Recent studies in the pulmonary circulation suggest a role for the endothelium-derived constricting factor, endothelin (ET), in mediating hypoxic vasoconstriction. However, the mechanism of action of ET in the pulmonary vasculature is unknown. Thus, the overall aim of this project is to characterize the mechanisms by which ET causes pulmonary vasoconstriction and to determine the effect of chronic hypoxia on this pathway.
The Specific Aims of this proposal are: 1) characterize ET- induced vasoconstriction and Ca2+ response, 2) determine intra- and extracellular Ca2+ sources involved in ET-1-induced Ca2+ response, 3) determine the ionic mechanisms of ET-1-induced membrane depolarization and 4) determine if the vasoconstrictory and Ca2+ responses are altered after chronic hypoxia. For these studies, a unique combination of techniques will be used, including isolated, cannulated arteries, whole cell patch clamp and microfluorescence measurement, to study the contractile effects of ET on isolated perfused microvessels and changes in ion currents, membrane potential and intracellular Ca2+in pulmonary artery smooth muscle cells, both before and after exposure to chronic hypoxia. For patients with chronic obstructive pulmonary disease, the structural and functional changes induced by hypoxia correlate with the development of pulmonary hypertension, considerably worsening the prognosis for patients. In this study, we hope to produce new information about the mechanisms by which ET regulates pulmonary vascular tone and elucidate a possible pathophysiologic role for endogenous ET, providing clinically useful information for the prevention and treatment of chronic obstructive airway disease and subsequent pulmonary hypertension.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Postdoctoral Individual National Research Service Award (F32)
Project #
5F32HL009543-02
Application #
2459909
Study Section
Special Emphasis Panel (ZRG2-PSF (02))
Project Start
1997-01-28
Project End
Budget Start
1997-08-01
Budget End
1998-06-30
Support Year
2
Fiscal Year
1997
Total Cost
Indirect Cost
Name
Johns Hopkins University
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
045911138
City
Baltimore
State
MD
Country
United States
Zip Code
21218
Shimoda, L A; Sylvester, J T; Booth, G M et al. (2001) Inhibition of voltage-gated K(+) currents by endothelin-1 in human pulmonary arterial myocytes. Am J Physiol Lung Cell Mol Physiol 281:L1115-22
Shimoda, L A; Sylvester, J T; Sham, J S (2000) Mobilization of intracellular Ca(2+) by endothelin-1 in rat intrapulmonary arterial smooth muscle cells. Am J Physiol Lung Cell Mol Physiol 278:L157-64
Shimoda, L A; Sylvester, J T; Sham, J S (1999) Chronic hypoxia alters effects of endothelin and angiotensin on K+ currents in pulmonary arterial myocytes. Am J Physiol 277:L431-9
Shimoda, L A; Sylvester, J T; Sham, J S (1998) Inhibition of voltage-gated K+ current in rat intrapulmonary arterial myocytes by endothelin-1. Am J Physiol 274:L842-53