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 |
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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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-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/ .</description><identifier>ISSN: 0363-6135</identifier><identifier>EISSN: 1522-1539</identifier><identifier>DOI: 10.1152/ajpheart.00212.2017</identifier><identifier>PMID: 29196344</identifier><language>eng</language><publisher>United States: American Physiological Society</publisher><subject>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</subject><ispartof>American journal of physiology. Heart and circulatory physiology, 2018-03, Vol.314 (3), p.H552-H562</ispartof><rights>Copyright American Physiological Society Mar 2018</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c444t-dc4aff34d996e3c7b904c9ee0107fc92813efb8b2f1548d5bcd41ddeda40d5913</citedby><cites>FETCH-LOGICAL-c444t-dc4aff34d996e3c7b904c9ee0107fc92813efb8b2f1548d5bcd41ddeda40d5913</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,3026,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29196344$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>You, Jieyun</creatorcontrib><creatorcontrib>Wu, Jian</creatorcontrib><creatorcontrib>Zhang, Qi</creatorcontrib><creatorcontrib>Ye, Yong</creatorcontrib><creatorcontrib>Wang, Shijun</creatorcontrib><creatorcontrib>Huang, Jiayuan</creatorcontrib><creatorcontrib>Liu, Haibo</creatorcontrib><creatorcontrib>Wang, Xiaoyan</creatorcontrib><creatorcontrib>Zhang, Weijing</creatorcontrib><creatorcontrib>Bu, Liping</creatorcontrib><creatorcontrib>Li, Jiming</creatorcontrib><creatorcontrib>Lin, Li</creatorcontrib><creatorcontrib>Ge, Junbo</creatorcontrib><creatorcontrib>Zou, Yunzeng</creatorcontrib><title>Differential cardiac hypertrophy and signaling pathways in pressure versus volume overload</title><title>American journal of physiology. Heart and circulatory physiology</title><addtitle>Am J Physiol Heart Circ Physiol</addtitle><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. 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Heart and circulatory physiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>You, Jieyun</au><au>Wu, Jian</au><au>Zhang, Qi</au><au>Ye, Yong</au><au>Wang, Shijun</au><au>Huang, Jiayuan</au><au>Liu, Haibo</au><au>Wang, Xiaoyan</au><au>Zhang, Weijing</au><au>Bu, Liping</au><au>Li, Jiming</au><au>Lin, Li</au><au>Ge, Junbo</au><au>Zou, Yunzeng</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Differential cardiac hypertrophy and signaling pathways in pressure versus volume overload</atitle><jtitle>American journal of physiology. Heart and circulatory physiology</jtitle><addtitle>Am J Physiol Heart Circ Physiol</addtitle><date>2018-03-01</date><risdate>2018</risdate><volume>314</volume><issue>3</issue><spage>H552</spage><epage>H562</epage><pages>H552-H562</pages><issn>0363-6135</issn><eissn>1522-1539</eissn><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/ .</abstract><cop>United States</cop><pub>American Physiological Society</pub><pmid>29196344</pmid><doi>10.1152/ajpheart.00212.2017</doi><oa>free_for_read</oa></addata></record> |
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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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