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压力与容量超负荷所致的心脏肥厚及信号通路的差异。

Differential cardiac hypertrophy and signaling pathways in pressure versus volume overload.

机构信息

Department of Cardiology, Shanghai East Hospital, Tongji University and Zhongshan Hospital, Fudan University , Shanghai , China.

Shanghai Institute of Cardiovascular Diseases, Zhongshan Hospital and Institutes of Biomedical Sciences, Fudan University , Shanghai , China.

出版信息

Am J Physiol Heart Circ Physiol. 2018 Mar 1;314(3):H552-H562. doi: 10.1152/ajpheart.00212.2017. Epub 2017 Dec 1.

Abstract

Mechanical overload can be classified into pressure overload and volume overload, causing concentric and eccentric cardiac hypertrophy, respectively. Here, we aimed to differentiate the load-mediated signaling pathways involved in pressure versus volume overload cardiac hypertrophy. Pressure or volume overload was imposed on C57BL/6J mice by transverse aortic constriction (TAC) or aortic regurgitation (AR), respectively. After surgery (2 wk), left ventricular structure and function were evaluated by echocardiographic, hemodynamic, and histological analyses. Signaling pathways related to hypertrophy, fibrosis, angiogenesis, and apoptosis were studied by histological analysis, RT-PCR, and Western blot analysis. Although mean wall stress was similar in both TAC and AR mice, systolic wall stress was significantly increased in TAC and diastolic wall stress was mainly elevated in AR. TAC or AR induced concentric or eccentric compensated hypertrophy, respectively. TAC was associated with more significant fibrosis and apoptosis, whereas AR was associated with more significant angiogenesis. MAPK kinase family, β-arrestin-2, Akt, and Ca-related signaling pathways were markedly activated in TAC but mildly upregulated or unchanged in AR. Pressure overload and volume overload induce different phenotypic and molecular adaptations in cardiac hypertrophy. Most load-related signaling pathways assessed in this study predominate in pressure but not volume overload. The stimulus-specific heterogeneity in the signaling pathways requires distinct manipulations for further mechanistic and pharmacological studies. NEW & NOTEWORTHY Using the transverse aortic constriction mouse model and the newly developed aortic regurgitation mouse model, we delineated the prominent differences between concentric and eccentric cardiac hypertrophy on morphological, functional, and molecular levels. Our findings are important for the precise diagnosis and treatment of these two types of cardiac hypertrophy. Listen to this article's corresponding podcast at http://ajpheart.podbean.com/e/chinese-english-language-podcast-on-differential-cardiac-remodeling-in-tac-vs-ar/ .

摘要

机械性过载可分为压力过载和容量过载,分别导致向心性和离心性心肌肥厚。在这里,我们旨在区分压力和容量过载心脏肥厚相关的负荷介导的信号通路。通过横主动脉缩窄(TAC)或主动脉瓣反流(AR)分别对 C57BL/6J 小鼠施加压力或容量过载。手术后(2 周),通过超声心动图、血流动力学和组织学分析评估左心室结构和功能。通过组织学分析、RT-PCR 和 Western blot 分析研究与肥大、纤维化、血管生成和细胞凋亡相关的信号通路。尽管 TAC 和 AR 小鼠的平均壁应力相似,但 TAC 中的收缩期壁应力显著增加,而 AR 中的舒张期壁应力主要升高。TAC 或 AR 分别诱导向心性或离心性代偿性肥厚。TAC 与更显著的纤维化和细胞凋亡相关,而 AR 与更显著的血管生成相关。MAPK 激酶家族、β-arrestin-2、Akt 和 Ca 相关信号通路在 TAC 中明显激活,但在 AR 中轻度上调或不变。压力过载和容量过载在心脏肥厚中引起不同的表型和分子适应性。本研究中评估的大多数与负荷相关的信号通路在压力过载中占主导地位,但在容量过载中占主导地位。信号通路中的刺激特异性异质性需要进行不同的操作,以进行进一步的机制和药理学研究。新的和值得注意的是,使用横主动脉缩窄小鼠模型和新开发的主动脉瓣反流小鼠模型,我们在形态、功能和分子水平上描绘了向心性和离心性心肌肥厚之间的显著差异。我们的发现对这两种类型的心脏肥厚的精确诊断和治疗非常重要。在 http://ajpheart.podbean.com/e/chinese-english-language-podcast-on-differential-cardiac-remodeling-in-tac-vs-ar/ 上收听这篇文章的相应播客。

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