Improved high-performance liquid chromatographic assay for the determination of "high-energy" phosphates in mammalian skeletal muscle. Application to a single-fibre study in man

J Chromatogr B Biomed Sci Appl. 1999 Jul 9;730(2):183-91. doi: 10.1016/s0378-4347(99)00221-2.

Abstract

A sensitive and reproducible method for the determination of adenine nucleotides (ATP, IMP) and creatine compounds [creatine (Cr), phosphocreatine (PCr)] in freeze-dried single human muscle fibre fragments is presented. The method uses isocratic reversed-phase high-performance liquid chromatography of methanol extracts. Average retention times (min) of ATP, IMP and PCr, Cr from standard solutions were 10.6+/-0.42, 2.11+/-0.06 (n=6) and 10.5+/-0.31 and 1.19+/-0.02 (n=9), respectively. Detection limits in extracts from muscle fibre fragments were 2.0, 1.0, 3.0 and 2.0 mmol/kg dm, respectively. The assay was found successful for analysis of fibre-fragments weighing > or = 1 microg.

MeSH terms

  • Adenine Nucleotides / analysis*
  • Animals
  • Chromatography, High Pressure Liquid / methods*
  • Creatine Kinase / analysis*
  • Humans
  • Muscle, Skeletal / chemistry*
  • Muscle, Skeletal / enzymology
  • Rats
  • Rats, Wistar
  • Reference Standards
  • Reproducibility of Results
  • Sensitivity and Specificity
  • Spectrophotometry, Ultraviolet

Substances

  • Adenine Nucleotides
  • Creatine Kinase