Ischemic postconditioning as a novel avenue to protect against brain injury after stroke

被引:166
作者
Zhao, Heng [1 ]
机构
[1] Stanford Univ, Sch Med, Dept Neurosurg, Stanford, CA 94305 USA
关键词
cerebral ischemia; focal ischemia; neuroprotection; preconditioning; postconditioning; stroke; FOCAL CEREBRAL-ISCHEMIA; ACUTE MYOCARDIAL-INFARCTION; ANTIOXIDANT ENZYME-ACTIVITY; REPERFUSION-INDUCED INJURY; IN-VIVO; POSTISCHEMIC HYPOPERFUSION; VENTRICULAR-FIBRILLATION; SUPEROXIDE-DISMUTASE; FOREBRAIN ISCHEMIA; SIGNALING PATHWAY;
D O I
10.1038/jcbfm.2009.13
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Ischemic postconditioning initially referred to a stuttering reperfusion performed immediately after reperfusion, for preventing ischemia/reperfusion injury in both myocardial and cerebral infarction. It has evolved into a concept that can be induced by a broad range of stimuli or triggers, and may even be performed as late as 6 h after focal ischemia and 2 days after transient global ischemia. The concept is thought to be derived from ischemic preconditioning or partial/gradual reperfusion, but in fact the first experiment for postconditioning was carried out much earlier than that of preconditioning or partial/gradual reperfusion, in the research on myocardial ischemia. This review first examines the protective effects and parameters of postconditioning in various cerebral ischemic models. Thereafter, it provides insights into the protective mechanisms of postconditioning associated with reperfusion injury and the Akt, mitogen-activated protein kinase (MAPK), protein kinase C (PKC), and ATP-sensitive K(+) (K(ATP)) channel cell signaling pathways. Finally, some open issues and future challenges regarding clinical translation of postconditioning are discussed. Journal of Cerebral Blood Flow & Metabolism (2009) 29, 873-885; doi:10.1038/jcbfm.2009.13; published online 25 February 2009
引用
收藏
页码:873 / 885
页数:13
相关论文
共 71 条
[1]   Remote ischaemic postconditioning protects the heart during acute myocardial infarction in pigs [J].
Andreka, Gyorgy ;
Vertesaljai, Marton ;
Szantho, Gergely ;
Font, Gusztav ;
Piroth, Zsolt ;
Fontos, Geza ;
Juhasz, Eszter D. ;
Szekely, Laszlo ;
Szelid, Zsolt ;
Turner, Mark S. ;
Ashrafian, Houman ;
Frenneaux, Michael P. ;
Andreka, Peter .
HEART, 2007, 93 (06) :749-752
[2]   Reperfusion injury: Demonstration of brain damage produced by reperfusion after transient focal ischemia in rats [J].
Aronowski, J ;
Strong, R ;
Grotta, JC .
JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 1997, 17 (10) :1048-1056
[3]   Prevention of inflammation is a mechanism of preconditioning-induced neuroprotection against focal cerebral ischemia [J].
Bowen, Kellie K. ;
Naylor, Michelle ;
Vemuganti, Raghu .
NEUROCHEMISTRY INTERNATIONAL, 2006, 49 (02) :127-135
[4]   SHORT-TERM POSTISCHEMIC HYPOPERFUSION IMPROVES RECOVERY OF PROTEIN-SYNTHESIS IN THE RAT-BRAIN CORTEX [J].
BURDA, J ;
GOTTLIEB, M ;
VANICKY, I ;
CHABKO, M ;
MARSALA, J .
MOLECULAR AND CHEMICAL NEUROPATHOLOGY, 1995, 25 (2-3) :189-198
[5]  
Burda J, 2006, CELL MOL NEUROBIOL, V26, P1139, DOI DOI 10.1007/S10571-006-9036-X
[6]   Delayed Postconditionig Initiates Additive Mechanism Necessary for Survival of Selectively Vulnerable Neurons After Transient Ischemia in Rat Brain [J].
Jozef Burda ;
Viera Danielisová ;
Miroslava Némethová ;
Miroslav Gottlieb ;
Milina Matiašová ;
Iveta Domoráková ;
Eva Mechírová ;
Marianna Feriková ;
Matilde Salinas ;
Rastislav Burda .
Cellular and Molecular Neurobiology, 2006, 26 (7) :1139-1149
[7]   POSTISCHEMIC MODERATE HYPOTHERMIA INHIBITS CA1 HIPPOCAMPAL ISCHEMIC NEURONAL INJURY [J].
BUSTO, R ;
DIETRICH, WD ;
GLOBUS, MYT ;
GINSBERG, MD .
NEUROSCIENCE LETTERS, 1989, 101 (03) :299-304
[8]   Intracellular signal modulation: A pivotal role for protein kinase C [J].
Casabona, G .
PROGRESS IN NEURO-PSYCHOPHARMACOLOGY & BIOLOGICAL PSYCHIATRY, 1997, 21 (03) :407-425
[9]   Role of oxidants in ischemic brain damage [J].
Chan, PH .
STROKE, 1996, 27 (06) :1124-1129
[10]  
Chen J, 1998, J NEUROSCI, V18, P4914