The objective of this program is to investigate the integrated function of respiration and circulation. Interaction between the respiratory and circulatory systems may be mediated through mechanical interdependence, changes in respiratory gas tensions, synthesis and release of chemical mediators, and shifts in body fluids. In order to study these interactions, seven interrelated projects are proposed by investigators with expertise in respiratory and cardiovascular physiology. These investigators are supported by co investigators with expertise in biochemistry, pathology, and immunology. Specific goals of the projects are: To assess the basis for mechanical interdependence between the cardiovascular and pulmonary systems (Project 1 - Permutt); To evaluate the regulation of the bronchial circulation and to determine its effects on airway tone and fluid movements in the lungs (Project 2 - Wagner); To characterize responses of the pulmonary circulation to hypoxia and to study mechanisms of hypoxia pulmonary vasoconstriction (Project 3 - Sylvester); To study the effects of stress on airway and vascular tone (Project 4 - Mitzner); To evaluate local mechanisms for the control of airway and vascular tone (Project 5 - Menkes); To assess neurotransmitter function in the control of ventilation (Project 6 - Fitzgerald). These projects are supported by a technical and consultative core with four components - (i) Machine shop, electronic facility, and animal handling (Mitzner), (ii) Pathology (Dannenberg), (iii) Statistic (Kimball), and (iv) Immunology (Liechtenstein). For the individual projects, a variety of approaches will be utilized and range from measurements of chemical mediators in excised smooth muscle tissue to assessments of temperature in exercising human subjects. Although each project is designed so that it can be carried out independently of the others, shared ideas, space, and equipment facilitate progress in the proposed research. This research should in improved understanding of cardiopulmonary interactions and provide a more sound basis for intervention in the acutely ill patient and for prevention of chronic disease.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Program Projects (P01)
Project #
5P01HL010342-27
Application #
3097442
Study Section
Heart, Lung, and Blood Research Review Committee A (HLBA)
Project Start
1978-06-01
Project End
1993-05-31
Budget Start
1992-06-03
Budget End
1993-05-31
Support Year
27
Fiscal Year
1992
Total Cost
Indirect Cost
Name
Johns Hopkins University
Department
Type
Schools of Public Health
DUNS #
045911138
City
Baltimore
State
MD
Country
United States
Zip Code
21218
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Zhong, Qiong; Jenkins, John; Moldobaeva, Aigul et al. (2016) Effector T Cells and Ischemia-Induced Systemic Angiogenesis in the Lung. Am J Respir Cell Mol Biol 54:394-401
Vigeland, Christine L; Collins, Samuel L; Chan-Li, Yee et al. (2016) Deletion of mTORC1 Activity in CD4+ T Cells Is Associated with Lung Fibrosis and Increased ?? T Cells. PLoS One 11:e0163288
D'Alessio, F R; Craig, J M; Singer, B D et al. (2016) Enhanced resolution of experimental ARDS through IL-4-mediated lung macrophage reprogramming. Am J Physiol Lung Cell Mol Physiol 310:L733-46

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