Neuman Manuela G, Seitz Helmut K, Teschke Rolf, Malnick Stephen, Johnson-Davis Kamisha L, Cohen Lawrence B, German Anit, Hohmann Nicolas, Moreira Bernhardo, Moussa George, Opris Mihai
In Vitro Drug Safety and Biotechnology and the Department of Pharmacology and Toxicology, Temerity Faculty of Medicine, University of Toronto, Toronto, ON M5G 1L5, Canada.
Centre of Liver and Alcohol Diseases, Ethianum Clinic and Department of Clinical Pharmacology and Pharmacoepidemiology, Faculty of Medicine, University of Heidelberg, 69115 Heidelberg, Germany.
Curr Issues Mol Biol. 2022 Mar 16;44(3):1294-1315. doi: 10.3390/cimb44030087.
Hepatic cells are sensitive to internal and external signals. Ethanol is one of the oldest and most widely used drugs in the world. The focus on the mechanistic engine of the alcohol-induced injury has been in the liver, which is responsible for the pathways of alcohol metabolism. Ethanol undergoes a phase I type of reaction, mainly catalyzed by the cytoplasmic enzyme, alcohol dehydrogenase (ADH), and by the microsomal ethanol-oxidizing system (MEOS). Reactive oxygen species (ROS) generated by cytochrome (CYP) 2E1 activity and MEOS contribute to ethanol-induced toxicity. We aimed to: (1) Describe the cellular, pathophysiological and clinical effects of alcohol misuse on the liver; (2) Select the biomarkers and analytical methods utilized by the clinical laboratory to assess alcohol exposure; (3) Provide therapeutic ideas to prevent/reduce alcohol-induced liver injury; (4) Provide up-to-date knowledge regarding the Corona virus and its affect on the liver; (5) Link rare diseases with alcohol consumption. The current review contributes to risk identification of patients with alcoholic, as well as non-alcoholic, liver disease and metabolic syndrome. Additional prevalence of ethnic, genetic, and viral vulnerabilities are presented.
肝细胞对内部和外部信号敏感。乙醇是世界上使用最久且最为广泛的药物之一。酒精性损伤的机制研究重点一直放在肝脏,肝脏负责酒精代谢途径。乙醇经历I相反应,主要由细胞质酶乙醇脱氢酶(ADH)和微粒体乙醇氧化系统(MEOS)催化。细胞色素(CYP)2E1活性和MEOS产生的活性氧(ROS)导致乙醇诱导的毒性。我们旨在:(1)描述酒精滥用对肝脏的细胞、病理生理和临床影响;(2)选择临床实验室用于评估酒精暴露的生物标志物和分析方法;(3)提供预防/减少酒精性肝损伤的治疗思路;(4)提供关于冠状病毒及其对肝脏影响的最新知识;(5)将罕见病与饮酒联系起来。本综述有助于识别酒精性和非酒精性肝病及代谢综合征患者的风险。还介绍了种族、遗传和病毒易感性的额外患病率。