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Updated: Dec 29, 2025

Assessment of Vascular Function in Patients With Chronic Kidney Disease
Published on: June 16, 2014
The Role of Endothelin and Endothelin Antagonists in Chronic Kidney Disease
Rupesh Raina1,2, Abigail Chauvin3, Ronith Chakraborty1
1Department of Nephrology, Cleveland Clinic Akron General/Akron Nephrology Associates, Akron, Ohio, USA.
Insights
Endothelin receptor antagonists (ERAs) show promise in treating chronic kidney disease (CKD) by reducing proteinuria and slowing disease progression. Further clinical trials are needed to confirm their therapeutic benefits in various kidney conditions.
Area of Science:
- Nephrology
- Cardiovascular Medicine
- Endocrinology
Background:
- Endothelins (ET) are potent vasoconstrictors and pro-fibrotic factors.
- ET-1 plays a critical role in renal and cardiovascular pathophysiology.
- ET-1 regulates renal perfusion, arteriole tone, and hemodynamics.
Purpose of the Study:
- To review the pathophysiology of ET-1 in chronic kidney disease (CKD).
- To discuss the role of ET and endothelin receptor antagonists (ERAs) in CKD management.
Main Methods:
- Review of existing literature on ET-1 and ERAs in CKD.
- Analysis of clinical trial data and observational studies.
Main Results:
- ERAs demonstrate potential in reducing proteinuria in hypertensive and diabetic nephropathy.
- ERAs may help restore glycocalyx thickness and slow tissue damage in FSGS.
- ET-1 is a potential biomarker for autosomal dominant polycystic kidney disease progression.
Conclusions:
- ERAs have shown utility in reducing blood pressure, proteinuria, and arterial stiffness in CKD.
- ERAs offer therapeutic promise for various CKD subtypes, including FSGS and ADPKD.
- Further clinical trials are essential to validate the efficacy and safety of ERAs in CKD.
Background:
Endothelins (ET) are a family of peptides that act as potent vasoconstrictors and pro-fibrotic growth factors. ET-1 is integral to renal and cardiovascular pathophysiology and exerts effects via autocrine, paracrine and endocrine signaling pathways tied to regulation of aldosterone, catecholamines, and angiotensin. In the kidney, ET-1 is critical to maintaining renal perfusion and controls glomerular arteriole tone and hemodynamics. It is hypothesized that ET-1 influences the progression of chronic kidney disease (CKD), and the objective of this review is to discuss the pathophysiology, and role of ET and endothelin receptor antagonists (ERAs) in CKD.
Summary:
The use of ERAs in hypertensive nephropathy has the potential to decrease proteinuria, and in diabetic nephropathy has the potential to restore glycocalyx thickness, also decreasing proteinuria. Focal segmental glomerular sclerosis has no specific Food and Drug Administration-approved therapy currently, however, ERAs show promise in decreasing proteinuria and slowing tissue damage. ET-1 is a potential biomarker for autosomal dominant polycystic kidney disease progression and so it is thought that ERAs may be of some therapeutic benefit.
Key Messages:
Multiple studies have shown the utility of ERAs in CKD. These agents have shown to reduce blood pressure, proteinuria, and arterial stiffness. However, more clinical trials are needed, and the results of active or recently concluded studies are eagerly awaited.
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