“…From a metabolic perspective, experimental diabetes in rats (model for Type 1 diabetes that causes chronic, severe hyperglycemia ϳ20 -40 mmol/l) results in increased nerve glucose, fructose, polyols, aldose reductase activity, protein kinase C activity, and monoenzymatic protein glycosylation as well as a reduction in nerve myoinositol and sodium potassium ATPase activity (13,15,29,32,51,63). From a vascular perspective, experimental diabetes is linked with reduced endothelial function (37, 50) and nerve blood flow (10,16,36,40,43,50,64). Together, these factors contribute to nerve dysfunction (10,16,40,64).…”