Myocardial insulin-like growth factor-I gene expression during recovery from heart failure after combined left ventricular assist device and clenbuterol therapy

Circulation. 2005 Aug 30;112(9 Suppl):I46-50. doi: 10.1161/01.CIRCULATIONAHA.105.525873.

Abstract

Background: Patients who undergo mechanical support with a left ventricular assist device (LVAD) exhibit reverse remodeling and in some cases recover from heart failure. We have developed a combination therapy using LVAD support combined with pharmacological therapy to maximize reverse remodeling, followed by the beta2 adrenergic agonist clenbuterol. We recently found that clenbuterol induces insulin-like growth factor I (IGF-I) in cardiac myocytes in vitro. The purpose of this study is to examine IGF-I expression in recovery patients after combination therapy.

Methods and results: Myocardial mRNA levels were determined by real-time quantitative polymerase chain reaction in 12 recovery patients (at LVAD implantation, explantation, and 1 year after explantation). IGF-I mRNA was elevated at the time of LVAD explantation relative to donors, with 2 groups distinguishable: Those with low IGF-I mRNA at implantation who showed significant increase during recovery and those with high IGF-I mRNA at implantation who remained high. Levels returned to normal by 1 year after explantation. Microarray analysis of implantation and explantation samples of recovery patients further revealed elevated IGF-II and IGF binding proteins IGFBP4 and IGFBP6. IGF-I levels correlated with stromal cell-derived factor mRNA measured both in LVAD patients and in a wider cohort of heart failure patients.

Conclusions: The data suggest involvement of elevated myocardial IGF-I mRNA in recovery. IGF-I may act to limit atrophy and apoptosis during reverse remodeling and to promote repair and regeneration in concert with stromal cell derived factor.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adrenergic beta-2 Receptor Agonists
  • Adrenergic beta-Agonists / therapeutic use*
  • Cardiomyopathy, Dilated / complications
  • Cardiomyopathy, Dilated / surgery
  • Chemokine CXCL12
  • Chemokines, CXC / biosynthesis
  • Chemokines, CXC / genetics
  • Clenbuterol / therapeutic use*
  • Combined Modality Therapy
  • Convalescence
  • Follow-Up Studies
  • Gene Expression Profiling
  • Heart Failure / drug therapy
  • Heart Failure / etiology
  • Heart Failure / genetics
  • Heart Failure / metabolism*
  • Heart Failure / surgery
  • Heart-Assist Devices*
  • Humans
  • Insulin-Like Growth Factor Binding Protein 4 / biosynthesis
  • Insulin-Like Growth Factor Binding Protein 4 / genetics
  • Insulin-Like Growth Factor Binding Protein 6 / biosynthesis
  • Insulin-Like Growth Factor Binding Protein 6 / genetics
  • Insulin-Like Growth Factor I / biosynthesis*
  • Insulin-Like Growth Factor I / genetics
  • Insulin-Like Growth Factor II / biosynthesis
  • Insulin-Like Growth Factor II / genetics
  • Myocardium / metabolism
  • Oligonucleotide Array Sequence Analysis
  • RNA, Messenger / biosynthesis
  • Regeneration
  • Reverse Transcriptase Polymerase Chain Reaction
  • Stroke Volume
  • Ventricular Remodeling / genetics

Substances

  • Adrenergic beta-2 Receptor Agonists
  • Adrenergic beta-Agonists
  • CXCL12 protein, human
  • Chemokine CXCL12
  • Chemokines, CXC
  • Insulin-Like Growth Factor Binding Protein 4
  • Insulin-Like Growth Factor Binding Protein 6
  • RNA, Messenger
  • Insulin-Like Growth Factor I
  • Insulin-Like Growth Factor II
  • Clenbuterol