A Histological Assessment of the Cell Death Induced by Haloperidol on Prefrontal Cortex

Neuroleptic drugs such as haloperidol has side effects on extrapyramidal pathways. Tardive Dyskinesia is the most important complication. The most characteristic feature of this Tardive Dyskinesia is involuntary movements of mouth and face. In regard to this problem, the induction of gliosis and cell death in the nervous tissue are considered. In this study, adult Sprague-Dawley rats were used as experimental models. Rats were divided into control and experimental groups. The rats were kept in the animal house under standard conditions during experiments. The control rats were intraperitoneally treated with normal saline for 6 days. The experimental samples were treated for the same time with 2, 5 and 10 mg haloperidol. After the trial period, the rats were killed following general anesthesia and their brains were removed after perfusion with a 4% formalin solution. Then, 1 mm cuts of the brains were obtained. After that, 5 µm tissue sections were prepared and stained with hematoxylin and eosin. The stained sections were examined by optical microscopy. The results showed that the short-term use of haloperidol does not lead to gliosis process in the rat cerebral cortex. The short-term use of 10 mg haloperidol results in cell death in the rat cerebral cortex. Cell death was not observed in the control group and the groups that had received 2 mg and 5 mg doses of haloperidol. According to previous studies, it can be concluded that the gliosis process is induced in the cerebral cortex only following the long-term use of haloperidol. It is considered as a secondary cause of the neuroleptic drugs side effects. The primary cause of these side effects is the induction of cell death in neurons.

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Main Authors: Ghanbari,Ali, Kakebaraei,Seyran, Khazaei,Mozafar
Format: Digital revista
Language:English
Published: Sociedad Chilena de Anatomía 2013
Online Access:http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0717-95022013000400046
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spelling oai:scielo:S0717-950220130004000462014-02-18A Histological Assessment of the Cell Death Induced by Haloperidol on Prefrontal CortexGhanbari,AliKakebaraei,SeyranKhazaei,Mozafar Haloperidol Cerebral cortex Optical microscopy Cell death Rat Neuroleptic drugs such as haloperidol has side effects on extrapyramidal pathways. Tardive Dyskinesia is the most important complication. The most characteristic feature of this Tardive Dyskinesia is involuntary movements of mouth and face. In regard to this problem, the induction of gliosis and cell death in the nervous tissue are considered. In this study, adult Sprague-Dawley rats were used as experimental models. Rats were divided into control and experimental groups. The rats were kept in the animal house under standard conditions during experiments. The control rats were intraperitoneally treated with normal saline for 6 days. The experimental samples were treated for the same time with 2, 5 and 10 mg haloperidol. After the trial period, the rats were killed following general anesthesia and their brains were removed after perfusion with a 4% formalin solution. Then, 1 mm cuts of the brains were obtained. After that, 5 µm tissue sections were prepared and stained with hematoxylin and eosin. The stained sections were examined by optical microscopy. The results showed that the short-term use of haloperidol does not lead to gliosis process in the rat cerebral cortex. The short-term use of 10 mg haloperidol results in cell death in the rat cerebral cortex. Cell death was not observed in the control group and the groups that had received 2 mg and 5 mg doses of haloperidol. According to previous studies, it can be concluded that the gliosis process is induced in the cerebral cortex only following the long-term use of haloperidol. It is considered as a secondary cause of the neuroleptic drugs side effects. The primary cause of these side effects is the induction of cell death in neurons.info:eu-repo/semantics/openAccessSociedad Chilena de AnatomíaInternational Journal of Morphology v.31 n.4 20132013-12-01text/htmlhttp://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0717-95022013000400046en10.4067/S0717-95022013000400046
institution SCIELO
collection OJS
country Chile
countrycode CL
component Revista
access En linea
databasecode rev-scielo-cl
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region America del Sur
libraryname SciELO
language English
format Digital
author Ghanbari,Ali
Kakebaraei,Seyran
Khazaei,Mozafar
spellingShingle Ghanbari,Ali
Kakebaraei,Seyran
Khazaei,Mozafar
A Histological Assessment of the Cell Death Induced by Haloperidol on Prefrontal Cortex
author_facet Ghanbari,Ali
Kakebaraei,Seyran
Khazaei,Mozafar
author_sort Ghanbari,Ali
title A Histological Assessment of the Cell Death Induced by Haloperidol on Prefrontal Cortex
title_short A Histological Assessment of the Cell Death Induced by Haloperidol on Prefrontal Cortex
title_full A Histological Assessment of the Cell Death Induced by Haloperidol on Prefrontal Cortex
title_fullStr A Histological Assessment of the Cell Death Induced by Haloperidol on Prefrontal Cortex
title_full_unstemmed A Histological Assessment of the Cell Death Induced by Haloperidol on Prefrontal Cortex
title_sort histological assessment of the cell death induced by haloperidol on prefrontal cortex
description Neuroleptic drugs such as haloperidol has side effects on extrapyramidal pathways. Tardive Dyskinesia is the most important complication. The most characteristic feature of this Tardive Dyskinesia is involuntary movements of mouth and face. In regard to this problem, the induction of gliosis and cell death in the nervous tissue are considered. In this study, adult Sprague-Dawley rats were used as experimental models. Rats were divided into control and experimental groups. The rats were kept in the animal house under standard conditions during experiments. The control rats were intraperitoneally treated with normal saline for 6 days. The experimental samples were treated for the same time with 2, 5 and 10 mg haloperidol. After the trial period, the rats were killed following general anesthesia and their brains were removed after perfusion with a 4% formalin solution. Then, 1 mm cuts of the brains were obtained. After that, 5 µm tissue sections were prepared and stained with hematoxylin and eosin. The stained sections were examined by optical microscopy. The results showed that the short-term use of haloperidol does not lead to gliosis process in the rat cerebral cortex. The short-term use of 10 mg haloperidol results in cell death in the rat cerebral cortex. Cell death was not observed in the control group and the groups that had received 2 mg and 5 mg doses of haloperidol. According to previous studies, it can be concluded that the gliosis process is induced in the cerebral cortex only following the long-term use of haloperidol. It is considered as a secondary cause of the neuroleptic drugs side effects. The primary cause of these side effects is the induction of cell death in neurons.
publisher Sociedad Chilena de Anatomía
publishDate 2013
url http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0717-95022013000400046
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