Department of Pathology, University of Miami Miller School of Medicine, Miami, FL 33125, United States.
Neurochem Int. 2012 Sep;61(4):575-80. doi: 10.1016/j.neuint.2012.01.012. Epub 2012 Jan 21.
Hepatic encephalopathy (HE) is the major neurological disorder associated with liver disease. It presents in chronic and acute forms, and astrocytes are the major neural cells involved. While the principal etiological factor in the pathogenesis of HE is increased levels of blood and brain ammonia, glutamine, a byproduct of ammonia metabolism, has also been implicated in its pathogenesis. This article reviews the current status of glutamine in the pathogenesis of HE, particularly its involvement in some of the events triggered by ammonia, including mitochondrial dysfunction, generation of oxidative stress, and alterations in signaling mechanisms, including activation of mitogen-activated protein kinases (MAPKs) and nuclear factor-kappaB (NF-κB). Mechanisms by which glutamine contributes to astrocyte swelling/brain edema associated with acute liver failure (ALF) will also be described.
肝性脑病(HE)是与肝脏疾病相关的主要神经障碍。它表现为慢性和急性两种形式,星形胶质细胞是主要涉及的神经细胞。虽然氨、谷氨酰胺等血脑氨水平升高是 HE 发病机制中的主要病因,但氨代谢的副产物谷氨酰胺也与发病机制有关。本文综述了谷氨酰胺在 HE 发病机制中的最新研究进展,特别是其在氨引发的一些事件中的作用,包括线粒体功能障碍、氧化应激的产生以及信号转导机制的改变,包括丝裂原活化蛋白激酶(MAPKs)和核因子-κB(NF-κB)的激活。本文还将描述谷氨酰胺如何导致与急性肝衰竭(ALF)相关的星形胶质细胞肿胀/脑水肿。