对两种已建立的海湾战争疾病小鼠模型的脑结构改变进行纵向评估

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC ACS Applied Electronic Materials Pub Date : 2024-09-06 DOI:10.3389/fnins.2024.1465701
Jessica M. Carpenter, Sarah N. Hughes, Nikolay M. Filipov
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引用次数: 0

摘要

海湾战争病(GWI)影响了近 30% 的 1990-1991 年海湾战争(GW)退伍军人,是一种多种症状的疾病,对神经系统的影响主要归咎于战时化学物质的过度暴露。以大脑为重点的研究显示,患有海湾战争综合症的退伍军人会出现持续的结构和功能改变,包括体积缩小、连通性降低和信号传递减少,这与认知和运动能力低下有关。在啮齿类动物模型中,GWI 的症状成分被再现为行为、神经化学和神经炎症畸变。然而,临床前结构成像研究仍然有限。本研究旨在描述两种已建立的 GWI 临床前模型在 12 个月内大脑结构改变的进展情况。在PB/PM模型中,雄性C57BL/6 J小鼠(8-9周)每天接触神经毒剂预防剂溴化吡啶斯的明(PB)和拟除虫菊酯杀虫剂氯菊酯(PM)10天。在 PB/DEET/CORT/DFP 模型中,小鼠每天接触 PB 和驱虫剂 DEET(第 1-14 天)以及皮质酮(CORT,第 7-14 天)。第 15 天,小鼠单次注射沙林代用品二异丙基氟磷酸盐(DFP)。使用瓦里安 7 T Bore MRI 系统,在暴露 GWI 后 6 个月、9 个月和 12 个月时进行结构(矢状 T2 加权)扫描。在 MATLAB 的开源 Aedes 工具箱中划定了感兴趣的区域,包括全脑、脑室、皮层、海马、小脑和脑干,然后在 ImageJ 中进行了脑容积和皮层厚度分析。在最后一次核磁共振成像后一个月,还进行了有限的行为测试。这项研究的结果比较了这些暴露范例之间的相似性和区别,有助于了解 GWI 的发病机制。这些模型的主要相似之处包括随着年龄的增长,脑室相对增大和海马体积缩小。PB/DEET/CORT/DFP模型的主要差异包括脑干体积缩小以及早期和持续的大脑总体积损失,而PB/PM模型随着年龄的增长会导致皮质厚度减少。在行为上,两个模型的小鼠在 13 个月大时运动功能基本保持不变。然而,PB/DEET/CORT/DFP 模型中的 GWI 小鼠表现出焦虑样行为的增加。
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Longitudinal evaluation of structural brain alterations in two established mouse models of Gulf War Illness
Gulf War Illness (GWI) affects nearly 30% of veterans from the 1990–1991 Gulf War (GW) and is a multi-symptom illness with many neurological effects attributed to in-theater wartime chemical overexposures. Brain-focused studies have revealed persistent structural and functional alterations in veterans with GWI, including reduced volumes, connectivity, and signaling that correlate with poor cognitive and motor performance. GWI symptomology components have been recapitulated in rodent models as behavioral, neurochemical, and neuroinflammatory aberrations. However, preclinical structural imaging studies remain limited. This study aimed to characterize the progression of brain structural alterations over the course of 12 months in two established preclinical models of GWI. In the PB/PM model, male C57BL/6 J mice (8–9 weeks) received daily exposure to the nerve agent prophylactic pyridostigmine bromide (PB) and the pyrethroid insecticide permethrin (PM) for 10 days. In the PB/DEET/CORT/DFP model, mice received daily exposure to PB and the insect repellent DEET (days 1–14) and corticosterone (CORT; days 7–14). On day 15, mice received a single injection of the sarin surrogate diisopropylfluorophosphate (DFP). Using a Varian 7 T Bore MRI System, structural (sagittal T2-weighted) scans were performed at 6-, 9-, and 12-months post GWI exposures. Regions of interest, including total brain, ventricles, cortex, hippocampus, cerebellum, and brainstem were delineated in the open source Aedes Toolbox in MATLAB, followed by brain volumetric and cortical thickness analyses in ImageJ. Limited behavioral testing 1 month after the last MRI was also performed. The results of this study compare similarities and distinctions between these exposure paradigms and aid in the understanding of GWI pathogenesis. Major similarities among the models include relative ventricular enlargement and reductions in hippocampal volumes with age. Key differences in the PB/DEET/CORT/DFP model included reduced brainstem volumes and an early and persistent loss of total brain volume, while the PB/PM model produced reductions in cortical thickness with age. Behaviorally, at 13 months, motor function was largely preserved in both models. However, the GWI mice in the PB/DEET/CORT/DFP model exhibited an elevation in anxiety-like behavior.
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