阿尔茨海默病特定区域海马区的性别差异:一种基于动物的方法

Jackson Sawyer, Syed Salman Shahid, Yu-Chien Wu
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摘要

背景:海马体萎缩是导致阿尔茨海默病(AD)患者记忆力和认知能力下降的原因。男性和女性阿尔茨海默病的进展和表现不同,海马及其亚区受到的影响也可能不同。通过确定海马体的哪些区域会受到性别影响,可以更好地利用诊断工具来临床识别和治疗老年痴呆症。目标:拟议研究的目标是(1)使用体内核磁共振成像技术在小鼠模型中分离海马;(2)使用数据分析比较 5xFAD 小鼠海马及其亚区的体积;(3)了解性别是否在不同海马体积中起作用;(4)评估使用结构性核磁共振成像测量海马完整性在未来体内人脑研究/临床实践中的转化效用。研究方法我们使用成像软件 FSLeyes 检查 MRI 图像并分离海马亚区掩膜。核磁共振成像图像是在淀粉样蛋白-B开始在前脑沉积的2个月大时拍摄的。在分离出每张核磁共振成像的海马掩膜后,确定了组别分类,并进行了定量分析以比较各组别。结果我们发现雌性小鼠海马颗粒层(SG)的空间体积明显低于雄性小鼠。海马颗粒层包含负责空间记忆的齿状颗粒细胞。除此以外,我们获得的数据并不显著,但确实表明,尽管雌性小鼠的TICV较大,但雌性小鼠的海马亚区和总体积主要较小。结论和影响:我们需要更多的数据来观察SG在一生中的退化情况,并评估这是否是雄性小鼠比雌性小鼠更能保持AD空间记忆的原因。否则,在AD早期阶段分析海马体积似乎不足以解释AD表现和发展过程中突出的性别差异。
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Sex differences in region-specific hippocampal areas in Alzheimer’s Disease: an animal-based approach
Background: Atrophy in the hippocampus is responsible for memory and cognitive decline in Alzheimer’s Disease (AD). Progression and presentation of AD in men and women are different, and the hippocampus and its subregions could be affected differently. By identifying what areas of the hippocampus are affected by sex, diagnostic tools can be better used to clinically identify and treat AD. Aims: The goals of the proposed research are: (1) use in vivo MRI techniques to isolate the hippocampus in a mouse model, (2) use data analysis to compare the volume of the hippocampus and its subregions in 5xFAD mice, and (3) see if sex plays a role in differing hippocampal volume, and (4) assess the translational utility of using structural MRI to measure hippocampal integrity for future in vivo human brain studies/clinical practice. Methods: We used the imaging software FSLeyes to examine MRI images and isolate hippocampal subregion masks. MRI images were taken at the 2-month age period when amyloid-B deposition begins in the forebrain. Upon isolation of the hippocampal mask of each MRI, group classification was identified, and quantitative analysis was performed to compare groups. Results: We found significant lower spatial volume in Stratum Granulosum (SG) of the hippocampus in female mice compared to male mice. The SG contains dentate granule cells, responsible for spatial memory. Apart from this, the data that we obtained was nonsignificant but did show that female mice contained mainly smaller hippocampus subregions and total volumes despite TICV being larger in females. Conclusion and Impact: More data is needed to observe the degeneration of SG over a lifetime and assess if it is the reason why males retain spatial memory in AD as opposed to females. Otherwise, analyzing hippocampal volume in the early stages of AD doesn’t appear to be sufficient in explaining outstanding sex differences in AD presentation and progression.
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