetrazole-kindled mice. METHODS: In the present experimental approach, we examined the efficacy of modulation of 5-HT(1A) and 5-HT(2A/2C) receptor in pentylenetetrazole-induced kindling in male Swiss mice (n=75). Mice were kindled by sub-convulsive dose of pentylenetetrazole (35 mg/kg, intraperitoneal injection), at the interval of 48±2 hours). Successfully kindled animals were treated with 5-HT(1A) and 5-HT(2A/2C) receptor modulators. The effect of different treatments on seizure severity score and memory impairment was analysed. RESULTS: 5-HT(1A) receptor agonist improved the memory functions while seizure severity was not improved, and the opposite effect was observed with 5-HT(1A) receptor antagonist. On the other hand, 5-HT(2A/2C) receptor agonist significantly improved memory deficit as well as seizure severity in the kindled animals. CONCLUSIONS: The outcome of the study indicates the possible involvement of 5-HT(2A/2C) receptor in the pathogenesis of epilepsy and associated memory deficit, which can be further explored for its management. Korean Epilepsy Society 2019-12-31 /pmc/articles/PMC7251343/ /pubmed/32509547 http://dx.doi.org/10.14581/jer.19012 Text en Copyright © 2019 Korean Epilepsy Society This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Mishra, Awanish
Goel, Rajesh Kumar
Modulatory Effect of Serotonergic System in Pentylenetetrazole-Induced Seizures and Associated Memory Deficit: Role of 5-HT(1A) and 5-HT(2A/2C)
title Modulatory Effect of Serotonergic System in Pentylenetetrazole-Induced Seizures and Associated Memory Deficit: Role of 5-HT(1A) and 5-HT(2A/2C)
title_full Modulatory Effect of Serotonergic System in Pentylenetetrazole-Induced Seizures and Associated Memory Deficit: Role of 5-HT(1A) and 5-HT(2A/2C)
title_fullStr Modulatory Effect of Serotonergic System in Pentylenetetrazole-Induced Seizures and Associated Memory Deficit: Role of 5-HT(1A) and 5-HT(2A/2C)
title_full_unstemmed Modulatory Effect of Serotonergic System in Pentylenetetrazole-Induced Seizures and Associated Memory Deficit: Role of 5-HT(1A) and 5-HT(2A/2C)
title_short Modulatory Effect of Serotonergic System in Pentylenetetrazole-Induced Seizures and Associated Memory Deficit: Role of 5-HT(1A) and 5-HT(2A/2C)
title_sort modulatory effect of serotonergic system in pentylenetetrazole-induced seizures and associated memory deficit: role of 5-ht(1a) and 5-ht(2a/2c)
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7251343/
https://www.ncbi.nlm.nih.gov/pubmed/32509547
http://dx.doi.org/10.14581/jer.19012
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