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肝硬化女性患者体内核黄素的代谢

The metabolism of riboflavin in female patients with liver cirrhosis.

作者信息

Zempleni J, Galloway J R, McCormick D B

机构信息

Dept. of Biochemistry, Rollins Research Center, Emory University School of Medicine, Atlanta, GA 30322, USA.

出版信息

Int J Vitam Nutr Res. 1996;66(3):237-43.

PMID:8899458
Abstract

The metabolism of vitamin B2 was studied in five female patients with liver cirrhosis of varying etiology. Following the oral administration of 40 mg (106.3 mumol) riboflavin, plasma concentrations of riboflavin and flavo-coenzymes as well as urinary riboflavin excretion were analyzed over a period of 48 h. Results were compared to data obtained for healthy controls (Zempleni J. et al, Am. J. Clin. Nutr., 1996 [15]). About 18% of the administered vitamin was recovered from patients' urine, indicating an absorption similar to healthy subjects (p > 0.05). The area under the riboflavin plasma concentration vs time curve was 1.2-fold larger among patients than controls, but the difference was not significant (p > 0.05). Riboflavin peak concentrations in plasma (315.6 nmol/l) and times when those concentrations were achieved (3.0 h) were similar to those found for healthy subjects (p > 0.05). Flavocoenzyme peak plasma concentrations were increased 1.4-fold above their baseline levels in cirrhotics which was equal to controls (p > 0.05). 7 alpha-Hydroxyriboflavin was detected in the plasma of patients. Distribution and elimination kinetics of riboflavin were analyzed by using a two-compartment open model; the riboflavin plasma disposition rate constants of the patients (k alpha = 0.7232 h-1; k beta = 0.0627 h-1) were not different from controls (p > 0.05). No differences between both groups were found regarding renal excretion (renal clearance, first-order rate constants for renal excretion; p > 0.05). In conclusion, patients with liver cirrhosis of varying etiology and varying medical treatment did not show alterations of riboflavin turnover.

摘要

对五名病因各异的女性肝硬化患者的维生素B2代谢情况进行了研究。口服40毫克(106.3微摩尔)核黄素后,在48小时内分析了血浆中核黄素和黄素辅酶的浓度以及尿核黄素排泄情况。将结果与健康对照者的数据进行了比较(Zempleni J.等人,《美国临床营养学杂志》,1996年[15])。从患者尿液中回收了约18%的给药维生素,表明其吸收情况与健康受试者相似(p>0.05)。患者的核黄素血浆浓度-时间曲线下面积比对照组大1.2倍,但差异不显著(p>0.05)。血浆中核黄素的峰值浓度(315.6纳摩尔/升)及其达到峰值的时间(3.0小时)与健康受试者相似(p>0.05)。肝硬化患者黄素辅酶的血浆峰值浓度比基线水平升高了1.4倍,与对照组相当(p>0.05)。在患者血浆中检测到了7α-羟基核黄素。采用二室开放模型分析了核黄素的分布和消除动力学;患者的核黄素血浆处置速率常数(kα = 0.7232小时-1;kβ = 0.0627小时-1)与对照组无差异(p>0.05)。两组在肾排泄方面未发现差异(肾清除率、肾排泄的一级速率常数;p>0.05)。总之,病因各异且接受不同治疗的肝硬化患者未表现出核黄素代谢的改变。

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