Experimental study of the protection of ischemic preconditioning to spinal cord ischemia

被引:33
作者
Fan, T
Wang, CC
Wang, FM
Cheng, F
Qiao, H
Liu, SL
Guo, W
Xiang, FY
机构
[1] Inst Neurosurg, Beijing 100050, Peoples R China
[2] Beijing Tian Tan Hosp, Neuroimaging Ctr, Beijing, Peoples R China
来源
SURGICAL NEUROLOGY | 1999年 / 52卷 / 03期
关键词
spinal cord; preconditioning; ischemia; blood flow; spinal cord evoked potentials (SCEPs);
D O I
10.1016/S0090-3019(99)00082-8
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
BACKGROUND Since the advent of ischemic preconditioning in myocardium, more and more attention has been paid to ischemic preconditioning in the central nervous system (CNS), This study was designed to evaluate the protective effect of ischemic preconditioning on spinal cord ischemia. METHODS Interventional neuroradiological techniques were used to induce spinal cord ischemia in a rabbit model. Hydrogen electrode technique was used to determine the regional blood flow of the spinal cord. Catecholamines and their metabolites were measured by high performance liquid chromatography (HPLA). Spinal cord evoked potentials were recorded to show spinal cord neurofunction. RESULTS After 5 minutes ischemic preconditioning with 20 minutes reperfusion, the regional spinal cord blood flow (rSCBF) was increased, as may be seen by the slight increase of catecholamine, especially NE. This is in positive proportion to the cAMP and indicates the enhancement of the metabolic activities of the spinal cord. After 30 minutes of irreversible ischemia, the great increase in catecholamine caused vascular spasm, endotheliocyte fissure, multiple hemorrhagic suffusion, and necrosis, which would injure the spinal cord as a result. The slight increase of the rSCBF and the maintenance of the rSCBF after irreversible ischemia may enhance the protection of ischemic preconditioning to the spinal cord neurofunction, which was proved by spinal cord evoked potentials (SCEPs). CONCLUSIONS Our study showed that 5 minutes of ischemic preconditioning can increase the rSCBF, enhance the tolerance of the spinal cord to irreversible ischemia, and protect the neurofunction of the spinal cord. The biological mechanism of the protective effect of ischemic preconditioning to spinal cord ischemia should be further studied. (C) 1999 by Elsevier Science Inc.
引用
收藏
页码:299 / 305
页数:7
相关论文
共 18 条
[1]
BERGUER R, 1992, J VASC SURG, V15, P26
[2]
CHARACTERIZATION OF PROTEIN-KINASE-C ISOTYPE EXPRESSION IN ADULT-RAT HEART - PROTEIN-KINASE C-EPSILON IS A MAJOR ISOTYPE PRESENT, AND IT IS ACTIVATED BY PHORBOL ESTERS, EPINEPHRINE, AND ENDOTHELIN [J].
BOGOYEVITCH, MA ;
PARKER, PJ ;
SUGDEN, PH .
CIRCULATION RESEARCH, 1993, 72 (04) :757-767
[3]
INHIBITION OF MONONUCLEAR PHAGOCYTES REDUCES ISCHEMIC-INJURY IN THE SPINAL-CORD [J].
GIULIAN, D ;
ROBERTSON, C .
ANNALS OF NEUROLOGY, 1990, 27 (01) :33-42
[4]
METHYLPREDNISOLONE TREATMENT OF EXPERIMENTAL SPINAL-CORD INJURY [J].
IWAI, A ;
MONAFO, WW ;
ELIASSON, SG .
PARAPLEGIA, 1993, 31 (07) :417-429
[5]
PRECONDITIONING MYOCARDIUM WITH ISCHEMIA [J].
JENNINGS, RB ;
MURRY, CE ;
REIMER, KA .
CARDIOVASCULAR DRUGS AND THERAPY, 1991, 5 (05) :933-938
[6]
INDUCTION OF TOLERANCE TO ISCHEMIA - ALTERATIONS IN 2ND-MESSENGER SYSTEMS IN THE GERBIL HIPPOCAMPUS [J].
KATO, H ;
ARAKI, T ;
MURASE, K ;
KOGURE, K .
BRAIN RESEARCH BULLETIN, 1992, 29 (05) :559-565
[7]
PROTECTION AGAINST INFARCTION AFFORDED BY PRECONDITIONING IS MEDIATED BY A1 ADENOSINE RECEPTORS IN RABBIT HEART [J].
LIU, GS ;
THORNTON, J ;
VANWINKLE, DM ;
STANLEY, AWH ;
OLSSON, RA ;
DOWNEY, JM .
CIRCULATION, 1991, 84 (01) :350-356
[8]
PROTECTION OF RAT HIPPOCAMPUS AGAINST ISCHEMIC NEURONAL DAMAGE BY PRETREATMENT WITH SUBLETHAL ISCHEMIA [J].
LIU, Y ;
KATO, H ;
NAKATA, N ;
KOGURE, K .
BRAIN RESEARCH, 1992, 586 (01) :121-124
[9]
ISCHEMIC PRECONDITIONING SLOWS ENERGY-METABOLISM AND DELAYS ULTRASTRUCTURAL DAMAGE DURING A SUSTAINED ISCHEMIC EPISODE [J].
MURRY, CE ;
RICHARD, VJ ;
REIMER, KA ;
JENNINGS, RB .
CIRCULATION RESEARCH, 1990, 66 (04) :913-931
[10]
NAFTCHI NE, 1982, SPINAL CORD INJURY, P67