Hagendorff A, Schumacher B, Kirchhoff S, Lüderitz B, Willecke K
Department of Cardiology, Institute of Genetics, University of Bonn, Germany.
Circulation. 1999 Mar 23;99(11):1508-15. doi: 10.1161/01.cir.99.11.1508.
Recently, it has been reported that connexin40 (Cx40) deficiency in targeted mouse mutants is associated with a prolongation of P-wave and QRS complex duration on surface electrograms. The specific effects of Cx40 deficiency on sinus node function, sinoatrial, and atrioventricular conduction properties as well as on atrial vulnerability have not yet been investigated systematically by electrophysiological analysis.
Fifty-two mice (18 Cx40(+/+), 15 Cx40(+/-), and 19 Cx40(-/-) mice) were subjected to rapid atrial transesophageal stimulation after anesthesia with avertin. A significant prolongation of sinus node recovery time was noticed in Cx40(-/-) mice compared with Cx40(+/-) and Cx40(+/+) mice (287.8+/-109.0 vs 211.1+/-61.8 vs 204.4+/-60.9 ms; P<0.05). In addition, Wenckebach periodicity occurred at significantly longer atrial pacing cycle lengths in Cx40(-/-) mice than in Cx40(+/-) or Cx40(+/+) mice (93. 3+/-11.8 vs 83.9+/-9.7 vs 82.8+/-8.0 ms, P<0.05). Analysis of 27 Cx40(-/-) mice showed a significant increase in intra-atrial conduction time and atrioventricular conduction time compared with 52 Cx40(+/-) and 31 wild-type (Cx40(+/+)) mice. Furthermore, in Cx40(-/-) mice, atrial tachyarrhythmias could be induced frequently by atrial burst pacing, whereas no atrial arrhythmias were inducible in heterozygous or wild-type mice.
This study demonstrates that Cx40 deficiency is associated with sinoatrial, intra-atrial, and atrioventricular conduction disturbances. In atrial myocardium of the mouse, Cx40 deficiency results in increased atrial vulnerability and might contribute to arrhythmogenesis.
最近有报道称,靶向小鼠突变体中连接蛋白40(Cx40)缺乏与体表心电图上P波和QRS波群时限延长有关。Cx40缺乏对窦房结功能、窦房结和房室传导特性以及心房易损性的具体影响尚未通过电生理分析进行系统研究。
52只小鼠(18只Cx40(+/+)、15只Cx40(+/-)和19只Cx40(-/-)小鼠)在经阿佛丁麻醉后接受快速心房经食管刺激。与Cx40(+/-)和Cx40(+/+)小鼠相比,Cx40(-/-)小鼠的窦房结恢复时间显著延长(287.8±109.0 vs 211.1±61.8 vs 204.4±60.9毫秒;P<0.05)。此外,Cx40(-/-)小鼠出现文氏周期时的心房起搏周期长度明显长于Cx40(+/-)或Cx40(+/+)小鼠(93.3±11.8 vs 83.9±9.7 vs 82.8±8.0毫秒,P<0.05)。对27只Cx40(-/-)小鼠的分析显示,与52只Cx40(+/-)小鼠和31只野生型(Cx40(+/+))小鼠相比,其心房内传导时间和房室传导时间显著增加。此外,在Cx40(-/-)小鼠中,心房猝发起搏可频繁诱发房性快速心律失常,而杂合子或野生型小鼠则不能诱发房性心律失常。
本研究表明,Cx40缺乏与窦房结、心房内和房室传导障碍有关。在小鼠心房肌中,Cx40缺乏会增加心房易损性,并可能导致心律失常的发生。