醛负荷作为轻度外伤性脑损伤的客观成像生物标志物。

Alexia Kirby, Cian Ward, Clara S Goulet, Nicholas D Calvert, Ryan Daniel, Joseph Wai-Hin Leung, Ashwin Sharma, Mojmír Suchý, Cassandra Donatelli, Jing Wang, Emily Standen, Adam J Shuhendler
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引用次数: 0

摘要

轻度创伤性脑损伤(mTBI)是由生物力学力引起的神经系统损伤,目前尚无客观的诊断工具。下游损伤源于氧化损伤导致神经毒性醛的产生。建立了一种基于胶原蛋白的三维模拟皮质的脑震荡体外模型,证实了撞击后醛的产生。使用一种新型cst - mri造影剂ProxyNA3,在一种新的闭头、清醒、单次冲击脑震荡模型中,对患有醛脱氢酶2 (ALDH2)缺乏症的老年和年轻小鼠进行mTBI后体内总醛水平的测定。在撞击前、撞击后第2天和第7天分别进行ProxyNA3-MRI检查。损伤后2天MRI信号增强显著,损伤后7天星形胶质细胞激活。数据表明高龄和ALDH2缺乏导致mTBI后醛负荷增加。总的来说,ProxyNA3能够定位脑震荡相关醛,支持其作为脑震荡客观诊断工具的应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Aldehydic load as an objective imaging biomarker of mild traumatic brain injury.

Mild traumatic brain injury (mTBI) is neurological impairment induced by biomechanical forces without structural brain damage, currently without an objective diagnostic tool. Downstream injury stems from oxidative damage leading to the production of neurotoxic aldehydes. A collagen-based 3D corticomimetic in vitro model of concussion was developed, confirming aldehyde production following impact. Total aldehyde levels were mapped in vivo following mTBI using a novel CEST-MRI contrast agent, ProxyNA3, in a new model of closed-head, awake, single-impact concussion in aged and young mice with aldehyde dehydrogenase 2 (ALDH2) deficiency. ProxyNA3-MRI was performed before impact, and on days two- and seven- post-impact. MRI signal enhancement significantly increased at two days post-injury prior to astrocyte activation at seven days post-injury. The data suggest that advanced age and ALDH2 deficiency contribute to increased aldehydic load following mTBI. Overall, ProxyNA3 was capable of mapping concussion-associated aldehydes, supporting its application as an objective diagnostic tool for concussion.

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