UPLC-Q/TOF质谱分析糖尿病冠心病气阴阳虚证血清代谢谱

Shenghua PIAO , Lei ZHANG , Ziqin ZHU , Huixia ZHAN , Xianglu RONG, Jiao GUO
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引用次数: 0

摘要

目的气阴虚证和阳虚证是两种常见的证候,临床表现为低热和寒症。不同的综合征表型在体内必须有不同的生物学基础。基于血清代谢组学,本研究旨在揭示上述两种糖尿病冠心病综合征的生物学特性。方法选择33例糖尿病性冠心病(DCHD)患者为研究对象,其中QYD 13例,YD证11例,平和体质9例。基于UPLC-Q/TOF质谱,采用代谢组学对上述三组血清样本进行检测和分析。利用PLS-DA(偏最小二乘判别分析)和数据库检索方法寻找具有差异的代谢物。同时,研究了各种代谢物的代谢途径。结果冠心病QYD证与YD证之间有17种代谢物差异。(YD)组的环GMP、LysoPE(20:3)、脯氨酸、异亮氨酸、n -乳酰酪氨酸、3-氧十六烷醇辅酶a和草酰琥珀酸含量低于PH组,而半乳糖醇、n -乳酰酪氨酸和草酰琥珀酸含量高于PH组。上述17种差异代谢物与多种途径相关,包括氨基酸代谢、嘌呤代谢、线粒体脂肪酸延伸、三羧酸循环、脂质代谢、能量代谢等。结论肝肾阴虚证、YD证等不同的冠心病证候,对同一疾病具有不同的生物学基础。本研究结果在一定程度上为中医对同一种疾病采取不同的治疗方法提供了科学依据。对指导临床使用草药也有重要意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Serum metabolic profile analysis of syndrome of Qi-yin deficiency and Yang deficiency in diabetic coronary heart disease by UPLC-Q/TOF MS

Aims

Qi-yin deficiency (QYD) and Yang-deficiency (YD) syndrome are two common syndromes with contrasting clinical manifestations of low fever and cold phobia. Different syndrome phenotypes must have distinct biological underpinnings in vivo. Based on serum metabolomics, this study aims to reveal the biological characteristics of the two diabetic coronary heart disease syndromes mentioned above.

Methods

A total of 33 diabetic coronary heart disease (DCHD) patients were included in the study, with 13 cases of QYD, 11 cases of YD syndrome, and 9 cases of Pinghe constitution (PH). Based on UPLC-Q/TOF MS, metabolomics was used to detect and analyze serum samples from the three groups mentioned above. To find differentiating metabolites, PLS-DA (Partial least squares discrimination analysis) and database searching were used. Meanwhile, the metabolic pathways of various metabolites were investigated.

Results

There were 17 different metabolites between QYD syndrome and YD syndrome of DCHD. Cyclic GMP, LysoPE (20:3), proline, isoleucine, N-lactoyl-tyrosine, 3-oxohexadecanoyl-CoA, and oxalosuccinic acid were lower in the (YD) group than those in the PH group, while galactitol, N-lactoyl-tyrosine, and oxalosuccinic acid were higher in the QYD group than in the PH group. The 17 differential metabolites mentioned above were linked to a variety of pathways, including amino acid metabolism, purine metabolism, fatty acid elongation in mitochondria, the tricarboxylic acid cycle, lipid metabolism, energy metabolism, etc.

Conclusion

Different DCHD syndromes, such as liver-kidney Yin deficiency and YD syndrome, have different biological bases for the same disease. To some extent, the findings of this study provide a scientific foundation for different approaches to treating the same disease in Traditional Chinese Medicine. It is also important for guiding the clinical use of herbal medicine.

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