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Kolaviron Protects the Prefrontal Cortex and Hippocampus against Histomorphological and Neurobehavioural Changes in Cuprizone Model of Multiple Sclerosis

BACKGROUND: This study explored the efficacy of kolaviron—a biflavonoid complex isolated from the seeds of Garcinia kola—in protecting against cuprizone (CPZ)-induced demyelination in both the prefrontal cortex and the hippocampus of Wistar rats. METHODOLOGY: Thirty rats were treated to receive 0.5...

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Autores principales: Omotoso, Gabriel Olaiya, Olajide, Olayemi Joseph, Gbadamosi, Ismail Temitayo, Rasheed, Mikail Abiodun, Izuogu, Chiazokam Tochukwu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Penerbit Universiti Sains Malaysia 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6422579/
https://www.ncbi.nlm.nih.gov/pubmed/30918455
http://dx.doi.org/10.21315/mjms2018.25.2.6
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author Omotoso, Gabriel Olaiya
Olajide, Olayemi Joseph
Gbadamosi, Ismail Temitayo
Rasheed, Mikail Abiodun
Izuogu, Chiazokam Tochukwu
author_facet Omotoso, Gabriel Olaiya
Olajide, Olayemi Joseph
Gbadamosi, Ismail Temitayo
Rasheed, Mikail Abiodun
Izuogu, Chiazokam Tochukwu
author_sort Omotoso, Gabriel Olaiya
collection PubMed
description BACKGROUND: This study explored the efficacy of kolaviron—a biflavonoid complex isolated from the seeds of Garcinia kola—in protecting against cuprizone (CPZ)-induced demyelination in both the prefrontal cortex and the hippocampus of Wistar rats. METHODOLOGY: Thirty rats were treated to receive 0.5 mL phosphate-buffered saline (group A, control), 0.5 mL corn oil (group B), 0.2% CPZ (group C), for 6 weeks, 0.2% CPZ for 3 weeks and then 200 mg/kg of Kv for 3 weeks (group D), or 200 mg/kg of Kv for 3 weeks followed by 0.2% CPZ for 3 weeks (group E). Rats were assessed for exploratory functions and anxiety-like behaviour before being euthanised and perfused transcardially with 4% paraformaldehyde. Prefrontal and hippocampal thin sections were stained in hematoxylin and eosin and cresyl fast violet stains. RESULTS: CPZ-induced demyelination resulted in behavioural impairment as seen by reduced exploratory activities, rearing behaviour, stretch attend posture, center square entry, and anxiogenic characteristics. Degenerative changes including pyknosis, karyorrhexis, neuronal hypertrophy, and reduced Nissl integrity were also seen. Animals treated with Kv showed significant improvement in behavioural outcomes and a comparatively normal cytoarchitectural profile. CONCLUSION: Kv provides protective roles against CPZ-induced neurotoxicity through prevention of ribosomal protein degradation.
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spelling pubmed-64225792019-03-27 Kolaviron Protects the Prefrontal Cortex and Hippocampus against Histomorphological and Neurobehavioural Changes in Cuprizone Model of Multiple Sclerosis Omotoso, Gabriel Olaiya Olajide, Olayemi Joseph Gbadamosi, Ismail Temitayo Rasheed, Mikail Abiodun Izuogu, Chiazokam Tochukwu Malays J Med Sci Original Article BACKGROUND: This study explored the efficacy of kolaviron—a biflavonoid complex isolated from the seeds of Garcinia kola—in protecting against cuprizone (CPZ)-induced demyelination in both the prefrontal cortex and the hippocampus of Wistar rats. METHODOLOGY: Thirty rats were treated to receive 0.5 mL phosphate-buffered saline (group A, control), 0.5 mL corn oil (group B), 0.2% CPZ (group C), for 6 weeks, 0.2% CPZ for 3 weeks and then 200 mg/kg of Kv for 3 weeks (group D), or 200 mg/kg of Kv for 3 weeks followed by 0.2% CPZ for 3 weeks (group E). Rats were assessed for exploratory functions and anxiety-like behaviour before being euthanised and perfused transcardially with 4% paraformaldehyde. Prefrontal and hippocampal thin sections were stained in hematoxylin and eosin and cresyl fast violet stains. RESULTS: CPZ-induced demyelination resulted in behavioural impairment as seen by reduced exploratory activities, rearing behaviour, stretch attend posture, center square entry, and anxiogenic characteristics. Degenerative changes including pyknosis, karyorrhexis, neuronal hypertrophy, and reduced Nissl integrity were also seen. Animals treated with Kv showed significant improvement in behavioural outcomes and a comparatively normal cytoarchitectural profile. CONCLUSION: Kv provides protective roles against CPZ-induced neurotoxicity through prevention of ribosomal protein degradation. Penerbit Universiti Sains Malaysia 2018-03 2018-04-27 /pmc/articles/PMC6422579/ /pubmed/30918455 http://dx.doi.org/10.21315/mjms2018.25.2.6 Text en © Penerbit Universiti Sains Malaysia, 2018 This work is licensed under the terms of the Creative Commons Attribution (CC BY) (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Original Article
Omotoso, Gabriel Olaiya
Olajide, Olayemi Joseph
Gbadamosi, Ismail Temitayo
Rasheed, Mikail Abiodun
Izuogu, Chiazokam Tochukwu
Kolaviron Protects the Prefrontal Cortex and Hippocampus against Histomorphological and Neurobehavioural Changes in Cuprizone Model of Multiple Sclerosis
title Kolaviron Protects the Prefrontal Cortex and Hippocampus against Histomorphological and Neurobehavioural Changes in Cuprizone Model of Multiple Sclerosis
title_full Kolaviron Protects the Prefrontal Cortex and Hippocampus against Histomorphological and Neurobehavioural Changes in Cuprizone Model of Multiple Sclerosis
title_fullStr Kolaviron Protects the Prefrontal Cortex and Hippocampus against Histomorphological and Neurobehavioural Changes in Cuprizone Model of Multiple Sclerosis
title_full_unstemmed Kolaviron Protects the Prefrontal Cortex and Hippocampus against Histomorphological and Neurobehavioural Changes in Cuprizone Model of Multiple Sclerosis
title_short Kolaviron Protects the Prefrontal Cortex and Hippocampus against Histomorphological and Neurobehavioural Changes in Cuprizone Model of Multiple Sclerosis
title_sort kolaviron protects the prefrontal cortex and hippocampus against histomorphological and neurobehavioural changes in cuprizone model of multiple sclerosis
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6422579/
https://www.ncbi.nlm.nih.gov/pubmed/30918455
http://dx.doi.org/10.21315/mjms2018.25.2.6
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