Analysis of Insulin Resistance in Nonalcoholic Steatohepatitis.
Hyunbae KimDeqiang ZhangZhenfeng SongXin TongKezhong ZhangPublished in: Methods in molecular biology (Clifton, N.J.) (2022)
Insulin resistance is a major phenotype observed in nonalcoholic steatohepatitis (NASH), the advanced stage of nonalcoholic fatty liver disease (NAFLD). Insulin resistance in NASH is characterized by reductions in whole body, hepatic, and adipose tissue insulin sensitivity. The mechanisms underlying hepatic insulin resistance is primarily associated with hepatic glucose production (HGP) rate. Hepatic insulin resistance can also be a consequence or a driving factor of hepatic lipid accumulation by increasing free fatty acid synthesis, delivery, and catabolism. The common method to assess hepatic insulin resistance is to measure hepatic glucose production (HGP) using isotope tracer distribution technique. However, non-radioactive approaches have been developed to assess hepatic insulin resistance in the context of NASH. In this chapter, we describe the methods to evaluate hepatic insulin resistance in animal models of NASH by examining insulin sensitivity and glucose tolerance as well as the key molecules in hepatic insulin signaling pathways.
Keyphrases
- insulin resistance
- adipose tissue
- type diabetes
- high fat diet
- metabolic syndrome
- fatty acid
- blood pressure
- blood glucose
- mass spectrometry
- oxidative stress
- cell proliferation
- epithelial mesenchymal transition
- high resolution
- glycemic control
- weight loss
- high fat diet induced
- pet imaging
- liver fibrosis
- gas chromatography