alexa Effects of Lidocaine on Ischemia/Reperfusion Injury in In vivo Rabbit Hearts | OMICS International | Abstract
ISSN: 2155-6148

Journal of Anesthesia & Clinical Research
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Research Article

Effects of Lidocaine on Ischemia/Reperfusion Injury in In vivo Rabbit Hearts

Uno Imaizumi1, Munetaka Furuya1, Shoko Itakura1, Hitoshi Yui1, Tsuyoshi Tagawa2, Shigeki Sakuraba1, Hirofumi Arisaka1 and Kazu-ichi Yoshida1*

1Division of Anesthesiology, Department of Clinical Care Medicine, Kanagawa Dental College, Kanagawa, Japan

2Division of Clinical Anesthesia, Mie University Hospital, Mie, Japan

*Corresponding Author:
Kazu-ichi Yoshida
Division of Anesthesiology
Department of Clinical Care Medicine, Kanagawa Dental College
82 Inaoka-Cho, Yokosuka, Kanagawa 238-8580, Japan
Tel: +81-46-822-8842
Fax: +81-46-822-8842
E-mail: [email protected]

Received date: October 14, 2012; Accepted date: November 17, 2012; Published date: November 27, 2012

Citation: Imaizumi U, Furuya M, Itakura S, Yui H, Tagawa T, et al. (2012) Effects of Lidocaine on Ischemia/Reperfusion Injury in In vivo Rabbit Hearts. J Anesth Clin Res 3:261. doi: 10.4172/2155-6148.1000261

Copyright: © 2012 Imaizumi U, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Abstract

Objective: The aim of this study was to investigate the cardioprotective effects of lidocaine administered at three different timings, as indexes of hemodynamics, infarct size, antiarrhythmic action, and changing activation time by electrocardiogram in in vivo rabbit hearts. Methods: Thirty two rabbits received regional ischemia by 30 min of left anterior descending coronary artery occlusion followed 3 hours of reperfusion under ketamine and xylazine anesthesia. The animals were randomly assigned to the following 4 treatment groups: a control group, a lidocaine-preconditioned group, a lidocainepostconditioned group, and a lidocaine-continuous administration group. Results: The ratio of areas at risk revealed no significant difference among all groups. Mean infarct size of the area at risk was significantly less in a lidocaine-continuous administration group than other 3 groups. The incidence of arrhythmias during myocardial ischemia was no significant difference between a control group and other 3 groups. The incidence of arrhythmias during reperfusion was no significant difference among all groups. However, lidocaine depressed the activation time which was prolonged by ischemia.

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