PMID- 9918534 OWN - NLM STAT- MEDLINE DCOM- 19990211 LR - 20190623 IS - 0009-7322 (Print) IS - 0009-7322 (Linking) VI - 99 IP - 3 DP - 1999 Jan 26 TI - Magnetic resonance imaging and invasive evaluation of development of heart failure in transgenic mice with myocardial expression of tumor necrosis factor-alpha. PG - 448-54 AB - BACKGROUND: Transgenic mice expressing tumor necrosis factor-alpha (TNF-alpha) in cardiac myocytes develop dilated cardiomyopathy, but the temporal progression to cardiac dysfunction is not well characterized. We asked (1) Does magnetic resonance imaging (MRI) provide a reproducible assessment of cardiac output in mice that correlates with invasive measurements obtained with thermodilution? (2) What is the time course of left ventricular (LV) remodeling in transgenic mice with myocardial expression of TNF-alpha? METHODS AND RESULTS: Transgenic mice from 2 different lineages with differing amounts of myocardial TNF-alpha expression [lineage 1 (L1) and lineage 2 (L2)] and littermate controls (LC) were studied. In protocol 1, cardiac output (CO) and stroke volume (SV) were measured by MRI and thermodilution (TD) in 15 mice (3 L1, 4 L2, 8 LC). In protocol 2, 23 mice (7 L1, 8 L2, 8 LC) were scanned at 1 month of life and every 4 weeks thereafter. In both protocols, cine-MRI was performed with the use of a 1.5-T clinical system (1.5-mm slices, 195x195 microm in-plane resolution). MRI CO and SV correlated well with TD [COTD (mL/min)=0.94*COMRI+0.72, r=0.84; SVTD( microL)=1. 01*SVMRI-1.07, r=0.94]. Serial MRI studies showed significant increase in LV mass and volumes over time and a significant decrease in ejection fraction in transgenic mice when compared with littermate controls. Compared with lineage 2, lineage 1 showed significantly larger LV mass and volumes and significantly lower ejection fraction. CONCLUSIONS: MRI assessment of cardiac function in mice correlates well with invasive measurements. Serial MRI studies in the TNF-alpha mouse model demonstrate that the rate of progression and severity of LV dysfunction are dependent on the degree of TNF-alpha overexpression. FAU - Franco, F AU - Franco F AD - Department of Radiology at the University of Texas Southwestern Medical Center at Dallas, 75235-9085, USA. FAU - Thomas, G D AU - Thomas GD FAU - Giroir, B AU - Giroir B FAU - Bryant, D AU - Bryant D FAU - Bullock, M C AU - Bullock MC FAU - Chwialkowski, M C AU - Chwialkowski MC FAU - Victor, R G AU - Victor RG FAU - Peshock, R M AU - Peshock RM LA - eng GR - 5R29-GM-51822-04/GM/NIGMS NIH HHS/United States GR - P01-HL-06296/HL/NHLBI NIH HHS/United States PT - Journal Article PT - Research Support, Non-U.S. Gov't PT - Research Support, U.S. Gov't, P.H.S. PL - United States TA - Circulation JT - Circulation JID - 0147763 RN - 0 (Tumor Necrosis Factor-alpha) SB - IM MH - Animals MH - Body Weight MH - Disease Models, Animal MH - Heart Failure/*diagnosis/*genetics/physiopathology MH - Heart Rate MH - *Magnetic Resonance Imaging MH - Mice MH - Mice, Inbred C57BL MH - Mice, Transgenic MH - Myocardium/*chemistry MH - Stroke Volume MH - Systole/physiology MH - Thermodilution MH - Tumor Necrosis Factor-alpha/*genetics MH - Ventricular Function, Left/physiology EDAT- 1999/01/26 00:00 MHDA- 1999/01/26 00:01 CRDT- 1999/01/26 00:00 PHST- 1999/01/26 00:00 [pubmed] PHST- 1999/01/26 00:01 [medline] PHST- 1999/01/26 00:00 [entrez] AID - 10.1161/01.cir.99.3.448 [doi] PST - ppublish SO - Circulation. 1999 Jan 26;99(3):448-54. doi: 10.1161/01.cir.99.3.448.