» Articles » PMID: 34867394

Therapy for Pulmonary Arterial Hypertension: Glance on Nitric Oxide Pathway

Overview
Journal Front Pharmacol
Date 2021 Dec 6
PMID 34867394
Citations 8
Authors
Affiliations
Soon will be listed here.
Abstract

Pulmonary arterial hypertension (PAH) is a severe disease with a resultant increase of the mean pulmonary arterial pressure, right ventricular hypertrophy and eventual death. Research in recent years has produced various therapeutic options for its clinical management but the high mortality even under treatment remains a big challenge attributed to the complex pathophysiology. Studies from clinical and non-clinical experiments have revealed that the nitric oxide (NO) pathway is one of the key pathways underlying the pathophysiology of PAH. Many of the essential drugs used in the management of PAH act on this pathway highlighting its significant role in PAH. Meanwhile, several novel compounds targeting on NO pathway exhibits great potential to become future therapy medications. Furthermore, the NO pathway is found to interact with other crucial pathways. Understanding such interactions could be helpful in the discovery of new drug that provide better clinical outcomes.

Citing Articles

Endothelial Function in Pulmonary Arterial Hypertension: From Bench to Bedside.

Correale M, Chirivi F, Bevere E, Tricarico L, DAlto M, Badagliacca R J Clin Med. 2024; 13(8).

PMID: 38673717 PMC: 11051060. DOI: 10.3390/jcm13082444.


An Unusual Etiology of Severe Right Heart Failure Deserving of Wider Recognition.

Kang W, Zong Y, Patel D, Mishra T, Afonso L JACC Case Rep. 2024; 29(5):102222.

PMID: 38464798 PMC: 10920146. DOI: 10.1016/j.jaccas.2024.102222.


Nitric Oxide Prevents Glioblastoma Stem Cells' Expansion and Induces Temozolomide Sensitization.

Salvatori L, Malatesta S, Illi B, Somma M, Fionda C, Stabile H Int J Mol Sci. 2023; 24(14).

PMID: 37511047 PMC: 10379318. DOI: 10.3390/ijms241411286.


Pharmacotherapy for Pulmonary Hypertension in Infants with Bronchopulmonary Dysplasia: Past, Present, and Future.

Fike C, Aschner J Pharmaceuticals (Basel). 2023; 16(4).

PMID: 37111262 PMC: 10141152. DOI: 10.3390/ph16040503.


Role of ryanodine receptor 2 and FK506-binding protein 12.6 dissociation in pulmonary hypertension.

Wang Y, Reyes-Garcia J, Di Mise A, Zheng Y J Gen Physiol. 2023; 155(3.

PMID: 36625865 PMC: 9836826. DOI: 10.1085/jgp.202213100.


References
1.
Vane J, Corin R . Prostacyclin: a vascular mediator. Eur J Vasc Endovasc Surg. 2003; 26(6):571-8. DOI: 10.1016/s1078-5884(03)00385-x. View

2.
Cogolludo A, Perez-Vizcaino F, Ibarra M, Lopez-Lopez G, Lopez-Miranda V, Tamargo J . Mechanisms involved in SNP-induced relaxation and [Ca+]i reduction in piglet pulmonary and systemic arteries. Br J Pharmacol. 2001; 132(4):959-67. PMC: 1572630. DOI: 10.1038/sj.bjp.0703894. View

3.
Chandra S, Razavi H, Kim J, Agrawal R, Kundu R, De Jesus Perez V . Disruption of the apelin-APJ system worsens hypoxia-induced pulmonary hypertension. Arterioscler Thromb Vasc Biol. 2011; 31(4):814-20. PMC: 3113525. DOI: 10.1161/ATVBAHA.110.219980. View

4.
Rubin L, Badesch D, Fleming T, Galie N, Simonneau G, Ghofrani H . Long-term treatment with sildenafil citrate in pulmonary arterial hypertension: the SUPER-2 study. Chest. 2011; 140(5):1274-1283. DOI: 10.1378/chest.10-0969. View

5.
Rosenkranz S . Pulmonary hypertension 2015: current definitions, terminology, and novel treatment options. Clin Res Cardiol. 2014; 104(3):197-207. DOI: 10.1007/s00392-014-0765-4. View