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Modulation of GABA(B) receptors in the insula bidirectionally affects associative memory of epilectic rats in both spatial and non-spatial operant tasks

BACKGROUND: Stimulation of gamma-aminobutyric acid (GABA) activity through GABA receptor agonists is the basic mechanism of many anticonvulsant drugs. Nevertheless, many of these GABergic drugs have adverse cognitive effects. We previously found that GABAB receptors (GABA(B)Rs) in the insula regulat...

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Autores principales: Wu, Nan, Sun, Tao, Wu, Xin, Chen, Hongguang, Zhang, Zhen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9846148/
https://www.ncbi.nlm.nih.gov/pubmed/36688127
http://dx.doi.org/10.3389/fnbeh.2022.1042227
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author Wu, Nan
Sun, Tao
Wu, Xin
Chen, Hongguang
Zhang, Zhen
author_facet Wu, Nan
Sun, Tao
Wu, Xin
Chen, Hongguang
Zhang, Zhen
author_sort Wu, Nan
collection PubMed
description BACKGROUND: Stimulation of gamma-aminobutyric acid (GABA) activity through GABA receptor agonists is the basic mechanism of many anticonvulsant drugs. Nevertheless, many of these GABergic drugs have adverse cognitive effects. We previously found that GABAB receptors (GABA(B)Rs) in the insula regulate operant associative memory in healthy rats. The present study aimed at investigating the effects of GABA(B)R modulation in the insula on operant associative memory in epileptic rats, along with the underlying mechanisms. METHODS: The lithium-pilocarpine model of temporal lobe epilepsy (TLE) was established in male Sprague–Dawley rats. A 22-gauge stainless-steel guide cannula was surgically implanted into the granular insula cortex of the epileptic rats. Baclofen (125 ng/μl, 1 μl), CGP35348 (12.5 μg/μl, 1 μl), or saline (1 μl) was slowly infused through the guide cannula. The Intellicage automated behavioral testing system was used to evaluate operant associative memory of the epileptic rats, including non-spatial operant tasks (basic nosepoke learning and skilled nosepoke learning) and spatial operant tasks (chamber position learning). The expression of the GABA(B)R subunits GB1 and GB2 in the insula was examined by immunofluorescence and Western blotting. RESULTS: The Intellicage tests demonstrated that baclofen significantly impaired basic nosepoke learning, skilled nosepoke learning and chamber position learning of the epileptic rats, while CGP35348 boosted these functions. Immunofluorescence staining revealed that GB1 and GB2 were expressed in the insula of the epileptic rats, and Western blotting analysis showed that baclofen enhanced while CGP35348 inhibited the expression of these subunits. CONCLUSION: GABA(B)Rs in the insula bidirectionally regulate both spatial and non-spatial operant associative memory of epileptic rats. Effects of GABA(B)Rs on cognition should be taken into account when evaluating new possible treatments for people with epilepsy.
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spelling pubmed-98461482023-01-19 Modulation of GABA(B) receptors in the insula bidirectionally affects associative memory of epilectic rats in both spatial and non-spatial operant tasks Wu, Nan Sun, Tao Wu, Xin Chen, Hongguang Zhang, Zhen Front Behav Neurosci Neuroscience BACKGROUND: Stimulation of gamma-aminobutyric acid (GABA) activity through GABA receptor agonists is the basic mechanism of many anticonvulsant drugs. Nevertheless, many of these GABergic drugs have adverse cognitive effects. We previously found that GABAB receptors (GABA(B)Rs) in the insula regulate operant associative memory in healthy rats. The present study aimed at investigating the effects of GABA(B)R modulation in the insula on operant associative memory in epileptic rats, along with the underlying mechanisms. METHODS: The lithium-pilocarpine model of temporal lobe epilepsy (TLE) was established in male Sprague–Dawley rats. A 22-gauge stainless-steel guide cannula was surgically implanted into the granular insula cortex of the epileptic rats. Baclofen (125 ng/μl, 1 μl), CGP35348 (12.5 μg/μl, 1 μl), or saline (1 μl) was slowly infused through the guide cannula. The Intellicage automated behavioral testing system was used to evaluate operant associative memory of the epileptic rats, including non-spatial operant tasks (basic nosepoke learning and skilled nosepoke learning) and spatial operant tasks (chamber position learning). The expression of the GABA(B)R subunits GB1 and GB2 in the insula was examined by immunofluorescence and Western blotting. RESULTS: The Intellicage tests demonstrated that baclofen significantly impaired basic nosepoke learning, skilled nosepoke learning and chamber position learning of the epileptic rats, while CGP35348 boosted these functions. Immunofluorescence staining revealed that GB1 and GB2 were expressed in the insula of the epileptic rats, and Western blotting analysis showed that baclofen enhanced while CGP35348 inhibited the expression of these subunits. CONCLUSION: GABA(B)Rs in the insula bidirectionally regulate both spatial and non-spatial operant associative memory of epileptic rats. Effects of GABA(B)Rs on cognition should be taken into account when evaluating new possible treatments for people with epilepsy. Frontiers Media S.A. 2023-01-04 /pmc/articles/PMC9846148/ /pubmed/36688127 http://dx.doi.org/10.3389/fnbeh.2022.1042227 Text en Copyright © 2023 Wu, Sun, Wu, Chen and Zhang. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Wu, Nan
Sun, Tao
Wu, Xin
Chen, Hongguang
Zhang, Zhen
Modulation of GABA(B) receptors in the insula bidirectionally affects associative memory of epilectic rats in both spatial and non-spatial operant tasks
title Modulation of GABA(B) receptors in the insula bidirectionally affects associative memory of epilectic rats in both spatial and non-spatial operant tasks
title_full Modulation of GABA(B) receptors in the insula bidirectionally affects associative memory of epilectic rats in both spatial and non-spatial operant tasks
title_fullStr Modulation of GABA(B) receptors in the insula bidirectionally affects associative memory of epilectic rats in both spatial and non-spatial operant tasks
title_full_unstemmed Modulation of GABA(B) receptors in the insula bidirectionally affects associative memory of epilectic rats in both spatial and non-spatial operant tasks
title_short Modulation of GABA(B) receptors in the insula bidirectionally affects associative memory of epilectic rats in both spatial and non-spatial operant tasks
title_sort modulation of gaba(b) receptors in the insula bidirectionally affects associative memory of epilectic rats in both spatial and non-spatial operant tasks
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9846148/
https://www.ncbi.nlm.nih.gov/pubmed/36688127
http://dx.doi.org/10.3389/fnbeh.2022.1042227
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