Journal of Molecular and Cellular Cardiology
Volume 48, Issue 3 , Pages 512-517, March 2010

Ventricular remodeling and function: Insights using murine echocardiography

  • Marielle Scherrer-Crosbie

      Affiliations

    • Corresponding Author InformationCorresponding author. Cardiac Ultrasound Laboratory, Massachusetts General Hospital, 55 Fruit Street, Boston, MA 02114, USA. Tel.: +1 617 726 7686; fax: +1 617 726 8383.
  • ,
  • Baptiste Kurtz

Cardiac Ultrasound Laboratory in the Cardiology Division of the Department of Medicine, Massachusetts General Hospital, Boston, MA, USA

Cardiovascular Research Center, Massachusetts General Hospital, Boston, MA, USA

Received 26 April 2009; received in revised form 19 June 2009; accepted 7 July 2009. published online 16 July 2009.

Abstract 

Extracellular matrix disturbances play an important role in the development of ventricular remodeling and failure. Genetically modified mice with abnormalities in the synthesis and degradation of extracellular matrix have been generated, in particular mice with deletion or overexpression of matrix metalloproteinases (MMPs) and tissue inhibitors of matrix metalloproteinases (TIMPs). Echocardiography is ideally suited to serially evaluate left ventricular (LV) size and function, thus defining the progression of LV remodeling and failure. This Review describes the echocardiographic parameters that may provide insights into the development of ventricular remodeling and heart failure. The application of echocardiography to study LV remodeling and function after myocardial infarction and LV pressure-overload in wild-type mice and mice deficient or overexpressing MMPs or TIMPs is then detailed. Finally, using the example of mice deficient in nitric oxide synthase 3, a cautionary example is given illustrating discrepancies between the cardiac echocardiographic phenotype and modifications of the extracellular matrix.

Keywords: Echocardiography, Heart failure, Mice, Ventricular remodeling, Nitric oxide, Myocardial perfusion, Ventricular function

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: S0022-2828(09)00278-8

doi:10.1016/j.yjmcc.2009.07.004

Journal of Molecular and Cellular Cardiology
Volume 48, Issue 3 , Pages 512-517, March 2010