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脊髓挫伤啮齿动物模型中的免疫和代谢生物标志物

Immune and Metabolic Biomarkers in a Rodent Model of Spinal Cord Contusion.

作者信息

Dos Santos E Santos Christiano, Welch Bradley A, Edwards Shelley R, Harris Kwamie K, Duncan Brittany C, Himel Alexandra R, Grayson Bernadette E

机构信息

University of Mississippi Medical Center, Jackson, MS, USA.

出版信息

Global Spine J. 2022 Jan;12(1):110-120. doi: 10.1177/2192568220950337. Epub 2020 Sep 23.

Abstract

STUDY DESIGN

Basic science animal research study.

OBJECTIVES

Using T10 spinal contused rats, we sought to identify molecular and circulating, metabolic and immune biomarkers during the subchronic and chronic recovery periods that may inform us concerning neurorehabilitation.

METHODS

Gene expression of the cord and ELISA were performed in 28 and 100 days in T10 injured rats and compared to sham-injured rats. Hundred-day injured rats were placed on either a low-fat or high-fat diet following the recovery phase. Linear regression analysis was performed between markers and locomotor score, body weight, body composition, and blood cholesterol and triglycerides.

RESULTS

Gene expression in the thoracic cord for complement marker, C1QC, dendritic cell marker, ITGAX, and cholesterol biosynthesis genes, FDFT1, HMCGR, LDLR, and SREBP1, were significantly associated with BBB score, body weight, composition, and other metabolic parameters. Circulating levels of these proteins, however, did not vary by injury or predict the level of locomotor recovery.

CONCLUSIONS

Identification of reliable circulating biomarkers that are durable and based on level of spinal injury are complicated by immune and metabolic comorbidities. Continued work is necessary to identify stable markers of disease progression.

摘要

研究设计

基础科学动物研究。

目的

利用T10脊髓挫伤大鼠,我们试图确定亚慢性和慢性恢复期的分子、循环、代谢和免疫生物标志物,这些标志物可能为神经康复提供信息。

方法

对T10损伤大鼠在28天和100天时进行脊髓基因表达检测及酶联免疫吸附测定(ELISA),并与假损伤大鼠进行比较。在恢复阶段后,将100天损伤大鼠置于低脂或高脂饮食中。对标志物与运动评分、体重、身体成分以及血液胆固醇和甘油三酯进行线性回归分析。

结果

胸段脊髓中补体标志物C1QC、树突状细胞标志物ITGAX以及胆固醇生物合成基因FDFT1、HMCGR、LDLR和SREBP1的基因表达与BBB评分、体重、身体成分及其他代谢参数显著相关。然而,这些蛋白质的循环水平并未因损伤而有所不同,也无法预测运动恢复水平。

结论

由于免疫和代谢合并症,识别基于脊髓损伤程度的持久可靠循环生物标志物变得复杂。有必要继续开展工作以确定疾病进展的稳定标志物。

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