We have utilized an established model of behavioral stress in Dahl salt-sensitive (DS) rats that indicates reactive oxygen species (ROS) mediate the stress-induced increase in blood pressure. We have hypothesized that stress triggers ROS production via mechanisms involving the endothelin (ET) and/or angiotensin II pathways through activation of NADPH oxidase and uncoupled NOS. Project 2's BPStress Cohort of young adults has shown that the response to stress was significantly greater in obese individuals or ones at a lower socioeconomic status that carry a specific ET polymorphism. Data in DS rats indicates that a high fat diet augments the stress-induced blood pressure response when compared to DS rats on a normal fat diet. Given the epidemic of childhood obesity that has contributed to the risk of hypertension, it is important to determine the mechanisms responsible for the augmented stress response. Lower childhood socioeconomic status is recognized to be associated with increased cardiovascular disease morbidity and mortality. We initiated preliminary studies with an established model of early life stress in rats. Pups are separated from their mothers for 3 hr/day from day 2-14 of life. The early life stress (separated) rats display a greater response to stress when compared to the non-separated rats. Rats with an impaired ET signaling pathway that are exposed to early life stress do not have an augmented response to stress in adulthood. These data have led us to predict that early life stress activates a component of the ET pathway that potentiates the stress response. We propose the following specific aims:
Specific Aim 1 : To test the hypothesis that air jet stress activates the ET and/or Ang II pathways, which stimulates NADPH oxidase and/or uncoupled NOS as the enzymatic source of ROS, increasing blood pressure;
Specific Aim 2 : To test the hypothesis that high fat diet augments the air jet stress induced increase in blood pressure via production of ROS;
Specific Aim 3 : To test the hypothesis that early life stress potentiates the air jet stress induced increase in blood pressure via the ET pathway. Relevance: The chronic stressors (high fat diet and early life stress) are models of established stressors that are known to sensitize humans to stress and increase the risk for hypertension. A complete understanding of the mechanisms involved in the blood pressure response to stress may disclose approaches for minimizing the risk of hypertension.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Program Projects (P01)
Project #
5P01HL069999-09
Application #
8235792
Study Section
Special Emphasis Panel (ZHL1)
Project Start
Project End
Budget Start
2011-03-01
Budget End
2012-02-29
Support Year
9
Fiscal Year
2011
Total Cost
$254,886
Indirect Cost
Name
Georgia Regents University
Department
Type
DUNS #
966668691
City
Augusta
State
GA
Country
United States
Zip Code
30912
Hao, Guang; Wang, Xiaoling; Treiber, Frank A et al. (2017) Blood Pressure Trajectories From Childhood to Young Adulthood Associated With Cardiovascular Risk: Results From the 23-Year Longitudinal Georgia Stress and Heart Study. Hypertension 69:435-442
Hao, G; Wang, X; Treiber, F A et al. (2017) Body mass index trajectories in childhood is predictive of cardiovascular risk: results from the 23-year longitudinal Georgia Stress and Heart study. Int J Obes (Lond) :
Kapuku, G; Treiber, F; Raouane, F et al. (2017) Race/ethnicity determines the relationships between oxidative stress markers and blood pressure in individuals with high cardiovascular disease risk. J Hum Hypertens 31:70-75
Youssef, Nagy A; Belew, Daniel; Hao, Guang et al. (2017) Racial/ethnic differences in the association of childhood adversities with depression and the role of resilience. J Affect Disord 208:577-581
Stewart, Deborah; Dong, Yanbin; Zhu, Haidong et al. (2017) Angiotensin II-Mediated Increases in Damage-Associated Molecular Patterns During Acute Mental Stress. Psychosom Med 79:112-114
De Miguel, Carmen; Speed, Joshua S; Kasztan, Malgorzata et al. (2016) Endothelin-1 and the kidney: new perspectives and recent findings. Curr Opin Nephrol Hypertens 25:35-41
Gohar, Eman Y; Giachini, Fernanda R; Pollock, David M et al. (2016) Role of the endothelin system in sexual dimorphism in cardiovascular and renal diseases. Life Sci 159:20-29
Saleh, Mohamed A; De Miguel, Carmen; Stevens, David I et al. (2016) Free radical scavenging decreases endothelin-1 excretion and glomerular albumin permeability during type 1 diabetes. Physiol Rep 4:
Davenport, Anthony P; Hyndman, Kelly A; Dhaun, Neeraj et al. (2016) Endothelin. Pharmacol Rev 68:357-418
Heimlich, J Brett; Speed, Joshua S; O'Connor, Paul M et al. (2016) Endothelin-1 contributes to the progression of renal injury in sickle cell disease via reactive oxygen species. Br J Pharmacol 173:386-95

Showing the most recent 10 out of 129 publications