The long term objective of this research is to improve our understanding of the mechanisms of adaptation to prolonged hypoxia, a condition which is a frequent feature of cardiopulmonary disease and which is also present in healthy individuals living at or sojourning to altitude for extended time periods. Hypoxia limits the delivery to and utilization of oxygen by the tissues, particularly in conditions of increased demand such as exercise, fever or other causes of increased metabolic activity. Hypoxia sets in motion several responses which appear to be directed to improve tissue oxygen supply: these include increased rate of red blood cell formation, increased ventilation, and changes in the oxygen affinity of hemoglobin. Although these features are well known, the underlying mechanisms, as well as their overall effectiveness in correcting the oxygen deprivation are poorly understood. The proposed studies will address two interrelated specific aims: 1. To study the mechanisms that limit maximal aerobic exercise capacity during acclimatization to hypoxia, in order to determine the role of changes in convective oxygen transport relative to other possible determinants of maximal oxygen uptake and 2. To determine the role of the sympathetic nervous system on the mechanisms of oxygen transport, uptake and utilization during exercise in prolonged hypoxia. These studies will be carried out in a rat model of acclimatization to hypoxia which has been in use in our laboratory for several years. This model allows a complete description of the oxygen transport system at rest and during hypoxic and normoxic exercise. The rat shares several features of acclimatization to hypoxia with humans, a fact that makes it an attractive animal model for these studies. The studies proposed will provide new information on the mechanisms of adaptation to prolonged hypoxia, and may increase our ability to manage conditions associated with oxygen deprivation.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project (R01)
Project #
5R01HL039443-10
Application #
6030575
Study Section
Special Emphasis Panel (ZRG2-PHY (01))
Project Start
1988-04-01
Project End
2001-06-30
Budget Start
1999-07-01
Budget End
2000-06-30
Support Year
10
Fiscal Year
1999
Total Cost
Indirect Cost
Name
University of Kansas
Department
Physiology
Type
Schools of Medicine
DUNS #
016060860
City
Kansas City
State
KS
Country
United States
Zip Code
66160
Chao, Jie; Viets, Zachary; Donham, Paula et al. (2012) Dexamethasone blocks the systemic inflammation of alveolar hypoxia at several sites in the inflammatory cascade. Am J Physiol Heart Circ Physiol 303:H168-77
Chao, Jie; Blanco, Gustavo; Wood, John G et al. (2011) Renin released from mast cells activated by circulating MCP-1 initiates the microvascular phase of the systemic inflammation of alveolar hypoxia. Am J Physiol Heart Circ Physiol 301:H2264-70
Chao, Jie; Wood, John G; Gonzalez, Norberto C (2011) Alveolar macrophages initiate the systemic microvascular inflammatory response to alveolar hypoxia. Respir Physiol Neurobiol 178:439-48
Gonzalez, Norberto C; Wood, John G (2010) Alveolar hypoxia-induced systemic inflammation: what low PO(2) does and does not do. Adv Exp Med Biol 662:27-32
Kirkton, Scott D; Howlett, Richard A; Gonzalez, Norberto C et al. (2009) Continued artificial selection for running endurance in rats is associated with improved lung function. J Appl Physiol (1985) 106:1810-8
Chao, Jie; Wood, John G; Gonzalez, Norberto C (2009) Alveolar hypoxia, alveolar macrophages, and systemic inflammation. Respir Res 10:54
Chao, Jie; Wood, John G; Blanco, Victor Gustavo et al. (2009) The systemic inflammation of alveolar hypoxia is initiated by alveolar macrophage-borne mediator(s). Am J Respir Cell Mol Biol 41:573-82
Howlett, Richard A; Kirkton, Scott D; Gonzalez, Norberto C et al. (2009) Peripheral oxygen transport and utilization in rats following continued selective breeding for endurance running capacity. J Appl Physiol (1985) 106:1819-25
Gonzalez, Norberto C; Allen, Julie; Blanco, V Gustavo et al. (2007) Alveolar macrophages are necessary for the systemic inflammation of acute alveolar hypoxia. J Appl Physiol 103:1386-94
Gonzalez, Norberto C; Allen, Julie; Schmidt, Eric J et al. (2007) Role of the renin-angiotensin system in the systemic microvascular inflammation of alveolar hypoxia. Am J Physiol Heart Circ Physiol 292:H2285-94

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