Key result
Focused ultrasound stimulation of the vagus nerve significantly reduced infarct size, ventricular arrhythmias, and inflammatory markers following acute myocardial ischemia/reperfusion injury in rats.
Why the study?
Invasive electrical vagus nerve stimulation attenuates acute myocardial I/R injury but carries risks of infection and complications, making a non-invasive stimulation method desirable.
Does non-invasive focused ultrasound stimulation of the vagus nerve reduce acute myocardial ischemia/reperfusion injury in a rat model?
Does non-invasive focused ultrasound stimulation of the vagus nerve reduce acute myocardial ischemia/reperfusion injury in a rat model?
Non-invasive focused ultrasound stimulation of the vagus nerve protects against acute myocardial ischemia/reperfusion injury in rats by inhibiting inflammation via the cholinergic pathway.
Hypothesis-generating for non-invasive vagus stimulation in myocardial I/R injury; prospective trials needed before clinical adoption.
Background The invasive method using electrically stimulating vagus nerve has been demonstrated to inhibit the inflammatory response against acute myocardial ischemia/reperfusion(I/R) injury. This neuro-regulatory technique used is invasive implantation of electrical stimulators which have the risk of infection and other complications. A non-invasive method of vagus nerve stimulation applying on acute myocardial I/R injury is particularly important and desirable. Objectives This study aimed to test the hypothesis that focused ultrasound stimulation(FUS) of vagus nerve attenuates acute myocardial I/R injury through cholinergic anti-inflammatory pathway. Methods This study was completed with two parts. In the first part, ischemia was induced by left anterior descending coronary artery (LAD) occlusion for 30 minutes (min), followed by 2 hours (h) of reperfusion, FUS lasted for 50 min after reperfusion for 10 min. Infammatory markers, arrhythmia score, histopathology, infammatory markers α7 nicotinic acetylcholine receptor (α7nAchR) protein were determined. In the second part, ischemia was induced by LAD occlusion for 30 min, followed by 24h of reperfusion, FUS lasted for 50 min after reperfusion for 10 min. Myocardial fibrosis, infarct size, echocardiographic measurements, biomarkers of pro-oxidative stress, antioxidant and myocardial apoptosis were determined. Results FUS of vagus nerve significantly decreased the level of infammatory markers in I/R+FUS group compared with the I/R group, I/R+vagotomy group and I/R+vagotomy+FUS group. FUS decreased the incidence of ventricular tachycardia (VT) and ventricular fibrillation (VF), while also reduced arrhythmia score in I/R+FUS group compared with the I/R group. These improvements were associated with the inhibition of acute inflammatory reaction through cholinergic anti-inflammatory pathway. FUS limited myocardial fibrosis and infarct size, preserved left ventricular function. This cardioprotective effect was associated with alleviation of apoptosis and oxidative stress. Conclusions The noninvasive method of ultrasonic neuromodulation using FUS of vagus nerve exerted protective effects on acute myocardial I/R injury. Its potential mechanisms involved the suppression of acute inflammatory reaction through cholinergic anti-inflammatory pathway.
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Zhang et al. (2023) studied Acute myocardial ischemia/reperfusion injury (n=72). Focused ultrasound stimulation of vagus nerve vs. I/R without FUS, sham, and vagotomy groups was evaluated on Myocardial ischemia/reperfusion injury (inflammatory markers, infarct size, arrhythmias) (p=<0.05). Focused ultrasound stimulation of the vagus nerve significantly reduced infarct size, ventricular arrhythmias, and inflammatory markers following acute myocardial ischemia/reperfusion injury in rats.
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