The metabolic basis of epilepsy
The brain is a highly energy-demanding organ and requires bioenergetic adaptability to
balance normal activity with pathophysiological fuelling of spontaneous recurrent seizures …
balance normal activity with pathophysiological fuelling of spontaneous recurrent seizures …
Pathoetiological model of delirium: a comprehensive understanding of the neurobiology of delirium and an evidence-based approach to prevention and treatment
JR Maldonado - Critical care clinics, 2008 - Elsevier
Delirium is the most common complication found in the general hospital setting. Yet, we
know relatively little about its actual pathophysiology. This article contains a summary of …
know relatively little about its actual pathophysiology. This article contains a summary of …
Experimental models of hepatic encephalopathy: ISHEN guidelines
RF Butterworth, MD Norenberg, V Felipo… - Liver …, 2009 - Wiley Online Library
Abstract Objectives of the International Society for Hepatic Encephalopathy and Nitrogen
Metabolism Commission were to identify well‐characterized animal models of hepatic …
Metabolism Commission were to identify well‐characterized animal models of hepatic …
Identifying the direct effects of ammonia on the brain
CR Bosoi, CF Rose - Metabolic brain disease, 2009 - Springer
Elevated concentrations of ammonia in the brain as a result of hyperammonemia leads to
cerebral dysfunction involving a spectrum of neuropsychiatric and neurological symptoms …
cerebral dysfunction involving a spectrum of neuropsychiatric and neurological symptoms …
Disturbance of the glutamate-glutamine cycle, secondary to hepatic damage, compromises memory function
ID Limón, I Angulo-Cruz, L Sánchez-Abdon… - Frontiers in …, 2021 - frontiersin.org
Glutamate fulfils many vital functions both at a peripheral level and in the central nervous
system (CNS). However, hyperammonemia and hepatic failure induce alterations in …
system (CNS). However, hyperammonemia and hepatic failure induce alterations in …
Neurological implications of urea cycle disorders
The urea cycle disorders constitute a group of rare congenital disorders caused by a
deficiency of the enzymes or transport proteins required to remove ammonia from the body …
deficiency of the enzymes or transport proteins required to remove ammonia from the body …
Refining the ammonia hypothesis: a physiology-driven approach to the treatment of hepatic encephalopathy
Hepatic encephalopathy (HE) is one of the most important complications of cirrhosis and
portal hypertension. Although the etiology is incompletely understood, it has been linked to …
portal hypertension. Although the etiology is incompletely understood, it has been linked to …
Three targets of branched-chain amino acid supplementation in the treatment of liver disease
M Holecek - Nutrition, 2010 - Elsevier
The article explains the pathogenesis of disturbances in branched-chain amino acid (BCAA;
valine, leucine, and isoleucine) and protein metabolism in various forms of hepatic injury …
valine, leucine, and isoleucine) and protein metabolism in various forms of hepatic injury …
[PDF][PDF] Hepatic encephalopathy, ammonia, glutamate, glutamine and oxidative stress
A Lemberg, MA Fernández - Annals of hepatology, 2009 - medigraphic.com
This review addresses recent and not so recent works that emphasize on the mechanisms
by which liver damage can induce encephalopathy. Hepatic encephalopathy constitutes an …
by which liver damage can induce encephalopathy. Hepatic encephalopathy constitutes an …
Current concepts in the pathogenesis of urea cycle disorders
O Braissant - Molecular genetics and metabolism, 2010 - Elsevier
The common feature of urea cycle diseases (UCD) is a defect in ammonium elimination in
liver, leading to hyperammonemia. This excess of circulating ammonium eventually reaches …
liver, leading to hyperammonemia. This excess of circulating ammonium eventually reaches …