Related Experiment Video
Updated: Jun 23, 2025

Induction of Atherosclerotic Plaques Through Activation of Mineralocorticoid Receptors in Apolipoprotein E-deficient Mice
Published on: September 26, 2018
Interplay between caveolin-1 and mineralocorticoid receptor in cardiometabolic disease
Katarzyna Czarzasta1, Luminita H Pojoga2
1Department of Experimental and Clinical Physiology, Laboratory of Center for Preclinical Research, Medical University of Warsaw, Warszawa, Poland.
Abstract:
Over the past decades, research has clearly established the important role of the mineralocorticoid receptor (MR) in both renal and extra-renal tissues. Recently, caveolin-1 (Cav-1) has emerged as a mediator of MR signaling in several tissues, with implications on cardiovascular and metabolic dysfunction. The main structural component of caveolae (plasma membrane invaginations with diverse functions), Cav-1 is a modulator of cardiovascular function, cellular glucose, and lipid homeostasis, via its effects on signal transduction pathways that mediate inflammatory responses and oxidative stress. In this review, we present evidence indicating an overlap between the roles of the MR and Cav-1 in cardiometabolic disease and the relevant signaling pathways involved. Furthermore, we discuss the potential use of Cav-1 as a biomarker and/or target for MR-mediated dysfunction.
Insights
Mineralocorticoid receptor (MR) and caveolin-1 (Cav-1) play key roles in cardiometabolic diseases. This review explores their overlapping functions and potential as therapeutic targets.
Area of Science:
- Cardiovascular biology
- Metabolic signaling
- Molecular medicine
Background:
- The mineralocorticoid receptor (MR) is crucial in renal and extra-renal tissues.
- Caveolin-1 (Cav-1), a structural protein of caveolae, influences cardiovascular function and metabolic homeostasis.
- MR and Cav-1 signaling pathways are implicated in cardiovascular and metabolic dysfunction.
Purpose of the Study:
- To review the overlapping roles of MR and Cav-1 in cardiometabolic diseases.
- To elucidate the signaling pathways involved in MR- and Cav-1-mediated effects.
- To discuss the potential of Cav-1 as a biomarker or therapeutic target for MR dysfunction.
Main Methods:
- Literature review of studies on MR and Cav-1 in cardiometabolic disease.
- Analysis of signaling pathways linking MR and Cav-1.
- Synthesis of evidence on the clinical implications of their interaction.
Main Results:
- Evidence suggests significant overlap in the functions of MR and Cav-1 in cardiometabolic disease.
- Both MR and Cav-1 modulate inflammatory responses and oxidative stress.
- Cav-1 influences cellular glucose and lipid homeostasis.
Conclusions:
- MR and Cav-1 signaling pathways are interconnected in the pathogenesis of cardiometabolic diseases.
- Cav-1 represents a potential biomarker and therapeutic target for conditions involving MR dysfunction.
- Further research is warranted to explore therapeutic strategies targeting Cav-1 in MR-mediated diseases.
More Related Videos
11:00Assessment of Sarcoplasmic Reticulum Calcium Reserve and Intracellular Diastolic Calcium Removal in Isolated Ventricular Cardiomyocytes
Published on: September 18, 2017
10:51Reverse Yeast Two-hybrid System to Identify Mammalian Nuclear Receptor Residues that Interact with Ligands and/or Antagonists
Published on: November 15, 2013
Related Concept Videos
Heart Failure Drugs: Inhibitors of Renin-Angiotensin System
Target Cell Response to Hormones
Notably, the cellular response can be regulated by altering the number of receptors expressed in the cell. For example, prolonged exposure to elevated hormone levels results in a gradual decline or down-regulation in the number of receptors for that specific hormone on the cell surface. Conversely, in response to low hormone levels, cells may use up-regulation, producing an...
Transducer Mechanism: Nuclear Receptors
About 48 different soluble family members of nuclear receptors are identified that can be divided into two main classes:
Antianginal Drugs: Calcium Channel Blockers and Ranolazine
CCBs, a diverse class that includes dihydropyridines (nifedipine) and diphenylalkylamines (verapamil and diltiazem), exert their effect by blocking calcium channels in cardiac and smooth muscle cells. This...
Calmodulin-dependent Signaling
The Ca2+-CaM complex does not have enzymatic activity by itself. Instead, the complex binds downstream target proteins, including membrane proteins or enzymes,...
Receptor Downregulation in MVBs
The EGFR can initiate signaling pathways that lead to cell proliferation, migration, and differentiation. Overexpression of EGFR stimulates cells to proliferate. Excessive EGFR...