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Kainic Acid-Induced Excitotoxicity Experimental Model: Protective Merits of Natural Products and Plant Extracts

Excitotoxicity is well recognized as a major pathological process of neuronal death in neurodegenerative diseases involving the central nervous system (CNS). In the animal models of neurodegeneration, excitotoxicity is commonly induced experimentally by chemical convulsants, particularly kainic acid...

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Autores principales: Mohd Sairazi, Nur Shafika, Sirajudeen, K. N. S., Asari, Mohd Asnizam, Muzaimi, Mustapha, Mummedy, Swamy, Sulaiman, Siti Amrah
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4697086/
https://www.ncbi.nlm.nih.gov/pubmed/26793262
http://dx.doi.org/10.1155/2015/972623
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author Mohd Sairazi, Nur Shafika
Sirajudeen, K. N. S.
Asari, Mohd Asnizam
Muzaimi, Mustapha
Mummedy, Swamy
Sulaiman, Siti Amrah
author_facet Mohd Sairazi, Nur Shafika
Sirajudeen, K. N. S.
Asari, Mohd Asnizam
Muzaimi, Mustapha
Mummedy, Swamy
Sulaiman, Siti Amrah
author_sort Mohd Sairazi, Nur Shafika
collection PubMed
description Excitotoxicity is well recognized as a major pathological process of neuronal death in neurodegenerative diseases involving the central nervous system (CNS). In the animal models of neurodegeneration, excitotoxicity is commonly induced experimentally by chemical convulsants, particularly kainic acid (KA). KA-induced excitotoxicity in rodent models has been shown to result in seizures, behavioral changes, oxidative stress, glial activation, inflammatory mediator production, endoplasmic reticulum stress, mitochondrial dysfunction, and selective neurodegeneration in the brain upon KA administration. Recently, there is an emerging trend to search for natural sources to combat against excitotoxicity-associated neurodegenerative diseases. Natural products and plant extracts had attracted a considerable amount of attention because of their reported beneficial effects on the CNS, particularly their neuroprotective effect against excitotoxicity. They provide significant reduction and/or protection against the development and progression of acute and chronic neurodegeneration. This indicates that natural products and plants extracts may be useful in protecting against excitotoxicity-associated neurodegeneration. Thus, targeting of multiple pathways simultaneously may be the strategy to maximize the neuroprotection effect. This review summarizes the mechanisms involved in KA-induced excitotoxicity and attempts to collate the various researches related to the protective effect of natural products and plant extracts in the KA model of neurodegeneration.
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spelling pubmed-46970862016-01-20 Kainic Acid-Induced Excitotoxicity Experimental Model: Protective Merits of Natural Products and Plant Extracts Mohd Sairazi, Nur Shafika Sirajudeen, K. N. S. Asari, Mohd Asnizam Muzaimi, Mustapha Mummedy, Swamy Sulaiman, Siti Amrah Evid Based Complement Alternat Med Review Article Excitotoxicity is well recognized as a major pathological process of neuronal death in neurodegenerative diseases involving the central nervous system (CNS). In the animal models of neurodegeneration, excitotoxicity is commonly induced experimentally by chemical convulsants, particularly kainic acid (KA). KA-induced excitotoxicity in rodent models has been shown to result in seizures, behavioral changes, oxidative stress, glial activation, inflammatory mediator production, endoplasmic reticulum stress, mitochondrial dysfunction, and selective neurodegeneration in the brain upon KA administration. Recently, there is an emerging trend to search for natural sources to combat against excitotoxicity-associated neurodegenerative diseases. Natural products and plant extracts had attracted a considerable amount of attention because of their reported beneficial effects on the CNS, particularly their neuroprotective effect against excitotoxicity. They provide significant reduction and/or protection against the development and progression of acute and chronic neurodegeneration. This indicates that natural products and plants extracts may be useful in protecting against excitotoxicity-associated neurodegeneration. Thus, targeting of multiple pathways simultaneously may be the strategy to maximize the neuroprotection effect. This review summarizes the mechanisms involved in KA-induced excitotoxicity and attempts to collate the various researches related to the protective effect of natural products and plant extracts in the KA model of neurodegeneration. Hindawi Publishing Corporation 2015 2015-12-17 /pmc/articles/PMC4697086/ /pubmed/26793262 http://dx.doi.org/10.1155/2015/972623 Text en Copyright © 2015 Nur Shafika Mohd Sairazi et al. https://creativecommons.org/licenses/by/4.0/ 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 Review Article
Mohd Sairazi, Nur Shafika
Sirajudeen, K. N. S.
Asari, Mohd Asnizam
Muzaimi, Mustapha
Mummedy, Swamy
Sulaiman, Siti Amrah
Kainic Acid-Induced Excitotoxicity Experimental Model: Protective Merits of Natural Products and Plant Extracts
title Kainic Acid-Induced Excitotoxicity Experimental Model: Protective Merits of Natural Products and Plant Extracts
title_full Kainic Acid-Induced Excitotoxicity Experimental Model: Protective Merits of Natural Products and Plant Extracts
title_fullStr Kainic Acid-Induced Excitotoxicity Experimental Model: Protective Merits of Natural Products and Plant Extracts
title_full_unstemmed Kainic Acid-Induced Excitotoxicity Experimental Model: Protective Merits of Natural Products and Plant Extracts
title_short Kainic Acid-Induced Excitotoxicity Experimental Model: Protective Merits of Natural Products and Plant Extracts
title_sort kainic acid-induced excitotoxicity experimental model: protective merits of natural products and plant extracts
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4697086/
https://www.ncbi.nlm.nih.gov/pubmed/26793262
http://dx.doi.org/10.1155/2015/972623
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