Norenberg M D, Jayakumar A R, Rama Rao K V, Panickar K S
Veterans Affairs Medical Center, Miami, FL 33101, USA.
Metab Brain Dis. 2007 Dec;22(3-4):219-34. doi: 10.1007/s11011-007-9062-5.
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.
一般认为,星形胶质细胞肿胀是急性肝衰竭(ALF)相关水肿的主要解剖学基础,而氨是其形成的主要病因。然而,导致这种肿胀的机制仍不清楚。最近的研究表明氧化应激在肝性脑病(HE)以及与ALF相关的脑水肿机制中发挥作用。本文总结了氧化应激作为HE/ALF主要致病因素的证据,并讨论了由氧化应激触发的机制,包括线粒体通透性转换(MPT)的诱导和信号激酶的激活。我们提出,由氨诱导的氧化应激引发的一系列事件导致细胞体积调节异常,进而导致细胞肿胀/脑水肿。阻断这一过程可能为与ALF相关的脑水肿提供新的治疗方法。