Differential cardiac hypertrophy and signaling pathways in pressure versus volume overload

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 volu...

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Veröffentlicht in:American journal of physiology. Heart and circulatory physiology 2018-03, Vol.314 (3), p.H552-H562
Hauptverfasser: You, Jieyun, Wu, Jian, Zhang, Qi, Ye, Yong, Wang, Shijun, Huang, Jiayuan, Liu, Haibo, Wang, Xiaoyan, Zhang, Weijing, Bu, Liping, Li, Jiming, Lin, Li, Ge, Junbo, Zou, Yunzeng
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container_title American journal of physiology. Heart and circulatory physiology
container_volume 314
creator You, Jieyun
Wu, Jian
Zhang, Qi
Ye, Yong
Wang, Shijun
Huang, Jiayuan
Liu, Haibo
Wang, Xiaoyan
Zhang, Weijing
Bu, Liping
Li, Jiming
Lin, Li
Ge, Junbo
Zou, Yunzeng
description 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/ .
doi_str_mv 10.1152/ajpheart.00212.2017
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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 &amp; 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. 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subjects Adaptation
Adaptation, Physiological
AKT protein
Angiogenesis
Animals
Aorta
Aorta - physiopathology
Aorta - surgery
Aortic Valve Insufficiency - complications
Aortic Valve Insufficiency - diagnostic imaging
Aortic Valve Insufficiency - metabolism
Aortic Valve Insufficiency - physiopathology
Apoptosis
Arrestin
Arterial Pressure
Biomechanical Phenomena
Calcium ions
Calcium signalling
Constriction
Disease Models, Animal
Fibrosis
Heart
Heart diseases
Hypertension
Hypertrophy
Hypertrophy, Left Ventricular - diagnostic imaging
Hypertrophy, Left Ventricular - etiology
Hypertrophy, Left Ventricular - metabolism
Hypertrophy, Left Ventricular - physiopathology
Male
MAP kinase
Mice
Mice, Inbred C57BL
Myocardial Contraction
Myocardium - metabolism
Myocardium - pathology
Pharmacology
Phenotype
Polymerase chain reaction
Pressure
Regurgitation
Signal Transduction
Stress
Stress, Mechanical
Stresses
Structure-function relationships
Surgery
Ventricle
Ventricular Function, Left
Ventricular Remodeling
title Differential cardiac hypertrophy and signaling pathways in pressure versus volume overload
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