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Memory-enhancing treatments reverse the impairment of inhibitory avoidance retention in sepsis-surviving rats

INTRODUCTION: Survivors from sepsis have presented with long-term cognitive impairment, including alterations in memory, attention, concentration, and global loss of cognitive function. Thus, we evaluated the effects of memory enhancers in sepsis-surviving rats. METHODS: The rats underwent cecal lig...

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Autores principales: Tuon, Lisiane, Comim, Clarissa M, Petronilho, Fabrícia, Barichello, Tatiana, Izquierdo, Ivan, Quevedo, João, Dal-Pizzol, Felipe
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2592772/
https://www.ncbi.nlm.nih.gov/pubmed/18957125
http://dx.doi.org/10.1186/cc7103
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author Tuon, Lisiane
Comim, Clarissa M
Petronilho, Fabrícia
Barichello, Tatiana
Izquierdo, Ivan
Quevedo, João
Dal-Pizzol, Felipe
author_facet Tuon, Lisiane
Comim, Clarissa M
Petronilho, Fabrícia
Barichello, Tatiana
Izquierdo, Ivan
Quevedo, João
Dal-Pizzol, Felipe
author_sort Tuon, Lisiane
collection PubMed
description INTRODUCTION: Survivors from sepsis have presented with long-term cognitive impairment, including alterations in memory, attention, concentration, and global loss of cognitive function. Thus, we evaluated the effects of memory enhancers in sepsis-surviving rats. METHODS: The rats underwent cecal ligation and perforation (CLP) (sepsis group) with 'basic support' (saline at 50 mL/kg immediately and 12 hours after CLP plus ceftriaxone at 30 mg/kg and clindamycin at 25 mg/kg 6, 12, and 18 hours after CLP) or sham-operated (control group). After 10 or 30 days, rats were submitted to an inhibitory avoidance task. After task training, animals received injections of saline, epinephrine, naloxone, dexamethasone, or glucose. Twenty-four hours afterwards, animals were submitted to the inhibitory avoidance test. RESULTS: We demonstrated that memory enhancers reversed impairment in the sepsis group 10 and 30 days after sepsis induction. This effect was of lower magnitude when compared with sham animals 10 days, but not 30 days, after sepsis. CONCLUSIONS: Using different pharmacologic approaches, we conclude that the adrenergic memory formation pathways are responsive in sepsis-surviving animals.
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spelling pubmed-25927722008-12-03 Memory-enhancing treatments reverse the impairment of inhibitory avoidance retention in sepsis-surviving rats Tuon, Lisiane Comim, Clarissa M Petronilho, Fabrícia Barichello, Tatiana Izquierdo, Ivan Quevedo, João Dal-Pizzol, Felipe Crit Care Research INTRODUCTION: Survivors from sepsis have presented with long-term cognitive impairment, including alterations in memory, attention, concentration, and global loss of cognitive function. Thus, we evaluated the effects of memory enhancers in sepsis-surviving rats. METHODS: The rats underwent cecal ligation and perforation (CLP) (sepsis group) with 'basic support' (saline at 50 mL/kg immediately and 12 hours after CLP plus ceftriaxone at 30 mg/kg and clindamycin at 25 mg/kg 6, 12, and 18 hours after CLP) or sham-operated (control group). After 10 or 30 days, rats were submitted to an inhibitory avoidance task. After task training, animals received injections of saline, epinephrine, naloxone, dexamethasone, or glucose. Twenty-four hours afterwards, animals were submitted to the inhibitory avoidance test. RESULTS: We demonstrated that memory enhancers reversed impairment in the sepsis group 10 and 30 days after sepsis induction. This effect was of lower magnitude when compared with sham animals 10 days, but not 30 days, after sepsis. CONCLUSIONS: Using different pharmacologic approaches, we conclude that the adrenergic memory formation pathways are responsive in sepsis-surviving animals. BioMed Central 2008 2008-10-28 /pmc/articles/PMC2592772/ /pubmed/18957125 http://dx.doi.org/10.1186/cc7103 Text en Copyright © 2008 Tuon et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Tuon, Lisiane
Comim, Clarissa M
Petronilho, Fabrícia
Barichello, Tatiana
Izquierdo, Ivan
Quevedo, João
Dal-Pizzol, Felipe
Memory-enhancing treatments reverse the impairment of inhibitory avoidance retention in sepsis-surviving rats
title Memory-enhancing treatments reverse the impairment of inhibitory avoidance retention in sepsis-surviving rats
title_full Memory-enhancing treatments reverse the impairment of inhibitory avoidance retention in sepsis-surviving rats
title_fullStr Memory-enhancing treatments reverse the impairment of inhibitory avoidance retention in sepsis-surviving rats
title_full_unstemmed Memory-enhancing treatments reverse the impairment of inhibitory avoidance retention in sepsis-surviving rats
title_short Memory-enhancing treatments reverse the impairment of inhibitory avoidance retention in sepsis-surviving rats
title_sort memory-enhancing treatments reverse the impairment of inhibitory avoidance retention in sepsis-surviving rats
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2592772/
https://www.ncbi.nlm.nih.gov/pubmed/18957125
http://dx.doi.org/10.1186/cc7103
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