Wang Xia, Zhu Xinxin, Shi Li, Wang Jingjing, Xu Qing, Yu Baoqi, Qu Aijuan
Beijing Key Laboratory for HIV/AIDS Research, Center for Infectious Diseases, Beijing Youan Hospital, Capital Medical University, Beijing, China.
Department of Physiology and Pathophysiology, School of Basic Medical Sciences, Capital Medical University, Beijing, China.
Front Cardiovasc Med. 2023 Feb 20;10:1110032. doi: 10.3389/fcvm.2023.1110032. eCollection 2023.
Transverse aortic constriction (TAC) is a widely-used animal model for pressure overload-induced cardiac hypertrophy and heart failure (HF). The severity of TAC-induced adverse cardiac remodeling is correlated to the degree and duration of aorta constriction. Most studies of TAC are performed with a 27-gauge needle, which is easy to cause a tremendous left ventricular overload and leads to a rapid HF, but it is accompanied by higher mortality attributed to tighter aortic arch constriction. However, a few studies are focusing on the phenotypes of TAC applied with a 25-gauge needle, which produces a mild overload to induce cardiac remodeling and has low post-operation mortality. Furthermore, the specific timeline of HF induced by TAC applied with a 25-gauge needle in C57BL/6 J mice remains unclear. In this study, C57BL/6 J mice were randomly subjected to TAC with a 25-gauge needle or sham surgery. Echocardiography, gross morphology, and histopathology were applied to evaluate time-series phenotypes in the heart after 2, 4, 6, 8, and 12 weeks. The survival rate of mice after TAC was more than 98%. All mice subjected to TAC maintained compensated cardiac remodeling during the first two weeks and began to exhibit heart failure characteristics after 4 weeks upon TAC. At 8 weeks post-TAC, the mice showed severe cardiac dysfunction, hypertrophy, and cardiac fibrosis compared to sham mice. Moreover, the mice raised a severe dilated HF at 12 weeks. This study provides an optimized method of the mild overload TAC-induced cardiac remodeling from the compensatory period to decompensatory HF in C57BL/6 J mice.
横向主动脉缩窄(TAC)是一种广泛应用于压力超负荷诱导的心脏肥大和心力衰竭(HF)的动物模型。TAC诱导的不良心脏重塑的严重程度与主动脉缩窄的程度和持续时间相关。大多数TAC研究使用27号针头进行,这容易导致巨大的左心室超负荷并导致快速的HF,但同时由于主动脉弓缩窄更紧而伴有更高的死亡率。然而,一些研究聚焦于使用25号针头进行TAC的表型,其产生轻度超负荷以诱导心脏重塑且术后死亡率低。此外,在C57BL/6 J小鼠中使用25号针头进行TAC诱导HF的具体时间线仍不清楚。在本研究中,将C57BL/6 J小鼠随机进行25号针头的TAC或假手术。应用超声心动图、大体形态学和组织病理学来评估2、4、6、8和12周后心脏的时间序列表型。TAC后小鼠的存活率超过98%。所有接受TAC的小鼠在最初两周内维持代偿性心脏重塑,并在TAC后4周开始表现出心力衰竭特征。与假手术小鼠相比,TAC后8周时,小鼠表现出严重的心脏功能障碍、肥大和心脏纤维化。此外,小鼠在12周时出现严重的扩张型HF。本研究提供了一种优化的方法,用于在C57BL/6 J小鼠中从代偿期到失代偿性HF的轻度超负荷TAC诱导的心脏重塑。