| Literature DB >> 28859482 |
Li Xiang1, Juntong Wei1, Xiao Yu Tian2, Bei Wang1, Wan Chan1, Shangfu Li1, Zhi Tang1, Hongsong Zhang2, Wai San Cheang2, Qian Zhao1, Hongzhi Zhao1, Zhiyi Yang1, Yanjun Hong1, Yu Huang2, Zongwei Cai1.
Abstract
Acylcarnitines are exerting a variety of biological functions depending on the differences in lengths, saturation levels, and conjugation groups, which to a great extent contribute to the challenges of acylcarnitines quantifications due to various kinds of isomers. Here, we describe a novel method by using high-resolution parallel reaction monitoring (PRM) liquid chromatography-tandem mass spectrometry (LC-MS/MS). Both reversed-phase and normal-phase column were used in order to get accurate, reliable, widespread quantification of acylcarnitines, and without tedious sample preparation procedure. The method provided the most comprehensive acylcarnitine profile with high-resolution MS and MS/MS confirmation to date. A total of 117 acylcarnitines were detected from plasma and urine samples. The application of targeted profiling of acylcarnitines in db/m+ control and db/db diabetic mice indicated incomplete amino acid and fatty acid oxidation on diabetic mice. Interestingly, the reduction of medium odd-numbered chain acylcarnitines in urine samples was first observed between db/m+ and db/db mice. The high-resolution PRM method makes it possible to monitor the widespread metabolic changes of the acylcarnitines in response to stimuli. Besides, the accurate MS and MS/MS spectra data of the 117 acylcarnitines could be used as mass spectrometric resources for the identification of acylcarnitines.Entities:
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Year: 2017 PMID: 28859482 DOI: 10.1021/acs.analchem.7b02283
Source DB: PubMed Journal: Anal Chem ISSN: 0003-2700 Impact factor: 6.986