高效液相色谱-荧光检测法测定大鼠骨骼肌组织内微量三甲基组氨酸

Determine the 3-methylhistidine level in skeletal muscle of rats by high performance liquid chromatographic

  • 摘要: 目的:建立快速检测肌肉组织内微量三甲基组氨酸(3-MH)含量的方法。方法:利用荧光胺与3-MH在酸性和高温条件下发生柱前衍生反应,在ZORBAX SB-C18(4.6×150mmol/L,5μm)柱上,用10mmol/L磷酸钠缓冲液(含30%乙腈,pH7.50)作流动相,以1.0ml/min的流速进行等度洗脱后,荧光(激发波长365nm/发射波长460nm)检测3-MH含量。结果:应用此方法检测骨骼肌组织内的氨基酸,仅见到3-MH和组氨酸的色谱峰,色谱保留时间分别约为(4.45±0.02) min和(6.92±0.05) min,分离度>16;线性检测范围是0.005~10.0nmol/ml (r=0.9999,P=0.00);衍生回收率为92.6%~96.8%;3-MH荧光衍生后15d分析与衍生后立即检测相比结果无显著差异(P=0.9095,n=24)。结论:本方法测定骨骼肌组织内3-MH,衍生步骤简单,重复性好,检测灵敏度高,适合快速、准确、经济地大批量检测肌组织内的微量3-MH,为开展骨骼肌肌纤维蛋白分解代谢研究提供了可行的方法。

     

    Abstract: Objective: To estabolish a quick and sensitive method for the determination of the trace amount 3-methylhisdine(3-MH) in skeletal muscle of rats Methods: After the formation of heat and stable fluorscanmine derivatives of 3-MH in skeletal muscle of rat, high performance liquid chromatographic separation and fluorescent detection (EX =365n m, Em =460nm) were used to determine the 3-MH levels in the samples The solvent system is 10 mmol/L sodium phosphate(pH7.5)and acetonitrile(30%) with a flow rate of 1.0ml/min Results: No amino acid peaks but two peaks, coeluting with histidine and 3-MH, were noted when standard sample and skeletal muscle sample were chromatographed The 3-MH was eluted completely with in 5 minutes and its peak could be easily distinguished from that of histidine (separation rate>16) The assay was linear over a range of 0.005~10.0nmol/ml (r=0.9999, P=0.0000) Conclusion: This method is not only very sensitive and accurate, but also quick and economical for determing the 3-MH amount in skeletal muscle of rats It is especially suited for analyzing samples in batches or with lower concentration of 3-MH

     

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