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The Potential Therapeutic Role of Celastrol in Patients With Heart Failure With Preserved Ejection Fraction
Maryam Ajmal1, Aisha Ajmal2, Lei Huang3,4
1GKT School of Medical Education, Faculty of Life Science and Medicine, King's College London, London, United Kingdom.
Insights
Celastrol, an anti-inflammatory compound, shows promise for treating heart failure with preserved ejection fraction (HFpEF). Its antioxidant properties may target key pathways involved in HFpEF development and progression.
Area of Science:
- Cardiology
- Pharmacology
- Molecular Biology
Background:
- Heart failure with preserved ejection fraction (HFpEF) affects over 50% of heart failure patients.
- Pathophysiology of HFpEF is poorly understood, with limited effective therapies.
- Pro-inflammatory and oxidative stress pathways, including Unfolded Protein Response (UPR), are implicated in HFpEF.
Purpose of the Study:
- To review the anti-inflammatory and antioxidant potential of Celastrol.
- To evaluate Celastrol's ability to impede HFpEF-associated pathways.
- To elucidate Celastrol's therapeutic role in treating HFpEF.
Main Methods:
- Literature review of Celastrol's properties and effects.
- Analysis of Celastrol's impact on inflammatory and oxidative stress pathways.
- Investigation of Celastrol's influence on pathways like JAK2/STAT.
Main Results:
- Celastrol exhibits potent anti-inflammatory and antioxidant activities.
- Celastrol may counteract dysregulated Unfolded Protein Response (UPR).
- Celastrol demonstrates potential to inhibit key pathways in HFpEF pathogenesis.
Conclusions:
- Celastrol presents a promising therapeutic candidate for HFpEF.
- Targeting inflammatory and oxidative stress pathways with Celastrol warrants further investigation.
- Celastrol's multifaceted actions offer a novel approach to HFpEF treatment.
Abstract:
Analysis of left ventricular systolic dysfunction remained at the centre of heart failure research for many years (also known as heart failure with reduced ejection fraction, HFrEF). Although more than 50% of all heart failure patients experience a form of heart failure characterised by preserved ejection fraction (HFpEF), the pathophysiological mechanisms leading to this form of heart failure remain not well-understood. Several evidence-based treatments for HFrEF are in routine use, but there are limited evidence-based therapies for HFpEF. The effects of these remain controversial, with current treatment options being limited to managing the associated symptoms and conditions. Accumulating evidence demonstrates that pro-inflammatory and oxidative stress pathways play key roles in the development and progression of HFpEF, such as the Unfolded Protein Response (UPR) and inducible nitric oxide synthase. Celastrol, derived from medicinal plants, is a bioactive compound with strong anti-inflammatory properties, which could deem it as fruitful in overcoming the effects of such dysregulated UPR. This literature review therefore focuses on Celastrol's anti-inflammatory and antioxidant activities, alongside its other potential therapeutic activities, and its ability to impede the pathways that are thought to be involved in the development of HFpEF, such as the JAK2/STAT pathway, to elucidate the potential therapeutic role of this bioactive compound, in the treatment of HFpEF.
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