The long-term goal of this project is explore the relationship between exercise and histamine receptor activation in order to improve overall health and cardiovascular wellness. The applicant's faculty mentor has recently documented that a single bout of exercise causes sustained peripheral vasodilation within the previously active skeletal muscle and is the result of histamine receptor activation. Specifically, histamine H1 and H2 receptor activation is considered as primary cause of the sustained postexercise vasodilation. The applicant speculates that histamine receptor activation is not only responsible for postexercise vasodilation but may also play a role in improving endothelial function, arterial compliance, and stimulate vascular remodeling. However, the histamine receptor agonist has yet to be identified, but several likely pathways have been identified. Possible histamine agonists that have been identified include: 1) carnosine released or leaked from skeletal muscle 2) histamine release via mast cell degranulation and 3) de novo production of histamine. Identification of the histamine agonist will be attempted by using single leg dynamic knee extension exercise along with the placement of microdialysis fibers to remove and infuse molecules and drugs of interest in the active skeletal muscle.
The specific aims for the proposed project are as follows: 1) determine the histamine H1 and H2 receptor agonist by measuring interstitial concentrations of carnosine, histamine, tryptase within previously active skeletal muscle 2) determine the role of de novo histamine production in previously active skeletal muscle. Data collected from this project will prove valuable on three fronts. First, these data will help to develop a better understanding of vascular regulation following exercise. Second, it is expected that carnosine will be identified as a significant new factor in peripheral vascular regulation. Alternatively, histamine that is usually associated with pathophysiological responses (e.g. asthma, allergies) may be established as an influential regulator of day-to-day regional blood flow. Last, data collected from this project will contribute to the understanding and development of exercise as a therapeutic modality for the treatment and prevention of cardiovascular disease. Taken together, this project will serve to enhance the health and well-being of many people through physical activity.

Public Health Relevance

Although exercise is known to improve cardiovascular health, many of the underlying mechanisms contributing to this improvement are not well understood or have yet to be identified. This project will attempt to identify another factor that contributes to the use of exercise as a prescription for the prevention and treatment of cardiovascular disease. Information from the proposed study has to potential to influence the health and well- being of many individuals.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Predoctoral Individual National Research Service Award (F31)
Project #
5F31HL107131-02
Application #
8490512
Study Section
Special Emphasis Panel (ZRG1-F10A-S (20))
Program Officer
Meadows, Tawanna
Project Start
2011-09-01
Project End
2013-08-31
Budget Start
2012-09-01
Budget End
2013-08-31
Support Year
2
Fiscal Year
2012
Total Cost
$37,336
Indirect Cost
Name
University of Oregon
Department
Physiology
Type
Schools of Arts and Sciences
DUNS #
948117312
City
Eugene
State
OR
Country
United States
Zip Code
97403