| Literature DB >> 2177815 |
K Fujimoto1, A Sakai, S Yoshikawa, S Shinozaki, Y Matsuzawa, K Kubo, T Kobayashi, G Ueda, M Sekiguchi, N F Voelkel.
Abstract
We examined, in isolated blood perfused rat lungs, the effect of the cell permeable 8-bromo derivative of cGMP on pulmonary vasoconstriction induced by either alveolar hypoxia or angiotensin II. 8-Bromo cGMP dose-dependently reduced both hypoxia-(IC50 = 2.2 X 10(-5) M) and angiotensin-II-induced pulmonary vasoconstriction (IC50 = 5.0 X 10(-5) M). This effect of 8-bromo cGMP on pulmonary vasoconstriction was not affected by cyclooxygenase blockade. M & B 22948 (0.1 mM), an inhibitor of cGMP-phosphodiesterase, reduced synergistically with 8-bromo cGMP the hypoxia or angiotensin-II-induced vasoconstriction. The cGMP-phosphodiesterase inhibitor M & B 22948, by itself, selectively reduced hypoxia-induced vasoconstriction, suggesting a modulating effect of endogenous cGMP during hypoxic vasoconstriction.Entities:
Mesh:
Substances:
Year: 1990 PMID: 2177815 DOI: 10.1007/BF02719710
Source DB: PubMed Journal: Lung ISSN: 0341-2040 Impact factor: 2.584