New concepts in the mechanism of ammonia-induced astrocyte swelling

被引:0
作者
M. D. Norenberg
A. R. Jayakumar
K. V. Rama Rao
K. S. Panickar
机构
[1] Veterans Affairs Medical Center,Department of Pathology
[2] University of Miami School of Medicine,Department of Biochemistry and Molecular Biology
[3] University of Miami School of Medicine,Nutrient Requirements & Functions Laboratory, Beltsville Human Nutrition Research Center
[4] United States Department of Agriculture,undefined
来源
Metabolic Brain Disease | 2007年 / 22卷
关键词
Acute liver failure; Ammonia; Astrocytes; Brain edema; Cell swelling; Glutamine; Hepatic encephalopathy; Mitochondrial permeability transition; Nitrosative stress; Oxidative stress; Signaling kinases;
D O I
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学科分类号
摘要
It is generally accepted that astrocyte swelling forms the major anatomic substrate of the edema associated with acute liver failure (ALF) and that ammonia represents a major etiological factor in its causation. The mechanisms leading to such swelling, however, remain elusive. Recent studies have invoked the role of oxidative stress in the mechanism of hepatic encephalopathy (HE), as well as in the brain edema related to ALF. This article summarizes the evidence for oxidative stress as a major pathogenetic factor in HE/ALF and discusses mechanisms that are triggered by oxidative stress, including the induction of the mitochondrial permeability transition (MPT) and activation of signaling kinases. We propose that a cascade of events initiated by ammonia-induced oxidative stress results in cell volume dysregulation leading to cell swelling/brain edema. Blockade of this cascade may provide novel therapies for the brain edema associated with ALF.
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页码:219 / 234
页数:15
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