胰岛素抵抗
肥胖
脂肪组织
糖异生
胰岛素
营养感应
生物
能源消耗
2型糖尿病
胰岛素受体
内科学
医学
生物信息学
糖尿病
信号转导
内分泌学
新陈代谢
细胞生物学
作者
Michael Roden,Gerald I. Shulman
出处
期刊:Nature
[Springer Nature]
日期:2019-12-04
卷期号:576 (7785): 51-60
被引量:807
标识
DOI:10.1038/s41586-019-1797-8
摘要
Obesity and type 2 diabetes are the most frequent metabolic disorders, but their causes remain largely unclear. Insulin resistance, the common underlying abnormality, results from imbalance between energy intake and expenditure favouring nutrient-storage pathways, which evolved to maximize energy utilization and preserve adequate substrate supply to the brain. Initially, dysfunction of white adipose tissue and circulating metabolites modulate tissue communication and insulin signalling. However, when the energy imbalance is chronic, mechanisms such as inflammatory pathways accelerate these abnormalities. Here we summarize recent studies providing insights into insulin resistance and increased hepatic gluconeogenesis associated with obesity and type 2 diabetes, focusing on data from humans and relevant animal models. A Review of studies into insulin resistance and hepatic gluconeogenesis associated with obesity and type 2 diabetes.
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