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Speckle tracking echocardiography in the assessment of mouse models of cardiac dysfunction.

Authors :
Yu Peng
Popović, Zoran B.
Sopko, Nikolai
Drinko, Jeannie
Zheng Zhang
Thomas, James D.
Penn, Marc S.
Source :
American Journal of Physiology: Heart & Circulatory Physiology. Aug2009, Vol. 297 Issue 2, pH811-H820. 10p.
Publication Year :
2009

Abstract

Two-dimensional (2-D) speckle tracking echocardiography (STE) accurately quantifies circumferential strain (Scirc) and radial strain (Srad) in humans and in large and small animals. This study was performed to assess sensitivity of Scirc and Srad to left ventricular (LV) dysfunction in mouse models. We performed 2-D and M-mode echocardiography 1) in 6 mice during superficial and profound isoflurane anesthesia, 2) serially in 12 mice to monitor the development of heart failure induced by transverse aortic constriction (TAC) and in 8 corresponding control mice, and 3) in 26 mice with varying degrees of TAC-induced heart failure and 12 corresponding control mice immediately before euthanasia. Fractional shortening (FS) and LV mass were measured from standard M-mode tracings, whereas Scirc and Srud were derived by STE. Percent fibrosis and myocyte diameters were assessed from whole heart cross-sectional specimens stained by Masson trichrome. Profound isoflurane anesthesia decreased Scirc (P = 0.027) but not Srad (P > 0.05). Mice subjected to TAC showed an immediate and sustained decrease in FS (P = 0.035), Scirc (P = 0.016), and Srad (P = 0.0 12). Scirc showed better correlation with FS (r = 0.56 and P < 0.0001) and LV mass (r = 0.42 and P = 0.0003) than Srad (r = 0.54 and P < 0.000 1 for FS and r = 0.37 and P = 0.0 14 for LV mass, respectively). Percent fibrosis correlated better with Scirc (r = 0.46 and P = 0.004) than with Srad (r = -0.32 and P = 0.05), whereas myocyte diameter showed similar correlation with both strains (r = 0.45 and r = -0.44, respectively, and P = 0.006 for both). STE correctly identifies LV dysfunction and histological changes in mice and can be used for the serial assessment of cardiac remodeling in murine models. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
03636135
Volume :
297
Issue :
2
Database :
Academic Search Index
Journal :
American Journal of Physiology: Heart & Circulatory Physiology
Publication Type :
Academic Journal
Accession number :
44143456
Full Text :
https://doi.org/10.1152/ajpheart.00385.2009