Related Experiment Video
Updated: Feb 15, 2026

Evaluation of Right Ventricular Function in Experimental Models of Pulmonary Arterial Hypertension
Published on: June 27, 2025
Emerging therapeutics in pulmonary hypertension
Matthew K Hensley1, Andrea Levine2,3, Mark T Gladwin2,3
1Division of Pulmonary and Critical Care Medicine, University of Michigan , Ann Arbor, Michigan.
Pulmonary hypertension (PH) is a serious condition with limited treatments. This review explores new therapeutic approaches for PH, focusing on pulmonary arterial hypertension (PAH) and future research directions.
Area of Science:
- Cardiovascular Medicine
- Pulmonary Medicine
- Pharmacology
Background:
- Pulmonary hypertension (PH) is a progressive, often fatal disease characterized by elevated pulmonary pressures.
- Endothelial dysfunction drives vascular remodeling, increasing pulmonary vascular resistance.
- Current FDA-approved treatments exist for pulmonary arterial hypertension (PAH) and chronic thromboembolic PH, but morbidity and mortality remain high.
Purpose of the Study:
- To provide an updated overview of novel therapeutic strategies for PH.
- To focus on emerging treatments for PAH, the most studied form of PH.
- To offer guidelines for future research in PH therapeutics.
Main Methods:
- Review of recent scientific literature and clinical studies.
- Analysis of molecular targets mediating vasodilation, anti-inflammatory, and antifibrotic effects.
- Synthesis of current understanding of PH pathophysiology and treatment landscape.
Main Results:
- Identification of promising molecular targets for PH treatment.
- Exploration of novel therapeutic approaches beyond current standards of care.
- Highlighting the need for expanded treatment options for non-PAH groups.
Conclusions:
- Emerging research offers potential for new PH therapies targeting specific molecular pathways.
- Further investigation is crucial to develop effective treatments for all forms of PH.
- Future studies should guide the clinical translation of these novel approaches.
Related Concept Videos
Pulmonary Hypertension: Classification and Pathogenesis
There are various classifications for PH, each relating to different underlying causes and also...
Treatment for Pulmonary Arterial Hypertension: Phosphodiesterase Inhibitors
Among the PDE5 inhibitors, sildenafil (Revatio) stands out as a competitive and selective inhibitor. It operates by elevating cellular levels of cGMP and augmenting signaling through the cGMP-PKG pathway, promoting vasodilation. Upon oral...
Treatment for Pulmonary Arterial Hypertension: Endothelin Receptor Antagonists
ETs are synthesized through a complex sequence of enzymatic steps, primarily involving an enzyme referred to as endothelin-converting enzyme...
Treatment for Pulmonary Arterial Hypertension: Prostacyclin Receptor Agonists
These agonists bind to the IPR receptor situated on the plasma membrane of the pulmonary artery smooth muscle cells. This binding triggers a cascade of reactions known as the GS-AC-cAMP-PKA pathway. This pathway results in the relaxation of smooth muscle...
Treatment for Pulmonary Arterial Hypertension: Oxygen Therapy for Respiratory Failure
Oxygen therapy is vital in increasing and maintaining blood oxygen levels in PAH patients. As a result, it aids in reducing fatigue,...
Emerging Adulthood

