UCL logo

UCL Discovery

UCL home » Library Services » Electronic resources » UCL Discovery

The molecular pathogenesis of hepatic encephalopathy

Jalan, R; Shawcross, D; Davies, N; (2003) The molecular pathogenesis of hepatic encephalopathy. INT J BIOCHEM CELL B , 35 (8) 1175 - 1181. 10.1016/S1357-2725(02)00396-5.

Full text not available from this repository.

Abstract

Hepatic encephalopathy (HE) incorporates a spectrum of neuropsychiatric abnormalities seen in patients with liver dysfunction with a potential for full reversibility. Distinct syndromes are identified in acute liver failure and cirrhosis. Rapid deterioration in consciousness level and increased intracranial pressure that may result in brain herniation and death are a feature of acute liver failure whereas manifestations of HE in cirrhosis include psychomotor dysfunction, impaired memory, increased reaction time, sensory abnormalities, poor concentration and in severe forms, coma. For over a 100 years ammonia has been considered central to its pathogenesis. In the brain, the astrocyte is the main site for ammonia detoxification, during the conversion of glutamate to glutamine. An increased ammonia level raises the amount of glutamine within astrocytes, causing an osmotic imbalance resulting in cell swelling and ultimately brain oedema. The present review focuses upon the molecular mechanisms involved in the pathogenesis of HE. Therapy of HE is directed primarily at reducing ammonia generation and increasing its detoxification. (C) 2003 Published by Elsevier Science Ltd.

Type:Article
Title:The molecular pathogenesis of hepatic encephalopathy
DOI:10.1016/S1357-2725(02)00396-5
Keywords:hepatic encephalopathy, ammonia, cirrhosis, acute liver failure, hypothermia, ACUTE LIVER-FAILURE, CEREBRAL EDEMA, AMMONIA, METABOLISM, RAT

Archive Staff Only: edit this record