Differential cerebral protein synthesis and heat shock protein 70 expression in the core and penumbra of rat brain after transient focal ischemia

被引:36
作者
Kokubo, Y
Liu, JL
Rajdev, S
Kayama, T
Sharp, FR
Weinstein, PR
机构
[1] Univ Calif San Francisco, Dept Neurol Surg, San Francisco, CA 94143 USA
[2] Yamagata Univ, Sch Med, Dept Neurosurg, Yamagata 990, Japan
[3] Univ Cincinnati, Dept Neurol, Cincinnati, OH USA
关键词
cerebral ischemia; heat shock proteins; ischemic penumbra; protein synthesis;
D O I
10.1227/01.NEU.0000069023.01440.D6
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
OBJECTIVE: The purpose of this study was to correlate the cerebral protein synthesis (CPS) reductions in the ischemic core and penumbra with the metabolic stress response indicated by heat shock protein 70 (HSP70) synthesis. METHODS: Rats were subjected to 90 minutes of temporary focal cerebral ischemia produced by occlusion of the middle cerebral artery, using the endovascular suture [S-35] model. Regional CPS was qualitatively evaluated, with methionine autoradiography, after reperfusion for 2 to 72 hours. The observed changes were correlated with HSP70 immunoreactivity, as assessed in the same brain sections. The ischemic core in the striatum was characterized by HSP70 expression only in endothelial and/or glial cells, with an absence of expression in neurons. The penumbra was delineated as the cortical middle cerebral artery territory region in which HSP70 was also expressed in metabolically stressed neurons. RESULTS: After 2 hours of reperfusion, CPS was reduced to 30 +/- 16% of the homologous contralateral hemisphere value in the core and to 75 +/- 22% in the penumbra (P < 0.05). This difference was still present at 72 hours, when CPS values were 62 +/- 21% and 98 +/- 29% of the nonischemic contralateral hemisphere values in the core and,penumbra, respectively (P < 0.05). CONCLUSION: Persistent inhibition of CPS in regions in which neuronal HSP70 expression is absent may distinguish core areas of infarction from penumbral regions in which neuronal HSP70 is present, which eventually recover from sublethal metabolic stress during reperfusion after temporary focal ischemia.
引用
收藏
页码:186 / 190
页数:5
相关论文
共 35 条
[21]   NEURONAL SURVIVAL IS ASSOCIATED WITH 72-KDA HEAT-SHOCK PROTEIN EXPRESSION AFTER TRANSIENT MIDDLE CEREBRAL-ARTERY OCCLUSION IN THE RAT [J].
LI, Y ;
CHOPP, M ;
ZHANG, ZG ;
ZHANG, RL ;
GARCIA, JH .
JOURNAL OF THE NEUROLOGICAL SCIENCES, 1993, 120 (02) :187-194
[22]   DISTRIBUTION OF THE 72-KD HEAT-SHOCK PROTEIN AS A FUNCTION OF TRANSIENT FOCAL CEREBRAL-ISCHEMIA IN RATS [J].
LI, Y ;
CHOPP, M ;
GARCIA, JH ;
YOSHIDA, Y ;
ZHANG, ZG ;
LEVINE, SR .
STROKE, 1992, 23 (09) :1292-1298
[23]   REVERSIBLE MIDDLE CEREBRAL-ARTERY OCCLUSION WITHOUT CRANIECTOMY IN RATS [J].
LONGA, EZ ;
WEINSTEIN, PR ;
CARLSON, S ;
CUMMINS, R .
STROKE, 1989, 20 (01) :84-91
[24]  
Massa SM, 1996, CEREBROVAS BRAIN MET, V8, P95
[25]   ISCHEMIC THRESHOLDS OF CEREBRAL PROTEIN-SYNTHESIS AND ENERGY-STATE FOLLOWING MIDDLE CEREBRAL-ARTERY OCCLUSION IN RAT [J].
MIES, G ;
ISHIMARU, S ;
XIE, Y ;
SEO, K ;
HOSSMANN, KA .
JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 1991, 11 (05) :753-761
[26]   CHANGES IN BRAIN ENERGY-METABOLISM AND PROTEIN-SYNTHESIS FOLLOWING TRANSIENT BILATERAL ISCHEMIA IN THE GERBIL [J].
NOWAK, TS ;
FRIED, RL ;
LUST, WD ;
PASSONNEAU, JV .
JOURNAL OF NEUROCHEMISTRY, 1985, 44 (02) :487-494
[27]  
NOWAK TS, 1990, CEREBROVAS BRAIN MET, V2, P345
[28]   LOCALIZATION OF 70-KDA STRESS PROTEIN MESSENGER-RNA INDUCTION IN GERBIL BRAIN AFTER ISCHEMIA [J].
NOWAK, TS .
JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 1991, 11 (03) :432-439
[29]   Radiolabelled tyrosine for the measurement of protein synthesis rate in vivo by positron emission tomography [J].
Paans, AMJ ;
Pruim, J ;
VanWaarde, A ;
Willemsen, ATM ;
Vaalburg, W .
BAILLIERES CLINICAL ENDOCRINOLOGY AND METABOLISM, 1996, 10 (04) :497-510
[30]   The heat shock stress response after brain lesions: Induction of 72 kda heat shock protein (cell types involved, axonal transport, transcriptional regulation) and protein synthesis inhibition [J].
Planas, AM ;
Soriano, MA ;
Estrada, A ;
Sanz, O ;
Martin, F ;
Ferrer, I .
PROGRESS IN NEUROBIOLOGY, 1997, 51 (06) :607-636