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Jujuboside A Exhibits an Antiepileptogenic Effect in the Rat Model via Protection against Traumatic Epilepsy-Induced Oxidative Stress and Inflammatory Responses

Traumatic brain injuries (TBI) are the greatest source of death in trauma, and post-traumatic epilepsy (PTE) is one of the common complications of TBI. Oxidative stress and inflammatory responses play an important role in the process of PTE. Many studies have shown that Jujuboside A has powerful ant...

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Autores principales: Lu, Wei, Wu, Zhangze, Zhang, Chong, Gao, Tingting, Ling, Xiaoyang, Xu, Min, Wang, Wenhua, Jin, Xuegang, Li, Keran, Chen, Long, Wang, Jinjuan, Sun, Zhongyang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9481365/
https://www.ncbi.nlm.nih.gov/pubmed/36118077
http://dx.doi.org/10.1155/2022/7792791
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author Lu, Wei
Wu, Zhangze
Zhang, Chong
Gao, Tingting
Ling, Xiaoyang
Xu, Min
Wang, Wenhua
Jin, Xuegang
Li, Keran
Chen, Long
Wang, Jinjuan
Sun, Zhongyang
author_facet Lu, Wei
Wu, Zhangze
Zhang, Chong
Gao, Tingting
Ling, Xiaoyang
Xu, Min
Wang, Wenhua
Jin, Xuegang
Li, Keran
Chen, Long
Wang, Jinjuan
Sun, Zhongyang
author_sort Lu, Wei
collection PubMed
description Traumatic brain injuries (TBI) are the greatest source of death in trauma, and post-traumatic epilepsy (PTE) is one of the common complications of TBI. Oxidative stress and inflammatory responses play an important role in the process of PTE. Many studies have shown that Jujuboside A has powerful antioxidant and anti-inflammatory properties. However, it is not known whether Jujuboside A has an anti-epileptic effect. The influences of Jujuboside A in the experimental FeCl(3)-induced model of PTE were tested by estimating the grade of seizures and performing behavioral tests. Following that, we detected oxidative stress indicators and inflammatory factors. Additionally, western blotting was used to test the protein levels of signaling molecules in MAPK pathways. In this study, Jujuboside A was found to have improved the recognition deficiency and epilepsy syndromes in the experimental rat model. Moreover, oxidative stress and inflammatory responses induced by FeCl(3) injection were relieved by Jujuboside A. In addition, Jujuboside A was found to be capable of reducing the increased expression of p-P38 and p-ERK1/2 caused by iron ions. Collectively, our results demonstrated that Jujuboside A exhibits an antiepileptogenic effect by alleviating oxidative stress and inflammatory responses via the p38 and ERK1/2 pathways.
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spelling pubmed-94813652022-09-17 Jujuboside A Exhibits an Antiepileptogenic Effect in the Rat Model via Protection against Traumatic Epilepsy-Induced Oxidative Stress and Inflammatory Responses Lu, Wei Wu, Zhangze Zhang, Chong Gao, Tingting Ling, Xiaoyang Xu, Min Wang, Wenhua Jin, Xuegang Li, Keran Chen, Long Wang, Jinjuan Sun, Zhongyang Evid Based Complement Alternat Med Research Article Traumatic brain injuries (TBI) are the greatest source of death in trauma, and post-traumatic epilepsy (PTE) is one of the common complications of TBI. Oxidative stress and inflammatory responses play an important role in the process of PTE. Many studies have shown that Jujuboside A has powerful antioxidant and anti-inflammatory properties. However, it is not known whether Jujuboside A has an anti-epileptic effect. The influences of Jujuboside A in the experimental FeCl(3)-induced model of PTE were tested by estimating the grade of seizures and performing behavioral tests. Following that, we detected oxidative stress indicators and inflammatory factors. Additionally, western blotting was used to test the protein levels of signaling molecules in MAPK pathways. In this study, Jujuboside A was found to have improved the recognition deficiency and epilepsy syndromes in the experimental rat model. Moreover, oxidative stress and inflammatory responses induced by FeCl(3) injection were relieved by Jujuboside A. In addition, Jujuboside A was found to be capable of reducing the increased expression of p-P38 and p-ERK1/2 caused by iron ions. Collectively, our results demonstrated that Jujuboside A exhibits an antiepileptogenic effect by alleviating oxidative stress and inflammatory responses via the p38 and ERK1/2 pathways. Hindawi 2022-09-09 /pmc/articles/PMC9481365/ /pubmed/36118077 http://dx.doi.org/10.1155/2022/7792791 Text en Copyright © 2022 Wei Lu 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 Research Article
Lu, Wei
Wu, Zhangze
Zhang, Chong
Gao, Tingting
Ling, Xiaoyang
Xu, Min
Wang, Wenhua
Jin, Xuegang
Li, Keran
Chen, Long
Wang, Jinjuan
Sun, Zhongyang
Jujuboside A Exhibits an Antiepileptogenic Effect in the Rat Model via Protection against Traumatic Epilepsy-Induced Oxidative Stress and Inflammatory Responses
title Jujuboside A Exhibits an Antiepileptogenic Effect in the Rat Model via Protection against Traumatic Epilepsy-Induced Oxidative Stress and Inflammatory Responses
title_full Jujuboside A Exhibits an Antiepileptogenic Effect in the Rat Model via Protection against Traumatic Epilepsy-Induced Oxidative Stress and Inflammatory Responses
title_fullStr Jujuboside A Exhibits an Antiepileptogenic Effect in the Rat Model via Protection against Traumatic Epilepsy-Induced Oxidative Stress and Inflammatory Responses
title_full_unstemmed Jujuboside A Exhibits an Antiepileptogenic Effect in the Rat Model via Protection against Traumatic Epilepsy-Induced Oxidative Stress and Inflammatory Responses
title_short Jujuboside A Exhibits an Antiepileptogenic Effect in the Rat Model via Protection against Traumatic Epilepsy-Induced Oxidative Stress and Inflammatory Responses
title_sort jujuboside a exhibits an antiepileptogenic effect in the rat model via protection against traumatic epilepsy-induced oxidative stress and inflammatory responses
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9481365/
https://www.ncbi.nlm.nih.gov/pubmed/36118077
http://dx.doi.org/10.1155/2022/7792791
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