Shi Yi-Xian, Huang Chen-Jie, Yang Zheng-Gang
Yi-Xian Shi, Chen-Jie Huang, Zheng-Gang Yang, State Key Lab of Diagnostic and Treatment of Infectious Diseases, Collaborative Innovation Center for Diagnosis and Treatment of Infectious Disease, The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou 310003, Zhejiang Province, China.
World J Gastroenterol. 2016 Sep 28;22(36):8161-7. doi: 10.3748/wjg.v22.i36.8161.
A growing body of epidemiologic research has demonstrated that metabolic derangement exists in patients with hepatitis B virus (HBV) infection, indicating that there are clinical associations between HBV infection and host metabolism. In order to understand the complex interplay between HBV and hepatic metabolism in greater depth, we systematically reviewed these alterations in different metabolic signaling pathways due to HBV infection. HBV infection interfered with most aspects of hepatic metabolic responses, including glucose, lipid, nucleic acid, bile acid and vitamin metabolism. Glucose and lipid metabolism is a particular focus due to the significant promotion of gluconeogenesis, glucose aerobic oxidation, the pentose phosphate pathway, fatty acid synthesis or oxidation, phospholipid and cholesterol biosynthesis affected by HBV. These altered metabolic pathways are involved in the pathological process of not only hepatitis B, but also metabolic disorders, increasing the occurrence of complications, such as hepatocellular carcinoma and liver steatosis. Thus, a clearer understanding of the hepatic metabolic pathways affected by HBV and its pathogenesis is necessary to develop more novel therapeutic strategies targeting viral eradication.
越来越多的流行病学研究表明,乙型肝炎病毒(HBV)感染患者存在代谢紊乱,这表明HBV感染与宿主代谢之间存在临床关联。为了更深入地了解HBV与肝脏代谢之间的复杂相互作用,我们系统地回顾了HBV感染导致的不同代谢信号通路的这些改变。HBV感染干扰了肝脏代谢反应的大多数方面,包括葡萄糖、脂质、核酸、胆汁酸和维生素代谢。由于HBV对糖异生、葡萄糖有氧氧化、磷酸戊糖途径、脂肪酸合成或氧化、磷脂和胆固醇生物合成有显著促进作用,葡萄糖和脂质代谢成为特别关注的焦点。这些改变的代谢途径不仅参与了乙型肝炎的病理过程,还参与了代谢紊乱,增加了并发症的发生,如肝细胞癌和肝脂肪变性。因此,更清楚地了解受HBV影响的肝脏代谢途径及其发病机制对于开发更多针对病毒根除的新型治疗策略是必要的。