Insulin resistance in type 2 diabetes mellitus

被引:0
作者
Accili, Domenico [1 ]
Deng, Zhaobing [1 ]
Liu, Qingli [1 ]
机构
[1] Columbia Univ, Vagelos Coll Phys & Surg, Dept Med, New York, NY 10027 USA
关键词
HEPATIC GLUCOSE-PRODUCTION; BETA-CELL DEDIFFERENTIATION; ACTIVATED PROTEIN-KINASE; PPAR-GAMMA; IN-VIVO; PHOSPHATIDYLINOSITOL; 3-KINASE; LIPID-METABOLISM; GENE-EXPRESSION; MICE LACKING; RECEPTOR;
D O I
10.1038/s41574-025-01114-y
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Insulin resistance is an integral pathophysiological feature of type 2 diabetes mellitus. Here, we review established and emerging cellular mechanisms of insulin resistance, their complex integrative features and their relevance to disease progression. While recognizing the heterogeneity of the elusive fundamental disruptions that cause insulin resistance, we endorse the view that effector mechanisms impinge on insulin receptor signalling and its relationship with plasma levels of insulin. We focus on hyperinsulinaemia and its consequences: acutely impaired but persistent insulin action, with reduced ability to lower glucose levels but preserved lipid synthesis and lipoprotein secretion. We emphasize the role of insulin sensitization as a therapeutic goal in type 2 diabetes mellitus.
引用
收藏
页码:413 / 426
页数:14
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