Direct visualization of trapped erythrocytes in rat brain after focal ischemia and reperfusion

被引:54
作者
Liu, SM
Connor, J
Peterson, S
Shuttleworth, CW
Liu, KJ
机构
[1] Univ New Mexico, Coll Pharm, Albuquerque, NM 87131 USA
[2] Univ New Mexico, Dept Neurosci, Albuquerque, NM 87131 USA
关键词
no-reflow; focal cerebral ischemia; erythrocyte; Fluorescence; sodium borohydride;
D O I
10.1097/01.wcb.0000037998.34930.83
中图分类号
R5 [内科学];
学科分类号
1002 [临床医学]; 100201 [内科学];
摘要
Partial microcirculatory stasis after cerebral ischemia and reperfusion is a potential factor in delayed cell death. Sometimes described as the "no-reflow" phenomenon, limitations in current detection techniques have left the extent and spatial distribution of the phenomenon undetermined, which has led to some doubt as to its actual existence. The authors describe a new method, based on erythrocyte autofluorescence, that allows the erythrocytes trapped in the microvasculature, and thus blocking recirculation, to be directly visualized. Using this method, the authors have examined the spatial and temporal characteristics of this phenomenon in the rat intraluminal model of cerebral ischemia and reperfusion. Up to 15% of the capillaries in the ischemic penumbra remained occluded at least 2 hours after reperfusion. The amount of capillary bed showing trapped erythrocytes was more severe in the ischemic penumbra region than in the ischemic core. These results indicate that the no-reflow phenomenon may contribute to the developing damage in ischemic penumbra region, leading to additional injury after reperfusion.
引用
收藏
页码:1222 / 1230
页数:9
相关论文
共 44 条
[1]
Redox reactions of hemoglobin and myoglobin: Biological and toxicological implications [J].
Alayash, AI ;
Patel, RP ;
Cashon, RE .
ANTIOXIDANTS & REDOX SIGNALING, 2001, 3 (02) :313-327
[2]
AMES A, 1968, AM J PATHOL, V52, P437
[3]
DO LEUKOCYTES HAVE A ROLE IN THE CEREBRAL NO-REFLOW PHENOMENON [J].
ASPEY, BS ;
JESSIMER, C ;
PEREIRA, S ;
HARRISON, MJG .
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 1989, 52 (04) :526-528
[4]
THRESHOLDS IN CEREBRAL-ISCHEMIA - THE ISCHEMIC PENUMBRA [J].
ASTRUP, J ;
SIESJO, BK ;
SYMON, L .
STROKE, 1981, 12 (06) :723-725
[5]
Intravenous basic fibroblast growth factor (bFGF) decreases DNA fragmentation and prevents downregulation of Bcl-2 expression in the ischemic brain following middle cerebral artery occlusion in rats [J].
Ay, I ;
Sugimori, H ;
Finklestein, SP .
MOLECULAR BRAIN RESEARCH, 2001, 87 (01) :71-80
[6]
Perfusion thresholds in human cerebral ischemia: Historical perspective and therapeutic implications [J].
Baron, JC .
CEREBROVASCULAR DISEASES, 2001, 11 :2-8
[7]
EVALUATION OF 2, 3, 5-TRIPHENYLTETRAZOLIUM CHLORIDE AS A STAIN FOR DETECTION AND QUANTIFICATION OF EXPERIMENTAL CEREBRAL INFARCTION IN RATS [J].
BEDERSON, JB ;
PITTS, LH ;
GERMANO, SM ;
NISHIMURA, MC ;
DAVIS, RL ;
BARTKOWSKI, HM .
STROKE, 1986, 17 (06) :1304-1308
[8]
Albumin therapy of transient focal cerebral ischemia - In vivo analysis of dynamic microvascular responses [J].
Belayev, L ;
Pinard, E ;
Nallet, H ;
Seylaz, J ;
Liu, YT ;
Riyamongkol, P ;
Zhao, WZ ;
Busto, R ;
Ginsberg, MD .
STROKE, 2002, 33 (04) :1077-1084
[9]
The cerebral 'no-reflow' phenomenon after cardiac arrest in rats - Influence of low-flow reperfusion [J].
Bottiger, BW ;
Krumnikl, JJ ;
Gass, P ;
Schmitz, B ;
Motsch, J ;
Martin, E .
RESUSCITATION, 1997, 34 (01) :79-87
[10]
Cerisoli M, 1981, J Neurosurg Sci, V25, P7