Wang D, Wu X, Zhong Y, Zhou Y, Shan G, Hu X, Li J, Liu Y, Qin X, Xia Z
Department of Anesthesiology, the First School of Clinical Medicine, China.
J Cardiothorac Vasc Anesth. 1999 Apr;13(2):176-80. doi: 10.1016/s1053-0770(99)90083-6.
To determine whether lidocaine can improve the neuropathologic results in canine brains after retrograde cerebral perfusion (RCP).
Randomized, blinded, experimental study.
University animal laboratory.
Mongrel dogs.
Fourteen mongrel dogs were placed on 120 minutes of hypothermic (20 degrees C) RCP. Following the RPC, they then resumed cardiopulmonary bypass and rewarming for 60 minutes. In the lidocaine group (n = 8), lidocaine was administered continuously; in the control group (n = 6), normal saline was administered. Cerebral perfusion fixation was performed at the end of the experiment.
The number of ischemic cells in 200 neurons was counted in the parietal cortex, CA1 sector of the hippocampus, CA3 sector of the hippocampus, ventral posterolateral nucleus of the thalamus, and Purkinje cells of the cerebellar cortex. Those in the parietal cortex, CA1 sector of the hippocampus, and ventral posterolateral nucleus of the thalamus were significantly less in the lidocaine group than in the control group (25.8+/-17.3 v 53.7+/-12.0; p < 0.01; 17.0+/-8.5 v 54.7+/-22.1; p < 0.01; and 16.9+/-17.8 v 49.7+/-28.4; p < 0.05, respectively). The total number of ischemic cells in the five examined regions was also significantly less in the lidocaine group than in the control group (89.5+/-19.4 v 219.5+/-45.5; p < 0.01).
Continuous lidocaine significantly alleviated the ischemic neuropathologic injury after RCP and thus possibly improved cerebral protection.
确定利多卡因能否改善犬逆行性脑灌注(RCP)后脑组织病理学结果。
随机、盲法实验研究。
大学动物实验室。
杂种犬。
14只杂种犬接受120分钟低温(20℃)RCP。RCP后,恢复体外循环并复温60分钟。利多卡因组(n = 8)持续输注利多卡因;对照组(n = 6)输注生理盐水。实验结束时进行脑灌注固定。
在顶叶皮质、海马CA1区、海马CA3区、丘脑腹后外侧核及小脑皮质浦肯野细胞中,计数200个神经元的缺血细胞数量。利多卡因组顶叶皮质、海马CA1区及丘脑腹后外侧核的缺血细胞数量显著少于对照组(分别为25.8±17.3对53.7±12.0;p < 0.01;17.0±8.5对54.7±22.1;p < 0.01;16.9±17.8对49.7±28.4;p < 0.05)。利多卡因组5个检测区域的缺血细胞总数也显著少于对照组(89.5±19.4对219.5±45.5;p < 0.01)。
持续输注利多卡因可显著减轻RCP后的缺血性神经病理损伤,从而可能改善脑保护作用。