Literature DB >> 1510935

The 31P NMR visibility of ATP in perfused rat liver remains about 90%, unaffected by changes of metabolic state.

S Masson1, B Quistorff.   

Abstract

The 31P NMR visibility of ATP of the perfused rat liver was tested over a wide range of metabolic conditions, including normoxic and hypoxic perfusions, fructose loads, and various intervals of normothermic ischemia, for both ad libitum fed and 24-h fasted rats. The 31P NMR signal of ATP was compared to the concentration of ATP determined by enzymatic assays on liver biopsies performed at the end of NMR acquisition. In a first series of experiments, the NMR resonance of intracellular ATP was quantitated in absolute terms by applying the 1H NMR water signal as internal reference: during normoxic and hypoxic perfusions, a constant amount of ATP (0.43 +/- 0.19 mM, mean +/- SD), approximately 12% of the cellular ATP, is not detected by NMR. Nevertheless, there is a high correlation (slope = 0.96 +/- 0.09; r2 = 0.93) between the measurements of ATP by 31P NMR spectroscopy and by biochemical analysis. In a second series of experiments, there was a highly significant correlation between the NMR and analytical biochemical measurements of ATP for whole range of metabolic states, i.e., fructose loads (1.0-10 mM) and various intervals of normothermic ischemia (ranging from 2 to 12 min), indicating unchanged ATP visibility. Thus, as opposed to the studies of Murphy et al. [Murphy, E., et al. (1988) Biochemistry 27, 526-528], it is concluded that ATP at 37 degrees C remains almost entirely visible in the perfused rat liver, also during ischemia.

Entities:  

Mesh:

Substances:

Year:  1992        PMID: 1510935     DOI: 10.1021/bi00148a008

Source DB:  PubMed          Journal:  Biochemistry        ISSN: 0006-2960            Impact factor:   3.162


  6 in total

1.  Hyperpolarized (13)C spectroscopy and an NMR-compatible bioreactor system for the investigation of real-time cellular metabolism.

Authors:  Kayvan R Keshari; John Kurhanewicz; Rex E Jeffries; David M Wilson; Brian J Dewar; Mark Van Criekinge; Matthew Zierhut; Daniel B Vigneron; Jeffrey M Macdonald
Journal:  Magn Reson Med       Date:  2010-02       Impact factor: 4.668

2.  Effect of phenylephrine on the compartmentation of inorganic phosphate in perfused rat liver during gluconeogenesis and urea synthesis: a 31P-n.m.r.-spectroscopic study.

Authors:  O Eriksson; P Pollesello; N E Saris
Journal:  Biochem J       Date:  1994-02-15       Impact factor: 3.857

3.  Effect of oxygen concentration on viability and metabolism in a fluidized-bed bioartificial liver using ³¹P and ¹³C NMR spectroscopy.

Authors:  Rex E Jeffries; Michael P Gamcsik; Kayvan R Keshari; Peter Pediaditakis; Andrey P Tikunov; Gregory B Young; Haakil Lee; Paul B Watkins; Jeffrey M Macdonald
Journal:  Tissue Eng Part C Methods       Date:  2012-09-28       Impact factor: 3.056

4.  Ischaemic ATP degradation studied by HPLC and 31P-NMR spectroscopy: do the two techniques observe the same ATP pools?

Authors:  P Herijgers; K Overloop; Y Toshima; P Van Hecke; F Vanstapel; K Mubagwa; W Flameng
Journal:  Basic Res Cardiol       Date:  1994 Jan-Feb       Impact factor: 17.165

5.  Kinetics of creatine uptake in the perfused mouse liver: a 31P-n.m.r. study of transgenic mice expressing creatine kinase (CKBB) in the liver.

Authors:  S Masson; B Quistorff
Journal:  Biochem J       Date:  1994-10-15       Impact factor: 3.857

6.  Biguanides suppress hepatic glucagon signalling by decreasing production of cyclic AMP.

Authors:  Russell A Miller; Qingwei Chu; Jianxin Xie; Marc Foretz; Benoit Viollet; Morris J Birnbaum
Journal:  Nature       Date:  2013-01-06       Impact factor: 49.962

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.