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A Rodent Model of Schizophrenia Reveals Increase in Creatine Kinase Activity with Associated Behavior Changes

Schizophrenia is a debilitating mental disorder characterized by positive (delusions, hallucinations, disorganized speech) and negative (affective flattering, avolition and social withdrawal) symptoms as well as cognitive deficits. The frequency, severity and topography characterize the disorder as...

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Autores principales: Canever, Leila, Oliveira, Larissa, de Luca, Renata D'Altoé, Correa, Paulo T. F., Fraga, Daiane de B., Matos, Maria Paula, Scaini, Giselli, Quevedo, João, Streck, Emílio L., Zugno, Alexandra I.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3154043/
https://www.ncbi.nlm.nih.gov/pubmed/21270541
http://dx.doi.org/10.4161/oxim.3.6.13446
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author Canever, Leila
Oliveira, Larissa
de Luca, Renata D'Altoé
Correa, Paulo T. F.
Fraga, Daiane de B.
Matos, Maria Paula
Scaini, Giselli
Quevedo, João
Streck, Emílio L.
Zugno, Alexandra I.
author_facet Canever, Leila
Oliveira, Larissa
de Luca, Renata D'Altoé
Correa, Paulo T. F.
Fraga, Daiane de B.
Matos, Maria Paula
Scaini, Giselli
Quevedo, João
Streck, Emílio L.
Zugno, Alexandra I.
author_sort Canever, Leila
collection PubMed
description Schizophrenia is a debilitating mental disorder characterized by positive (delusions, hallucinations, disorganized speech) and negative (affective flattering, avolition and social withdrawal) symptoms as well as cognitive deficits. The frequency, severity and topography characterize the disorder as heterogeneous, the pathophysiology of schizophrenia is poorly understood. Sub-anesthetic doses of ketamine produce hyperactivity, stereotypy and abnormal social interaction and it is used as a model of schizophrenia. In this study, we induced an animal model by acute sub-anesthetic doses of ketamine and tested different behavioral parameters. We also evaluated the activity of creatine kinase (CK) in brain of rats treated with ketamine. Our results demonstrated that administration of 10, 25 and 50 mg/kg of ketamine induced an increase of covered distance in habituated and non-habituated rats to the behavioral apparatus. Ketamine administration induced significant social deficits and stereotypic behavioral in all doses tested. Finally we evaluated the effect of different doses of ketamine on creatinine kinase (CK) activity and we observed that CK activity is increased inspecific regions of the brain. Our study suggests that our animal model may be used as a model of schizophrenia and that cerebral energy metabolism might be altered in the brain of schizophrenic patients, probably leading to alterations that might be involved in the pathogenesis of schizophrenia.
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spelling pubmed-31540432011-08-29 A Rodent Model of Schizophrenia Reveals Increase in Creatine Kinase Activity with Associated Behavior Changes Canever, Leila Oliveira, Larissa de Luca, Renata D'Altoé Correa, Paulo T. F. Fraga, Daiane de B. Matos, Maria Paula Scaini, Giselli Quevedo, João Streck, Emílio L. Zugno, Alexandra I. Oxid Med Cell Longev Research Paper Schizophrenia is a debilitating mental disorder characterized by positive (delusions, hallucinations, disorganized speech) and negative (affective flattering, avolition and social withdrawal) symptoms as well as cognitive deficits. The frequency, severity and topography characterize the disorder as heterogeneous, the pathophysiology of schizophrenia is poorly understood. Sub-anesthetic doses of ketamine produce hyperactivity, stereotypy and abnormal social interaction and it is used as a model of schizophrenia. In this study, we induced an animal model by acute sub-anesthetic doses of ketamine and tested different behavioral parameters. We also evaluated the activity of creatine kinase (CK) in brain of rats treated with ketamine. Our results demonstrated that administration of 10, 25 and 50 mg/kg of ketamine induced an increase of covered distance in habituated and non-habituated rats to the behavioral apparatus. Ketamine administration induced significant social deficits and stereotypic behavioral in all doses tested. Finally we evaluated the effect of different doses of ketamine on creatinine kinase (CK) activity and we observed that CK activity is increased inspecific regions of the brain. Our study suggests that our animal model may be used as a model of schizophrenia and that cerebral energy metabolism might be altered in the brain of schizophrenic patients, probably leading to alterations that might be involved in the pathogenesis of schizophrenia. Hindawi Publishing Corporation 2010 /pmc/articles/PMC3154043/ /pubmed/21270541 http://dx.doi.org/10.4161/oxim.3.6.13446 Text en Copyright © 2010 Hindawi Publishing Corporation. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Paper
Canever, Leila
Oliveira, Larissa
de Luca, Renata D'Altoé
Correa, Paulo T. F.
Fraga, Daiane de B.
Matos, Maria Paula
Scaini, Giselli
Quevedo, João
Streck, Emílio L.
Zugno, Alexandra I.
A Rodent Model of Schizophrenia Reveals Increase in Creatine Kinase Activity with Associated Behavior Changes
title A Rodent Model of Schizophrenia Reveals Increase in Creatine Kinase Activity with Associated Behavior Changes
title_full A Rodent Model of Schizophrenia Reveals Increase in Creatine Kinase Activity with Associated Behavior Changes
title_fullStr A Rodent Model of Schizophrenia Reveals Increase in Creatine Kinase Activity with Associated Behavior Changes
title_full_unstemmed A Rodent Model of Schizophrenia Reveals Increase in Creatine Kinase Activity with Associated Behavior Changes
title_short A Rodent Model of Schizophrenia Reveals Increase in Creatine Kinase Activity with Associated Behavior Changes
title_sort rodent model of schizophrenia reveals increase in creatine kinase activity with associated behavior changes
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3154043/
https://www.ncbi.nlm.nih.gov/pubmed/21270541
http://dx.doi.org/10.4161/oxim.3.6.13446
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