Study on the effect of spinal anesthesia on ventricular arrhythmias in acute myocardial ischemia-reperfusion in rats
10.12092/j.issn.1009-2501.2023.03.002
- Author:
Huabin ZHANG
1
;
Zhongxu LUO
1
;
Deguo WANG
1
;
Huabin ZHANG
2
;
Zhongxu LUO
2
;
Min ZHONG
2
;
Deguo WANG
2
;
Huabin ZHANG
3
;
Zongyuan HONG
3
Author Information
1. Department of Geriatrics, The First Affiliated Hospital of Wannan Medical College, Yijishan Hospital
2. Key Laboratory of Non-coding RNA Transformation Research of Anhui Higher Education Institution of Yijishan Hospital
3. Department of Pharmacy, Wannan Medical College
- Publication Type:Journal Article
- Keywords:
bupivacaine;
cardiac function;
ischemia-reperfusion;
neuroelectrical activity;
spinal anesthesia;
ventricular arrhythmias
- From:
Chinese Journal of Clinical Pharmacology and Therapeutics
2023;28(3):249-256
- CountryChina
- Language:Chinese
-
Abstract:
AIM: To explore the effect of spinal anesthesia on ventricular arrhythmia and involved mechanisms in myocardial ischemia-reperfusion (MIR) rats. METHODS: The rat MIR model was made by occlusion the left anterior descending coronary artery for 30 minutes and reperfusion for 45 minutes. Bupivacaine (0.05 mL / 100 g, 1 mg / kg) was injected slowly via intrathecal for spinal anesthesia. The electromyelogram at T2 thoracic spinal cord was recorded. Ventricular arrhythmias, cardiac function, myocardial damage were assessed by electrocardiography, echocardiography and TTC or HE staining. RESULTS: MIR reduced left ventricular short-axis shortening (LVFS) and left ventricular ejection fraction (LVEF), caused myocardial histological damage and ventricular arrhythmias, promoted spinal electrical discharge frequency and amplitude in T2 dorsal horn. Spinal injection of bupivacaine could significantly reduce spinal cord electrical activities and eliminate MIR-induced arrhythmias. Moreover, bupivacaine also significantly improved MIR-induced myocardial histological damage and cardiac function inhibition. CONCLUSION: Spinal anesthesia can reduce ventricular arrhythmias induced by MIR. The mechanism may be related to the effect of abolishing spinal nerve excitability.
