Department of Biochemistry, School of Medicine, Tzu Chi University, Hualien 97004, Taiwan.
Institute of Medical Sciences, Tzu Chi University, Hualien 97004, Taiwan.
Int J Mol Sci. 2022 Mar 31;23(7):3897. doi: 10.3390/ijms23073897.
Hepatitis is defined as inflammation of the liver; it can be acute or chronic. In chronic cases, the prolonged inflammation gradually damages the liver, resulting in liver fibrosis, cirrhosis, and sometimes liver failure or cancer. Hepatitis is often caused by viral infections. The most common causes of viral hepatitis are the five hepatitis viruses-hepatitis A virus (HAV), hepatitis B virus (HBV), hepatitis C virus (HCV), hepatitis D virus (HDV), and hepatitis E virus (HEV). While HAV and HEV rarely (or do not) cause chronic hepatitis, a considerable proportion of acute hepatitis cases caused by HBV (sometimes co-infected with HDV) and HCV infections become chronic. Thus, many medical researchers have focused on the treatment of HBV and HCV. It has been documented that host lipid metabolism, particularly cholesterol metabolism, is required for the hepatitis viral infection and life cycle. Thus, manipulating host cholesterol metabolism-related genes and proteins is a strategy used in fighting the viral infections. Efforts have been made to evaluate the efficacy of cholesterol-lowering drugs, particularly 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) reductase inhibitors, in the treatment of hepatitis viral infections; promising results have been obtained. This review provides information on the relationships between hepatitis viruses and host cholesterol metabolism/homeostasis, as well as the discovery/development of cholesterol-lowering natural phytochemicals that could potentially be applied in the treatment of viral hepatitis.
肝炎是肝脏炎症的定义;它可以是急性的或慢性的。在慢性病例中,长期的炎症逐渐损害肝脏,导致肝纤维化、肝硬化,有时还会导致肝功能衰竭或癌症。肝炎通常由病毒感染引起。病毒性肝炎最常见的原因是五种肝炎病毒——甲型肝炎病毒(HAV)、乙型肝炎病毒(HBV)、丙型肝炎病毒(HCV)、丁型肝炎病毒(HDV)和戊型肝炎病毒(HEV)。虽然 HAV 和 HEV 很少(或不)引起慢性肝炎,但由 HBV(有时与 HDV 共同感染)和 HCV 感染引起的相当一部分急性肝炎病例会变成慢性。因此,许多医学研究人员专注于治疗 HBV 和 HCV。已有文献记载,宿主脂质代谢,特别是胆固醇代谢,是肝炎病毒感染和生命周期所必需的。因此,操纵宿主胆固醇代谢相关基因和蛋白质是对抗病毒感染的一种策略。人们已经努力评估降脂药物,特别是 3-羟基-3-甲基戊二酰辅酶 A(HMG-CoA)还原酶抑制剂,在治疗肝炎病毒感染方面的疗效;已经取得了有希望的结果。本综述提供了有关肝炎病毒与宿主胆固醇代谢/平衡之间关系的信息,以及发现/开发可能应用于治疗病毒性肝炎的降胆固醇天然植物化学物质的信息。