Sun Hui, Zhang Shuxiang, Zhang Aihua, Yan Guangli, Wu Xiuhong, Han Ying, Wang Xijun
Department of Pharmaceutical Analysis, Key Lab of Metabolomics and Chinmedomics, National TCM Key Laboratory of Serum Pharmacochemistry, Heilongjiang University of Chinese Medicine, Harbin, China.
PLoS One. 2014 Mar 26;9(3):e93384. doi: 10.1371/journal.pone.0093384. eCollection 2014.
Metabolomics represents an emerging discipline concerned with comprehensive assessment of small molecule endogenous metabolites in biological systems and provides a powerful approach insight into the mechanisms of diseases. Type 2 diabetes (T2D), called the burden of the 21st century, is growing with an epidemic rate. However, its precise molecular mechanism has not been comprehensively explored. In this study, we applied urinary metabolomics based on the UPLC/MS integrated with pattern recognition approaches to discover differentiating metabolites, to characterize and explore metabolic pathway disruption in an experimental model for high-fat-diet induced T2D. Six differentiating urinary metabolites were found in the negative mode, and two (2-(4-hydroxy-3-methoxy-phenyl) acetaldehyde sulfate, 2-phenylethanol glucuronide) of which were identified involving the key metabolic pathways linked to pentose and glucuronate interconversions, starch, sucrose metabolism and tyrosine metabolism. Our study provides new insight into pathophysiologic mechanisms and may enhance the understanding of T2D pathogenesis.
代谢组学是一门新兴学科,致力于全面评估生物系统中的小分子内源性代谢物,并为洞察疾病机制提供了一种强大的方法。2型糖尿病(T2D)被称为21世纪的负担,正以流行的速度增长。然而,其精确的分子机制尚未得到全面探索。在本研究中,我们应用基于超高效液相色谱/质谱联用并结合模式识别方法的尿液代谢组学,来发现差异代谢物,表征并探索高脂饮食诱导的T2D实验模型中的代谢途径破坏情况。在负离子模式下发现了六种差异尿液代谢物,其中两种(硫酸2-(4-羟基-3-甲氧基苯基)乙醛、2-苯乙醇葡萄糖醛酸苷)被鉴定涉及与戊糖和葡萄糖醛酸相互转化、淀粉、蔗糖代谢以及酪氨酸代谢相关的关键代谢途径。我们的研究为病理生理机制提供了新的见解,并可能增进对T2D发病机制的理解。