Hepatic insulin receptor: new views on the mechanisms of liver disease

被引:20
|
作者
Lee, Wang-Hsin [1 ]
Najjar, Sonia M. [2 ,3 ]
Kahn, C. Ronald [4 ]
Hinds, Terry D. [1 ,5 ,6 ,7 ]
机构
[1] Univ Kentucky, Coll Med, Dept Pharmacol & Nutr Sci, Lexington, KY USA
[2] Ohio Univ, Heritage Coll Osteopath Med, Dept Biomed Sci, Athens, OH USA
[3] Ohio Univ, Diabet Inst, Heritage Coll Osteopath Med, Athens, OH USA
[4] Harvard Med Sch, Sect Integrat Physiol & Metab, Joslin Diabet Ctr, Boston, MA 02215 USA
[5] Univ Kentucky, Barnstable Brown Diabet Ctr, Coll Med, Lexington, KY USA
[6] Univ Kentucky, Markey Canc Ctr, Lexington, KY USA
[7] Univ Kentucky, Coll Med, Dept Pharmacol & Nutr Sci, 760 Press Ave,Hlth Kentucky Res Bldg HKRB 221, Lexington, KY 40508 USA
来源
基金
美国国家卫生研究院;
关键词
Fatty liver; NAFLD; MAFLD; NASH; MASH; Cirrhosis; Hepatocytes; Hepatic stellate cells; Lipogenesis; Insulin resistance; Insulin clearance; GLUCOCORTICOID-RECEPTOR; GENE-EXPRESSION; STELLATE CELLS; NONALCOHOLIC STEATOHEPATITIS; BILIVERDIN REDUCTASE; LIPID-METABOLISM; OBESE MICE; BILIRUBIN; CLEARANCE; RESISTANCE;
D O I
10.1016/j.metabol.2023.155607
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Over 65 % of people with obesity display the metabolic-associated fatty liver disease (MAFLD), which can manifest as steatohepatitis, fibrosis, cirrhosis, or liver cancer. The development and progression of MAFLD involve hepatic insulin resistance and reduced insulin clearance. This review discusses the relationships between altered insulin signaling, hepatic insulin resistance, and reduced insulin clearance in the development of MAFLD and how this provides the impetus for exploring the use of insulin sensitizers to curb this disease. The review also explores the role of the insulin receptor in hepatocytes and hepatic stellate cells and how it signals in metabolic and end-stage liver diseases. Finally, we discuss new research findings that indicate that advanced hepatic dis-eases may be an insulin-sensitive state in the liver and deliberate whether insulin sensitizers should be used to manage late-stage liver diseases.
引用
收藏
页数:10
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