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首页> 外文期刊>Pediatric Research >Changes of Liver Metabolite Concentrations in Adults with Disorders of Fructose Metabolism after Intravenous Fructose by 31P Magnetic Resonance Spectroscopy
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Changes of Liver Metabolite Concentrations in Adults with Disorders of Fructose Metabolism after Intravenous Fructose by 31P Magnetic Resonance Spectroscopy

机译:31P磁共振波谱分析静脉注射果糖后成年果糖代谢紊乱的成年人肝脏代谢物浓度的变化

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A novel 31P 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 (Pi 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-1-phosphate (F-1-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. Pi was 1.4 ± 0.3 mmol/L and represented the one fourth of Pi 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-l-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 Pi from 1.4 to 0.3 mmol/L. The subsequent decrease of F-l-P, mediated by fructaldolase, was accompanied by an overshooting rise of Pi to 2.7 mmol/L. In the patient with essential fructosuria, the concentrations of F-l-P, ATP, and Pi 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.
机译:一种新颖的31P磁共振波谱方法可以估算肝脏中某些含磷化合物的绝对浓度。我们通过在健康成年人和三名果糖代谢异常的成年人中测量ATP,磷酸单酯和无机磷酸盐(禁食期间和静脉果糖推注后的Pi)并将结果与​​化学测量的已知代谢物浓度进行比较,从而验证了该方法的有效性。 ATP的平均浓度为2.7±0.3(SD,n = 9)mmol / L,经对其他三磷酸核苷的校正后,为2.1 mmol / L,与已知浓度相当。 P)不能在空腹时测量;果糖后的浓度是根据果糖之前(2.9±0.2 mmol / L)和果糖后的磷酸单酯信号的差计算得出的,Pi为1.4±0.3 mmol / L,占Pi的四分之一在果糖(200 mg / kg,20%溶液,2.5分钟)注射后的三个健康对照中,果糖激酶介导的FlP迅速增加,在3分钟内达到4.9 mmol / L,而t他的未校正ATP从2.7降至1.8 mmol / L,Pi则从1.4降至0.3 mmol / L。随后由果糖醇酶介导的F-1-P的降低伴随着Pi的超调升高至2.7mmol / L。在患有原发性果糖尿症的患者中,F-1-P,ATP和Pi的浓度保持不变,证实果糖激酶确实没有活性。具有遗传性果糖耐受不良的患者,初始代谢变化与对照组相同,但7小时后基线浓度尚未恢复,表明果糖醇酶活性较弱。在果糖-1,6-二磷酸酶缺乏症患者中,初始代谢变化与对照组相同,但正常化略有延迟。

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