Suppr超能文献

托吡酯对热惊厥实验模型中颞叶新皮质突触终末的影响:一项超微结构研究

Influence of Topiramate on the Synaptic Endings of the Temporal Lobe Neocortex in an Experimental Model of Hyperthermia-Induced Seizures: An Ultrastructural Study.

作者信息

Sobaniec Piotr, Lotowska Joanna Maria, Sobaniec-Lotowska Maria Elzbieta, Zochowska-Sobaniec Milena

机构信息

Department of Pediatric Neurology and Rehabilitation, Faculty of Health Sciences, Medical University of Bialystok, 15-274 Białystok, Poland.

Department of Medical Pathomorphology, Faculty of Medicine with the Division of Dentistry and Division of Medical Education in English, Medical University of Bialystok, 15-269 Białystok, Poland.

出版信息

Brain Sci. 2021 Oct 28;11(11):1433. doi: 10.3390/brainsci11111433.

Abstract

The objective of this pioneering study was to assess potentially neuroprotective properties of topiramate (TPM), a broad spectrum and newer-generation antiepileptic used against damage to synaptic endings of the temporal lobe neocortex in experimental hyperthermia-induced seizures (HS). TPM (80 mg/kg b.m.) was administered in young male Wistar rats with an intragastric tube before and immediately after HS. Specimens (1 mm) collected from the neocortex, fixed via transcardial perfusion with paraformaldehyde and glutaraldehyde solution, were routinely processed for transmission-electron microscopic study, i.e., for descriptive and morphometric analysis. The ultrastructure of neocortical neuropil components affected by hyperthermic stress showed distinct swelling of pre and post-synaptic axodendritic and axospinal endings, including total disintegration. Mitochondria were markedly damaged in synaptic structures. Axoplasm of presynaptic boutons contained a decreased number of synaptic vesicles. Synaptic junctions showed active zone-shortening. Preventive administration of TPM before HS induction demonstrated neuroprotective effects against synaptic damage in approximately 1/4 of these structures. Interestingly, beneficial effects on synapsis morphology were more common in perivascular zones close to well-preserved capillaries. They were demonstrated by smaller swelling of both presynaptic and postsynaptic parts, well-preserved mitochondria, an increased number and regular distribution of synaptic vesicles within axoplasm, and a significantly increased synaptic active zones. However, topiramate used directly after HS was ineffective in the prevention of hyperthermia-evoked synaptic injury. Our findings support the hypothesis that topiramate applied before HS can protect some neocortical synapses via the vascular factor by enhancing blood-brain barrier components and improving the blood supply of gray matter in the temporal lobe, which may be significant in febrile seizure-prevention in children.

摘要

这项开创性研究的目的是评估托吡酯(TPM)潜在的神经保护特性。TPM是一种广谱新一代抗癫痫药物,用于对抗实验性热惊厥(HS)中颞叶新皮质突触末梢的损伤。在年轻雄性Wistar大鼠热惊厥发作前及发作后立即通过胃管给予TPM(80mg/kg体重)。从新皮质采集1mm的标本,经心脏灌注多聚甲醛和戊二醛溶液固定后,常规处理用于透射电子显微镜研究,即进行描述性和形态计量学分析。受热应激影响的新皮质神经毡成分的超微结构显示,突触前和突触后的轴树突和轴棘末梢明显肿胀,包括完全崩解。突触结构中的线粒体明显受损。突触前终扣的轴浆中突触小泡数量减少。突触连接显示活性区缩短。在热惊厥诱导前预防性给予TPM对约四分之一的这些结构的突触损伤具有神经保护作用。有趣的是,对突触形态的有益影响在靠近保存完好的毛细血管的血管周围区域更为常见。表现为突触前和突触后部分肿胀较小、线粒体保存完好、轴浆内突触小泡数量增加且分布规则,以及突触活性区显著增加。然而,在热惊厥发作后直接使用托吡酯对预防热惊厥诱发的突触损伤无效。我们的研究结果支持这样的假设,即在热惊厥发作前应用托吡酯可通过血管因子保护一些新皮质突触,通过增强血脑屏障成分和改善颞叶灰质的血液供应,这可能对预防儿童热性惊厥具有重要意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/14cc/8615765/c34c73d2008b/brainsci-11-01433-g001.jpg

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