Adenosine Receptors As Drug Targets for Treatment of Pulmonary Arterial Hypertension

Pulmonary arterial hypertension (PAH) is a clinical condition characterized by pulmonary arterial remodeling and vasoconstriction, which promote chronic vessel obstruction and elevation of pulmonary vascular resistance. Long-term right ventricular (RV) overload leads to RV dysfunction and failure, w...

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Detalles Bibliográficos
Autores principales: Alencar, Allan K. N., Montes, Guilherme C., Barreiro, Eliezer J., Sudo, Roberto T., Zapata-Sudo, Gisele
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Pharmacology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5722832/
https://www.ncbi.nlm.nih.gov/pubmed/29255415
http://dx.doi.org/10.3389/fphar.2017.00858

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5722832/
https://www.ncbi.nlm.nih.gov/pubmed/29255415
http://dx.doi.org/10.3389/fphar.2017.00858

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