EXPERIMENTAL BASIS OF MULTIINFARCT DEMENTIA - MEMORY IMPAIRMENTS IN RODENT MODELS OF ISCHEMIA

被引:54
作者
NARITOMI, H [1 ]
机构
[1] NATL CARDIOVASC CTR,DIV CEREBRAL CIRCULAT RES,SUITA,OSAKA 565,JAPAN
关键词
D O I
10.1097/00002093-199100520-00007
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Memory is an intellectual function that is initially and consistently impaired in patients with vascular dementia. Experimental approaches to vascular dementia have so far been confined to investigations of memory impairments in rodent ischemic models. Unilateral middle cerebral artery (MCA) occlusion, multiple small embolization or transient four-vessel occlusion in rats produced acute single or multiple infarctions. In such rats, significant memory impairments occurred during the subacute or chronic phases, but were partially reversible. Permanent stenosis of both common carotid arteries in gerbils caused no ischemic changes at 1 day after stenosis but induced multiple infarctions after 1 week of stenosis, probably due either to chronic recurrent ischemia resulting from transient repetitive obstruction of the carotid arteries or to chronic low perfusion. The memory impairments in this model were persistent. Permanent bilateral common carotid artery occlusion in rats produced multiple infarctions plus white matter changes after 1 week of occlusion. Marked memory impairment was also observed in this model. The results of the above studies suggest that memory impairments due to ischemic causes may be partially reversible provided that the infarctions occur only once and are followed by flow recovery. Memory impairments, however, appear to persist if the brain is exposed to chronic recurrent ischemia or chronic moderately low perfusion. A repetitive or persistent low-flow state appears to be an important factor in determining the irreversibility of cognitive impairments.
引用
收藏
页码:103 / 111
页数:9
相关论文
共 28 条
[1]   LEUKOENCEPHALOPATHY IN PATIENTS WITH ISCHEMIC STROKE [J].
BOGOUSSLAVSKY, J ;
REGLI, F ;
USKE, A .
STROKE, 1987, 18 (05) :896-899
[2]   REGIONAL CEREBRAL BLOOD-FLOW AND HISTOPATHOLOGIC CHANGES AFTER MIDDLE CEREBRAL-ARTERY OCCLUSION IN RATS [J].
BOLANDER, HG ;
PERSSON, L ;
HILLERED, L ;
DARGY, R ;
PONTEN, U ;
OLSSON, Y .
STROKE, 1989, 20 (07) :930-937
[3]   PERIVENTRICULAR LESIONS ON MRI - FACTS AND THEORIES (REPRINTED FROM CURRENT CONCEPTS OF CEREBROVASCULAR-DISEASE AND STROKE, VOL 24, PG 7-12, 1989) [J].
CHIMOWITZ, MI ;
AWAD, IA ;
FURLAN, AJ .
STROKE, 1989, 20 (07) :963-967
[4]   REFERENCE AND WORKING MEMORY OF RATS FOLLOWING HIPPOCAMPAL DAMAGE INDUCED BY TRANSIENT FOREBRAIN ISCHEMIA [J].
DAVIS, HP ;
TRIBUNA, J ;
PULSINELLI, WA ;
VOLPE, BT .
PHYSIOLOGY & BEHAVIOR, 1986, 37 (03) :387-392
[5]   RETENTION OF REFERENCE MEMORY FOLLOWING ISCHEMIC HIPPOCAMPAL DAMAGE [J].
DAVIS, HP ;
BARANOWSKI, JR ;
PULSINELLI, WA ;
VOLPE, BT .
PHYSIOLOGY & BEHAVIOR, 1987, 39 (06) :783-786
[6]   LEUKOENCEPHALOPATHY IN DIFFUSE HEMORRHAGIC CEREBRAL AMYLOID ANGIOPATHY [J].
GRAY, F ;
DUBAS, F ;
ROULLET, E ;
ESCOUROLLE, R .
ANNALS OF NEUROLOGY, 1985, 18 (01) :54-59
[7]   LEUKOARAIOSIS [J].
HACHINSKI, VC ;
POTTER, P ;
MERSKEY, H .
ARCHIVES OF NEUROLOGY, 1987, 44 (01) :21-23
[8]   FLOW THRESHOLDS OF FUNCTIONAL AND MORPHOLOGICAL DAMAGE OF BRAIN-TISSUE [J].
HEISS, WD .
STROKE, 1983, 14 (03) :329-331
[9]  
HELPER DJ, 1985, BRAIN RES, V346, P8
[10]   DELAYED NEURONAL DEATH IN THE GERBIL HIPPOCAMPUS FOLLOWING ISCHEMIA [J].
KIRINO, T .
BRAIN RESEARCH, 1982, 239 (01) :57-69