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代谢组学在识别心肌肥厚中的作用:对过去 20 年发展的综述及未来展望。

Role of metabolomics in identifying cardiac hypertrophy: an overview of the past 20 years of development and future perspective.

机构信息

Centre of Biomedical Research, SGPGIMS Campus, Lucknow, India.

Department of Cardiology, King George's Medical University, Lucknow, India.

出版信息

Expert Rev Mol Med. 2021 Aug 11;23:e8. doi: 10.1017/erm.2021.12.

DOI:10.1017/erm.2021.12
PMID:34376261
Abstract

Cardiac hypertrophy (CH) is an augmentation of either the right ventricular or the left ventricular mass in order to compensate for the increase of work load on the heart. Metabolic abnormalities lead to histological changes of cardiac myocytes and turn into CH. The molecular mechanisms that lead to initiate CH have been of widespread concern, hence the development of the new field of research, metabolomics: one 'omics' approach that can reveal comprehensive information of the paradigm shift of metabolic pathways network in contrast to individual enzymatic reaction-based metabolites, have attempted and until now only 19 studies have been conducted using experimental animal and human specimens. Nuclear magnetic resonance spectroscopy and mass spectrometry-based metabolomics studies have found that CH is a metabolic disease and is mainly linked to the harmonic imbalance of glycolysis, citric acid cycle, amino acids and lipid metabolism. The current review will summarise the main outcomes of the above mentioned 19 studies that have expanded our understanding of the molecular mechanisms that may lead to CH and eventually to heart failure.

摘要

心脏肥厚(CH)是指右心室或左心室质量的增加,以代偿心脏工作量的增加。代谢异常导致心肌细胞的组织学变化,并转化为 CH。导致 CH 发生的分子机制一直受到广泛关注,因此新的研究领域——代谢组学得以发展:一种可以揭示代谢途径网络范式转变的综合信息的“组学”方法,与基于单个酶促反应的代谢物相比,到目前为止,只有 19 项研究使用实验动物和人体标本进行了尝试。基于核磁共振波谱和质谱的代谢组学研究发现,CH 是一种代谢疾病,主要与糖酵解、柠檬酸循环、氨基酸和脂质代谢的和谐失衡有关。本综述将总结上述 19 项研究的主要结果,这些研究加深了我们对可能导致 CH 并最终导致心力衰竭的分子机制的理解。

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