Glutathione kinetics in normal man and in patients with liver cirrhosis

被引:36
作者
Bianchi, G
Bugianesi, E
Ronchi, M
Fabbri, A
Zoli, M
Marchesini, G
机构
[1] Dipartimento di Medicina Interna, Cardioangiologia Ed Epatologia, C., Bologna
关键词
cirrhosis; cysteine; glutathione; liver failure; sulfur-containing amino acids; GAMMA-GLUTAMYL-TRANSPEPTIDASE; EXTRACELLULAR WATER; TOTAL-BODY; PLASMA; RAT; METABOLISM; ELIMINATION; DEFICIENCY; PROTECTION; DISULFIDE;
D O I
10.1016/S0168-8278(97)80426-6
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background/Aims: The dynamics of glutathione in plasma has always been studied by bolus injections. Data are available suggesting that the low plasma levels of cirrhosis are due to decreased production in glutathione-producing tissues, mainly the liver, We aimed to measure the kinetics of glutathione during controlled steady-state conditions, and to determine the reasons for its reduced plasma levels in advanced cirrhosis. Methods: The plasma clearance of glutathione was measured in six control subjects and in ten patients with cirrhosis during a 2-step infusion study, producing steady-state levels approximately 5 and 10 times basal values, The plasma disappearance curve after infusion stop was used to determine the apparent volume of distribution and half-life of glutathione, and the estimated basal appearance rate. Results: The clearance of glutathione did not reject Ist-order kinetics, i.e., it was concentration-independent, and was nearly doubled in cirrhosis. The half-life of exogenous glutathione was not different, whereas the volume of distribution was larger in cirrhosis, in the same range as extracellular water, The endogenous basal appearance rate of glutathione was reduced by 50%, and correlated with liver function, measured by routine and dynamic tests. Conclusions: The data confirm that the primary defect responsible for reduced glutathione in liver disease is a reduced production, possibly related to hepatocyte dysfunction and a block along the pathway of methionine metabolism.
引用
收藏
页码:606 / 613
页数:8
相关论文
共 28 条
[11]   PROMOTION OF CYSTINE UPTAKE AND ITS UTILIZATION FOR GLUTATHIONE BIOSYNTHESIS INDUCED BY CYSTEAMINE AND N-ACETYLCYSTEINE [J].
ISSELS, RD ;
NAGELE, A ;
ECKERT, KG ;
WILMANNS, W .
BIOCHEMICAL PHARMACOLOGY, 1988, 37 (05) :881-888
[12]   HEPATIC GLUTATHIONE HOMEOSTASIS IN THE RAT - EFFLUX ACCOUNTS FOR GLUTATHIONE TURNOVER [J].
LAUTERBURG, BH ;
ADAMS, JD ;
MITCHELL, JR .
HEPATOLOGY, 1984, 4 (04) :586-590
[13]   GLUTATHIONE DEFICIENCY IN ALCOHOLICS - RISK FACTOR FOR PARACETAMOL HEPATOTOXICITY [J].
LAUTERBURG, BH ;
VELEZ, ME .
GUT, 1988, 29 (09) :1153-1157
[14]  
MARCHESINI G, 1992, HEPATOLOGY, V16, P149
[15]  
MARCHESINI G, 1990, LIVER, V10, P65
[16]   MEASUREMENTS OF TOTAL-BODY AND EXTRACELLULAR WATER IN CIRRHOTIC-PATIENTS WITH AND WITHOUT ASCITES [J].
MCCULLOUGH, AJ ;
MULLEN, KD ;
KALHAN, SC .
HEPATOLOGY, 1991, 14 (06) :1102-1111
[17]  
Meister A., 1989, GLUTATHIONE, P367
[18]   ELIMINATION OF GLUTATHIONE-INDUCED PROTECTION FROM HYPERBARIC HYPEROXIA BY ACIVICIN [J].
PEACOCK, MD ;
SCHENK, DA ;
LAWRENCE, RA ;
MORGAN, JA ;
JENKINSON, SG .
JOURNAL OF APPLIED PHYSIOLOGY, 1994, 76 (03) :1279-1284
[19]   THE HEPATIC GLUTATHIONE CONTENT IN LIVER-DISEASES [J].
POULSEN, HE ;
RANEK, L ;
ANDREASEN, PB .
SCANDINAVIAN JOURNAL OF CLINICAL & LABORATORY INVESTIGATION, 1981, 41 (06) :573-576
[20]   TRANSECTION OF ESOPHAGUS FOR BLEEDING ESOPHAGEAL VARICES [J].
PUGH, RNH ;
MURRAYLY.IM ;
DAWSON, JL ;
PIETRONI, MC ;
WILLIAMS, R .
BRITISH JOURNAL OF SURGERY, 1973, 60 (08) :646-649