Heavy ion radiation up-regulates Cx43 and ameliorates arrhythmogenic substrates in hearts after myocardial infarction

被引:79
作者
Amino, Mari
Yoshioka, Koichiro
Tanabe, Teruhisa
Tanaka, Etsuro
Mori, Hidezo
Furusawa, Yoshiya
Zareba, Wojciech
Yamazaki, Masatoshi
Nakagawa, Harumichi
Honjo, Haruo
Yasui, Kenji
Kamiya, Kaichiro
Kodama, Itsuo [1 ]
机构
[1] Nagoya Univ, Res Inst Environm Med, Nagoya, Aichi, Japan
[2] Tokai Univ, Sch Med, Dept Cardiol, Isehara, Kanagawa 25911, Japan
[3] Tokyo Univ Agr, Dept Nutr Sci, Tokyo, Japan
[4] Natl Cardiovasc Ctr Hosp & Res Inst, Dept Cardiac Physiol, Osaka, Japan
[5] Natl Inst Radiol Sci, Chiba 260, Japan
[6] Univ Rochester, Cardiol Unit, Rochester, NY 14627 USA
基金
日本学术振兴会;
关键词
gap junctions; connexin43; heavy ion radiaton; myocardial infarction; ventricular arrhythmias; arrhythmia (mechanisms); epicardial mapping;
D O I
10.1016/j.cardiores.2006.09.010
中图分类号
R5 [内科学];
学科分类号
1002 [临床医学]; 100201 [内科学];
摘要
Objective: Radiation has been shown to enhance intercellular communication in the skin and lungs through an increase of connexin43 (Cx43) expression. If analogous Cx43 up-regulation is induced in the diseased heart, it would provide a new perspective in radiation therapy for arrhythmias. The aim of the present study is to test this hypothesis. \ Methods: Non-transmural myocardial infarction (MI) was created in 24 rabbits by microsphere injection into the coronary arteries. Twenty-four rabbits without MI were used as controls. Targeted external heavy ion beam irradiation (THIR; 15 Gy) was applied 2 weeks after MI with an accelerator (HIMAC, Chiba, Japan). Results: The THIR was associated with an increase of Cx43 mRNA and protein levels in the left ventricle in control as well as in MI rabbits. THIR also increased lateralization of Cx43, which was no longer colocalized with cadherins. In MI hearts, immunoreactive Cx43 signals were reduced in the peri-infarct zone, and the reduction was reversed by THIR. In-vivo epicardial potential mapping on the free wall (64 unipolar electrodes to cover 7 x 7 mm) in MI hearts revealed reduced conduction velocity, whereas dispersion of the activation-recovery interval (ARI) was increased compared with controls, and these changes were reversed by TIER. The vulnerability for ventricular tachyarrhythmias (VT/VF), which was estimated by programmed stimulation, was increased in MI hearts, and this increased vulnerability to arrhythmias was reversed by THIR. Conclusions: THIR increases Cx43 expression, improves the conductivity, decreases the spatial heterogeneity of repolarization, and reduces the vulnerability of rabbit hearts to ventricular arrhythmias after MI. THIR could have an antiarrhythmic potential through an improvement of electrical coupling. (c) 2006 European Society of Cardiology. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:412 / 421
页数:10
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