Cranial irradiation induces cognitive decline associated with altered dendritic spine morphology in the young rat hippocampus.

IF 1.2
Xin Ding, Hai-Bo Zhang, Hui Qiu, Xin Wen, Long-Zhen Zhang
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引用次数: 2

Abstract

Objective: Therapeutic irradiation is commonly used to treat brain cancers but can induce cognitive dysfunction, especially in children. The mechanism is unknown but likely involves alterations in dendritic spine number and structure.

Methods: To explore the impact of radiation exposure on the alteration of dendritic spine morphology in the hippocampus of young brains, 21-day-old Sprague-Dawley rats received cranial irradiation (10 Gy), and changes in spine density and morphology in dentate gyrus (DG) granules and CA1 pyramidal neurons were detected 1 and 3 months later by using Golgi staining. Moreover, we analyzed synapse-associated proteins within dendritic spines after irradiation.

Result: Our data showed that cognitive deficits were detected in young rats at both time points postirradiation, accompanied by morphological changes in dendritic spines. Our results revealed significant reductions in spine density in the DG at both 1 month (40.58%) and 3 months (28.92%) postirradiation. However, there was a decrease in spine density only at 1 month (33.29%) postirradiation in the basal dendrites of CA1 neurons and no significant changes in the apical dendrites of CA1 neurons at either time point. Notably, among our findings were the significant dynamic changes in spine morphology that persisted 3 months following cranial irradiation. Meanwhile, we found that depletion of the synapse-associated proteins PSD95 and Drebrin coincided with alterations in dendritic spines.

Conclusion: These data suggest that the decreased levels of PSD95 and Drebrin after ionizing radiation may cause changes in synaptic plasticity by affecting the morphological structure of dendritic spines, blocking the functional connectivity pathways of the brain and leading to cognitive impairment. Although the mechanism involved is unclear, understanding how ionizing radiation affects young brain hippocampal tissue may be useful to gain new mechanistic insights into radiation-induced cognitive dysfunction.

在幼龄大鼠海马中,颅照射诱导认知能力下降并改变树突棘形态。
目的:治疗性放疗常用于脑癌的治疗,但可引起认知功能障碍,尤其是儿童。机制尚不清楚,但可能涉及到树突棘数目和结构的改变。方法:为探讨辐射暴露对幼龄大鼠脑海马区树突棘形态改变的影响,采用10 Gy颅脑照射21日龄大鼠,分别于1、3个月后采用高尔基染色法检测棘密度、齿状回(DG)颗粒和CA1锥体神经元形态的变化。此外,我们分析了辐照后树突棘内的突触相关蛋白。结果:我们的数据显示,在辐射后的两个时间点,年轻大鼠都检测到认知缺陷,并伴有树突棘的形态学改变。我们的结果显示放射后1个月(40.58%)和3个月(28.92%)DG脊柱密度显著降低。然而,仅在放疗后1个月CA1神经元基底树突的脊柱密度下降(33.29%),CA1神经元顶端树突在两个时间点均无明显变化。值得注意的是,在我们的研究结果中,脊柱形态的显著动态变化持续了颅骨照射后3个月。同时,我们发现突触相关蛋白PSD95和Drebrin的缺失与树突棘的改变一致。结论:电离辐射后PSD95和Drebrin水平降低可能通过影响树突棘形态结构,阻断大脑功能连接通路,导致突触可塑性改变,从而导致认知功能障碍。虽然所涉及的机制尚不清楚,但了解电离辐射如何影响年轻的大脑海马组织可能有助于获得辐射诱发认知功能障碍的新机制见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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