Trends in Cardiovascular Medicine
Volume 19, Issue 4 , Pages 111-118, May 2009

Na/K-ATPase—An Integral Player in the Adrenergic Fight-or-Flight Response

  • Donald M. Bers

      Affiliations

    • Corresponding Author InformationAddress correspondence to: Donald M. Bers, Department of Pharmacology, University of California, Davis, 1 Shields Ave, Genome Building 3511, Davis, CA 95616-8636, USA. Tel.: (+1) 530 752 6517; fax: (+1) 530 752 7710.
  • ,
  • Sanda Despa

Department of Pharmacology, University of California, Davis, CA 95616-8636, USA

During activation of the sympathetic nervous system, cardiac performance is increased as part of the fight-or-flight stress response. The increase in contractility with sympathetic stimulation is an orchestrated combination of intrinsic inotropic, lusitropic, and chronotropic effects, mediated in part by activation of β-adrenergic receptors and protein kinase A. This causes phosphorylation of several Ca cycling proteins in cardiac myocytes (increasing Ca entry via L-type Ca channels, sarcoplasmic reticulum Ca pumping, and the dissociation rate of Ca from the myofilaments). Here, we discuss how stimulation of the Na/K-ATPase, mediated by phosphorylation of phospholemman (a small sarcolemmal protein that associates with and modulates Na/K-ATPase), is an additional important player in the sympathetic fight-or-flight response. Enhancement of Na/K- ATPase activity limits the rise in [Na]i caused by the higher level of Na influx and by doing so limits the rise in cellular and sarcoplasmic reticulum Ca load by favoring Ca extrusion via the Na/Ca exchanger. Thus, phospholemman-mediated activation of the Na/K-ATPase may prevent Ca overload and triggered arrhythmias during stress.

To access this article, please choose from the options below

Login to an existing account or Register a new account.

  • Purchase this article for 31.50 USD (You must login/register to purchase this article)

    Online access for 24 hours. The PDF version can be downloaded as your permanent record.

  • Subscribe to this title

    Get unlimited online access to this article and all other articles in this title 24/7 for one year.

  • Claim access now

    For current subscribers with Society Membership or Account Number.

  • Visit SciVerse ScienceDirect to see if you have access via your institution.
 

PII: S1050-1738(09)00104-2

doi:10.1016/j.tcm.2009.07.001

Trends in Cardiovascular Medicine
Volume 19, Issue 4 , Pages 111-118, May 2009