T. Walther, A. Schubert, V. Falk, C. Binner, C. Walther, N. Doll, A. Fabricius, S. Dhein, J. Gummert, F. Mohr
{"title":"主动脉狭窄手术治疗后左心室反向重构:与肾素-血管紧张素系统基因表达的关系","authors":"T. Walther, A. Schubert, V. Falk, C. Binner, C. Walther, N. Doll, A. Fabricius, S. Dhein, J. Gummert, F. Mohr","doi":"10.1161/01.CIR.0000032919.33237.4D","DOIUrl":null,"url":null,"abstract":"BackgroundSurgical therapy for aortic stenosis leads to reverse remodeling, with normalization of left ventricular hypertrophy (LVH). The aim of this study was to examine Renin-Angiotensin system (RAS) gene expression in this setting. MethodsGrowing sheep (n=44) underwent supracoronary aortic banding for controlled induction of LVH at the age of 6 to 8 months (A=baseline). Surgical revision to completely release the pressure gradient was performed 8.3±1 months later (B). The animals were sacrificed after another 10.1±2 months (C). Along with hemodynamic measurements, subtractive hybridization and competitive polymerase chain reaction were applied to quantify mRNA expression for angiotensin-converting enzyme (ACE) and angiotensin receptors 1 and 2 (AT1-R and AT2-R). ResultsLeft ventricular mass index was 82±21 g (A), 150±33 g (B), and 78±18 g (C), P <0.01. Left ventricular function and cardiac index remained stable. Myocardial fiber diameter was 11.3±0.8 (A), 15.9±1.2 (B), and 11.4±1 (C) &mgr;m, P <0.01. Gene expression was as follows: ACE 0.8±0.05 (A), 1.3±0.08 (B), and 0.9±0.06 (C), P <0.01; AT1-R 0.7±0.06 (A), 0.9±0.07 (B), and 0.3±0.04 (C), P <0.01; AT2-R 0.5±0.05 (A), 0.2±0.04 (B), and 0.5±0.05 (C), P <0.01. ConclusionLVH in aortic stenosis coincides with significant alterations of the RAS. Surgical therapy leads to reverse remodeling, which is paralleled by regression of RAS gene expression.","PeriodicalId":10194,"journal":{"name":"Circulation: Journal of the American Heart Association","volume":"6 1","pages":"I-23-I-26"},"PeriodicalIF":0.0000,"publicationDate":"2002-09-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"33","resultStr":"{\"title\":\"Left Ventricular Reverse Remodeling After Surgical Therapy for Aortic Stenosis: Correlation to Renin-Angiotensin System Gene Expression\",\"authors\":\"T. Walther, A. Schubert, V. Falk, C. Binner, C. Walther, N. Doll, A. Fabricius, S. Dhein, J. Gummert, F. Mohr\",\"doi\":\"10.1161/01.CIR.0000032919.33237.4D\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"BackgroundSurgical therapy for aortic stenosis leads to reverse remodeling, with normalization of left ventricular hypertrophy (LVH). The aim of this study was to examine Renin-Angiotensin system (RAS) gene expression in this setting. MethodsGrowing sheep (n=44) underwent supracoronary aortic banding for controlled induction of LVH at the age of 6 to 8 months (A=baseline). Surgical revision to completely release the pressure gradient was performed 8.3±1 months later (B). The animals were sacrificed after another 10.1±2 months (C). Along with hemodynamic measurements, subtractive hybridization and competitive polymerase chain reaction were applied to quantify mRNA expression for angiotensin-converting enzyme (ACE) and angiotensin receptors 1 and 2 (AT1-R and AT2-R). ResultsLeft ventricular mass index was 82±21 g (A), 150±33 g (B), and 78±18 g (C), P <0.01. Left ventricular function and cardiac index remained stable. Myocardial fiber diameter was 11.3±0.8 (A), 15.9±1.2 (B), and 11.4±1 (C) &mgr;m, P <0.01. Gene expression was as follows: ACE 0.8±0.05 (A), 1.3±0.08 (B), and 0.9±0.06 (C), P <0.01; AT1-R 0.7±0.06 (A), 0.9±0.07 (B), and 0.3±0.04 (C), P <0.01; AT2-R 0.5±0.05 (A), 0.2±0.04 (B), and 0.5±0.05 (C), P <0.01. ConclusionLVH in aortic stenosis coincides with significant alterations of the RAS. Surgical therapy leads to reverse remodeling, which is paralleled by regression of RAS gene expression.\",\"PeriodicalId\":10194,\"journal\":{\"name\":\"Circulation: Journal of the American Heart Association\",\"volume\":\"6 1\",\"pages\":\"I-23-I-26\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2002-09-24\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"33\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Circulation: Journal of the American Heart Association\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1161/01.CIR.0000032919.33237.4D\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Circulation: Journal of the American Heart Association","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1161/01.CIR.0000032919.33237.4D","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 33
摘要
背景:主动脉瓣狭窄的手术治疗导致了左心室肥厚(LVH)的正常化,导致了反向重构。本研究的目的是检测肾素-血管紧张素系统(RAS)基因在这种情况下的表达。方法:生长中的绵羊(n=44)在6 ~ 8月龄时(A=基线)行冠状动脉上束带术以控制LVH诱导。8.3±1个月后进行手术翻修以完全释放压力梯度(B)。再过10.1±2个月后处死动物(C)。在进行血流动力学测量的同时,采用减法杂交和竞争性聚合酶链反应定量血管紧张素转换酶(ACE)和血管紧张素受体1和2 (AT1-R和AT2-R)的mRNA表达。结果左室质量指数分别为82±21 g (A)、150±33 g (B)和78±18 g (C), P <0.01。左心室功能和心脏指数保持稳定。心肌纤维直径分别为11.3±0.8 (A)、15.9±1.2 (B)、11.4±1 (C), P <0.01。基因表达:ACE 0.8±0.05 (A)、1.3±0.08 (B)、0.9±0.06 (C), P <0.01;AT1-R 0.7±0.06 (A), 0.9±0.07 (B)和0.3±0.04 (C), P < 0.01;AT2-R 0.5±0.05 (A), 0.2±0.04 (B)和0.5±0.05 (C), P < 0.01。结论主动脉瓣狭窄患者lvh与RAS变化一致。手术治疗导致逆转重塑,这与RAS基因表达的回归是平行的。
Left Ventricular Reverse Remodeling After Surgical Therapy for Aortic Stenosis: Correlation to Renin-Angiotensin System Gene Expression
BackgroundSurgical therapy for aortic stenosis leads to reverse remodeling, with normalization of left ventricular hypertrophy (LVH). The aim of this study was to examine Renin-Angiotensin system (RAS) gene expression in this setting. MethodsGrowing sheep (n=44) underwent supracoronary aortic banding for controlled induction of LVH at the age of 6 to 8 months (A=baseline). Surgical revision to completely release the pressure gradient was performed 8.3±1 months later (B). The animals were sacrificed after another 10.1±2 months (C). Along with hemodynamic measurements, subtractive hybridization and competitive polymerase chain reaction were applied to quantify mRNA expression for angiotensin-converting enzyme (ACE) and angiotensin receptors 1 and 2 (AT1-R and AT2-R). ResultsLeft ventricular mass index was 82±21 g (A), 150±33 g (B), and 78±18 g (C), P <0.01. Left ventricular function and cardiac index remained stable. Myocardial fiber diameter was 11.3±0.8 (A), 15.9±1.2 (B), and 11.4±1 (C) &mgr;m, P <0.01. Gene expression was as follows: ACE 0.8±0.05 (A), 1.3±0.08 (B), and 0.9±0.06 (C), P <0.01; AT1-R 0.7±0.06 (A), 0.9±0.07 (B), and 0.3±0.04 (C), P <0.01; AT2-R 0.5±0.05 (A), 0.2±0.04 (B), and 0.5±0.05 (C), P <0.01. ConclusionLVH in aortic stenosis coincides with significant alterations of the RAS. Surgical therapy leads to reverse remodeling, which is paralleled by regression of RAS gene expression.