Rationale: Diabetes is epidemic in our society. Type-2 Diabetes Mellitus (T2DM) is a progressive pathology characterized by insulin resistance and hyperinsulinemia. Cardiovascular pathologies that are the sequelae of this disorder are the leading cause of morbidity and mortality in our Veteran population. Atherosclerosis is a major consequence of diabetes and one particular characteristic of atherosclerois is inflammation. Studies suggest that chronic insulin resistance and hyperinsulinemia contribute to atherogenesis by augmenting the effects of the inflammatory cytokines, thereby increasing the secretion of additonal inflammatory cytokines and expression of cellular adhesion molecules (CAMs). Tumor Necrosis Factor-alpha (TNF?) activity has been shown to be linked to insulin resistance. Pathways that mediate the effects of TNF? may also regulate intracellular insulin signaling and thus correlated to atherogenesis. TNF? is known to increase the expression of vascular cell adhesion molecule-1 (VCAM-1). In contrast, insulin's role in atherogenesis is debated. Some contend that insulin stimulates the increase of nitric oxide (NO). Others argue that hyperinsulinemia increases the proliferaton of vascular cells and the inflammatory response. The question we asked here is, does insulin dampen or augment the effects of TNF? on VCAM-1 expression and what mechanisms are attributed to these effects? In vitro and in vivo animal model experiments have examined some of the signaling pathways that mediate CAM expression, but there is a significant gap in our understanding between identifying pathways and their molecular interactions or cross talk within cells and tissues in the presence of hyperinsulinemia and inflammatory cytokines. Significance: We are interested in determining the molecular mechanisms that regulate insulin and TNF? stimulation of VCAM-1 expression and thereby help define novel drug targets. These findings may provide healthcare strategies that will allay vascular inflammation and atherosclerosis in Veterans. We hypothesize - that in the state of metabolic insulin resistance hyperinsulinemia exaggerates the effects of TNF?-associated inflammation via increased expression of VCAM-1. These effects are mediated in part by multiple signal pathways, in which ERK5 plays an important role in VCAM-1 expression, NF?B activation and vascular inflammation. Goals of Research: To further our knowledge of vascular inflammation we plan to use the findings from the current proposal to advance our understanding of the molecular mechanisms of vascular inflammation by characterizing the roles of key players in insulin and TNF?-stimulated VCAM-1 expression.
Specific Aims : (1) Determine the role of kinase pathway crosstalk in hyperinsulinemia and TNF?-stimulated increases in VCAM-1 expression. (2) Determine the role of ERK5 in hyperinsulinemia and TNF? stimulated increases in VCAM-1 expression. (3) Determine the role that hyprerinsulinemia plays in VCAM-1 expression in carotids of diabetic rats.

Public Health Relevance

- Diabetes is a common disorder in Veterans. As Veterans age, their sedentary lifestyle and poor eating habits contribute to a slow acting, but insidious disease called Type-2 Diabetes Mellitus; a form of diabetes that is associated with insulin resistance and higher than normal concentrations of sugar and insulin in the blood. Among the more common effects of high blood sugar and insulin is the occurrence of atherosclerosis. Atherosclerosis is characterized by constriction of important blood vessels that lead to and from the heart and brain, and eventual closer of blood vessels, which can lead to heart attacks and strokes. Associated with atherosclerosis is a condition called vascular inflammation. Inflammation aggravates atherosclerosis. This study examines some of the causes of vascular inflammation in vascular tissue and tries to determine the role that high concentrations of insulin play in atherosclerosis and vascular inflammation. Additionally, this research will determine drug targets and therapeutic strategies to slow or allay the effects of atherosclerosis.

Agency
National Institute of Health (NIH)
Institute
Veterans Affairs (VA)
Type
Non-HHS Research Projects (I01)
Project #
5I01BX002019-04
Application #
9339515
Study Section
Endocriniology A (ENDA)
Project Start
2014-04-01
Project End
2018-03-31
Budget Start
2017-04-01
Budget End
2018-03-31
Support Year
4
Fiscal Year
2017
Total Cost
Indirect Cost
Name
VA Eastern Colorado Health Care System
Department
Type
DUNS #
003252830
City
Aurora
State
CO
Country
United States
Zip Code
80045