Simultaneous determination of choline, L-carnitine, betaine, trimethylamine, trimethylamine N-oxide, and creatinine in plasma, liver, and feces of hyperlipidemic rats by UHPLC-MS/MS

IF 2.8 3区 医学 Q2 BIOCHEMICAL RESEARCH METHODS Journal of Chromatography B Pub Date : 2024-06-25 DOI:10.1016/j.jchromb.2024.124210
Changqian Xu , Min Zhang , Shuo Zhang , Pengjiao Wang , Chencen Lai , Duo Meng , Zhiyu Chen , Xinxin Yi , Xiuli Gao
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Abstract

Background

Due to the close correlation between choline, L-carnitine, betaine and their intestinal microbial metabolites, including trimethylamine (TMA) and trimethylamine N-oxide (TMAO), and creatinine, there has been an increasing interest in the study of these compounds in vivo.

Methods

In this study, a rapid stable isotope dilution (SID)-UHPLC-MS/MS method was developed for the simultaneous determination of choline, L-carnitine, betaine, TMA, TMAO and creatinine in plasma, liver and feces of rats. The method was validated using quality control (QC) samples spiked at low, medium and high levels. Second, we applied the method to quantify the effects of Rosa Roxburghii Tratt juice (RRTJ) on plasma, liver, and fecal levels of choline, L-carnitine, betaine, TMA, TMAO, and creatinine in high-fat diet-induced hyperlipidemic rats, demonstrating the utility of the method.

Results

The limits of detection (LOD) were 0.04–0.027 µM and the limits of quantification (LOQ) were 0.009–0.094 µM. The linear ranges for each metabolite in plasma were choline1.50–96 µM; L-carnitine: 2–128 µM; betaine: 3–192 µM; TMA: 0.01–40.96 µM; TMAO: 0.06–61.44 µM and creatinine: 1–64 µM (R2 ≥ 0.9954). The linear ranges for each metabolite in liver were Choline: 12–768 µM; L-carnitine: 1.5–96 µM; betaine: 10–640 µM; TMA: 0.5–32 µM; TMAO: 0.02–81.92 µM and creatinine: 0.2–204.8 µM (R2 ≥ 0.9938). The linear ranges for each metabolite in feces were choline: 1.5–96 µM; L-carnitine: 0.01–40.96 µM; Betaine: 1.5–96 µM; TMA: 1–64 µM; TMAO: 0.02–81.92 µM and Creatinine: 0.02–81.92 µM (R2 ≥ 0.998). The intra-day and inter-day coefficients of variation were < 8 % for all analytes. The samples were stabilized after multiple freeze–thaw cycles (3 freeze–thaw cycles), 24 h at room temperature, 24 h at 4 °C and 20 days at −80 °C. The samples were stable. The average recovery was 89 %-99 %. This method was used to quantify TMAO and its related metabolites and creatinine levels in hyperlipidemic rats. The results showed that high-fat diet led to the disorder of TMAO and its related metabolites and creatinine in rats, which was effectively improved after the intervention of Rosa Roxburghii Tratt juice(RRTJ).

Conclusions

A method for the determination of choline, L-carnitine, betaine, TMA, TMAO and creatinine in plasma, liver and feces samples was established, which is simple, time-saving, high precision, accuracy and recovery.

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利用超高效液相色谱-质谱/质谱法同时测定高脂血症大鼠血浆、肝脏和粪便中的胆碱、左旋肉碱、甜菜碱、三甲胺、三甲胺 N-氧化物和肌酐。
背景:由于胆碱、左旋肉碱、甜菜碱及其肠道微生物代谢产物(包括三甲胺(TMA)和三甲胺N-氧化物(TMAO))与肌酐之间的密切相关性,人们对这些化合物在体内的研究越来越感兴趣:本研究建立了一种快速稳定同位素稀释(SID)-UHPLC-MS/MS 法,用于同时测定大鼠血浆、肝脏和粪便中的胆碱、左旋肉碱、甜菜碱、TMA、TMAO 和肌酐。使用低、中、高添加水平的质量控制(QC)样品对该方法进行了验证。其次,我们应用该方法定量检测了Rosa Roxburghii Tratt果汁(RRTJ)对高脂饮食诱导的高脂血症大鼠血浆、肝脏和粪便中胆碱、左旋肉碱、甜菜碱、TMA、TMAO和肌酐水平的影响,证明了该方法的实用性:检测限(LOD)为 0.04-0.027 µM,定量限(LOQ)为 0.009-0.094 µM。血浆中各代谢物的线性范围分别为:胆碱:1.50-96 µM;左旋肉碱:2-128 µM;甜菜碱:3-192 µM;TMA:0.01-40.96 µM;TMAO:0.06-61.44 µM;肌酐:1-64 µM(R2 ≥ 0.9954)。肝脏中各代谢物的线性范围分别为:胆碱:12-768 µM;左旋肉碱:1.5-96 µM;肌酐:1-64 µM(R2≥0.9954):1.5-96 µM;甜菜碱:10-640 µM;TMA:0.5-32 µM;TMAO:0.02-81.92 µM;肌酐:0.2-204.8 µM(R2 ≥ 0.9938)。粪便中每种代谢物的线性范围分别为胆碱:1.5-96 µM;左旋肉碱:0.01-40.96 µM:0.01-40.96 µM;甜菜碱:1.5-96 µM;TMA:1-64 µM;TMAO:0.02-81.92 µM;肌酐:0.02-81.92 µM(R2 ≥ 0.998)。日内和日间变异系数为结论:建立了血浆、肝脏和粪便样品中胆碱、左旋肉碱、甜菜碱、TMA、TMAO和肌酐的测定方法,该方法简便、省时、精密度高、准确度好、回收率高。
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来源期刊
Journal of Chromatography B
Journal of Chromatography B 医学-分析化学
CiteScore
5.60
自引率
3.30%
发文量
306
审稿时长
44 days
期刊介绍: The Journal of Chromatography B publishes papers on developments in separation science relevant to biology and biomedical research including both fundamental advances and applications. Analytical techniques which may be considered include the various facets of chromatography, electrophoresis and related methods, affinity and immunoaffinity-based methodologies, hyphenated and other multi-dimensional techniques, and microanalytical approaches. The journal also considers articles reporting developments in sample preparation, detection techniques including mass spectrometry, and data handling and analysis. Developments related to preparative separations for the isolation and purification of components of biological systems may be published, including chromatographic and electrophoretic methods, affinity separations, field flow fractionation and other preparative approaches. Applications to the analysis of biological systems and samples will be considered when the analytical science contains a significant element of novelty, e.g. a new approach to the separation of a compound, novel combination of analytical techniques, or significantly improved analytical performance.
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