15155270

pubmed:Citation

3

We previously reported that angiotensin II stimulates an increase in nitric oxide production in pulmonary artery endothelial cells. The aims of this study were to determine which receptor subtype mediates the angiotensin II-dependent increase in nitric oxide production and to investigate the roles of the angiotensin type 1 and type 2 receptors in modulating angiotensin II-dependent vasoconstriction in pulmonary arteries. Pulmonary artery endothelial cells express both angiotensin II type 1 and type 2 receptors as assessed by RT-PCR, Western blot analysis, and flow cytometry. Treatment of the endothelial cells with PD-123319, a type 2 receptor antagonist, prevented the angiotensin II-dependent increase in nitric oxide synthase mRNA, protein levels, and nitric oxide production. In contrast, the type 1 receptor antagonist losartan enhanced nitric oxide synthase mRNA levels, protein expression, and nitric oxide production. Pretreatment of the endothelial cells with either PD-123319 or an anti-angiotensin II antibody prevented this losartan enhancement of nitric oxide production. Angiotensin II-dependent enhanced hypoxic contractions in pulmonary arteries were blocked by the type 1 receptor antagonist candesartan; however, PD-123319 enhanced hypoxic contractions in angiotensin II-treated endothelium-intact vessels. These data demonstrate that angiotensin II stimulates an increase in nitric oxide synthase mRNA, protein expression, and nitric oxide production via the type 2 receptor, whereas signaling via the type 1 receptor negatively regulates nitric oxide production in the pulmonary endothelium. This endothelial, type 2 receptor-dependent increase in nitric oxide may serve to counterbalance the angiotensin II-dependent vasoconstriction in smooth muscle cells, ultimately regulating pulmonary vascular tone.

eng

IM

MEDLINE

1040-0605

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NLM

L559-68

pubmed-meshheading:15155270-Angiotensin I, pubmed-meshheading:15155270-Angiotensin II, pubmed-meshheading:15155270-Animals, pubmed-meshheading:15155270-Antihypertensive Agents, pubmed-meshheading:15155270-Cattle, pubmed-meshheading:15155270-Cells, Cultured, pubmed-meshheading:15155270-Dithiothreitol, pubmed-meshheading:15155270-Dose-Response Relationship, Drug, pubmed-meshheading:15155270-Endothelium, Vascular, pubmed-meshheading:15155270-Muscle, Smooth, Vascular, pubmed-meshheading:15155270-Nitric Oxide, pubmed-meshheading:15155270-Nitric Oxide Synthase, pubmed-meshheading:15155270-Nitric Oxide Synthase Type III, pubmed-meshheading:15155270-Peptide Fragments, pubmed-meshheading:15155270-Pulmonary Artery, pubmed-meshheading:15155270-Receptor, Angiotensin, Type 1, pubmed-meshheading:15155270-Receptor, Angiotensin, Type 2, pubmed-meshheading:15155270-Signal Transduction, pubmed-meshheading:15155270-Vasoconstriction, pubmed-meshheading:15155270-Vasoconstrictor Agents

Angiotensin II stimulates nitric oxide production in pulmonary artery endothelium via the type 2 receptor.

Journal Article, Research Support, U.S. Gov't, P.H.S.