Swift increase in alcohol metabolism (SIAM): understanding the phenomenon of hypermetabolism in liver

被引:26
作者
Bradford, BU
Rusyn, I [1 ]
机构
[1] Univ N Carolina, Sch Med, Bowles Ctr Alcohol Studies, Chapel Hill, NC 27599 USA
[2] Univ N Carolina, Dept Environm Sci & Engn, Sch Publ Hlth, Chapel Hill, NC 27599 USA
关键词
alcohol metabolism; swift increase in alcohol metabolism; SIAM; perfused liver; hypermetabolism;
D O I
10.1016/j.alcohol.2004.12.001
中图分类号
R194 [卫生标准、卫生检查、医药管理];
学科分类号
摘要
The swift increase in alcohol metabolism (SIAM) is a phenomenon defined as a rapid increase in hepatic respiration and alcohol metabolism after administration of a bolus dose of alcohol. Continuous exposure to alcohol is known to produce adaptive changes in liver alcohol and oxygen metabolism. A considerable burst of hepatic respiration can also occur after administration of a single large dose of alcohol and results in a near doubling of alcohol metabolism, a high demand for oxygen, and downstream or pericentral hypoxia. These dramatic changes in rates of alcohol metabolism and tissue concentrations of oxygen are not due to induced enzyme activity in liver. This phenomenon depends on activation of mitochondrial function, an increase in co-factor supply for nicotinamide adenine dinucleotide-dependent alcohol metabolism, depletion of glycogen reserves, liberation of fatty acids through activation of an adrenergic response to alcohol providing substrate for catalase, and activation of Kupffer cells, the hepatic resident macrophages responsible for production of cytokines and prostaglandins. An understanding of the mechanisms of hypermetabolism in liver can have vital ramifications for knowledge of both alcohol-related and alcohol-unrelated liver injury because hypoxia that is a result of hypermetabolism can compound effects of pharmaceuticals and environmental agents on the liver. Swift increase in alcohol metabolism is an excellent example of the complexity of cell-cell interactions in liver and extrahepatic regulation of biochemical and molecular events in this organ, and this important phenomenon shall be considered in studies of liver disease and biochemistry. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:13 / 17
页数:5
相关论文
共 35 条
[1]   Acute alcohol produces hypoxia directly in rat liver tissue in vivo: Role of Kupffer cells [J].
Arteel, GE ;
Raleigh, JA ;
Bradford, BU ;
Thurman, RG .
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY, 1996, 271 (03) :G494-G500
[2]  
BERNSTEIN J, 1975, J PHARMACOL EXP THER, V192, P583
[3]  
Bleyman M A, 1979, Curr Alcohol, V7, P115
[4]  
BRADFORD BU, 1995, HEPATOLOGY, V22, P550
[5]  
Bradford BU, 1999, J PHARMACOL EXP THER, V288, P254
[6]  
BRADFORD BU, 1993, RES COMMUN SUBSTANCE, V14, P1
[7]   EVIDENCE THAT CATALASE IS A MAJOR PATHWAY OF ETHANOL OXIDATION INVIVO - DOSE-RESPONSE STUDIES IN DEER MICE USING METHANOL AS A SELECTIVE SUBSTRATE [J].
BRADFORD, BU ;
SEED, CB ;
HANDLER, JA ;
FORMAN, DT ;
THURMAN, RG .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1993, 303 (01) :172-176
[8]  
BRADFORD BU, 1993, MOL PHARMACOL, V43, P115
[9]   AN INTERMEDIATE COMPOUND IN THE CATALASE-HYDROGEN PEROXIDE REACTION [J].
CHANCE, B .
ACTA CHEMICA SCANDINAVICA, 1947, 1 (02) :236-267
[10]   OXIDOREDUCTION OF BUTANOL IN DEERMICE (PEROMYSCUS-MANICULATUS) LACKING HEPATIC CYTOSOLIC ALCOHOL-DEHYDROGENASE [J].
CRONHOLM, T ;
NORSTENHOOG, C ;
EKSTROM, G ;
HANDLER, JA ;
THURMAN, RG ;
INGELMANSUNDBERG, M .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1992, 204 (01) :353-357