基于体素的形态和功能连通性对辐射诱导认知功能障碍的非侵入性和敏感性MRI评估。

IF 5.7 2区 医学 Q1 NEUROSCIENCES
Long Zhu, Yaolei Ma, Ao Kong, Xiangjun Wu, Yanming Ren, Wei Zhou, Chaoji Huangfu, Yue Gao
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引用次数: 0

摘要

背景:放射治疗不可避免地引起认知功能障碍。我们的目标是利用基于体素的形态测量(VBM)和功能连接(FC),探索一种非侵入性的、敏感的策略来评估辐射诱导的认知功能障碍,并从行为、组织学和分子角度阐明潜在的机制。方法:我们采用多模态交叉验证策略来评估C57BL/6j小鼠在60Co γ辐射源中单剂量暴露于5 Gy或15 Gy时的认知功能障碍。放射线照射后第18、19、21天分别进行空地、新物体识别和Morris水迷宫测试,第27天进行fMRI扫描。VBM和FC分析用于评估放射后的认知功能损害。进行组织病理学分析(HE和尼氏染色)和神经损伤标志物(Iba-1和GFAP)的免疫组化评估。结果:辐射组(5 Gy、15 Gy)小鼠的逃避潜伏期增加,穿越平台次数减少,对新旧物体的探索偏好无差异。辐射组海马DG区神经元排列紊乱,尼索小体明显减少。放疗后,Iba1 (CA1、CA2和CA3区)和GFAP (CA1和CA3区)的表达增加。海马组织促炎因子ifn - γ、il -1 β水平升高,抗炎因子IL-4、IL-10表达降低。5gy组脑灰质体积增加的区域为右侧海马DG区。24对海马亚区(如CA1)之间的功能连接值增加。R和DG-mo。而CA3等29对之间则呈下降趋势。R和ent1。R在5gy基团中。在15 Gy组,功能连接值在31对之间增加,如DG-mo。L和HATA。R,在20对之间减少,如CA2。R和DG-po.L。与5gy组相比,15gy组有33对功能连接值增加,23对功能连接值降低。结论:功能磁共振成像可以无创、更有效地评估辐射剂量后脑认知功能损伤。这为用非侵入性和敏感的方法评估认知功能提供了新的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Non-invasive and sensitive MRI assessment of radiation-induced cognitive dysfunction via voxel-based morphological and functional connectivity.

Background: Radiotherapy inevitably cause cognitive dysfunction. We aim to explore a non-invasive, sensitive strategy for assessing radiation-induced cognitive dysfunction, using voxel-based morphometry (VBM) and functional connectivity (FC), and to clarify the potential mechanisms from behavioral, histological, and molecular perspectives.

Methods: We employed a multimodal cross-validation strategy to evaluate cognitive dysfunction of C57BL/6j mice exposed to a single dose of 5 Gy or 15 Gy using a 60Co γ radiation source. The open field, novel object recognition, and Morris water maze tests were conducted on days 18, 19, and 21 after radiation, respectively, followed by fMRI scanning on day 27. VBM and FC analysis are used to assess cognitive function impairment after radiation. Histopathological analyses (HE and Nissl staining) and immunohistochemical assessments of neural damage markers (Iba-1 and GFAP) were conducted.

Results: The radiation group (5 Gy, 15 Gy) showed an increased escape latency, decreased number of platform crossings, and no difference in exploration preference for old versus new objects. In the radiation group, the arrangement of neurons in the hippocampal DG region was disordered, and a significant reduction of Nissl bodies was observed. The expression of Iba1 (in CA1, CA2, and CA3 regions) and GFAP (in CA1 and CA3 regions) was increased after radiation. The levels of pro-inflammatory factors such as IFN-gamma and IL-1beta were increased in the hippocampal tissue, while the expression of anti-inflammatory factors (IL-4 and IL-10) were decreased. The brain region with increased gray matter volume in the 5 Gy group was the right hippocampal DG region. Functional connectivity values were increased between 24 pairs of hippocampal subregions, such as CA1.R and DG-mo.L, while decreased between 29 pairs, such as CA3.R and ENTl1.R in the 5 Gy group. In the 15 Gy group, functional connectivity values increased between 31 pairs, such as DG-mo.L and HATA.R, and decreased between 20 pairs, such as CA2.R and DG-po.L. Compared to the 5 Gy group, the 15 Gy group had 33 pairs with increased functional connectivity values and 23 pairs with decreased values.

Conclusion: Functional magnetic resonance imaging can non-invasively and more efficiently assess cognitive function impairment in the brain after radiation doses using VBM and FC comparative methods. This provides new insights into the evaluation of cognitive function with non-invasive and sensitive methods.

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来源期刊
Acta Neuropathologica Communications
Acta Neuropathologica Communications Medicine-Pathology and Forensic Medicine
CiteScore
11.20
自引率
2.80%
发文量
162
审稿时长
8 weeks
期刊介绍: "Acta Neuropathologica Communications (ANC)" is a peer-reviewed journal that specializes in the rapid publication of research articles focused on the mechanisms underlying neurological diseases. The journal emphasizes the use of molecular, cellular, and morphological techniques applied to experimental or human tissues to investigate the pathogenesis of neurological disorders. ANC is committed to a fast-track publication process, aiming to publish accepted manuscripts within two months of submission. This expedited timeline is designed to ensure that the latest findings in neuroscience and pathology are disseminated quickly to the scientific community, fostering rapid advancements in the field of neurology and neuroscience. The journal's focus on cutting-edge research and its swift publication schedule make it a valuable resource for researchers, clinicians, and other professionals interested in the study and treatment of neurological conditions.
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