| Literature DB >> 31384108 |
Sanjay Tyagi1,2, Vishal Batra2.
Abstract
Pulmonary arterial hypertension (PAH) is an uncommon disease characterized progressive remodeling of pulmonary vasculature. Although treatment for PAH have improved in last two decades but the outcome remains fatal. Currently, the therapies for PAH target three well-established pathways the nitric oxide (NO) pathway, endothelin receptors, and prostanoids. There are multiple potential targets for development of newer drugs in PAH which requires meticulous research and clinical trials.Entities:
Keywords: endothelin receptor; nitric oxide; novel; phosphodiesterase; prostaglandins; pulmonary arterial hypertension; therapeutic
Year: 2019 PMID: 31384108 PMCID: PMC6679998 DOI: 10.1055/s-0039-1692140
Source DB: PubMed Journal: Int J Angiol ISSN: 1061-1711