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Determination of Coenzyme A and Acetyl-Coenzyme A in Biological Samples Using HPLC with UV Detection

机译:高效液相色谱-紫外检测法测定生物样品中的辅酶A和乙酰辅酶A

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摘要

Coenzyme A (CoA) and acetyl-coenzyme A (acetyl-CoA) play essential roles in cell energy metabolism. Dysregulation of the biosynthesis and functioning of both compounds may contribute to various pathological conditions. We describe here a simple and sensitive HPLC-UV based method for simultaneous determination of CoA and acetyl-CoA in a variety of biological samples, including cells in culture, mouse cortex, and rat plasma, liver, kidney, and brain tissues. The limits of detection for CoA and acetyl-CoA are >10-fold lower than those obtained by previously described HPLC procedures, with coefficients of variation <1% for standard solutions, and 1–3% for deproteinized biological samples. Recovery is 95–97% for liver extracts spiked with Co-A and acetyl-CoA. Many factors may influence the tissue concentrations of CoA and acetyl-CoA (e.g., age, fed, or fasted state). Nevertheless, the values obtained by the present HPLC method for the concentration of CoA and acetyl-CoA in selected rodent tissues are in reasonable agreement with literature values. The concentrations of CoA and acetyl-CoA were found to be very low in rat plasma, but easily measurable by the present HPLC method. The method should be useful for studying cellular energy metabolism under normal and pathological conditions, and during targeted drug therapy treatment.
机译:辅酶A(CoA)和乙酰辅酶A(乙酰CoA)在细胞能量代谢中起重要作用。这两种化合物的生物合成和功能失调可能导致各种病理状况。我们在这里描述了一种简单而灵敏的基于HPLC-UV的方法,用于同时测定多种生物样品(包括培养物中的细胞,小鼠皮层以及大鼠血浆,肝,肾和脑组织)中的CoA和乙酰辅酶A。 CoA和乙酰辅酶A的检出限比以前描述的HPLC方法低10倍以上,标准溶液的变异系数<1%,去蛋白的生物样品的变异系数<1-3%。掺有Co-A和乙酰辅酶A的肝提取物的回收率为95–97%。许多因素可能会影响CoA和乙酰CoA的组织浓度(例如年龄,进食或禁食状态)。然而,通过本发明的HPLC方法获得的在选定啮齿动物组织中CoA和乙酰-CoA的浓度值与文献值合理地一致。发现在大鼠血浆中CoA和乙酰基-CoA的浓度非常低,但是可以通过本发明的HPLC方法容易地测量。该方法对于研究正常和病理条件下以及靶向药物治疗期间的细胞能量代谢应该是有用的。

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