Abstract

Transverse aortic constriction (TAC) is a well-established model of pressure overload-induced cardiac hypertrophy and failure in mice. The degree of constriction “tightness” dictates the TAC severity and is determined by the gauge (G) of needle used. Though many reports use the TAC model, few studies have directly compared the range of resulting phenotypes. In this study adult male mice were randomized to receive TAC surgery with varying degrees of tightness: mild (25G), moderate (26G) or severe (27G) for 4 weeks, alongside sham-operated controls. Weekly echocardiography and terminal haemodynamic measurements determined cardiac remodelling and function. All TAC models induced significant, severity-dependent left ventricular hypertrophy and diastolic dysfunction compared to sham mice. Mice subjected to 26G TAC additionally exhibited mild systolic dysfunction and cardiac fibrosis, whereas mice in the 27G TAC group had more severe systolic and diastolic dysfunction, severe cardiac fibrosis, and were more likely to display features of heart failure, such as elevated plasma BNP. We also observed renal atrophy in 27G TAC mice, in the absence of renal structural, functional or gene expression changes. 25G, 26G and 27G TAC produced different responses in terms of cardiac structure and function. These distinct phenotypes may be useful in different preclinical settings.

Highlights

  • Transverse aortic constriction (TAC) is one of the most common surgical models of pressure overload-induced cardiac hypertrophy and heart failure[9,10]

  • The trans-TAC gradient was significantly higher in 26G TAC compared to 25G TAC (P < 0.01), and significantly higher in 27 gauge (27G) TAC compared to 26G TAC (P < 0.01), representing a distinct, graded phenotype

  • The remaining 25G and 26G TAC mice had 100% survival after the 8-hour perioperative period, whereas 2 of 13 mice (15.4%) subjected to 27G TAC died within 4 days (Fig. 1c; P > 0.05)

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Summary

Introduction

Transverse aortic constriction (TAC) is one of the most common surgical models of pressure overload-induced cardiac hypertrophy and heart failure[9,10]. The potentially different effects of varying degrees of pressure overload on LV haemodynamics, as well as on renal structure and function, remain unknown. This is important since the selection of an informative model is critical to successful analysis of genetic or pharmacologic interventions in heart failure. We found a largely graded response to TAC severity in terms of cardiac hypertrophy, dysfunction and fibrosis, representing the transition from compensated to decompensated heart failure phenotypes

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