Key result
Immune cell mineralocorticoid receptor activation drives vascular inflammation and atherosclerosis, highlighting a novel MRA target.
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Review reveals that mineralocorticoid receptor activation in immune cells drives cardiovascular inflammation, highlighting receptor antagonists as promising therapies.
Chronic low-grade inflammation and immune cell activation are important mechanisms in the pathophysiology of cardiovascular disease (CVD). Therefore, targeted immunosuppression is a promising novel therapy to reduce cardiovascular risk. In this review, we identify the mineralocorticoid receptor (MR) on immune cells as a potential target to modulate inflammation. The MR is present in almost all cells of the cardiovascular system, including immune cells. Activation of the MRs in innate and adaptive immune cells induces inflammation which can contribute to CVD, by inducing endothelial dysfunction and hypertension. Moreover, it accelerates atherosclerotic plaque formation and destabilization and impairs tissue regeneration after ischaemic events. Identifying the molecular targets for these non-renal actions of the MR provides promising novel cardiovascular drug targets for mineralocorticoid receptor antagonists (MRAs), which are currently mainly applied in hypertension and heart failure. LINKED ARTICLES: This article is part of a themed issue on Emerging Fields for Therapeutic Targeting of the Aldosterone-Mineralocorticoid Receptor Signaling Pathway. To view the other articles in this section visit http://onlinelibrary.wiley.com/doi/10.1111/bph.v179.13/issuetoc.
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Heijden et al. (2021) conducted a review in Cardiovascular disease. Mineralocorticoid receptor antagonists (MRAs) was evaluated. Mineralocorticoid receptor activation on immune cells induces inflammation, endothelial dysfunction, hypertension, and atherosclerosis, making it a promising novel drug target for MRAs in CVD.
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