Literature DB >> 12878176

DNA microarray analysis of in vivo progression mechanism of heart failure.

Shuichi Ueno1, Ruri Ohki, Toru Hashimoto, Toshihiro Takizawa, Koichi Takeuchi, Yoshihiro Yamashita, Jun Ota, Young Lim Choi, Tomoaki Wada, Koji Koinuma, Keiji Yamamoto, Uichi Ikeda, Kazuyuki Shimada, Hiroyuki Mano.   

Abstract

Dahl salt-sensitive rats are genetically hypersensitive to sodium intake. When fed a high sodium diet, they develop systemic hypertension, followed by cardiac hypertrophy and finally heart failure within a few months. Therefore, Dahl rats represent a good model with which to study how heart failure is developed in vivo. By using DNA microarray, we here monitored the transcriptome of >8000 genes in the left ventricular muscles of Dahl rats during the course of cardiovascular damage. Expression of the atrial natriuretic peptide gene was, for instance, induced in myocytes by sodium overload and further enhanced even at the heart failure stage. Interestingly, expression of the gene for the D-binding protein, an apoptotic-related transcriptional factor, became decreased upon the transition to heart failure. To our best knowledge, this is the first report to describe the transcriptome of cardiac myocytes during the disease progression of heart failure.

Entities:  

Mesh:

Year:  2003        PMID: 12878176     DOI: 10.1016/s0006-291x(03)01252-x

Source DB:  PubMed          Journal:  Biochem Biophys Res Commun        ISSN: 0006-291X            Impact factor:   3.575


  7 in total

1.  Dynamic gene expression patterns in animal models of early and late heart failure reveal biphasic-bidirectional transcriptional activation of signaling pathways.

Authors:  Janelle Rowell; Norimichi Koitabashi; David A Kass; Andreas S Barth
Journal:  Physiol Genomics       Date:  2014-08-26       Impact factor: 3.107

2.  Reciprocal transcriptional regulation of metabolic and signaling pathways correlates with disease severity in heart failure.

Authors:  Andreas S Barth; Ami Kumordzie; Constantine Frangakis; Kenneth B Margulies; Thomas P Cappola; Gordon F Tomaselli
Journal:  Circ Cardiovasc Genet       Date:  2011-08-09

3.  A gene expression profile of the myocardial response to clenbuterol.

Authors:  Enrique Lara-Pezzi; Cesare M N Terracciano; Gopal K R Soppa; Ryszard T Smolenski; Leanne E Felkin; Magdi H Yacoub; Paul J R Barton
Journal:  J Cardiovasc Transl Res       Date:  2009-03-13       Impact factor: 4.132

4.  Alteration of gene expression during progression of hypertension-induced cardiac dysfunction in rats.

Authors:  Tomoyoshi Koyanagi; Lily Y Wong; Koichi Inagaki; Olga V Petrauskene; Daria Mochly-Rosen
Journal:  Am J Physiol Heart Circ Physiol       Date:  2008-05-16       Impact factor: 4.733

5.  Deep RNA sequencing reveals novel cardiac transcriptomic signatures for physiological and pathological hypertrophy.

Authors:  Hong Ki Song; Seong-Eui Hong; Taeyong Kim; Do Han Kim
Journal:  PLoS One       Date:  2012-04-16       Impact factor: 3.240

6.  Rnd3 haploinsufficient mice are predisposed to hemodynamic stress and develop apoptotic cardiomyopathy with heart failure.

Authors:  X Yue; X Yang; X Lin; T Yang; X Yi; Y Dai; J Guo; T Li; J Shi; L Wei; G-C Fan; C Chen; J Chang
Journal:  Cell Death Dis       Date:  2014-06-05       Impact factor: 8.469

7.  Quantitative Real-Time Analysis of Differentially Expressed Genes in Peripheral Blood Samples of Hypertension Patients.

Authors:  Fawad Ali; Arifullah Khan; Syed Aun Muhammad; Syed Shams Ul Hassan
Journal:  Genes (Basel)       Date:  2022-01-21       Impact factor: 4.096

  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.