Literature DB >> 15309249

Current perspectives of electrical remodeling and its therapeutic implications.

Sanjeev Wasson1, H K Reddy, Mary L Dohrmann.   

Abstract

Electrical remodeling involves alterations in the electrophysiologic milieu of myocardium in various disease states, such as ventricular hypertrophy, heart failure, atrial tachyarrhythmias, myocardial ischemia, and infarction that are associated with cardiac arrhythmias. Although research in this area dates back to early part of the 19th century, we still lack the exact knowledge of ionic remodeling, the role of various genes and channel proteins, and their relevance for the newer antiarrhythmic therapies. Structural remodeling may also have an impact on the electrical remodeling process, although differences in both structural and electrical remodeling are associated with different disease states. Various electrophysiologic, cellular, and structural alterations, including anisotropic conduction, increased intracellular calcium levels, and gap junction remodeling predispose to increased dispersion of action potential duration and refractoriness. This constitutes a favorable substrate for early and late afterdepolarizations and reentrant arrhythmias. Studying the role of ionic remodeling in the initiation and propagation of cardiac arrhythmias has significant relevance for developing newer antiarrhythmic therapies, for identifying patients at risk of developing fatal arrhythmias, and for implementing effective preventive measures. Further research is required to understand the specific effects of individual ion channel remodeling, to understand the signal transduction mechanisms, and to address whether detrimental effects of electrical remodeling can be altered.

Entities:  

Mesh:

Substances:

Year:  2004        PMID: 15309249     DOI: 10.1177/107424840400900208

Source DB:  PubMed          Journal:  J Cardiovasc Pharmacol Ther        ISSN: 1074-2484            Impact factor:   2.457


  6 in total

1.  SERCA2a superinhibition by human phospholamban triggers electrical and structural remodeling in mouse hearts.

Authors:  Hong-Sheng Wang; Demetrios A Arvanitis; Min Dong; Paul J Niklewski; Wen Zhao; Chi Keung Lam; Evangelia G Kranias; Despina Sanoudou
Journal:  Physiol Genomics       Date:  2011-01-25       Impact factor: 3.107

2.  Expression of skeletal but not cardiac Na+ channel isoform preserves normal conduction in a depolarized cardiac syncytium.

Authors:  Lev Protas; Wen Dun; Zhiheng Jia; Jia Lu; Annalisa Bucchi; Sindhu Kumari; Ming Chen; Ira S Cohen; Michael R Rosen; Emilia Entcheva; Richard B Robinson
Journal:  Cardiovasc Res       Date:  2008-10-31       Impact factor: 10.787

3.  Microtubule-Dependent Mitochondria Alignment Regulates Calcium Release in Response to Nanomechanical Stimulus in Heart Myocytes.

Authors:  Michele Miragoli; Jose L Sanchez-Alonso; Anamika Bhargava; Peter T Wright; Markus Sikkel; Sophie Schobesberger; Ivan Diakonov; Pavel Novak; Alessandra Castaldi; Paola Cattaneo; Alexander R Lyon; Max J Lab; Julia Gorelik
Journal:  Cell Rep       Date:  2015-12-24       Impact factor: 9.423

Review 4.  Altered Mitochondrial Metabolism and Mechanosensation in the Failing Heart: Focus on Intracellular Calcium Signaling.

Authors:  Aderville Cabassi; Michele Miragoli
Journal:  Int J Mol Sci       Date:  2017-07-10       Impact factor: 5.923

5.  Shensong Yangxin Protects Against Metabolic Syndrome-Induced Ventricular Arrhythmias by Inhibiting Electrical Remodeling.

Authors:  Hong-Jie Yang; Bin Kong; Wei Shuai; Jing-Jing Zhang; He Huang
Journal:  Front Pharmacol       Date:  2020-07-09       Impact factor: 5.810

6.  Protective effects of Dapagliflozin on the vulnerability of ventricular arrhythmia in rats with pulmonary artery hypertension induced by monocrotaline.

Authors:  Tianyou Qin; Bin Kong; Chang Dai; Zheng Xiao; Jin Fang; Wei Shuai; He Huang
Journal:  Bioengineered       Date:  2022-02       Impact factor: 3.269

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.