Literature DB >> 8184946

In vivo assessment of LV mass in mice using high-frequency cardiac ultrasound: necropsy validation.

W J Manning1, J Y Wei, S E Katz, S E Litwin, P S Douglas.   

Abstract

Left ventricular (LV) mass is an important descriptor of cardiac status that increases with normal aging and may be affected by a variety of disease processes. There are currently limited noninvasive techniques that permit accurate determination of in vivo LV mass in very small animals, such as the mouse, a frequently used model for cardiac research. We sought to evaluate the ability of high-frequency (7.0 or 7.5 MHz), two-dimensional (2-D) guided M-mode echocardiography to estimate in vivo LV mass in the mouse. Fifteen adult mice weighing 22-45 g were studied, including six young adult (2- to 3-mo-old), two adult (12- to 14-mo-old), and seven senescent (18- to 20-mo-old) animals. Resting heart rate varied up to 450 beats/min. Anterior wall, inferior wall, and end-diastolic dimensions were measured, and echocardiographic LV mass (LVMe) was calculated using an uncorrected cube approximation. Autopsy LV mass was determined within 4 h of echocardiographic examination. Autopsy LV mass ranged from 88 to 211 mg. LV chamber dimensions included anterior wall (1.0 +/- 0.2 mm), inferior wall (1.1 +/- 0.3 mm), and end-diastolic dimension (3.7 +/- 0.5 mm). There was a very good correlation between LVMe (x) and autopsy LV mass (y):y = 0.96x - 7, r = 0.94, standard error of the estimate = 18 mg, P < 0.001. This correlation was stronger than that for autopsy LV mass and body weight (r = 0.70) or age (r = 0.74), indexes which until now were the only noninvasive correlates available for this very small animal model. We conclude that, despite the rapid heart rate and small size of the mouse heart, these results demonstrate the potential of high-frequency 2-D guided M-mode transthoracic echocardiography for the in vivo assessment of LV dimensions and mass in the mouse and may prove useful for cardiac research on aging and cardiomyopathies.

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Year:  1994        PMID: 8184946     DOI: 10.1152/ajpheart.1994.266.4.H1672

Source DB:  PubMed          Journal:  Am J Physiol        ISSN: 0002-9513


  36 in total

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2.  The conserved phosphoinositide 3-kinase pathway determines heart size in mice.

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Journal:  EMBO J       Date:  2000-06-01       Impact factor: 11.598

3.  Characterization of the failing murine heart in a desmin knock-out model using a clinical 3 T MRI scanner.

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4.  Controlled dual delivery of fibroblast growth factor-2 and Interleukin-10 by heparin-based coacervate synergistically enhances ischemic heart repair.

Authors:  William C W Chen; Brandon G Lee; Dae Woo Park; Kyobum Kim; Hunghao Chu; Kang Kim; Johnny Huard; Yadong Wang
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5.  Endoplasmic reticulum chaperon tauroursodeoxycholic acid alleviates obesity-induced myocardial contractile dysfunction.

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6.  SR-targeted CaMKII inhibition improves SR Ca²+ handling, but accelerates cardiac remodeling in mice overexpressing CaMKIIδC.

Authors:  Sabine Huke; Jaime Desantiago; Marcia A Kaetzel; Shikha Mishra; Joan H Brown; John R Dedman; Donald M Bers
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7.  Cardiomyocyte-specific deletion of endothelin receptor A rescues aging-associated cardiac hypertrophy and contractile dysfunction: role of autophagy.

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8.  The Src homology and collagen A (ShcA) adaptor protein is required for the spatial organization of the costamere/Z-disk network during heart development.

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Journal:  J Biol Chem       Date:  2014-12-08       Impact factor: 5.157

9.  Ablation of Akt2 protects against lipopolysaccharide-induced cardiac dysfunction: role of Akt ubiquitination E3 ligase TRAF6.

Authors:  Yingmei Zhang; Xihui Xu; Asli F Ceylan-Isik; Maolong Dong; Zhaohui Pei; Yan Li; Jun Ren
Journal:  J Mol Cell Cardiol       Date:  2014-05-05       Impact factor: 5.000

10.  Adiponectin knockout accentuates high fat diet-induced obesity and cardiac dysfunction: role of autophagy.

Authors:  Rui Guo; Yingmei Zhang; Subat Turdi; Jun Ren
Journal:  Biochim Biophys Acta       Date:  2013-03-21
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