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Transcardiac extraction of circulating endothelin-1 across the failing heart
1First Department of Internal Medicine, Shiga University of Medical Science, Seta, Otsu, Japan. tutamoto@belle.shiga-med.ac.jp
Insights
In congestive heart failure (CHF), the failing heart extracts endothelin-1 (ET-1). This extraction correlates with left ventricular remodeling, suggesting ET-1 receptor upregulation in severe CHF.
Area of Science:
- Cardiology
- Vascular Biology
- Biochemistry
Background:
- Congestive heart failure (CHF) involves complex cardiovascular changes.
- Endothelin-1 (ET-1) is a potent vasoconstrictor implicated in heart disease.
- Understanding ET-1's role in the failing heart is crucial for therapeutic development.
Purpose of the Study:
- To investigate the transcardiac gradient of plasma endothelin-1 (ET-1) in patients with congestive heart failure (CHF).
- To determine the relationship between ET-1 gradient and indicators of cardiac dysfunction and remodeling.
Main Methods:
- Plasma ET-1 levels were measured in the aortic root and coronary sinus of normal subjects and CHF patients.
- Transcardiac ET-1 gradient was calculated and correlated with clinical parameters.
- Statistical analyses, including stepwise multivariate analysis, were performed.
Main Results:
- Normal subjects and mild CHF patients showed ET-1 spillover into the coronary sinus.
- Severe CHF patients exhibited significant ET-1 extraction across the heart.
- The transcardiac ET-1 gradient correlated with left ventricular end-diastolic volume index and myocardial fibrosis markers.
Conclusions:
- Elevated circulating ET-1 is extracted by the failing heart in severe CHF.
- The transcardiac ET-1 gradient is independently associated with left ventricular remodeling.
- Upregulated ET-1 receptors in the failing ventricle may mediate ET-1's role in left ventricular remodeling.
Abstract:
To determine the transcardiac gradient of plasma endothelin-1 (ET-1) in patients with congestive heart failure (CHF), we measured plasma levels of ET-1 in both the aortic root and the coronary sinus in 14 normal subjects and 79 consecutive patients with CHF. In normal subjects, plasma ET-1 was significantly higher in the coronary sinus than in the aortic root; these findings were also shown in patients with mild CHF, suggesting that there was ET-1 spillover across the heart. In contrast, plasma ET-1 was significantly lower in the coronary sinus than in the aortic root in patients with severe CHF, suggesting there was ET-1 extraction across the heart in patients with severe CHF. The transcardiac gradient of plasma ET-1 was correlated with the left ventricular end-diastolic volume index (r = 0.501, p <0.0001) and plasma level of procollagen type III amino terminal peptide in the coronary sinus (r = 0.54, p = 0.0008), a marker of myocardial fibrosis. Stepwise multivariate analysis showed that the transcardiac gradient of plasma ET-1 was an independent and significant relation with the left ventricular end-diastolic volume index in patients with CHF (r = 0.665, p <0.0001). These findings suggest that elevated circulating ET-1 is extracted across the failing heart with a significant correlation between the transcardiac gradient of plasma ET-1 and the left ventricular end-diastolic volume index, suggesting that ET receptors are upregulated in the failing ventricle and that the elevated circulating ET-1 might stimulate the process of left ventricular remodeling in patients with severe CHF.
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