Effects of cerebral ischemia on neuronal hemoglobin

被引:46
作者
He, Yangdong [1 ]
Hua, Ya [1 ]
Liu, Wenquan [1 ]
Hu, Haitao [1 ]
Keep, Richard F. [1 ]
Xi, Guohua [1 ]
机构
[1] Univ Michigan, Dept Neurosurg, Ann Arbor, MI 48109 USA
基金
美国国家卫生研究院;
关键词
cerebral ischemia; hemoglobin; ischemic preconditioning; oxygen-glucose deprivation; INTRACEREBRAL HEMORRHAGE; BRAIN EDEMA; GENE-EXPRESSION; NEONATAL-RAT; INJURY; TOLERANCE; NEUROGLOBIN; OXYGEN; NEUROPROTECTION; ATTENUATION;
D O I
10.1038/jcbfm.2008.145
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
This study examined whether neuronal hemoglobin (Hb) is present in rats. It then examined whether cerebral ischemia or ischemic preconditioning (IPC) affects neuronal Hb levels in vivo and in vitro. In vivo, male Sprague-Dawley rats were subjected to either 15 mins of transient middle cerebral artery occlusion (MCAO) with 24 h of reperfusion, an IPC stimulus, or 24 h of permanent MCAO (pMCAO), or IPC followed 3 days later by 24 h of pMCAO. In vitro, primary cultured neurons were exposed to 2 h of oxygen-glucose deprivation (OGD) with 22 h of reoxygenation. Results showed that Hb is widely expressed in rat cerebral neurons but not astrocytes. Hemoglobin expression was significantly upregulated in the ipsilateral caudate and the cortical core of the middle cerebral artery territory after IPC. Hemoglobin levels also increased more in the penumbral cortex and the contralateral hemisphere 24 h after pMCAO, but expressions in the ipsilateral caudate and the cortical core area were decreased. Ischemic preconditioning modified pMCAO-induced brain Hb changes. Neuronal Hb levels in vitro were increased by 2 h of OGD and 22 h of reoxygenation. These results indicate that Hb is synthesized in neurons and can be upregulated by ischemia.
引用
收藏
页码:596 / 605
页数:10
相关论文
共 36 条
[1]   The protective effects of preconditioning on cerebral endothelial cells in vitro [J].
Andjelkovic, AV ;
Stamatovic, SM ;
Keep, RF .
JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 2003, 23 (11) :1348-1355
[2]  
Bergeron M, 2000, ANN NEUROL, V48, P285, DOI 10.1002/1531-8249(200009)48:3<285::AID-ANA2>3.0.CO
[3]  
2-8
[4]   Oxygen tension modulates β-globin switching in embryoid bodies [J].
Bichet, S ;
Wenger, RH ;
Camenisch, G ;
Rolfs, A ;
Ehleben, W ;
Porwol, T ;
Acker, H ;
Fandrey, J ;
Bauer, C ;
Gassmann, M .
FASEB JOURNAL, 1999, 13 (02) :285-295
[5]  
Blalock EM, 2003, J NEUROSCI, V23, P3807
[6]   FUNCTIONING HEMOGLOBIN GENES IN NON-NODULATING PLANTS [J].
BOGUSZ, D ;
APPLEBY, CA ;
LANDSMANN, J ;
DENNIS, ES ;
TRINICK, MJ ;
PEACOCK, WJ .
NATURE, 1988, 331 (6152) :178-180
[7]   Use of a spectrophotometric hemoglobin assay to objectively quantify intracerebral hemorrhage in mice [J].
Choudhri, TF ;
Hoh, BL ;
Solomon, RA ;
Connolly, ES ;
Pinsky, DJ .
STROKE, 1997, 28 (11) :2296-2302
[8]   Ischemic tolerance and endogenous neuroprotection [J].
Dirnagl, U ;
Simon, RP ;
Hallenbeck, JM .
TRENDS IN NEUROSCIENCES, 2003, 26 (05) :248-254
[9]   NEUROPROTECTION FROM ISCHEMIC BRAIN INJURY BY HYPOXIC PRECONDITIONING IN THE NEONATAL RAT [J].
GIDDAY, JM ;
FITZGIBBONS, JC ;
SHAH, AR ;
PARK, TS .
NEUROSCIENCE LETTERS, 1994, 168 (1-2) :221-224
[10]  
GOLDBERG MP, 1993, J NEUROSCI, V13, P3510