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Videomorphometric Analysis of Hypoxic Pulmonary Vasoconstriction of Intra-pulmonary Arteries Using Murine Precision Cut Lung Slices
Published on: January 14, 2014
Dopamine receptor subtypes in the human pulmonary arterial tree
A Ricci1, F Mignini, D Tomassoni
1Sezione Malattie dell'Apparato Respiratorio, Dipartimento di Scienze Cardiovascolari e Respiratorie, II Facoltà di Medicina e Chirurgia, Policlinico S. Andrea, Università 'La Sapienza', 00189 Rome, Italy.
Dopamine receptors, particularly D1, are found in human pulmonary arteries, influencing vasorelaxation. Dopamine D2-like receptors are located in the sympathetic nerve supply, suggesting distinct roles in pulmonary circulation.
Area of Science:
- Cardiovascular Pharmacology
- Neuropharmacology
- Pulmonary Circulation Research
Background:
- Dopamine induces pulmonary artery vasodilation via endothelium-dependent pathways.
- The specific dopamine receptor subtypes mediating this effect in the pulmonary artery remain unidentified.
Purpose of the Study:
- To investigate the expression and localization of dopamine receptor subtypes (D1, D5, D2, D3, D4) in the human pulmonary artery.
- To elucidate the role of these receptors in dopamine-induced pulmonary vasorelaxation.
Main Methods:
- Immunoblotting and immunohistochemistry were used to detect dopamine receptor subtypes.
- Analysis was performed on hilar, lobar, and intrapulmonary branches of the human pulmonary artery.
Main Results:
- Human pulmonary arteries express dopamine D1, D2, D4, and D5 receptor subtypes, but not D3.
- Dopamine D1 and D5 receptors are concentrated in the endothelium of extrapulmonary arteries.
- Dopamine D2 and D4 receptors are located in the adventitia, associated with sympathetic nerve plexuses.
Conclusions:
- Dopamine receptors play a role in endothelium-dependent pulmonary vasorelaxation, with the D1 subtype being most significant.
- Dopamine D2-like receptors are prejunctional, located on sympathetic nerve endings.
- The varied distribution of dopamine receptors suggests differential functions in the pulmonary arterial tree.
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