Overexpression of the cardiac β2-adrenergic receptor and expression of a β-adrenergic receptor kinase-1 (βARK1) inhibitor both increase myocardial contractility but have differential effects on susceptibility to ischemic injury

Heather R. Cross, Charles Steenbergen, Robert J. Lefkowitz, Walter J. Koch, Elizabeth Murphy

Research output: Contribution to journalArticlepeer-review

Abstract

Cardiac β2-adrenergic receptor (β2AR) overexpression is a potential contractile therapy for heart failure. Cardiac contractility was elevated in mice overexpressing β2ARs (TG4s) with no adverse effects under normal conditions. To assess the consequences of β2AR overexpression during ischemia, perfused hearts from TG4 and wild-type mice were subjected to 20- minute ischemia and 40-minute reperfusion. During ischemia, ATP and pH fell lower in TG4 hearts than wild type. Ischemic injury was greater in TG4 hearts, as indicated by lower postischemic recoveries of contractile function, ATP, and phosphocreatine. Because β2ARs, unlike β1ARs, couple to G(i) as well as G(s), we pretreated mice with the G(i) inhibitor pertussis toxin (PTX). PTX treatment increased basal contractility in TG4 hearts and abolished the contractile resistance to isoproterenol. During ischemia, ATP fell lower in TG4+PTX than in TD4 hearts. Recoveries of contractile function and ATP were lower in TG4+PTX than in TG4 hearts. We also studied mice that overexpressed either βARK1 (TGβARK1) or a βARK1 inhibitor (TGβARKct). Recoveries of function, ATP, and phosphocreatine were higher in TGβARK1 hearts than in wild-type hearts. Despite basal contractility being elevated in TGβARKct hearts to the same level as that of TG4s, ischemic injury was not increased. In summary, β2AR overexpression increased ischemic injury, whereas βARK1 overexpression was protective. Ischemic injury in the β2AR overexpressors was exacerbated by PTX treatment, implying that it was G(s) not G(i) activity that enhanced injury. Unlike β2AR overexpression, basal contractility was increased by βARK1 inhibitor expression without increasing ischemic injury, thus implicating a safer potential therapy for heart failure.

Original languageEnglish (US)
Pages (from-to)1077-1084
Number of pages8
JournalCirculation research
Volume85
Issue number11
DOIs
StatePublished - Nov 26 1999

Keywords

  • Adrenergic signaling
  • Energetics
  • G proteins
  • Ischemia
  • NMPC spectroscopy

ASJC Scopus subject areas

  • Physiology
  • Cardiology and Cardiovascular Medicine

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