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Protective Role of L-3-n-Butylphthalide in Cognitive Function and Dysthymic Disorders in Mouse With Chronic Epilepsy

Epilepsy is a common neurological disease with recurrent seizures and neurobehavioral comorbidities, including cognitive impairment and psychiatric disorders. Recent studies suggest that L-3-n-butylphthalide (NBP), an extract from the seeds of Apium graveolens Linn. (Chinese celery), ameliorates cog...

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Autores principales: Ye, Xiaowen, Rong, Zhouyi, Li, Yanfang, Wang, Xintian, Cheng, Baoying, Cheng, Yiyun, Luo, Haijuan, Ti, Yue, Huang, Xiaohua, Liu, Zhaoji, Zhang, Yun-wu, Zheng, Weihong, Zheng, Honghua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6051017/
https://www.ncbi.nlm.nih.gov/pubmed/30050437
http://dx.doi.org/10.3389/fphar.2018.00734
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author Ye, Xiaowen
Rong, Zhouyi
Li, Yanfang
Wang, Xintian
Cheng, Baoying
Cheng, Yiyun
Luo, Haijuan
Ti, Yue
Huang, Xiaohua
Liu, Zhaoji
Zhang, Yun-wu
Zheng, Weihong
Zheng, Honghua
author_facet Ye, Xiaowen
Rong, Zhouyi
Li, Yanfang
Wang, Xintian
Cheng, Baoying
Cheng, Yiyun
Luo, Haijuan
Ti, Yue
Huang, Xiaohua
Liu, Zhaoji
Zhang, Yun-wu
Zheng, Weihong
Zheng, Honghua
author_sort Ye, Xiaowen
collection PubMed
description Epilepsy is a common neurological disease with recurrent seizures and neurobehavioral comorbidities, including cognitive impairment and psychiatric disorders. Recent studies suggest that L-3-n-butylphthalide (NBP), an extract from the seeds of Apium graveolens Linn. (Chinese celery), ameliorates cognitive dysfunction in ischemia and/or Alzheimer’s disease animal models. However, little is known about the role of NBP in epilepsy and the associated comorbidities. Here, using a pilocarpine-induced chronic epileptic mouse model, we found that NBP supplement not only alleviated seizure severity and abnormal electroencephalogram, but also rescued cognitive and emotional impairments in these epileptic mice. The possible underlying mechanisms may be associated with the protective role of NBP in reducing neuronal loss and in restoring the expression of neural synaptic proteins such as postsynaptic density protein 95 (PSD95) and glutamic acid decarboxylase 65/67 (GAD65/67). In addition, NBP treatment increased the transcription of neuroprotective factors, brain-derived neurotrophic factor and Klotho. These findings suggest that NBP treatment may be a potential strategy for ameliorating epileptogenesis and the comorbidities of cognitive and psychological impairments.
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spelling pubmed-60510172018-07-26 Protective Role of L-3-n-Butylphthalide in Cognitive Function and Dysthymic Disorders in Mouse With Chronic Epilepsy Ye, Xiaowen Rong, Zhouyi Li, Yanfang Wang, Xintian Cheng, Baoying Cheng, Yiyun Luo, Haijuan Ti, Yue Huang, Xiaohua Liu, Zhaoji Zhang, Yun-wu Zheng, Weihong Zheng, Honghua Front Pharmacol Pharmacology Epilepsy is a common neurological disease with recurrent seizures and neurobehavioral comorbidities, including cognitive impairment and psychiatric disorders. Recent studies suggest that L-3-n-butylphthalide (NBP), an extract from the seeds of Apium graveolens Linn. (Chinese celery), ameliorates cognitive dysfunction in ischemia and/or Alzheimer’s disease animal models. However, little is known about the role of NBP in epilepsy and the associated comorbidities. Here, using a pilocarpine-induced chronic epileptic mouse model, we found that NBP supplement not only alleviated seizure severity and abnormal electroencephalogram, but also rescued cognitive and emotional impairments in these epileptic mice. The possible underlying mechanisms may be associated with the protective role of NBP in reducing neuronal loss and in restoring the expression of neural synaptic proteins such as postsynaptic density protein 95 (PSD95) and glutamic acid decarboxylase 65/67 (GAD65/67). In addition, NBP treatment increased the transcription of neuroprotective factors, brain-derived neurotrophic factor and Klotho. These findings suggest that NBP treatment may be a potential strategy for ameliorating epileptogenesis and the comorbidities of cognitive and psychological impairments. Frontiers Media S.A. 2018-07-11 /pmc/articles/PMC6051017/ /pubmed/30050437 http://dx.doi.org/10.3389/fphar.2018.00734 Text en Copyright © 2018 Ye, Rong, Li, Wang, Cheng, Cheng, Luo, Ti, Huang, Liu, Zhang, Zheng and Zheng. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pharmacology
Ye, Xiaowen
Rong, Zhouyi
Li, Yanfang
Wang, Xintian
Cheng, Baoying
Cheng, Yiyun
Luo, Haijuan
Ti, Yue
Huang, Xiaohua
Liu, Zhaoji
Zhang, Yun-wu
Zheng, Weihong
Zheng, Honghua
Protective Role of L-3-n-Butylphthalide in Cognitive Function and Dysthymic Disorders in Mouse With Chronic Epilepsy
title Protective Role of L-3-n-Butylphthalide in Cognitive Function and Dysthymic Disorders in Mouse With Chronic Epilepsy
title_full Protective Role of L-3-n-Butylphthalide in Cognitive Function and Dysthymic Disorders in Mouse With Chronic Epilepsy
title_fullStr Protective Role of L-3-n-Butylphthalide in Cognitive Function and Dysthymic Disorders in Mouse With Chronic Epilepsy
title_full_unstemmed Protective Role of L-3-n-Butylphthalide in Cognitive Function and Dysthymic Disorders in Mouse With Chronic Epilepsy
title_short Protective Role of L-3-n-Butylphthalide in Cognitive Function and Dysthymic Disorders in Mouse With Chronic Epilepsy
title_sort protective role of l-3-n-butylphthalide in cognitive function and dysthymic disorders in mouse with chronic epilepsy
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6051017/
https://www.ncbi.nlm.nih.gov/pubmed/30050437
http://dx.doi.org/10.3389/fphar.2018.00734
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