Sepehrinezhad Ali, Shahbazi Ali, Sahab Negah Sajad, Joghataei Mohammad Taghi, Larsen Fin Stolze
Department of Neuroscience, Faculty of Advanced Technologies in Medicine, Iran University of Medical Sciences, Tehran, Iran.
Neuroscience Research Center, Mashhad University of Medical Sciences, Mashhad, Iran.
Toxicol Rep. 2021 Apr 30;8:962-970. doi: 10.1016/j.toxrep.2021.04.011. eCollection 2021.
Hepatic encephalopathy (HE) following acute and chronic liver failure is defined as a complex of neuropsychiatric abnormalities, such as discrete personal changes, sleep disorder, forgetfulness, confusion, and decreasing the level of consciousness to coma. The use and design of suitable animal models that represent clinical features and pathological changes of HE are valuable to map the molecular mechanisms that result in HE. Among different types of animal models, thioacetamide (TAA) has been used extensively for the induction of acute liver injury and HE. This agent is not directly hepatotoxic but its metabolites induce liver injury through the induction of oxidative stress and produce systemic inflammation similar to that seen in acute HE patients. In this short review article, we shortly review the most important pathological findings in animal models of acute HE following the administration of TAA.
急性和慢性肝衰竭后的肝性脑病(HE)被定义为一种神经精神异常的综合征,如性格改变、睡眠障碍、健忘、意识混乱以及意识水平下降至昏迷。使用和设计能够体现HE临床特征和病理变化的合适动物模型,对于明确导致HE的分子机制具有重要价值。在不同类型的动物模型中,硫代乙酰胺(TAA)已被广泛用于诱导急性肝损伤和HE。该药物本身并无直接肝毒性,但其代谢产物通过诱导氧化应激引发肝损伤,并产生与急性HE患者相似的全身炎症反应。在这篇简短的综述文章中,我们简要回顾了给予TAA后急性HE动物模型中最重要的病理发现。