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Effects of resveratrol and oxyresveratrol on hippocampal cell death induced by kainic acid

In the present study, we have examined the possible neuroprotective effects of resveratrol and oxyresveratrol against kainic-acid (KA)-induced hippocampal neuronal cell death. Either resveratrol or oxyresvertrol was orally administered 30 min prior to intracerebroventricular (i.c.v.) administration...

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Autores principales: Lee, Hee-Jung, Feng, Jing-Hui, Sim, Su-Min, Lim, Soon-Sung, Lee, Jae-Yong, Suh, Hong-Won
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2019
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6711029/
https://www.ncbi.nlm.nih.gov/pubmed/31489245
http://dx.doi.org/10.1080/19768354.2019.1620853
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author Lee, Hee-Jung
Feng, Jing-Hui
Sim, Su-Min
Lim, Soon-Sung
Lee, Jae-Yong
Suh, Hong-Won
author_facet Lee, Hee-Jung
Feng, Jing-Hui
Sim, Su-Min
Lim, Soon-Sung
Lee, Jae-Yong
Suh, Hong-Won
author_sort Lee, Hee-Jung
collection PubMed
description In the present study, we have examined the possible neuroprotective effects of resveratrol and oxyresveratrol against kainic-acid (KA)-induced hippocampal neuronal cell death. Either resveratrol or oxyresvertrol was orally administered 30 min prior to intracerebroventricular (i.c.v.) administration with KA (0.05 μg). Oral pretreatment with oxyresveratrol (50 mg/kg) significantly protected KA-induced hippocampal CA3 neuronal cell death. However, the same dose (50 mg/kg) or a higher dose (100 mg/kg) pretreatment with resveratrol did not affect KA-induced hippocampal neuronal cell death. Furthermore, the i.c.v. pretreatment with 30 μg of oxyresveratrol or resveratrol did not show the protective effect against KA-induced hippocampal neuronal cell death. In the immunohistochemical analysis, FoxO3a and pFoxO3a expressions in the hippocampal CA3 region were significantly increased 30 min after KA administration. Oral pretreatment with oxyresveratrol (50 mg/kg) significantly reduced KA-induced Forkhead homeobox type O3a (FoxO3a) and pFoxO3a expression in CA3 region of the hippocampus, suggesting that oxyresveratrol may exert a neuroprotective effect against KA-induced hippocampal neuronal cell death by reducing the levels of FoxO3a and pFoxO3a protein expression in the hippocampal CA3 region. Furthermore, it is suggested that the neuroprotective effect of orally administered oxyresveratrol against KA-induced neurotoxicity might be possibly mediated by some metabolites rather than direct action of oxyresveratrol on the central nervous system.
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spelling pubmed-67110292019-09-05 Effects of resveratrol and oxyresveratrol on hippocampal cell death induced by kainic acid Lee, Hee-Jung Feng, Jing-Hui Sim, Su-Min Lim, Soon-Sung Lee, Jae-Yong Suh, Hong-Won Anim Cells Syst (Seoul) Molecular & Cellular Biology In the present study, we have examined the possible neuroprotective effects of resveratrol and oxyresveratrol against kainic-acid (KA)-induced hippocampal neuronal cell death. Either resveratrol or oxyresvertrol was orally administered 30 min prior to intracerebroventricular (i.c.v.) administration with KA (0.05 μg). Oral pretreatment with oxyresveratrol (50 mg/kg) significantly protected KA-induced hippocampal CA3 neuronal cell death. However, the same dose (50 mg/kg) or a higher dose (100 mg/kg) pretreatment with resveratrol did not affect KA-induced hippocampal neuronal cell death. Furthermore, the i.c.v. pretreatment with 30 μg of oxyresveratrol or resveratrol did not show the protective effect against KA-induced hippocampal neuronal cell death. In the immunohistochemical analysis, FoxO3a and pFoxO3a expressions in the hippocampal CA3 region were significantly increased 30 min after KA administration. Oral pretreatment with oxyresveratrol (50 mg/kg) significantly reduced KA-induced Forkhead homeobox type O3a (FoxO3a) and pFoxO3a expression in CA3 region of the hippocampus, suggesting that oxyresveratrol may exert a neuroprotective effect against KA-induced hippocampal neuronal cell death by reducing the levels of FoxO3a and pFoxO3a protein expression in the hippocampal CA3 region. Furthermore, it is suggested that the neuroprotective effect of orally administered oxyresveratrol against KA-induced neurotoxicity might be possibly mediated by some metabolites rather than direct action of oxyresveratrol on the central nervous system. Taylor & Francis 2019-05-31 /pmc/articles/PMC6711029/ /pubmed/31489245 http://dx.doi.org/10.1080/19768354.2019.1620853 Text en © 2019 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Molecular & Cellular Biology
Lee, Hee-Jung
Feng, Jing-Hui
Sim, Su-Min
Lim, Soon-Sung
Lee, Jae-Yong
Suh, Hong-Won
Effects of resveratrol and oxyresveratrol on hippocampal cell death induced by kainic acid
title Effects of resveratrol and oxyresveratrol on hippocampal cell death induced by kainic acid
title_full Effects of resveratrol and oxyresveratrol on hippocampal cell death induced by kainic acid
title_fullStr Effects of resveratrol and oxyresveratrol on hippocampal cell death induced by kainic acid
title_full_unstemmed Effects of resveratrol and oxyresveratrol on hippocampal cell death induced by kainic acid
title_short Effects of resveratrol and oxyresveratrol on hippocampal cell death induced by kainic acid
title_sort effects of resveratrol and oxyresveratrol on hippocampal cell death induced by kainic acid
topic Molecular & Cellular Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6711029/
https://www.ncbi.nlm.nih.gov/pubmed/31489245
http://dx.doi.org/10.1080/19768354.2019.1620853
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