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- W2016671134 abstract "The mineralocorticoid receptor (MR), a steroid-hormone-activated transcription factor, plays a substantial role in cardiovascular diseases. MR antagonists (MRAs) have long been appreciated as effective treatments for heart failure and hypertension; however, recent research suggests that additional patient populations may also benefit from MRA therapy. Experimental evidence demonstrates that in addition to its classic role in the regulating sodium handling in the kidney, functional MR is expressed in the blood vessels and contributes to hypertension, vascular inflammation and remodeling, and atherogenesis. MR activation drives pathological phenotypes in smooth muscle cells, endothelial cells, and inflammatory cells, whereas MRAs inhibit these effects. Collectively, these studies demonstrate a new role for extrarenal MR in cardiovascular disease. This review summarizes these new lines of evidence and how they contribute to the mechanisms of atherosclerosis, pulmonary and systemic hypertension, and vein graft failure, and describes new patient populations that may benefit from MRA therapy." @default.
- W2016671134 created "2016-06-24" @default.
- W2016671134 creator A5010237095 @default.
- W2016671134 creator A5015102832 @default.
- W2016671134 creator A5019926661 @default.
- W2016671134 creator A5052354859 @default.
- W2016671134 date "2013-05-30" @default.
- W2016671134 modified "2023-10-16" @default.
- W2016671134 title "Mineralocorticoid Receptors in Vascular Disease: Connecting Molecular Pathways to Clinical Implications" @default.
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- W2016671134 doi "https://doi.org/10.1007/s11883-013-0340-x" @default.
- W2016671134 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/4264110" @default.
- W2016671134 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/23719923" @default.