Rama Rao K V, Norenberg M D
Department of Pathology, University of Miami School of Medicine, Miami, FL 33101, USA.
Metab Brain Dis. 2007 Dec;22(3-4):265-75. doi: 10.1007/s11011-007-9063-4.
Brain edema is a critical component of hepatic encephalopathy (HE) associated with acute liver failure and such edema appears to be principally due to astrocyte swelling (cytotoxic edema). Ammonia is believed to represent a major factor responsible for astrocyte swelling, although the mechanisms by which ammonia causes such swelling are not completely understood. Recent studies have implicated potential role of oxidative stress, and the mitochondrial permeability transition (mPT). While it is not known how oxidative stress and the mPT cause astrocyte swelling, it is reasonable to suggest that these events may affect one or more plasma membrane proteins involved in water and ion homeostasis in astrocytes. One such protein strongly implicated in brain edema in other neurological conditions is the water channel protein aquaporin-4 (AQP-4), which is abundantly expressed in astrocytes. This article summarizes the potential role of AQP-4 in brain edema in in vivo models of HE, as well as in ammonia-induced cell swelling in cultured astrocytes. The involvement of AQP-4 in the effects of manganese, another toxin implicated in HE, will also be discussed.
脑水肿是与急性肝衰竭相关的肝性脑病(HE)的一个关键组成部分,这种水肿似乎主要是由于星形胶质细胞肿胀(细胞毒性水肿)所致。氨被认为是导致星形胶质细胞肿胀的一个主要因素,尽管氨导致这种肿胀的机制尚未完全明确。最近的研究表明氧化应激和线粒体通透性转换(mPT)可能发挥作用。虽然尚不清楚氧化应激和mPT如何导致星形胶质细胞肿胀,但有理由认为这些事件可能会影响星形胶质细胞中参与水和离子稳态的一种或多种质膜蛋白。在其他神经疾病中,一种与脑水肿密切相关的蛋白是水通道蛋白4(AQP-4),它在星形胶质细胞中大量表达。本文总结了AQP-4在HE体内模型脑水肿以及氨诱导的培养星形胶质细胞肿胀中的潜在作用。还将讨论AQP-4在锰(另一种与HE有关的毒素)作用中的参与情况。