Related Experiment Video
Updated: Sep 3, 2026

A Model of Chronic Nutrient Infusion in the Rat
Published on: August 14, 2013
High glucose condition activates protein tyrosine phosphatases and deactivates insulin receptor function in
1Third Department of Medicine, Shiga University of Medical Science, Japan.
Abstract:
To investigate the mechanism for the impairment of insulin receptor kinase activity induced by high glucose (HG) in Rat 1 fibroblasts that expressed human insulin receptors (HIRc), we measured protein tyrosine phosphatase (PTPase) activity in HG cells. Incubating HIRc cells for 4 days in 27 mM D-glucose (HG) stimulated cytosolic PTPase activities, but not particulate PTPase activity as determined by two methods using the dephosphorylation of insulin receptors. Furthermore, PTP1B, a major non-transmembrane PTPase in the cytosolic fraction, was increased in HG cells according to Western blots. These results indicate that desensitization of insulin receptor function by a high glucose condition is associated with the activation of PTPase activity.
More Related Videos
Related Concept Videos
Insulin Secretory Vesicles
cAMP-dependent Protein Kinase Pathways
Hormones Regulating Blood Glucose
In addition to accelerating glucose uptake and utilization, insulin has...
Glucose Homeostasis: Pancreatic Islets and Insulin Secretion
Insulin and C-peptide are co-secreted in...
Insulin: The Receptor and Signaling Pathways
Type II Diabetes II: Pathophysiology

