Mitigation of Acute Seizures and Neuropathology after Traumatic Brain Injury by Structure-Based Discovery-Identified Drugs.

IF 3.9 2区 医学 Q1 CLINICAL NEUROLOGY
Natallie Kajevu, Ivette Banuelos, Pedro Andrade, Elina Hämäläinen, Laureano Sabatier, Manuel Couyoupetrou, María Luisa Villalba, Luciana Gavernet, Anssi Lipponen, Teemu Natunen, Noora Puhakka, Mikko Hiltunen, Alan Talevi, Asla Pitkänen
{"title":"Mitigation of Acute Seizures and Neuropathology after Traumatic Brain Injury by Structure-Based Discovery-Identified Drugs.","authors":"Natallie Kajevu, Ivette Banuelos, Pedro Andrade, Elina Hämäläinen, Laureano Sabatier, Manuel Couyoupetrou, María Luisa Villalba, Luciana Gavernet, Anssi Lipponen, Teemu Natunen, Noora Puhakka, Mikko Hiltunen, Alan Talevi, Asla Pitkänen","doi":"10.1089/neu.2024.0070","DOIUrl":null,"url":null,"abstract":"<p><p>Our objective was to test the hypothesis that structure-based identified or designed compounds exhibiting neuroprotective, antioxidant, and anti-inflammatory properties <i>in vitro</i> will mitigate early seizures and neuropathology after traumatic brain injury (TBI) <i>in vivo</i>. The neuroprotective and anti-inflammatory effects of 11 compounds identified by computer-assisted approximations were tested <i>in vitro</i> in neuronal microglial co-cultures. Among these, compound FBA exhibited the best neuroprotective (MAP-2, microtubule-associated-protein 2, a neuronal damage biomarker), antioxidative (nitrite production), and anti-inflammatory effects <i>in vitro</i> (all <i>p</i> < 0.01). Consequently, its neuroprotective and antiseizure effects were assessed <i>in vivo</i> in adult male Sprague-Dawley rats exposed to severe lateral fluid-percussion-induced TBI. Rats under continuous video-electroencephalogram monitoring received prophylactic treatment with an intraperitoneal (i.p.) injection of FBA (FBApro, 30 mg/kg) or vehicle (VEH, 48% PEG in 0.9% saline, 3 mL/kg) at 2 and 24 h post-TBI. Rats that developed status epilepticus received 1-2 additional on-demand FBA doses (FBApro+, 100 mg/kg, i.p.) to stop epileptiform activity. FBApro treatment reduced the cortical lesion area (18.9 ± 4.1 mm<sup>2</sup>, <i>n</i> = 7) compared with VEH treatment (24.8 ± 5.7 mm<sup>2</sup>, <i>n</i> = 10, <i>p</i> < 0.05). FBApro treatment also showed a favorable effect on the white matter by reducing plasma levels of pNF-H, a biomarker of axonal injury, compared with VEH treatment (Cohen's delta 0.657). Both FBApro (368 ± 407 s) and FBApro+ (256 ± 327 s) treatments reduced the average cumulative seizure duration compared with VEH (896 ± 703 s, both <i>p</i> < 0.05). The FBApro+ treatment regimen also reduced the mean relative theta and alpha power and increased the mean relative gamma power in the electroencephalogram (<i>p</i> < 0.05). Our data identified FBA as a novel structure-based discovered compound with promising favorable effects on structural and functional recovery after TBI.</p>","PeriodicalId":16512,"journal":{"name":"Journal of neurotrauma","volume":" ","pages":""},"PeriodicalIF":3.9000,"publicationDate":"2025-04-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of neurotrauma","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1089/neu.2024.0070","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CLINICAL NEUROLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Our objective was to test the hypothesis that structure-based identified or designed compounds exhibiting neuroprotective, antioxidant, and anti-inflammatory properties in vitro will mitigate early seizures and neuropathology after traumatic brain injury (TBI) in vivo. The neuroprotective and anti-inflammatory effects of 11 compounds identified by computer-assisted approximations were tested in vitro in neuronal microglial co-cultures. Among these, compound FBA exhibited the best neuroprotective (MAP-2, microtubule-associated-protein 2, a neuronal damage biomarker), antioxidative (nitrite production), and anti-inflammatory effects in vitro (all p < 0.01). Consequently, its neuroprotective and antiseizure effects were assessed in vivo in adult male Sprague-Dawley rats exposed to severe lateral fluid-percussion-induced TBI. Rats under continuous video-electroencephalogram monitoring received prophylactic treatment with an intraperitoneal (i.p.) injection of FBA (FBApro, 30 mg/kg) or vehicle (VEH, 48% PEG in 0.9% saline, 3 mL/kg) at 2 and 24 h post-TBI. Rats that developed status epilepticus received 1-2 additional on-demand FBA doses (FBApro+, 100 mg/kg, i.p.) to stop epileptiform activity. FBApro treatment reduced the cortical lesion area (18.9 ± 4.1 mm2, n = 7) compared with VEH treatment (24.8 ± 5.7 mm2, n = 10, p < 0.05). FBApro treatment also showed a favorable effect on the white matter by reducing plasma levels of pNF-H, a biomarker of axonal injury, compared with VEH treatment (Cohen's delta 0.657). Both FBApro (368 ± 407 s) and FBApro+ (256 ± 327 s) treatments reduced the average cumulative seizure duration compared with VEH (896 ± 703 s, both p < 0.05). The FBApro+ treatment regimen also reduced the mean relative theta and alpha power and increased the mean relative gamma power in the electroencephalogram (p < 0.05). Our data identified FBA as a novel structure-based discovered compound with promising favorable effects on structural and functional recovery after TBI.

基于结构的新发现药物减轻创伤性脑损伤后的急性发作和神经病理。
我们的目的是验证基于结构的鉴定或设计的化合物在体外具有神经保护、抗氧化和抗炎特性,可以减轻体内创伤性脑损伤(TBI)后的早期癫痫发作和神经病理。通过计算机辅助近似鉴定的11种化合物的神经保护和抗炎作用在体外神经小胶质共培养中进行了测试。其中,化合物FBA在体外表现出最好的神经保护(MAP-2,微管相关蛋白2,神经元损伤生物标志物)、抗氧化(亚硝酸盐产生)和抗炎作用(均p < 0.01)。因此,在暴露于严重外侧液体撞击性TBI的成年雄性Sprague-Dawley大鼠体内评估其神经保护和抗癫痫作用。连续视频脑电图监测的大鼠在脑外伤后2和24小时分别腹腔注射FBA (FBApro, 30 mg/kg)或载药(VEH, 48% PEG, 0.9%生理盐水,3 mL/kg)进行预防性治疗。发生癫痫持续状态的大鼠接受1-2次额外的按需FBA剂量(FBApro+, 100 mg/kg, i.p)以停止癫痫样活动。与VEH组相比,FBApro组皮质损伤面积减少(18.9±4.1 mm2, n = 7)(24.8±5.7 mm2, n = 10, p < 0.05)。与VEH治疗相比,FBApro治疗还显示出通过降低血浆pNF-H水平(轴突损伤的生物标志物)对白质的有利影响(Cohen’s δ 0.657)。与VEH(896±703 s)相比,FBApro(368±407 s)和FBApro+(256±327 s)治疗组平均累积癫痫发作时间缩短(p < 0.05)。FBApro+治疗方案降低了脑电图平均相对θ和α功率,增加了平均相对γ功率(p < 0.05)。我们的数据表明,FBA是一种基于结构的新型化合物,对TBI后的结构和功能恢复有良好的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Journal of neurotrauma
Journal of neurotrauma 医学-临床神经学
CiteScore
9.20
自引率
7.10%
发文量
233
审稿时长
3 months
期刊介绍: Journal of Neurotrauma is the flagship, peer-reviewed publication for reporting on the latest advances in both the clinical and laboratory investigation of traumatic brain and spinal cord injury. The Journal focuses on the basic pathobiology of injury to the central nervous system, while considering preclinical and clinical trials targeted at improving both the early management and long-term care and recovery of traumatically injured patients. This is the essential journal publishing cutting-edge basic and translational research in traumatically injured human and animal studies, with emphasis on neurodegenerative disease research linked to CNS trauma.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信