• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

拉科酰胺治疗对颞叶癫痫大鼠模型癫痫发生、神经元损伤和行为共病的影响。

Effects of Lacosamide Treatment on Epileptogenesis, Neuronal Damage and Behavioral Comorbidities in a Rat Model of Temporal Lobe Epilepsy.

机构信息

Department of Pharmacology Toxicology and Pharmacotherapy, Medical University-Plovdiv, 4002 Plovdiv, Bulgaria.

Institute of Neurobiology, Bulgarian Academy of Sciences (BAS), 1113 Sofia, Bulgaria.

出版信息

Int J Mol Sci. 2021 Apr 28;22(9):4667. doi: 10.3390/ijms22094667.

DOI:10.3390/ijms22094667
PMID:33925082
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8124899/
Abstract

Clinically, temporal lobe epilepsy (TLE) is the most prevalent type of partial epilepsy and often accompanied by various comorbidities. The present study aimed to evaluate the effects of chronic treatment with the antiepileptic drug (AED) lacosamide (LCM) on spontaneous motor seizures (SMS), behavioral comorbidities, oxidative stress, neuroinflammation, and neuronal damage in a model of TLE. Vehicle/LCM treatment (30 mg/kg, p.o.) was administered 3 h after the pilocarpine-induced status epilepticus (SE) and continued for up to 12 weeks in Wistar rats. Our study showed that LCM attenuated the number of SMS and corrected comorbid to epilepsy impaired motor activity, anxiety, memory, and alleviated depressive-like responses measured in the elevated plus maze, object recognition test, radial arm maze test, and sucrose preference test, respectively. This AED suppressed oxidative stress through increased superoxide dismutase activity and glutathione levels, and alleviated catalase activity and lipid peroxidation in the hippocampus. Lacosamide treatment after SE mitigated the increased levels of IL-1β and TNF-α in the hippocampus and exerted strong neuroprotection both in the dorsal and ventral hippocampus, basolateral amygdala, and partially in the piriform cortex. Our results suggest that the antioxidant, anti-inflammatory, and neuroprotective activity of LCM is an important prerequisite for its anticonvulsant and beneficial effects on SE-induced behavioral comorbidities.

摘要

临床上,颞叶癫痫(TLE)是最常见的部分性癫痫类型,常伴有各种合并症。本研究旨在评估抗癫痫药物(AED)拉科酰胺(LCM)慢性治疗对 TLE 模型中自发性运动性发作(SMS)、行为合并症、氧化应激、神经炎症和神经元损伤的影响。在匹罗卡品诱导的癫痫持续状态(SE)后 3 小时给予载体/LCM 治疗(30mg/kg,po),并在 Wistar 大鼠中持续治疗长达 12 周。我们的研究表明,LCM 减轻了 SMS 的数量,并纠正了与癫痫相关的运动活动受损、焦虑、记忆和抑郁样反应,这些反应分别在高架十字迷宫、物体识别测试、放射臂迷宫测试和蔗糖偏好测试中进行测量。这种 AED 通过增加超氧化物歧化酶活性和谷胱甘肽水平来抑制氧化应激,并减轻海马中的过氧化氢酶活性和脂质过氧化。SE 后 LCM 治疗减轻了海马中 IL-1β和 TNF-α水平的升高,并在背侧和腹侧海马、基底外侧杏仁核以及部分梨状皮质中发挥了强烈的神经保护作用。我们的结果表明,LCM 的抗氧化、抗炎和神经保护活性是其抗惊厥作用和对 SE 诱导的行为合并症有益作用的重要前提。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f6e/8124899/9918c52814cd/ijms-22-04667-g017.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f6e/8124899/3d9a5659e25e/ijms-22-04667-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f6e/8124899/89bf0791b374/ijms-22-04667-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f6e/8124899/5288dc777992/ijms-22-04667-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f6e/8124899/a849f835d3a6/ijms-22-04667-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f6e/8124899/3df17d1a4bb7/ijms-22-04667-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f6e/8124899/6029f99f5606/ijms-22-04667-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f6e/8124899/7bf1802be9a5/ijms-22-04667-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f6e/8124899/c4c1c14fb399/ijms-22-04667-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f6e/8124899/ee2f0811e8fe/ijms-22-04667-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f6e/8124899/a4cbfaea8913/ijms-22-04667-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f6e/8124899/6ace8fb0e146/ijms-22-04667-g011.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f6e/8124899/66d612cc5e8b/ijms-22-04667-g012.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f6e/8124899/66e5510a1ab2/ijms-22-04667-g013.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f6e/8124899/71cad607752a/ijms-22-04667-g014.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f6e/8124899/dfd259d28063/ijms-22-04667-g015.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f6e/8124899/0b4c9cacec32/ijms-22-04667-g016.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f6e/8124899/9918c52814cd/ijms-22-04667-g017.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f6e/8124899/3d9a5659e25e/ijms-22-04667-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f6e/8124899/89bf0791b374/ijms-22-04667-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f6e/8124899/5288dc777992/ijms-22-04667-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f6e/8124899/a849f835d3a6/ijms-22-04667-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f6e/8124899/3df17d1a4bb7/ijms-22-04667-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f6e/8124899/6029f99f5606/ijms-22-04667-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f6e/8124899/7bf1802be9a5/ijms-22-04667-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f6e/8124899/c4c1c14fb399/ijms-22-04667-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f6e/8124899/ee2f0811e8fe/ijms-22-04667-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f6e/8124899/a4cbfaea8913/ijms-22-04667-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f6e/8124899/6ace8fb0e146/ijms-22-04667-g011.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f6e/8124899/66d612cc5e8b/ijms-22-04667-g012.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f6e/8124899/66e5510a1ab2/ijms-22-04667-g013.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f6e/8124899/71cad607752a/ijms-22-04667-g014.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f6e/8124899/dfd259d28063/ijms-22-04667-g015.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f6e/8124899/0b4c9cacec32/ijms-22-04667-g016.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f6e/8124899/9918c52814cd/ijms-22-04667-g017.jpg

相似文献

1
Effects of Lacosamide Treatment on Epileptogenesis, Neuronal Damage and Behavioral Comorbidities in a Rat Model of Temporal Lobe Epilepsy.拉科酰胺治疗对颞叶癫痫大鼠模型癫痫发生、神经元损伤和行为共病的影响。
Int J Mol Sci. 2021 Apr 28;22(9):4667. doi: 10.3390/ijms22094667.
2
Anticonvulsant Effects of Topiramate and Lacosamide on Pilocarpine-Induced Status Epilepticus in Rats: A Role of Reactive Oxygen Species and Inflammation.托吡酯和拉考沙胺对匹罗卡品诱导的大鼠癫痫持续状态的抗惊厥作用:活性氧和炎症的作用。
Int J Mol Sci. 2021 Feb 25;22(5):2264. doi: 10.3390/ijms22052264.
3
Inverted-U response of lacosamide on pilocarpine-induced status epilepticus and oxidative stress in C57BL/6 mice is independent of hippocampal collapsin response mediator protein-2.拉科酰胺对毛果芸香碱诱导的C57BL/6小鼠癫痫持续状态和氧化应激的倒U型反应独立于海马塌陷反应介导蛋白-2。
Epilepsy Res. 2018 Sep;145:93-101. doi: 10.1016/j.eplepsyres.2018.06.009. Epub 2018 Jun 18.
4
Neuroprotective potential of topiramate, pregabalin and lacosamide combination in a rat model of acute SE and intractable epilepsy: Perspectives from electroencephalographic, neurobehavioral and regional degenerative analysis.托吡酯、普瑞巴林和拉科酰胺联合治疗急性 SE 和耐药性癫痫大鼠模型的神经保护作用:脑电图、神经行为和区域性退行性分析的观点。
Eur J Pharmacol. 2024 Sep 5;978:176792. doi: 10.1016/j.ejphar.2024.176792. Epub 2024 Jun 29.
5
The anticonvulsant effect of chronic treatment with topiramate after pilocarpine-induced status epilepticus is accompanied by a suppression of comorbid behavioral impairments and robust neuroprotection in limbic regions in rats.匹罗卡品诱导癫痫持续状态后,托吡酯慢性治疗的抗惊厥作用伴随着对大鼠边缘区域共病行为障碍的抑制和强大的神经保护作用。
Epilepsy Behav. 2022 Sep;134:108802. doi: 10.1016/j.yebeh.2022.108802. Epub 2022 Jul 2.
6
Time course evaluation of lacosamide alone and in polypharmacy on behavioral manifestations and oxidative stress in lithium-pilocarpine-induced model.左乙拉西坦单药和联合用药对锂-匹罗卡品诱导模型行为表现和氧化应激的时间进程评估。
J Physiol Pharmacol. 2020 Aug;71(4). doi: 10.26402/jpp.2020.4.10. Epub 2020 Dec 12.
7
Agomelatine protects against neuronal damage without preventing epileptogenesis in the kainate model of temporal lobe epilepsy.阿戈美拉汀在红藻氨酸颞叶癫痫模型中可预防神经元损伤,但不能阻止癫痫发生。
Neurobiol Dis. 2017 Aug;104:1-14. doi: 10.1016/j.nbd.2017.04.017. Epub 2017 Apr 21.
8
Lacosamide modulates interictal spiking and high-frequency oscillations in a model of mesial temporal lobe epilepsy.拉科酰胺在颞叶内侧癫痫模型中调节发作间期棘波和高频振荡。
Epilepsy Res. 2015 Sep;115:8-16. doi: 10.1016/j.eplepsyres.2015.05.006. Epub 2015 May 19.
9
Neuroprotective effects of chlorogenic acid against oxidative stress in rats subjected to lithium-pilocarpine-induced status epilepticus.绿原酸对锂-匹罗卡品诱导癫痫持续状态大鼠氧化应激的神经保护作用。
Naunyn Schmiedebergs Arch Pharmacol. 2024 Sep;397(9):6989-6999. doi: 10.1007/s00210-024-03080-0. Epub 2024 Apr 16.
10
Treatment with melatonin after status epilepticus attenuates seizure activity and neuronal damage but does not prevent the disturbance in diurnal rhythms and behavioral alterations in spontaneously hypertensive rats in kainate model of temporal lobe epilepsy.癫痫持续状态后给予褪黑素治疗可减轻癫痫发作活动和神经元损伤,但不能预防在颞叶癫痫的海人酸模型中自发性高血压大鼠的昼夜节律紊乱和行为改变。
Epilepsy Behav. 2014 Feb;31:198-208. doi: 10.1016/j.yebeh.2013.12.013. Epub 2014 Jan 16.

引用本文的文献

1
Probiotics Co-administered with LCM Enhance Antiepileptic Efficacy in the Experimental Post-traumatic Epilepsy Model.益生菌与左乙拉西坦联合使用可增强实验性创伤后癫痫模型的抗癫痫疗效。
Neurochem Res. 2025 Sep 6;50(5):290. doi: 10.1007/s11064-025-04541-5.
2
BDNF/Cyclin D1 Signaling System and Cognitive Performance After Perampanel and Lacosamide Treatment Singly or in Combination in an Experimental Model of Temporal Lobe Epilepsy.在颞叶癫痫实验模型中,单药或联合使用吡仑帕奈和拉科酰胺治疗后,BDNF/细胞周期蛋白D1信号系统与认知表现
Curr Issues Mol Biol. 2024 Dec 11;46(12):14010-14032. doi: 10.3390/cimb46120838.
3
Evaluation of the Influence of Extract on Cognitive Functions and Hippocampal BDNF Expression.

本文引用的文献

1
The Genetics of Epilepsy.癫痫的遗传学
Annu Rev Genomics Hum Genet. 2020 Aug 31;21:205-230. doi: 10.1146/annurev-genom-120219-074937. Epub 2020 Apr 27.
2
Effect of acute pentylenetetrazol injection induced epileptic seizures on rat dentate gyrus at different postnatal ages.急性注射戊四氮诱导癫痫发作对不同出生后年龄大鼠齿状回的影响。
Anat Cell Biol. 2020 Mar;53(1):84-94. doi: 10.5115/acb.19.083. Epub 2020 Feb 3.
3
Anti-Epileptogenic Effects of Antiepileptic Drugs.抗癫痫药物的抗癫痫作用。
提取物对认知功能及海马脑源性神经营养因子表达的影响评估
Molecules. 2024 Dec 4;29(23):5723. doi: 10.3390/molecules29235723.
4
Cognitive comorbidities in the rat pilocarpine model of epilepsy.癫痫大鼠匹罗卡品模型中的认知共病
Front Neurol. 2024 May 30;15:1392977. doi: 10.3389/fneur.2024.1392977. eCollection 2024.
5
The therapeutic effects of lacosamide on epilepsy-associated comorbidities.拉科酰胺对癫痫相关合并症的治疗作用。
Front Neurol. 2023 Mar 16;14:1063703. doi: 10.3389/fneur.2023.1063703. eCollection 2023.
6
Pre- and Post-Endurance Training Mitigates the Rat Pilocarpine-Induced Status Epilepticus and Epileptogenesis-Associated Deleterious Consequences.耐力训练前后可减轻匹罗卡品诱导的大鼠癫痫持续状态和癫痫发生相关的有害后果。
Int J Mol Sci. 2022 Oct 29;23(21):13188. doi: 10.3390/ijms232113188.
7
Aqueous extract of (Jacq.) R. Br. (Fabaceae) exerts antiepileptogenic, anti-amnesic, and anxiolytic-like effects in mice mechanisms involving antioxidant and anti-inflammatory pathways.(豆科)R. Br.(豆科)的水提取物在小鼠中发挥抗癫痫发生、抗遗忘和抗焦虑样作用,其机制涉及抗氧化和抗炎途径。
Front Pharmacol. 2022 Oct 24;13:995881. doi: 10.3389/fphar.2022.995881. eCollection 2022.
8
The Role of the Negative Regulation of Microglia-Mediated Neuroinflammation in Improving Emotional Behavior After Epileptic Seizures.小胶质细胞介导的神经炎症负调控在改善癫痫发作后情绪行为中的作用
Front Neurol. 2022 Apr 14;13:823908. doi: 10.3389/fneur.2022.823908. eCollection 2022.
9
Baicalin Rescues Cognitive Dysfunction, Mitigates Neurodegeneration, and Exerts Anti-Epileptic Effects Through Activating TLR4/MYD88/Caspase-3 Pathway in Rats.黄芩苷通过激活大鼠体内的TLR4/MYD88/半胱天冬酶-3通路来挽救认知功能障碍、减轻神经退行性变并发挥抗癫痫作用。
Drug Des Devel Ther. 2021 Jul 20;15:3163-3180. doi: 10.2147/DDDT.S314076. eCollection 2021.
Int J Mol Sci. 2020 Mar 28;21(7):2340. doi: 10.3390/ijms21072340.
4
Ultrastructural and functional changes at the tripartite synapse during epileptogenesis in a model of temporal lobe epilepsy.在颞叶癫痫模型中癫痫发生过程中三突触复合体的超微结构和功能变化。
Exp Neurol. 2020 Apr;326:113196. doi: 10.1016/j.expneurol.2020.113196. Epub 2020 Jan 11.
5
Kainic acid-induced status epilepticus decreases mGlu receptor and phase-specifically downregulates Homer1b/c expression.海人酸诱导的癫痫持续状态会降低 mGlu 受体,并在特定时相下调 Homer1b/c 的表达。
Brain Res. 2020 Mar 1;1730:146640. doi: 10.1016/j.brainres.2019.146640. Epub 2019 Dec 28.
6
Evaluation of the impact of compound C11 a new anticonvulsant candidate on cognitive functions and hippocampal neurogenesis in mouse brain.评估新型抗惊厥候选药物 C11 复合物对小鼠大脑认知功能和海马神经发生的影响。
Neuropharmacology. 2020 Feb;163:107849. doi: 10.1016/j.neuropharm.2019.107849. Epub 2019 Nov 9.
7
The Impact of Prophylactic Lacosamide on LPS-Induced Neuroinflammation in Aged Rats.预防性拉考沙胺对 LPS 诱导的老年大鼠神经炎症的影响。
Inflammation. 2019 Oct;42(5):1913-1924. doi: 10.1007/s10753-019-01053-7.
8
Inflammation and reactive oxygen species in status epilepticus: Biomarkers and implications for therapy.癫痫持续状态中的炎症和活性氧:生物标志物及治疗意义。
Epilepsy Behav. 2019 Dec;101(Pt B):106275. doi: 10.1016/j.yebeh.2019.04.028. Epub 2019 Jun 4.
9
Targeting oxidative stress improves disease outcomes in a rat model of acquired epilepsy.靶向氧化应激可改善获得性癫痫大鼠模型的疾病转归。
Brain. 2019 Jul 1;142(7):e39. doi: 10.1093/brain/awz130.
10
Neuroprotective Effects of Lacosamide in Experimental Traumatic Spinal Cord Injury in Rats.拉科酰胺对大鼠实验性创伤性脊髓损伤的神经保护作用。
Turk Neurosurg. 2019;29(5):718-723. doi: 10.5137/1019-5149.JTN.25891-19.2.