Future targets and cascades for neuroprotective strategies

被引:43
作者
Chan, PH
机构
[1] Stanford Univ, Neurosurg Labs, Dept Neurosurg, Sch Med, Stanford, CA 94305 USA
[2] Stanford Univ, Sch Med, Dept Neurol & Neurol Sci, Stanford, CA 94305 USA
[3] Stanford Univ, Sch Med, Program Neurosci, Stanford, CA 94305 USA
关键词
apoptosis; cell survival signaling; mitochondria; neuroprotection; stroke;
D O I
10.1161/01.STR.0000143325.25610.ac
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Cumulative evidence suggests that apoptosis plays a pivotal role in neuronal death after cerebral ischemia in various experimental animal models. The time-dependent molecular and biochemical sequelae that lead to apoptotic cell death after the interruption of cerebral blood flow have been established. Many neuroprotective agents that target cell death pathways have been failures, and alternative strategies need to be considered. One such strategy is to target the neuronal survival signaling pathway, which involves the phosphatidylinositol 3-kinase (PI3-K)/Akt (protein kinase B) pathway. It has been demonstrated that PI3-K/Akt and downstream phosphorylated Bad and proline-rich Akt substrate survival signaling cascades are upregulated in surviving neurons in the ischemic brain that overexpresses copper-zinc superoxide dismutase activity. These studies provide an impetus for novel therapeutic targets in neuroprotective strategies in stroke.
引用
收藏
页码:2748 / 2750
页数:3
相关论文
共 25 条
[1]   Reactive oxygen radicals in signaling and damage in the ischemic brain [J].
Chan, PH .
JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 2001, 21 (01) :2-14
[2]   Overexpression of SOD1 in transgenic rats protects vulnerable neurons against ischemic damage after global cerebral ischemia and reperfusion [J].
Chan, PH ;
Kawase, M ;
Murakami, K ;
Chen, SF ;
Li, YB ;
Calagui, B ;
Reola, L ;
Carlson, E ;
Epstein, CJ .
JOURNAL OF NEUROSCIENCE, 1998, 18 (20) :8292-8299
[3]  
Chen J, 1998, J NEUROSCI, V18, P4914
[4]   Poly(ADP-ribose) polymerase gene disruption renders mice resistant to cerebral ischemia [J].
Eliasson, MJL ;
Sampei, K ;
Mandir, AS ;
Hurn, PD ;
Traystman, RJ ;
Bao, J ;
Pieper, A ;
Wang, ZQ ;
Dawson, TM ;
Snyder, SH ;
Dawson, VL .
NATURE MEDICINE, 1997, 3 (10) :1089-1095
[5]   Ischemic brain injury is mediated by the activation of poly(ADP-ribose)polymerase [J].
Endres, M ;
Wang, ZQ ;
Namura, S ;
Waeber, C ;
Moskowitz, MA .
JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 1997, 17 (11) :1143-1151
[6]   Cytosolic redistribution of cytochrome c after transient focal cerebral ischemia in rats [J].
Fujimura, M ;
Morita-Fujimura, Y ;
Murakami, K ;
Kawase, M ;
Chan, PH .
JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 1998, 18 (11) :1239-1247
[7]  
Fujimura M, 2000, J NEUROSCI, V20, P2817
[8]  
Fujimura M, 1999, J NEUROSCI, V19, P3414
[9]   Cytochrome c associated apoptosis during ATP recovery after hypoxia in neonatal rat cerebrocortical slices [J].
Hirai, K ;
Sugawara, T ;
Chan, PH ;
Basus, VJ ;
James, TL ;
Litt, L .
JOURNAL OF NEUROCHEMISTRY, 2002, 83 (02) :309-319
[10]  
Kondo T, 1997, ACT NEUR S, V70, P62