Obesity which has become common in the US and among the VA population is a major cause of hypertension, a principal reversible risk factor for cardiovascular disease. However, the mechanisms underlying the relationship between obesity and hypertension remain largely unknown. The goal of this proposal is to identify the neuronal and molecular processes that control sympathetic activity and blood pressure and how dysregulation in these processes contribute to obesity-associated cardiovascular risks. This proposal is based on the hypothesis that mTORC1 signaling in the hypothalamic arcuate nucleus neurons are critical for sympathetic and blood pressure regulation with important pathophysiological implications in obesity. We will use a multidisciplinary strategy combining unique genetically engineered mouse models that permit selective modulation of key pathways in defined neurons with novel and cutting edge neuro-technologies to precisely and remotely modulate the firing of distinct arcuate nucleus neuronal populations in freely moving animals with sophisticated integrative physiology for sympathetic and cardiovascular phenotyping. We will investigate the contribution of mTORC1 signaling in arcuate nucleus neurons that express proopiomelanocortin (POMC) or agouti-related protein (AgRP) to the regulation of sympathetic activity and arterial pressure and obesity- associated hypertension and sympathetic nerve activation. We will also use chemogenetic and optogenetics to probe the functional relevance of arcuate nucleus POMC and AgRP neurons for the regulation of arterial pressure and sympathetic activity in normal and obese states. This work should unravel novel mechanisms that underlie obesity-associated sympathetic activation and hypertension, making our work of high clinical relevance. Insights into the cellular and molecular processes that control the sympathetic tone that regulates cardiovascular function may make it possible to selectively interfere with the damage obesity inflicts on cardiovascular sympathetic functions.

Public Health Relevance

Veterans who receive care at the VA have high rates of obesity. This is a problem because obesity is a major risk factor for the development of many serious medical problems including high blood pressure (hypertension), a condition that promotes cardiovascular diseases including stroke, coronary artery disease and heart failure. However, the mechanisms underlying obesity-induced hypertension remain poorly understood, hindering therapy. The focus of this project is to explore the processes by which the brain influence blood pressure and understand how dysregulation in these processes lead to hypertension in obesity. Thus, this proposal should fundamentally advance our understanding of the causes of cardiovascular diseases in obesity. This information can then be exploited for therapeutic purposes to benefit obese people including the veterans.

Agency
National Institute of Health (NIH)
Institute
Veterans Affairs (VA)
Type
Non-HHS Research Projects (I01)
Project #
1I01BX004249-01A1
Application #
9658979
Study Section
Special Emphasis Panel (ZRD1)
Project Start
2019-01-01
Project End
2022-12-31
Budget Start
2019-01-01
Budget End
2019-12-31
Support Year
1
Fiscal Year
2019
Total Cost
Indirect Cost
Name
Iowa City VA Medical Center
Department
Type
DUNS #
028084333
City
Iowa City
State
IA
Country
United States
Zip Code
52246