Effect of fasting and acute ethanol administration on the energy state of in vivo liver as measured by 31P-NMR spectroscopy.
Effect of fasting and acute ethanol administration on the energy state of in vivo liver as measured by 31P-NMR spectroscopy.
复制标题
通过 31P-NMR 波谱测量禁食和急性乙醇给药对体内肝脏能量状态的影响。
DOI:
10.1016/0167-4889(86)90033-9
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发表时间:
1986
期刊:
影响因子:
--
通讯作者:
Radda,GK
中科院分区:
文献类型:
--
作者:
Cunningham,CC;Malloy,CR;Radda,GK
The effects of 48 h fasting, administration of ethanol or 2, 4-dinitrophenol, on the phosphorus-containing metabolites in liver in vivo have been determined utilizing 31 P nuclear magnetic resonance spectroscopy. These measurements were combined with determinations of metabolite concentrations in livers which were freeze-clamped immediately after the NMR measurements were completed. Administration of sub-lethal amounts of dinitrophenol dramatically decreased ATP and increased P i concentrations in liver in vivo as indicated by a 2.7-fold increase in the NMR-derived [P i][ATP] ratio. Ethanol administration to fed animals increased the NMR-derived [P i][ATP] ratio 27%; in contrast, the same amount of ethanol administered to fasted animals decreased the NMR-derived [P i][ATP] ratio 30%. The NMR visible P i and ADP represent about 50% and 15% of the total P i and ADP, respectively. The phosphorylation potentials calculated from the NMR visible P i and ADP were an order of magnitude higher than those obtained from metabolite concentrations in freeze-clamped tissue. There was no apparent correlation between the phosphorylation potentials derived from either the NMR spectral analyses or from metabolite concentrations and the hepatic [NAD+][NADH] ratio. The chemical shift of P i indicated that ethanol administration elicited a decrease in pH of 0.1 unit in liver in vivo. Hepatic free [Mg 2+] was increased 21% in fasted animals, but was unaffected by ethanol administration.