Resistance to Cholesterol Gallstone Disease: Hepatic Cholesterol Metabolism

被引:0
|
作者
Zhang, Chenghao [1 ]
Dai, Wanlin [2 ]
Yang, Shaojie [1 ]
Wu, Shuodong [1 ]
Kong, Jing [1 ]
机构
[1] China Med Univ, Shengjing Hosp, Dept Gen Surg, Biliary Surg Gen Unit 2, 36 Sanhao St, Shenyang 110004, Liaoning, Peoples R China
[2] China Med Univ, Innovat Inst, Shenyang 110122, Peoples R China
来源
关键词
cholesterol gallstone disease; hepatic cholesterol metabolism; key molecules; therapeutic targets; treatments; gallstone patients; FATTY LIVER-DISEASE; BINDING CASSETTE TRANSPORTER; BILE-ACID SYNTHESIS; RECEPTOR CLASS-B; SR-BI; ANIMAL-MODEL; RISK; PREVENTION; BIOSYNTHESIS; INHIBITION;
D O I
10.1210/clinem/dgad528
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Cholesterol gallstone disease (CGD) is one of the most common digestive diseases, and it is closely associated with hepatic cholesterol metabolism. Cholesterol gallstones may be caused by abnormal hepatic cholesterol metabolism, such as excessive cholesterol biosynthesis within the liver, interfering with the uptake or export of cholesterol in the liver, and abnormal hepatic cholesterol esterification. In this review, we begin with a brief overview of the clinical diagnosis and treatment of gallstone disease (GSD). Then, we briefly describe the major processes of hepatic cholesterol metabolism and summarize the key molecular expression changes of hepatic cholesterol metabolism in patients with gallstones. We review and analyze the recent advances in elucidating the relationships between these key molecules and CGD, and some targets significantly impacting on CGD via hepatic cholesterol metabolism are also listed. We also provide a significant discussion on the relationship between CGD and nonalcoholic fatty liver disease (NAFLD). Finally, the new discoveries of some therapeutic strategies associated with hepatic cholesterol metabolism to prevent and treat CGD are summarized.
引用
收藏
页码:912 / 923
页数:12
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