Key result
Left stellate ganglion ablation significantly increased the ventricular fibrillation threshold (7.1 V vs 3.0 V, P<0.001) and reduced ventricular tachycardia inducibility in canines with acute ischemic stroke.
Why the study?
To investigate the mechanism of ventricular arrhythmias following acute ischemic stroke and explore the effects of left stellate ganglion ablation on stroke-induced ventricular arrhythmias.
Does left stellate ganglion ablation reduce ventricular arrhythmia vulnerability in a canine model of acute ischemic stroke?
Does left stellate ganglion ablation reduce ventricular arrhythmia vulnerability in a canine model of acute ischemic stroke?
Absolute Event Rate: 7.1% vs 3%
p-value: p=<0.001
Left stellate ganglion ablation reduces ventricular arrhythmia vulnerability after acute ischemic stroke in a canine model by modulating sympathetic hyperactivity and macrophage polarization.
LSG ablation may attenuate post-stroke VAs in canines; leaves open any role in human stroke patients.
Aims: To investigate the potential mechanism of ventricular arrhythmias (VAs) after acute ischemic stroke and explore the effects of left stellate gangling (LSG) ablation on VAs induced by stroke in canines. Materials and Methods: Twenty canines were randomly divided into the sham-operated group (n=6), AS group (n=7) and SGA group (n=7). Cerebral ischemic model was established in the AS group and the SGA group by right acute middle cerebral artery occlusion (MCAO). LSG ablation was performed in the SGA group as soon as MCAO. After 3 days, atrial electrophysiology and neural activity were measured in vivo. The levels of norepinephrine (NE) in plasma and ventricle were detected by ELISA. The levels of monocyte chemotactic protein-1 (MCP-1), tumor necrosis factor- (TNF-) and NF-B p65 in ventricle were detected by western blotting. The pro-inflammatory polarization of macrophages in ventricle was detected by immunofluorescence. Results: Higher ventricular tachycardia (VT) inducibility and lower ventricular fibrillation threshold (VFT) were observed in the AS group compared with those in the sham-operated group, associated with higher LSG activity and NE levels, increased number of M1 macrophages and secretion of inflammatory cytokines in ventricle (all P<0.001). Compared with the AS group, the SGA group had lower VT inducibility and higher VFT, combined with lower NE levels, and reduced number of M1 macrophages and secretion of inflammatory cytokines in ventricle (all P<0.001). Conclusion: LSG ablation could reduce VAs vulnerability after acute stroke by preventing the macrophages polarization and activation induced by sympathetic hyperactivity.
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Wang et al. (2021) studied Acute ischemic stroke (n=20). Left stellate ganglion (LSG) ablation vs. Acute stroke without ablation (AS group) was evaluated on Ventricular fibrillation threshold (VFT) (p=<0.001). Left stellate ganglion ablation significantly increased the ventricular fibrillation threshold (7.1 V vs 3.0 V, P<0.001) and reduced ventricular tachycardia inducibility in canines with acute ischemic stroke.
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