Decreased connexin 40 expression of the sinoatrial node mediates ischemic stroke-induced arrhythmia in mice

Arrhythmia is the most common cardiac complication after ischemic stroke. Connexin 40 is the staple component of gap junctions, which influences the propagation of cardiac electrical signals in the sinoatrial node. However, the role of connexin 40 in post-stroke arrhythmia remains unclear. In this s...

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Veröffentlicht in:Experimental neurology 2024-06, Vol.376, p.114773-114773, Article 114773
Hauptverfasser: Yao, Zhi-Jun, Jiang, Yan-Pin, Yuan, Dan, Hong, Pu, He, Meng-Jiao, Li, Feng-Xian, Xu, Shi-Yuan, Lin, Hong-Bin, Zhang, Hong-Fei
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Sprache:eng
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Zusammenfassung:Arrhythmia is the most common cardiac complication after ischemic stroke. Connexin 40 is the staple component of gap junctions, which influences the propagation of cardiac electrical signals in the sinoatrial node. However, the role of connexin 40 in post-stroke arrhythmia remains unclear. In this study, a permanent middle cerebral artery occlusion model was used to simulate the occurrence of an ischemic stroke. Subsequently, an electrocardiogram was utilized to record and assess variations in electrocardiogram measures. In addition, optical tissue clearing and whole-mount immunofluorescence staining were used to confirm the anatomical localization of the sinoatrial node, and the sinoatrial node tissue was collected for RNA sequencing to screen for potential pathological mechanisms. Lastly, the rAAV9-Gja5 virus was injected with ultrasound guidance into the heart to increase Cx40 expression in the sinoatrial node. We demonstrated that the mice suffering from a permanent middle cerebral artery occlusion displayed significant arrhythmia, including atrial fibrillation, premature ventricular contractions, atrioventricular block, and abnormal electrocardiogram parameters. Of note, we observed a decrease in connexin 40 expression within the sinoatrial node after the ischemic stroke via RNA sequencing and western blot. Furthermore, rAAV9-Gja5 treatment ameliorated the occurrence of arrhythmia following stroke. In conclusion, decreased connexin 40 expression in the sinoatrial node contributed to the ischemic stroke-induced cardiac arrhythmia. Therefore, enhancing connexin 40 expression holds promise as a potential therapeutic approach for ischemic stroke-induced arrhythmia. Role of Cx40 in the sinoatrial node in ischemic stroke-induced arrhythmia. Decreased Cx40 expression was presented in the sinoatrial node in the context of ischemic stroke, which leads to impaired intercellular communication among cardiac pacemaker cells, resulting in cardiac arrhythmias after ischemic stroke. [Display omitted] •Stroke induced arrhythmia•Cx40 abnormality caused stroke-related arrhythmia.•Stroke induced genetic alteration in SAN
ISSN:0014-4886
1090-2430
DOI:10.1016/j.expneurol.2024.114773