Abstract
We have examined the effects of Y-27632, a specific inhibitor of Rho-activated kinases (ROCK I and ROCK II) upon sustained hypoxic pulmonary vasoconstriction (HPV) in both rat isolated small intrapulmonary arteries (IPA) and perfused rat lungs in situ. Y-27632 (100 nM - 3 microM) was found to cause a concentration-dependent inhibition of acute sustained HPV in rat IPA. Application of Y-27632 (10-600 nM) in perfused rat lungs caused no change in basal perfusion pressure, but was found to inhibit HPV in a concentration-dependent manner, resulting in complete ablation of the pressor response to hypoxia at a concentration of 600 nM. Furthermore, addition of Y-27632 at any point during hypoxia caused a reversal of HPV in perfused rat lungs. These results suggest that activation of Rho-associated kinase may be a pivotal step in the generation of sustained HPV.
MeSH Terms
Amides/pharmacology
Animals
Calcium/metabolism
Dose-Response Relationship, Drug
Enzyme Inhibitors/pharmacology
Hypoxia/physiopathology
Intracellular Signaling Peptides and Proteins
Lung/drug effects,physiology
Male
Perfusion
Protein Serine-Threonine Kinases/antagonists & inhibitors,physiology
Pulmonary Artery/drug effects,physiology
Pyridines/pharmacology
Rats
Rats, Wistar
Vasoconstriction/drug effects
rho-Associated Kinases
Chemicals
Amides
Enzyme Inhibitors
Intracellular Signaling Peptides and Proteins
Pyridines
Y 27632
Protein Serine-Threonine Kinases
rho-Associated Kinases
Calcium
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Robertson T P
Department of Respiratory Medicine and Allergy, GKT School of Medicine, King's College London, Guy's Campus, London SE1 9RT.
[email protected]
Dipp M
Ward J P
Aaronson P I
Evans A M
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