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创伤性脑损伤亚急性期大鼠模型中海马和皮层的代谢组学分析

Metabolomics Analysis of Hippocampus and Cortex in a Rat Model of Traumatic Brain Injury in the Subacute Phase.

作者信息

Zheng Fei, Zhou Yan-Tao, Li Peng-Fei, Hu En, Li Teng, Tang Tao, Luo Jie-Kun, Zhang Wei, Ding Chang-Song, Wang Yang

机构信息

College of Electrical and Information Engineering, Hunan University, Changsha, China.

Laboratory of Ethnopharmacology, Institute of Integrated Traditional Chinese and Western Medicine, Xiangya Hospital, Central South University, Changsha, China.

出版信息

Front Neurosci. 2020 Sep 4;14:876. doi: 10.3389/fnins.2020.00876. eCollection 2020.

DOI:10.3389/fnins.2020.00876
PMID:33013291
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7499474/
Abstract

Traumatic brain injury (TBI) is a complex and serious disease as its multifaceted pathophysiological mechanisms remain vague. The molecular changes of hippocampal and cortical dysfunction in the process of TBI are poorly understood, especially their chronic effects on metabolic profiles. Here we utilize metabolomics-based liquid chromatography coupled with tandem mass spectrometry coupled with bioinformatics method to assess the perturbation of brain metabolism in rat hippocampus and cortex on day 7. The results revealed a signature panel which consisted of 13 identified metabolites to facilitate targeted interventions for subacute TBI discrimination. Purine metabolism change in cortical tissue and taurine and hypotaurine metabolism change in hippocampal tissue were detected. Furthermore, the associations between the metabolite markers and the perturbed pathways were analyzed based on databases: 64 enzyme and one pathway were evolved in TBI. The findings represented significant profiling changes and provided unique metabolite-protein information in a rat model of TBI following the subacute phase. This study may inspire scientists and doctors to further their studies and provide potential therapy targets for clinical interventions.

摘要

创伤性脑损伤(TBI)是一种复杂且严重的疾病,因为其多方面的病理生理机制仍不明确。TBI过程中海马体和皮质功能障碍的分子变化了解甚少,尤其是它们对代谢谱的慢性影响。在此,我们利用基于代谢组学的液相色谱-串联质谱联用生物信息学方法,评估大鼠海马体和皮质在第7天的脑代谢扰动情况。结果揭示了一个由13种已鉴定代谢物组成的特征面板,有助于对亚急性TBI进行靶向干预鉴别。检测到皮质组织中的嘌呤代谢变化以及海马体组织中的牛磺酸和亚牛磺酸代谢变化。此外,基于数据库分析了代谢物标记与受干扰途径之间的关联:TBI中有64种酶和一条途径发生了变化。这些发现代表了显著的谱图变化,并在亚急性期后的TBI大鼠模型中提供了独特的代谢物-蛋白质信息。本研究可能会激励科学家和医生进一步开展研究,并为临床干预提供潜在的治疗靶点。

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Decreased static and increased dynamic global signal topography in major depressive disorder.
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