Detailseite
Projekt Druckansicht

Vaskuläres Anti- und Reverse-Remodelling bei pharmakologischer Aktivierung der löslichen Guanylatzyklase bei pulmonaler Hypertonie

Fachliche Zuordnung Pneumologie,Thoraxchirurgie
Förderung Förderung von 2010 bis 2014
Projektkennung Deutsche Forschungsgemeinschaft (DFG) - Projektnummer 165239704
 
Erstellungsjahr 2014

Zusammenfassung der Projektergebnisse

Impaired nitric oxide (NO) bioavailability, soluble guanylate cyclase (sGC) activity and cGMP production have been implicated in the pathogenesis of pulmonary hypertension (PH). The focus of this project was centered on the role of sGC in pulmonary vascular remodeling and the development of therapeutic strategies focusing on pharmacological sGC activation. Within the project, we performed preclinical studies addressing the role of the sGC-signaling pathway in PH. We have demonstrated the localization of the sGC-subunits in healthy and hypertensive lungs. In several animal models of PH, we demonstrated the effects of sGC stimulators on hemodynamics, pulmonary vascular and RV remodeling. Further, we locally delivered a sGC stimulator to the lung and demonstrated regression of PH. Early clinical trials addressing safety and efficacy of the sGC stimulator riociguat in patients with pulmonary arterial hypertension (PAH) and non-operable chronic thromboembolic pulmonary hypertension (CTEPH) were followed by two phase 3 trials in PAH and CTEPH. These randomized controlled trials demonstrated efficacy of this compound in both PH forms and led to the approval of riociguat for the treatment of PAH and CTEPH.

Projektbezogene Publikationen (Auswahl)

 
 

Zusatzinformationen

Textvergrößerung und Kontrastanpassung