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Induction of Atherosclerotic Plaques Through Activation of Mineralocorticoid Receptors in Apolipoprotein E-deficient Mice
Published on: September 26, 2018
Mineralocorticoid Receptor and Endothelial Dysfunction in Hypertension
Jessica L Faulkner1, Eric J Belin de Chantemèle2
1Vascular Biology Center, Department of Medicine (Cardiology), Medical College of Georgia, Augusta University, 1460 Laney Walker Blvd., Augusta, GA, 30912, USA.
Endothelial mineralocorticoid receptors are elevated in females, contributing to endothelial dysfunction and hypertension, particularly in obesity. Targeting this pathway may offer new hypertension treatments.
Area of Science:
- Cardiovascular Research
- Endocrinology
- Vascular Biology
Background:
- Endothelial mineralocorticoid receptor (eMR) plays a role in endothelial function.
- Sex-specific differences in eMR expression and its link to dysfunction are increasingly recognized.
Purpose of the Study:
- To review recent findings on the endothelial mineralocorticoid receptor's role in endothelial dysfunction and hypertension.
- To explore the clinical potential of targeting the eMR pathway for hypertension treatment.
Main Methods:
- Review of current scientific literature on endothelial mineralocorticoid receptors.
- Analysis of sex-specific expression patterns and signaling pathways.
Main Results:
- Endothelial mineralocorticoid receptor expression is higher in females, influenced by progesterone.
- eMR deletion protects against obesity- and diabetes-associated endothelial dysfunction in female models.
- Intact eMR and progesterone receptor signaling are crucial for obesity-associated endothelial dysfunction in females.
- The signaling pathway involves alpha-epithelial sodium channels (αENaC) in endothelial cells.
Conclusions:
- Sex-specific upregulation of eMR in females, driven by progesterone, is a key mediator of endothelial dysfunction.
- This eMR pathway is implicated in hypertension, especially in obese females.
- The endothelial mineralocorticoid receptor pathway presents a potential target for novel hypertension therapies.
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