P2X7 purinergic receptor: A potential target in heart diseases (Review)
Anfal F Bin Dayel1, Asma S Alonazi1, Tahani K Alshammari1
1Department of Pharmacology and Toxicology, College of Pharmacy, King Saud University, 12371 Riyadh, Kingdom of Saudi Arabia.
Abstract:
The P2X7 purinergic receptor (P2X7R) is a non‑selective cation channel activated by high levels of adenosine triphosphate that are commonly present in serious conditions. Activation of this purinergic receptor is closely related to the development of various disease states including inflammatory and neurodegenerative disorders, orthopedic diseases and types of cancer. Accumulating evidence has shown that the P2X7R plays a crucial role in the development of various heart diseases. For example, activation of P2X7Rs may alleviate myocardial ischemia‑reperfusion injury by releasing endogenous cardiac protective substances. In contrast to these findings, activation of P2X7Rs can promote the development of acute myocardial infarction and myocarditis by inducing inflammatory responses. Activation of these receptors can also contribute to the development of different types of cardiomyopathies including diabetic cardiomyopathy, dilated cardiomyopathy and hypertrophic cardiomyopathy by inducing cardiac hypertrophy, fibrosis and apoptosis. Notably, inhibition of P2X7Rs can improve cardiac structure and function abnormalities following acute myocardial infarction, reduction of inflammatory responses following myocarditis and attenuation of the cardiomyopathy process. Furthermore, recent evidence has demonstrated that P2X7Rs are highly active in patients infected with coronavirus disease‑2019 (COVID‑19). Hyperactivation of P2X7Rs in COVID‑19 may induce severe myocardial injury through the activation of several signaling pathways. The present study reviewed the important role of the P2X7R in cardiac dysfunctions and discusses its use as a possible new therapeutic approach for the prevention and treatment of several myocardial diseases.
Insights
The P2X7 purinergic receptor (P2X7R) is implicated in heart diseases. Inhibiting P2X7R shows therapeutic potential for conditions like myocardial infarction, myocarditis, and COVID-19-related heart injury.
Area of Science:
- Cardiology
- Molecular Biology
- Pathology
Background:
- The P2X7 purinergic receptor (P2X7R) is a cation channel activated by extracellular ATP.
- P2X7R activation is linked to inflammatory, neurodegenerative, orthopedic diseases, and cancer.
- Evidence suggests P2X7R plays a significant role in various heart conditions.
Purpose of the Study:
- To review the role of P2X7R in cardiac dysfunction.
- To discuss P2X7R as a potential therapeutic target for myocardial diseases.
Main Methods:
- Literature review of studies investigating P2X7R in cardiovascular diseases.
- Analysis of P2X7R involvement in myocardial ischemia-reperfusion injury, infarction, myocarditis, and cardiomyopathies.
- Examination of P2X7R activity in COVID-19 patients and its impact on myocardial injury.
Main Results:
- P2X7R activation can be protective (alleviating ischemia-reperfusion injury) or detrimental (promoting myocardial infarction and myocarditis).
- P2X7R contributes to cardiomyopathies (diabetic, dilated, hypertrophic) by inducing hypertrophy, fibrosis, and apoptosis.
- P2X7R inhibition improves cardiac function post-infarction and reduces inflammation in myocarditis.
- Hyperactivated P2X7R in COVID-19 may cause severe myocardial injury via specific signaling pathways.
Conclusions:
- P2X7R has a complex, dual role in heart diseases.
- Targeting P2X7R inhibition offers a promising therapeutic strategy for managing diverse myocardial pathologies.
- Further research into P2X7R modulation is warranted for cardiovascular disease treatment.
More Related Videos
16:36Proteomics to Identify Proteins Interacting with P2X2 Ligand-Gated Cation Channels
Published on: May 18, 2009
05:41Left Anterior Descending Coronary Artery Ligation for Ischemia-Reperfusion Research: Model Improvement via Technical Modifications and Quality Control
Published on: December 16, 2022
Related Concept Videos
Transducer Mechanism: Enzyme-Linked Receptors
Major types that are helpful drug targets include:
G-Protein Gated Ion Channels
Sensory...
Coronary Artery Disease II: Pathophysiology
Heart Failure Drugs: Inhibitors of Renin-Angiotensin System
Treatment for Pulmonary Arterial Hypertension: Receptor Tyrosine Kinase Inhibitors and Calcium Channel Blockers
TKIs, such as imatinib (Gleevec), are particularly effective in tackling the growth and mitogenic factors that become upregulated in PAH patients. These factors contribute to the...
Heart Failure II: Pathophysiology
