CHANGES OF LIVER METABOLITE CONCENTRATIONS IN ADULTS WITH DISORDERS OF FRUCTOSE METABOLISM AFTER INTRAVENOUS FRUCTOSE BY P-31 MAGNETIC-RESONANCE SPECTROSCOPY

被引:42
作者
BOESIGER, P
BUCHLI, R
MEIER, D
STEINMANN, B
GITZELMANN, R
机构
[1] UNIV ZURICH,INST BIOMED ENGN & INFORMAT,ZURICH,SWITZERLAND
[2] UNIV ZURICH,DEPT PEDIAT,DIV METAB,ZURICH,SWITZERLAND
[3] ETH ZURICH,ZURICH,SWITZERLAND
关键词
D O I
10.1203/00006450-199410000-00004
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
A novel P-31 magnetic resonance spectroscopy procedure allows the estimation of absolute concentrations of certain phosphorus-containing compounds in liver. We have validated this approach by measuring ATP, phosphomonesters, and inorganic phosphate (P-i) during fasting and after an i.v. fructose bolus in healthy adults and in three adults with disorders of fructose metabolism and by comparing results with known metabolite concentrations measured chemically. During fasting, the ATP concentration averaged 2.7 +/- 0.3 (SD, n = 9) mmol/L, which, after due correction for other nucleoside triphosphates, was 2.1 mmol/L and corresponded well with known concentrations. Fructose-l-phosphate (Fl-P) could not be measured during fasting; its concentration after fructose was calculated from the difference of the phosphomonester signals before (2.9 +/- 0.2 mmol/L) and after fructose. P-i was 1.4 +/- 0.3 mmol/L and represented the one fourth of P-i visible in magnetic resonance spectra. In the three healthy controls after fructose (200 mg/kg, 20% solution, 2.5 min), the fructokinase-mediated increase of F-1-P was rapid, reaching 4.9 mmol/L within 3 min, whereas the uncorrected ATP decreased from 2.7 to 1.8 mmol/L and the P-i from 1.4 to 0.3 mmol/L. The subsequent decrease of F-1-P, mediated by fructaldolase, was accompanied by an overshooting rise of P-i to 2.7 mmol/L. In the patient with essential fructosuria, the concentrations of F-1-P, ATP, and P-i remained unchanged, confirming that fructokinase was indeed inactive. In the patient with hereditary fructose intolerance, initial metabolic changes were the same as in the controls, but baseline concentrations were not yet reestablished after 7 h, indicating weak fructaldolase activity. In the patient with fructose-1,6-diphosphatase deficiency, initial metabolic changes were the same as in the controls, but normalization was slightly delayed.
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页码:436 / 440
页数:5
相关论文
共 23 条
[1]  
BAERLOCHER K, 1971, HELV PAEDIATR ACTA, V26, P489
[2]   DEPLETION OF LIVER ADENOSINE PHOSPHATES AND METABOLIC EFFECTS OF INTRAVENOUS INFUSION OF FRUCTOSE OR SORBITOL IN MAN AND IN RAT [J].
BODE, JC ;
ZELDER, O ;
RUMPELT, HJ ;
WITTKAMP, U .
EUROPEAN JOURNAL OF CLINICAL INVESTIGATION, 1973, 3 (05) :436-441
[3]   COMPARISON OF METHODS FOR THE DETERMINATION OF ABSOLUTE METABOLITE CONCENTRATIONS IN HUMAN MUSCLES BY P-31 MRS [J].
BUCHLI, R ;
BOESIGER, P .
MAGNETIC RESONANCE IN MEDICINE, 1993, 30 (05) :552-558
[4]   TOWARD FULLY-AUTOMATIC ESTIMATION OF INVIVO P-31 SPECTRA [J].
BURGER, C ;
MCKINNON, G ;
BUCHLI, R ;
BOESIGER, P .
MAGNETIC RESONANCE IN MEDICINE, 1991, 21 (02) :216-221
[5]   ALTERATIONS IN HEPATIC FRUCTOSE METABOLISM IN CIRRHOTIC-PATIENTS DEMONSTRATED BY DYNAMIC P-31 SPECTROSCOPY [J].
DUFOUR, JF ;
STOUPIS, C ;
LAZEYRAS, F ;
VOCK, P ;
TERRIER, F ;
REICHEN, J .
HEPATOLOGY, 1992, 15 (05) :835-842
[6]  
Gitzelmann R, 1989, METABOLIC BASIS INHE, P399
[7]   Fructosuria [J].
Heeres, PA ;
Vos, H .
ARCHIVES OF INTERNAL MEDICINE, 1929, 44 (01) :47-64
[8]   PHOSPHORYLATION STATUS OF LIVER BY P-31-NMR SPECTROSCOPY, AND ITS IMPLICATIONS FOR METABOLIC CONTROL - A COMPARISON OF P-31-NMR SPECTROSCOPY (INVIVO AND INVITRO) WITH CHEMICAL AND ENZYMIC DETERMINATIONS OF ATP, ADP AND PI [J].
ILES, RA ;
STEVENS, AN ;
GRIFFITHS, JR ;
MORRIS, PG .
BIOCHEMICAL JOURNAL, 1985, 229 (01) :141-151
[9]   THERAPEUTIC RESPONSE OF BREAST-CARCINOMA MONITORED BY P-31 MRS INSITU [J].
NG, TC ;
GRUNDFEST, S ;
VIJAYAKUMAR, S ;
BALDWIN, NJ ;
MAJORS, AW ;
KARALIS, I ;
MEANEY, TF ;
SHIN, KH ;
THOMAS, FJ ;
TUBBS, R .
MAGNETIC RESONANCE IN MEDICINE, 1989, 10 (01) :125-134
[10]  
OBERHAENSLI RD, 1987, LANCET, V2, P931