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Role of Neurohormonal Modulators in Reducing Adverse Outcomes in Patients with Ischemic Heart Disease
Arjun Talukdar1, Prasanti Sharma1, Sayak Khawas1
1Department of Pharmaceutical Sciences and Technology, Birla Institute of Technology, Mesra, Ranchi, Jharkhand, India.
Insights
Neurohormonal modulators, including ACE inhibitors and ARNIs, effectively manage ischemic heart disease (IHD) by targeting the renin-angiotensin-aldosterone system (RAAS) and sympathetic nervous system (SNS). These treatments improve cardiac function and survival rates in IHD patients.
Area of Science:
- Cardiology
- Pharmacology
- Internal Medicine
Background:
- Ischemic heart disease (IHD) progression is driven by maladaptive activation of the renin-angiotensin-aldosterone system (RAAS) and sympathetic nervous system (SNS).
- Neurohormonal modulators are crucial for mitigating adverse outcomes in IHD by targeting these overactive systems.
Purpose of the Study:
- To critically review conventional and emerging neurohormonal modulators used in managing ischemic heart disease (IHD).
- To evaluate the mechanisms, benefits, limitations, and future directions of these therapeutic agents.
Main Methods:
- This narrative review synthesizes current literature on neurohormonal modulators for IHD.
- Key drug classes discussed include ACE inhibitors, ARBs, beta-blockers, MRAs, ARNIs, and SGLT2 inhibitors.
Main Results:
- ACE inhibitors and ARBs reduce RAAS-mediated injury; beta-blockers attenuate SNS overactivation.
- MRAs and ARNIs target aldosterone and natriuretic peptides, respectively, to combat fibrosis and remodeling.
- SGLT2 inhibitors offer additional benefits by improving metabolic efficiency and hemodynamic stability.
Conclusions:
- Neurohormonal modulators significantly improve cardiac function, reduce hospitalizations, and enhance survival in IHD patients.
- These agents have complementary mechanisms and are central to contemporary IHD management, improving quality of life.
- Further research into their limitations and future therapeutic applications is warranted.
Abstract:
Neurohormonal modulators mitigate adverse outcomes in ischemic heart disease (IHD) by targeting maladaptive activation of the renin-angiotensin-aldosterone system (RAAS) and sympathetic nervous system (SNS), both of which contribute to disease progression. This narrative review summarizes and critically evaluates conventional and emerging neurohormonal modulators in IHD management. Angiotensin-converting enzyme (ACE) inhibitors, angiotensin II receptor blockers (ARBs), beta-blockers, mineralocorticoid receptor antagonists (MRAs), and angiotensin receptor-neprilysin inhibitors (ARNIs) counteract vasoconstriction, inflammation, fibrosis, and adverse ventricular remodelling. ACE inhibitors and ARBs reduce RAAS-mediated injury, while beta-blockers limit myocardial oxygen demand and arrhythmia risk by attenuating SNS overactivation. MRAs block aldosterone-mediated sodium retention and myocardial fibrosis, whereas ARNIs enhance natriuretic peptide signaling to mitigate fluid overload and structural remodeling. In addition, sodium- glucose cotransporter-2 (SGLT2) inhibitors improve metabolic efficiency and hemodynamic stability, extending the benefits of neurohormonal modulation beyond traditional pathways. Collectively, these agents improve cardiac function, reduce hospitalizations, and enhance survival, as demonstrated in clinical trials. This review highlights their complementary mechanisms, current limitations, and future therapeutic directions, underscoring their central role in contemporary IHD management and in improving quality of life.
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