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Published in: Journal of Cardiothoracic Surgery 1/2013

Open Access 01-12-2013 | Research article

Intracellular lactate signaling cascade in atrial remodeling of mitral valvular patients with atrial fibrillation

Authors: Jing Xu, Xiaohan Xu, Linjie Si, Lei Xue, Shijiang Zhang, Jianwei Qin, Yanhu Wu, Yongfeng Shao, Yijiang Chen, Xiaowei Wang

Published in: Journal of Cardiothoracic Surgery | Issue 1/2013

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Abstract

Background

Atrial remodeling has emerged as the structural basis for the maintenance and recurrence of atrial fibrillation. Lactate signaling cascade was recently linked to some cardiovascular disorders for its regulatory functions to myocardial structural remodeling. It was hypothesized that lactate signaling cascade was involved in the maintenance and recurrence of atrial fibrillation by regulating atrial structural remodeling.

Methods

Biopsies of right atrial appendage and clinical data were collected from sex- and age-matched 30 persistent atrial fibrillation, 30 paroxysmal atrial fibrillation, 30 sinus rhythm patients undergoing isolated mitral valve surgery and 10 healthy heart donors.

Results

Atrial fibrillation groups had higher atrial lactate expression and this upregulated expression was positively correlated with regulatory indicators of atrial structural remodeling as reflected by severe oxidative stress injury and mitochondrial control of apoptosis.

Conclusions

The present findings suggest a potential role for lactate signaling cascade in the maintenance and recurrence of atrial fibrillation and possibly represent new targets for therapeutic intervention in this disorder.
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Metadata
Title
Intracellular lactate signaling cascade in atrial remodeling of mitral valvular patients with atrial fibrillation
Authors
Jing Xu
Xiaohan Xu
Linjie Si
Lei Xue
Shijiang Zhang
Jianwei Qin
Yanhu Wu
Yongfeng Shao
Yijiang Chen
Xiaowei Wang
Publication date
01-12-2013
Publisher
BioMed Central
Published in
Journal of Cardiothoracic Surgery / Issue 1/2013
Electronic ISSN: 1749-8090
DOI
https://doi.org/10.1186/1749-8090-8-34

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