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Pharmacological modulation of brain levels of glutamate and GABA in rats exposed to total sleep deprivation

Modulation of gamma-aminobutyric acid (GABA) and glutamate by selected antidepressants and anticonvulsants could play a beneficial role in total sleep deprivation (TSD) caused by depressed mood. In the present study, albino rats were exposed to TSD for five days. On the sixth day, the brains were re...

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Autor principal: Kamal, Sahar Mohamed
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4863290/
https://www.ncbi.nlm.nih.gov/pubmed/27186093
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author Kamal, Sahar Mohamed
author_facet Kamal, Sahar Mohamed
author_sort Kamal, Sahar Mohamed
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description Modulation of gamma-aminobutyric acid (GABA) and glutamate by selected antidepressants and anticonvulsants could play a beneficial role in total sleep deprivation (TSD) caused by depressed mood. In the present study, albino rats were exposed to TSD for five days. On the sixth day, the brains were removed, and GABA and glutamate levels were measured in the prefrontal cortex and thalamus to identify TSD-induced changes in untreated rats and in rats treated with carbamazepine 40 mg/kg intraperitoneally (IP), fluoxetine 20 mg/kg IP, or desipramine 10 mg/kg IP. Carbamazepine and fluoxetine significantly increased GABA and reduced glutamate levels in both brain areas. Desipramine administration did not affect GABA or glutamate concentrations in the tested brain areas; levels were comparable with those induced by TSD without treatment. These results suggest that administration of carbamazepine or fluoxetine could have a beneficial effect by increasing GABA levels during TSD.
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spelling pubmed-48632902016-05-16 Pharmacological modulation of brain levels of glutamate and GABA in rats exposed to total sleep deprivation Kamal, Sahar Mohamed J Exp Pharmacol Original Research Modulation of gamma-aminobutyric acid (GABA) and glutamate by selected antidepressants and anticonvulsants could play a beneficial role in total sleep deprivation (TSD) caused by depressed mood. In the present study, albino rats were exposed to TSD for five days. On the sixth day, the brains were removed, and GABA and glutamate levels were measured in the prefrontal cortex and thalamus to identify TSD-induced changes in untreated rats and in rats treated with carbamazepine 40 mg/kg intraperitoneally (IP), fluoxetine 20 mg/kg IP, or desipramine 10 mg/kg IP. Carbamazepine and fluoxetine significantly increased GABA and reduced glutamate levels in both brain areas. Desipramine administration did not affect GABA or glutamate concentrations in the tested brain areas; levels were comparable with those induced by TSD without treatment. These results suggest that administration of carbamazepine or fluoxetine could have a beneficial effect by increasing GABA levels during TSD. Dove Medical Press 2010-06-03 /pmc/articles/PMC4863290/ /pubmed/27186093 Text en © 2010 Kamal, publisher and licensee Dove Medical Press Ltd This is an Open Access article which permits unrestricted noncommercial use, provided the original work is properly cited.
spellingShingle Original Research
Kamal, Sahar Mohamed
Pharmacological modulation of brain levels of glutamate and GABA in rats exposed to total sleep deprivation
title Pharmacological modulation of brain levels of glutamate and GABA in rats exposed to total sleep deprivation
title_full Pharmacological modulation of brain levels of glutamate and GABA in rats exposed to total sleep deprivation
title_fullStr Pharmacological modulation of brain levels of glutamate and GABA in rats exposed to total sleep deprivation
title_full_unstemmed Pharmacological modulation of brain levels of glutamate and GABA in rats exposed to total sleep deprivation
title_short Pharmacological modulation of brain levels of glutamate and GABA in rats exposed to total sleep deprivation
title_sort pharmacological modulation of brain levels of glutamate and gaba in rats exposed to total sleep deprivation
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4863290/
https://www.ncbi.nlm.nih.gov/pubmed/27186093
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