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Phosphodiesterase-5 Inhibitors As Therapeutics for Cardiovascular Diseases: A Brief Review

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Date 2023 Jul 24
PMID 37484720
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Abstract

Background: Three selective and most used inhibitors of PDE-5-sildenafil, vardenafil and tadalafil- have been successfully used for the treatment of erectile dysfunction. Erectile dysfunction and cardiovascular diseases might be considered as two dissimilar clinical signs of the identical systemic disease. PDE-5 inhibitors can through different models and mechanisms induce vasodilation, decrease apoptosis and cell proliferation, and they are widely present in various tissues that make them promising targets in a range of cardiovascular diseases.

Methods: PubMed was explored to identify papers published from 1990-2019, presenting data for the most used PDE-5 inhibitors (sildenafil, tadalafil or vardenafil) in treatment of cardiovascular diseases.

Results: This article analyses the therapeutic potentials of PDE-5 inhibitors in cardiovascular diseases and discusses mechanisms, possible risks and limitations. Comparable to earlier studies, newer studies suggest cardioprotective effects of PDE-5 inhibitors, which include different models and mechanisms and do not indicate an increased rate of significant cardiovascular adverse reactions. Dissimilarity in the pharmacokinetics and pharmacodynamics of PDE-5 inhibitors are significant to their risk- benefit profile and clinical use. Some of the studies suggesting infarct size reduction after PDE-5 inhibition described the especially close dose-effect relation, other studies dosage adaptation in drug- drug interactions.

Conclusion: PDE-5 inhibitors indicate the encouraging useful effects by ischemia/reperfusion injury, myocar-dial infarction, cardiac hypertrophy, cardiomyopathy and systolic and diastolic congestive heart failure. Therefore, this and similar reviews can help for additional clinical targeting in the therapy of cardiovascular diseases.

References
1.
Nagy O, Hajnal A, Parratt J, Vegh A . Sildenafil (Viagra) reduces arrhythmia severity during ischaemia 24 h after oral administration in dogs. Br J Pharmacol. 2004; 141(4):549-51. PMC: 1574240. DOI: 10.1038/sj.bjp.0705658. View

2.
Seo K, Rainer P, Lee D, Hao S, Bedja D, Birnbaumer L . Hyperactive adverse mechanical stress responses in dystrophic heart are coupled to transient receptor potential canonical 6 and blocked by cGMP-protein kinase G modulation. Circ Res. 2014; 114(5):823-32. PMC: 3963144. DOI: 10.1161/CIRCRESAHA.114.302614. View

3.
McAlindon E, Bucciarelli-Ducci C, Suleiman M, Baumbach A . Infarct size reduction in acute myocardial infarction. Heart. 2014; 101(2):155-60. DOI: 10.1136/heartjnl-2013-304289. View

4.
Chiang C, Luk H, Wang T, Ding P . Effects of sildenafil on cardiac repolarization. Cardiovasc Res. 2002; 55(2):290-9. DOI: 10.1016/s0008-6363(02)00438-8. View

5.
Salloum F, Yin C, Xi L, Kukreja R . Sildenafil induces delayed preconditioning through inducible nitric oxide synthase-dependent pathway in mouse heart. Circ Res. 2003; 92(6):595-7. DOI: 10.1161/01.RES.0000066853.09821.98. View