Skip to main content

Advertisement

Log in

Regulation of myocardial Na+/H+ exchanger activity

  • Focussed issue: Na+/H+-exchange
  • Published:
Basic Research in Cardiology Aims and scope Submit manuscript

Abstract

The Na+/H+ exchanger is a plasma membrane protein, present in the myocardium, which removes intracellular protons and exchanges them with extracellular Na+. The protein comprises an N-terminal, hydrophobic, integral membrane domain that transports the ions and a C-terminal, hydrophilic region that regulates the N-terminal domain. The C-terminal domain has several sub-domains, including one region that binds calmodulin and another that is phosphorylated by protein kinases. The Na+/H+ exchanger is activated by angiotensin, endothelin and α1-adrenergic stimulation. These effectors increase phosphorylation of the C-terminal domain by protein kinases, and G proteins have been implicated in this, but their role remains to be defined. It has recently been shown that ischemia and other stimuli lead to an increased expression of the Na+/H+ exchanger in the myocardium. The role of this increased expression in the pathology of ischemia and reperfusion-mediated myocardial damage has yet to be determined. Recent evidence suggests that the Na+/H+ exchanger may play a key role in hypertrophy of the myocardium, and that its activation through G protein-coupled receptors may be important in mediating its effects.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

Author information

Authors and Affiliations

Authors

Additional information

Received: 23 April 2001 / Accepted: 14 May 2001

Rights and permissions

Reprints and permissions

About this article

Cite this article

Fliegel, L. Regulation of myocardial Na+/H+ exchanger activity. Basic Res Cardiol 96, 301–305 (2001). https://doi.org/10.1007/s003950170036

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1007/s003950170036

Navigation