Electrical forepaw stimulation during reversible forebrain ischemia decreases infarct volume

被引:41
作者
Burnett, MG
Shimazu, T
Szabados, T
Muramatsu, H
Detre, JA
Greenberg, JH
机构
[1] Univ Penn, Dept Neurol, Sch Med, Philadelphia, PA 19104 USA
[2] Univ Penn, Dept Neurosurg, Sch Med, Philadelphia, PA 19104 USA
关键词
cerebral ischemia; focal; electrical stimulation therapy; middle cerebral artery occlusion;
D O I
10.1161/01.STR.0000217305.82123.d8
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background and Purpose-Functional stimulation is accompanied by increases in regional cerebral blood flow which exceed metabolic demands under normal circumstances, but it is unknown whether functional stimulation is beneficial or detrimental in the setting of acute ischemia. The aim of this study was to determine the effect of forepaw stimulation during temporary focal ischemia on neurological and tissue outcome in a rat model of reversible focal forebrain ischemia. Methods-Sprague-Dawley rats were prepared for temporary occlusion of the right middle cerebral artery (MCA) using the filament model. Cerebral blood flow in the MCA territory was continuously monitored with a laser-Doppler flowmeter. Subdermal electrodes were inserted into the dorsal forepaw to stimulate either the forepaw ipsilateral or contralateral to the occlusion starting 1 minute into ischemia and continuing throughout the ischemic period. A neurological evaluation was undertaken after 24 hours of reperfusion, and animals were then euthanized and brain slices stained with 2,3,5-triphenyltetrazolium chloride. Cortical and striatal damage was measured separately. Results-The cortical and striatal infarct volumes were both significantly reduced in the contralateral stimulated group compared with the ipsilateral stimulated group (48% total reduction). There were no statistically significant differences in the neurobehavioral scores between the 2 groups, or in the laser-Doppler flow measurements from the MCA core. Conclusions-Functional stimulation of ischemic tissue may decrease tissue damage and improve outcome from stroke. Although the precise mechanism of this effect remains to be determined, functional stimulation could readily be translated to clinical practice.
引用
收藏
页码:1327 / 1331
页数:5
相关论文
共 38 条
[1]   Acute carotid occlusion alters the activation flow coupling response to forepaw stimulation in a rat model [J].
Ances, BM ;
Greenberg, JH ;
Detre, JA .
STROKE, 2000, 31 (04) :955-960
[2]   The effects of graded hypercapnia on the activation flow coupling response due to forepaw stimulation in α-chloralose anesthetized rats [J].
Ances, BM ;
Greenberg, JH ;
Detre, JA .
BRAIN RESEARCH, 2001, 911 (01) :82-88
[3]  
Auer RN, 2001, ANN NY ACAD SCI, V939, P271
[4]   SENSITIVITY OF CALCIUM-BINDING IN CEREBRAL TISSUE TO WEAK ENVIRONMENTAL ELECTRIC-FIELDS OSCILLATING AT LOW-FREQUENCY [J].
BAWIN, SM ;
ADEY, WR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1976, 73 (06) :1999-2003
[5]   Activation-flow coupling during graded cerebral ischemia [J].
Burnett, MG ;
Detre, JA ;
Greenberg, JH .
BRAIN RESEARCH, 2005, 1047 (01) :112-118
[6]  
DELZOPPO GJ, 1995, J INTERN MED, V237, P79
[7]   PHOTOCHEMICAL STROKE MODEL - FLUNARIZINE PREVENTS SENSORIMOTOR DEFICITS AFTER NEOCORTICAL INFARCTS IN RATS [J].
DERYCK, M ;
VANREEMPTS, J ;
BORGERS, M ;
WAUQUIER, A ;
JANSSEN, PAJ .
STROKE, 1989, 20 (10) :1383-1390
[8]   Dynamic changes of brain-derived neurotrophic factor protein levels in the rat forebrain after single and recurring kindling-induced seizures [J].
Elmér, E ;
Kokaia, Z ;
Kokaia, M ;
Carnahan, J ;
Nawa, H ;
Lindvall, O .
NEUROSCIENCE, 1998, 83 (02) :351-362
[9]   Ischemic brain damage in mice after selectively modifying BDNF or NT4 gene expression [J].
Endres, M ;
Fan, GP ;
Hirt, L ;
Fujii, M ;
Matsushita, K ;
Liu, X ;
Jaenisch, R ;
Moskowitz, MA .
JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 2000, 20 (01) :139-144
[10]   BDNF stimulates expression, activity and release of tissue-type plasminogen activator in mouse cortical neurons [J].
Fiumelli, H ;
Jabaudon, D ;
Magistretti, PJ ;
Martin, JL .
EUROPEAN JOURNAL OF NEUROSCIENCE, 1999, 11 (05) :1639-1646