Current and future strategies for targeting the endothelin pathway in cardiovascular disease.
George R AbrahamThomas L WilliamsJanet J MaguirePeter J GreasleyPhilip AmberyAnthony P DavenportPublished in: Nature cardiovascular research (2023)
The first endothelin (ET)-1 receptor antagonist was approved for clinical use over 20 years ago, but to date this class of compounds has been limited to treating pulmonary arterial hypertension, a rare disease. Translational research over the last 5 years has reignited interest in the ET system as a therapeutic target across the spectrum of cardiovascular diseases including resistant hypertension, microvascular angina and post-coronavirus disease 2019 conditions. Notable developments include approval of a new ET A receptor antagonist and, intriguingly, combining the actions of ET A and an angiotensin II type 1 receptor antagonist within the same novel small molecule. Combinations of ET receptor blockers with other drugs, including phosphodiesterase-5 inhibitors and sodium-glucose co-transporter-2 antagonists, may drive synergistic benefits with the prospect of alleviating side effects. These new therapeutic strategies have the potential to dramatically widen the scope of indications targeting the ET-1 pathway.
Keyphrases
- pulmonary arterial hypertension
- angiotensin ii
- cardiovascular disease
- angiotensin converting enzyme
- small molecule
- coronavirus disease
- cancer therapy
- pulmonary artery
- pulmonary hypertension
- vascular smooth muscle cells
- current status
- blood pressure
- coronary artery
- coronary artery disease
- drug administration
- type diabetes
- cardiovascular events
- protein protein
- percutaneous coronary intervention
- drug delivery
- human health
- binding protein
- sars cov
- climate change