MICROVASCULATURE IN BRAIN BIOPSY SPECIMENS FROM PATIENTS WITH ALZHEIMERS-DISEASE - AN IMMUNOHISTOCHEMICAL AND ULTRASTRUCTURAL-STUDY

被引:114
作者
VINTERS, HV
SECOR, DL
READ, SL
FRAZEE, JG
TOMIYASU, U
STANLEY, TM
FERREIRO, JA
AKERS, MA
机构
[1] UNIV CALIF LOS ANGELES,MED CTR,BRAIN RES INST,LOS ANGELES,CA 90024
[2] JOHN DOUGLAS FRENCH CTR,LOS ALAMITOS,CA
[3] W LOS ANGELES VET AFFAIRS MED CTR,LOS ANGELES,CA 90073
关键词
ALZHEIMERS DISEASE; AMYLOID ANGIOPATHY; BLOOD-BRAIN BARRIER; BRAIN BIOPSY; CEREBRAL MICROVASCULATURE;
D O I
10.3109/01913129409023202
中图分类号
TH742 [显微镜];
学科分类号
摘要
Brain biopsy specimens from five patients with Alzheimer's disease obtained in the course of a trial of intracerebroventricular bethanechol were studied by immunohistochemical (antibody to A, peptide) and ultrastructural techniques, with particular emphasis on the microvessels. In some cases, numbers of A(4)-immunoreactive lesions (senile plaques) correlated well with numbers of plaques demonstrable by silver stains. Prominent A(4)-immunoreactive amyloid angiopathy was seen in one patient. The patient with severe cerebral amyloid angiopathy (CAA) showed extensive arteriolar deposition of amyloid filaments with apparent destruction of the media but remarkably intact endothelium. A cell of origin for amyloid filaments was not apparent, although close proximity to smooth muscle cell remnants in the arteriolar media suggested this as one possible cell of origin. Frequent vessels showed medial or adventitial collagen deposition, even when the amount of amyloid was minimal or negligible. Thus relatively severe CAA can exist in the absence of overt endothelial injury, although related studies on this tissue indicate definite abnormalities of the blood-brain barrier. Conversely, destruction of smooth muscle cells and collagen deposition in vessel walls may be the cellular correlates of arteriolar weakening that can lead to CAA-related brain hemorrhage.
引用
收藏
页码:333 / 348
页数:16
相关论文
共 74 条
[1]   AN IMMUNOHISTOCHEMICAL STUDY OF BETA-PROTEIN IN ALZHEIMER-TYPE DEMENTIA BRAINS [J].
ARAI, H ;
SAGI, N ;
NOGUCHI, I ;
HAGA, S ;
ISHII, T ;
MAKINO, Y ;
KOSAKA, K .
JOURNAL OF NEUROLOGY, 1989, 236 (04) :214-217
[2]   NEURITIC PLAQUES AND VESSELS OF VISUAL-CORTEX IN AGING AND ALZHEIMERS DEMENTIA [J].
BELL, MA ;
BALL, MJ .
NEUROBIOLOGY OF AGING, 1990, 11 (04) :359-370
[3]   PHENOTYPIC HETEROGENEITY IN FAMILIAL ALZHEIMERS-DISEASE - A STUDY OF 24 KINDREDS [J].
BIRD, TD ;
SUMI, SM ;
NEMENS, EJ ;
NOCHLIN, D ;
SCHELLENBERG, G ;
LAMPE, TH ;
SADOVNICK, A ;
CHUI, H ;
MINER, GW ;
TINKLENBERG, J .
ANNALS OF NEUROLOGY, 1989, 25 (01) :12-25
[4]   ALZHEIMERS-DISEASE - MISMATCH BETWEEN AMYLOID PLAQUES AND NEURITIC PLAQUES [J].
BRAAK, H ;
BRAAK, E ;
OHM, T ;
BOHL, J .
NEUROSCIENCE LETTERS, 1989, 103 (01) :24-28
[5]  
CANCILLA PA, 1972, LAB INVEST, V26, P376
[6]   THE AMYLOID PROTEINS OF ALZHEIMERS-DISEASE AS POTENTIAL TARGETS FOR DRUG-THERAPY [J].
CAPUTO, CB ;
SALAMA, AI .
NEUROBIOLOGY OF AGING, 1989, 10 (05) :451-461
[7]  
CASTANO EM, 1988, LAB INVEST, V58, P122
[8]  
Claudio L., 1992, Society for Neuroscience Abstracts, V18, P1493
[9]   OBSERVATION OF MORPHOLOGICAL RELATIONSHIPS BETWEEN ANGIOPATHIC BLOOD-VESSELS AND DEGENERATIVE NEURITES IN ALZHEIMERS-DISEASE [J].
DELACOURTE, A ;
DEFOSSEZ, A ;
PERSUY, P ;
PEERS, MC .
VIRCHOWS ARCHIV A-PATHOLOGICAL ANATOMY AND HISTOPATHOLOGY, 1987, 411 (03) :199-204
[10]   LOW CEREBROSPINAL-FLUID CONCENTRATIONS OF SOLUBLE AMYLOID BETA-PROTEIN PRECURSOR IN HEREDITARY ALZHEIMERS-DISEASE [J].
FARLOW, M ;
GHETTI, B ;
BENSON, MD ;
FARROW, JS ;
VANNOSTRAND, WE ;
WAGNER, SL .
LANCET, 1992, 340 (8817) :453-454