In vivo cardiac 1H-MRS in the mouse

✍ Scribed by Jürgen E. Schneider; Damian J. Tyler; Michiel ten Hove; A. Elizabeth Sang; Paul J. Cassidy; Alexandra Fischer; Julie Wallis; Liam M. Sebag-Montefiore; Hugh Watkins; Dirk Isbrandt; Kieran Clarke; Stefan Neubauer

• Publisher: John Wiley and Sons
• Year: 2004
• Tongue: English
• Weight: 292 KB
• Volume: 52
• Category: Article
• ISSN: 0740-3194
• DOI: 10.1002/mrm.20257

✦ Synopsis

Abstract

The mouse is the predominant animal model to study the effect of gene manipulations. Imaging techniques to define functional effects on the heart caused by genomic alterations are becoming increasingly routine in mice, yet methods for in vivo investigation of metabolic phenotypes in the mouse heart are lacking. In this work, cardiac ^1^H‐MRS was developed and applied in mouse hearts in vivo using a single‐voxel technique (PRESS). In normal C57Bl/6J mice, stability and reproducibility achieved by dedicated cardiac and respiratory gating was demonstrated by measuring amplitude and zero‐order phase changes of the unsuppressed water signal. Various cardiac metabolites, such as creatine, taurine, carnitine, or intramyocardial lipids were successfully detected and quantified relative to the total water content in voxels as small as 2 μl, positioned in the interventricular septum. The method was applied to a murine model of guanidinoacetate N‐methyltransferase (GAMT) deficiency, which is characterized by substantially decreased myocardial creatine levels. Creatine deficiency was confirmed noninvasively in myocardium of anesthetized GAMT^‐/‐^ mice. This is the first study to report the application of cardiac ^1^H‐MRS in mice in vivo. Magn Reson Med 52:1029–1035, 2004. © 2004 Wiley‐Liss, Inc.