The brain in acute liver failure. A tortuous path from hyperammonemia to cerebral edema

被引:59
作者
Bjerring, Peter Nissen [1 ]
Eefsen, Martin [1 ]
Hansen, Bent Adel [1 ]
Larsen, Fin Stolze [1 ]
机构
[1] Univ Copenhagen Hosp, Rigshosp, Dept Hepatol, Sect A 2121, DK-2100 Copenhagen, Denmark
关键词
Acute liver failure; Cerebral edema; Hyperammonemia; Intracranial hypertension; FULMINANT HEPATIC-FAILURE; MITOCHONDRIAL PERMEABILITY TRANSITION; BLOOD-FLOW AUTOREGULATION; CULTURED ASTROCYTES; INTRACRANIAL HYPERTENSION; PORTACAVAL ANASTOMOSIS; GLUTAMINE-SYNTHETASE; AMMONIA METABOLISM; OXIDATIVE STRESS; AMINO-ACIDS;
D O I
10.1007/s11011-008-9116-3
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Acute liver failure (ALF) is a condition with an unfavourable prognosis. Multiorgan failure and circulatory collapse are frequent causes of death, but cerebral edema and intracranial hypertension (ICH) are also common complications with a high risk of fatal outcome. The underlying pathogenesis has been extensively studied and although the development of cerebral edema and ICH is of a complex and multifactorial nature, it is well established that ammonia plays a pivotal role. This review will focus on the effects of hyperammonemia on neurotransmission, mitochondrial function, oxidative stress, inflammation and regulation of cerebral blood flow. Finally, potential therapeutic targets and future perspectives are briefly discussed.
引用
收藏
页码:5 / 14
页数:10
相关论文
共 68 条
[1]  
Albrecht J, 1998, ACTA NEUROBIOL EXP, V58, P169, DOI 10.55782/ane-1998-1271
[2]   Glutamine: A Trojan horse in ammonia neurotoxicity [J].
Albrecht, Jan ;
Norenberg, Michael D. .
HEPATOLOGY, 2006, 44 (04) :788-794
[3]   Interstitial adenosine, inosine, and hypoxanthine are increased after experimental traumatic brain injury in the rat [J].
Bell, MJ ;
Kochanek, PM ;
Carcillo, JA ;
Mi, ZC ;
Schiding, JK ;
Wisniewski, SR ;
Clark, RSB ;
Dixon, CE ;
Marion, DW ;
Jackson, E .
JOURNAL OF NEUROTRAUMA, 1998, 15 (03) :163-170
[4]  
Bender AS, 1998, J NEUROSCI RES, V54, P673, DOI 10.1002/(SICI)1097-4547(19981201)54:5<673::AID-JNR12>3.3.CO
[5]  
2-G
[6]   Carbon dioxide stimulates peroxynitrite-mediated nitration of tyrosine residues and inhibits oxidation of methionine residues of glutamine synthetase: Both modifications mimic effects of adenylylation [J].
Berlett, BS ;
Levine, RL ;
Stadtman, ER .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (06) :2784-2789
[7]   The mitochondrial permeability transition from in vitro artifact to disease target [J].
Bernardi, P ;
Krauskopf, A ;
Basso, E ;
Petronilli, V ;
Blalchy-Dyson, E ;
Di Lisa, F ;
Forte, MA .
FEBS JOURNAL, 2006, 273 (10) :2077-2099
[8]   Xanthine oxicloreductase and cardiovascular disease: molecular mechanisms and pathophysiological implications [J].
Berry, CE ;
Hare, JM .
JOURNAL OF PHYSIOLOGY-LONDON, 2004, 555 (03) :589-606
[9]  
BJERRING PN, 2008, CEREBRAL GLUTAMINE C
[10]   THE BLOOD-BRAIN-BARRIER [J].
BRADBURY, MWB .
EXPERIMENTAL PHYSIOLOGY, 1993, 78 (04) :453-472