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Curative Effect of Aqueous Leaf Extract of Crinum Giganteum on NMDA-Receptor Antagonist-Induced Schizophrenic Wistar Rat Model

AIM: This study evaluated the curative potential of Crinum giganteum in the treatment of schizophrenia using an NMDA-receptor antagonist-induced schizophrenic Wistar rat model. METHODS: Twenty-five adult Wistar rats of both sexes of average weights 180 g were divided into two groups: control and sch...

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Autores principales: Finbarrs-Bello, Elizabeth, Obikili, Emmanuel Nebeuwa, Anayochukwu, Esom Emmanuel, Godson, Anyanwu Emeka
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Institute of Immunobiology and Human Genetics 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5042612/
https://www.ncbi.nlm.nih.gov/pubmed/27703552
http://dx.doi.org/10.3889/oamjms.2016.061
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author Finbarrs-Bello, Elizabeth
Obikili, Emmanuel Nebeuwa
Anayochukwu, Esom Emmanuel
Godson, Anyanwu Emeka
author_facet Finbarrs-Bello, Elizabeth
Obikili, Emmanuel Nebeuwa
Anayochukwu, Esom Emmanuel
Godson, Anyanwu Emeka
author_sort Finbarrs-Bello, Elizabeth
collection PubMed
description AIM: This study evaluated the curative potential of Crinum giganteum in the treatment of schizophrenia using an NMDA-receptor antagonist-induced schizophrenic Wistar rat model. METHODS: Twenty-five adult Wistar rats of both sexes of average weights 180 g were divided into two groups: control and schizophrenic rat models. The controls received 0.1 ml of 0. 9% saline, while schizophrenia was induced in models using 25 mg/kg of ketamine hydrochloride (i.p.) for 7 days. On the 8 day models were divided into group’s k1, k2, k3 and k4 of 5 rats each. K1 and the controls were sacrificed then, groups k2 and k3 were treated with 5 mg/kg and 10 mg/kg aqueous leaf extract of Crinum giganteum while, k4 (standard) received 25 mg/kg of chlorpromazine orally for 28 days. Amygdala were harvested, processed and stained with Haematoxylin and Eosin (H &E) stain, Neuron-specific enolase (NSE) marker was also used to monitor the curative effect on the amygdala. RESULTS: Degenerative changes and increased NSE immunoreactivity were observed in the untreated models. Extract-treated models showed normal amygdala and negative NSE immunoreactivity while chlorpromazine treated models revealed decreased NSE immunoreactivity. CONCLUSION: Crinum giganteum extracts exhibits better curative effect than the standard antipsychotic agent.
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spelling pubmed-50426122016-10-04 Curative Effect of Aqueous Leaf Extract of Crinum Giganteum on NMDA-Receptor Antagonist-Induced Schizophrenic Wistar Rat Model Finbarrs-Bello, Elizabeth Obikili, Emmanuel Nebeuwa Anayochukwu, Esom Emmanuel Godson, Anyanwu Emeka Open Access Maced J Med Sci Basic Science AIM: This study evaluated the curative potential of Crinum giganteum in the treatment of schizophrenia using an NMDA-receptor antagonist-induced schizophrenic Wistar rat model. METHODS: Twenty-five adult Wistar rats of both sexes of average weights 180 g were divided into two groups: control and schizophrenic rat models. The controls received 0.1 ml of 0. 9% saline, while schizophrenia was induced in models using 25 mg/kg of ketamine hydrochloride (i.p.) for 7 days. On the 8 day models were divided into group’s k1, k2, k3 and k4 of 5 rats each. K1 and the controls were sacrificed then, groups k2 and k3 were treated with 5 mg/kg and 10 mg/kg aqueous leaf extract of Crinum giganteum while, k4 (standard) received 25 mg/kg of chlorpromazine orally for 28 days. Amygdala were harvested, processed and stained with Haematoxylin and Eosin (H &E) stain, Neuron-specific enolase (NSE) marker was also used to monitor the curative effect on the amygdala. RESULTS: Degenerative changes and increased NSE immunoreactivity were observed in the untreated models. Extract-treated models showed normal amygdala and negative NSE immunoreactivity while chlorpromazine treated models revealed decreased NSE immunoreactivity. CONCLUSION: Crinum giganteum extracts exhibits better curative effect than the standard antipsychotic agent. Institute of Immunobiology and Human Genetics 2016-09-15 2016-08-06 /pmc/articles/PMC5042612/ /pubmed/27703552 http://dx.doi.org/10.3889/oamjms.2016.061 Text en Copyright: © 2016 Elizabeth Finbarrs-Bello, Emmanuel Nebeuwa Obikili, Esom Emmanuel Anayochukwu, Anyanwu Emeka Godson. http://creativecommons.org/licenses/by/2.5/ This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Basic Science
Finbarrs-Bello, Elizabeth
Obikili, Emmanuel Nebeuwa
Anayochukwu, Esom Emmanuel
Godson, Anyanwu Emeka
Curative Effect of Aqueous Leaf Extract of Crinum Giganteum on NMDA-Receptor Antagonist-Induced Schizophrenic Wistar Rat Model
title Curative Effect of Aqueous Leaf Extract of Crinum Giganteum on NMDA-Receptor Antagonist-Induced Schizophrenic Wistar Rat Model
title_full Curative Effect of Aqueous Leaf Extract of Crinum Giganteum on NMDA-Receptor Antagonist-Induced Schizophrenic Wistar Rat Model
title_fullStr Curative Effect of Aqueous Leaf Extract of Crinum Giganteum on NMDA-Receptor Antagonist-Induced Schizophrenic Wistar Rat Model
title_full_unstemmed Curative Effect of Aqueous Leaf Extract of Crinum Giganteum on NMDA-Receptor Antagonist-Induced Schizophrenic Wistar Rat Model
title_short Curative Effect of Aqueous Leaf Extract of Crinum Giganteum on NMDA-Receptor Antagonist-Induced Schizophrenic Wistar Rat Model
title_sort curative effect of aqueous leaf extract of crinum giganteum on nmda-receptor antagonist-induced schizophrenic wistar rat model
topic Basic Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5042612/
https://www.ncbi.nlm.nih.gov/pubmed/27703552
http://dx.doi.org/10.3889/oamjms.2016.061
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