Na+/H+ exchanger and cardiac hypertrophy

Hipertens Riesgo Vasc. 2020 Jan-Mar;37(1):22-32. doi: 10.1016/j.hipert.2019.09.002. Epub 2019 Oct 7.

Abstract

Reactive cardiac hypertrophy (CH) is an increase in heart mass in response to hemodynamic overload. Exercise-induced CH emerges as an adaptive response with improved cardiac function, in contrast to pathological CH that represents a risk factor for cardiovascular health. The Na+/H+ exchanger (NHE-1) is a membrane transporter that not only regulates intracellular pH but also intracellular Na+ concentration. In the scenario of cardiovascular diseases, myocardial NHE-1 is activated by a variety of stimuli, such as neurohumoral factors and mechanical stress, leading to intracellular Na+ overload and activation of prohypertrophic cascades. NHE-1 hyperactivity is intimately linked to heart diseases, including ischemia-reperfusion injury, maladaptive CH and heart failure. In this review, we will present evidence to support that the NHE-1 hyperactivity constitutes a "switch on/off" for the pathological phenotype during CH development. We will also discuss some classical and novel strategies to avoid NHE-1 hyperactivity, and that are therefore worthwhile to improve cardiovascular health.

Keywords: Estiramiento; Hipertrofia; Hypertrophy; IGF-1, ejercicio; IGF-1, exercise; Intercambiador sodio/hidrógeno; Sodium hydrogen exchanger; Stretching.

Publication types

  • Review

MeSH terms

  • Animals
  • Cardiomegaly / physiopathology*
  • Cardiomegaly, Exercise-Induced / physiology
  • Cardiovascular Diseases / physiopathology
  • Heart Failure / physiopathology*
  • Humans
  • Myocardial Reperfusion Injury / physiopathology
  • Risk Factors
  • Sodium-Hydrogen Exchanger 1 / metabolism*

Substances

  • SLC9A1 protein, human
  • Sodium-Hydrogen Exchanger 1