Mineralocorticoid receptor antagonists and the metabolic syndrome

Curr Hypertens Rep. 2010 Aug;12(4):252-7. doi: 10.1007/s11906-010-0126-2.

Abstract

Key components of the metabolic syndrome (MetS), ie, obesity and insulin resistance, are associated with increased aldosterone production and mineralocorticoid receptor (MR) activation. Both MetS and hyperaldosteronism are proinflammatory and pro-oxidative states associated with cardiovascular disease. This review discusses emerging data that MR activation may contribute to abnormalities seen in MetS. In view of these data, MR antagonists may be beneficial in MetS, not only by controlling hypertension but also by reversing inflammation, oxidative stress, and defective insulin signaling at the cellular-molecular level. Clinical trials have demonstrated benefits of MR antagonists in heart failure, hypertension, and diabetic nephropathy, but additional trials are needed to demonstrate the clinical significance of MR blockade in MetS.

Publication types

  • Research Support, N.I.H., Extramural
  • Review

MeSH terms

  • Aldosterone*
  • Antihypertensive Agents / therapeutic use*
  • Eplerenone
  • Humans
  • Hypertension / drug therapy*
  • Hypertension / physiopathology
  • Inflammation / physiopathology
  • Insulin Resistance
  • Lipid Metabolism
  • Lipids
  • Metabolic Syndrome / drug therapy*
  • Metabolic Syndrome / physiopathology
  • Mineralocorticoid Receptor Antagonists* / therapeutic use
  • Obesity / physiopathology*
  • Signal Transduction / drug effects
  • Spironolactone / analogs & derivatives
  • Spironolactone / therapeutic use

Substances

  • Antihypertensive Agents
  • Lipids
  • Mineralocorticoid Receptor Antagonists
  • Spironolactone
  • Aldosterone
  • Eplerenone