Electroacupuncture regulates NMDA receptor NR1 subunit expression via PI3-K pathway in a rat model of cerebral ischemia-reperfusion

被引:38
作者
Sun, N [1 ]
Zou, XJ [1 ]
Shi, J [1 ]
Liu, XC [1 ]
Li, LL [1 ]
Zhao, L [1 ]
机构
[1] Huazhong Univ Sci & Technol, Tongji Med Coll, Dept Neurobiol, Wuhan 430030, Peoples R China
基金
中国国家自然科学基金;
关键词
cerebral ischemia; electroacupuncture; NMDA receptor subunit; TrkA; MAP kinase; PI3-kinase;
D O I
10.1016/j.brainres.2005.09.060
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Cell survival is regulated by the balance between death and survival signals. Previous studies have shown that the N-methyl-D-aspartate receptors (NMDARs) are responsible for the glutamate-induced excitotoxicity in the postischemic brain. Meanwhile, nerve growth factor (NGF) is critically involved in cell survival and neuroprotective effects via the extracellular signal-related kinase (ERK) pathway or the phosphatidylinositol 3-kinase (PI3-K) pathway mediated by the high affinity NGF receptor, tropomyosin-related kinase A (TrkA). Clinically, electroacupuncture (EA) has been shown to produce beneficial effects on stroke patients. However, the detailed mechanisms mediating the beneficial effects of EA on stroke are still unknown. In the present study, we found that EA treatment reversed the high expression of NR1 subunit and up-regulated the level of TrkA in a rat model of middle cerebral artery occlusion. Using protein kinase inhibitors of specific intracellular signaling pathways, we found that the neuroprotective effects of EA appear to be mediated by stimulation of the PI3-K pathway, but not ERK pathway. These findings may provide important experimental evidence for the clinical application of EA treatment for stroke patients. (C) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:98 / 107
页数:10
相关论文
共 40 条
[1]   Nerve growth factor up-regulates the N-methyl-D-aspartate receptor subunit 1 promoter in PC12 cells [J].
Bai, G ;
Kusiak, JW .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (09) :5936-5942
[2]   Structural and functional properties of the TRK family of neurotrophin receptors [J].
Barbacid, M .
RECEPTOR ACTIVATION BY ANTIGENS, CYTOKINES, HORMONES, AND GROWTH FACTORS, 1995, 766 :442-458
[3]   Expression of messenger RNA coding for the nerve growth factor receptor trkA in the hippocampus of the adult rat [J].
Cellerino, A .
NEUROSCIENCE, 1996, 70 (03) :613-616
[4]  
CHOMCZYNSKI P, 1987, ANAL BIOCHEM, V162, P156, DOI 10.1016/0003-2697(87)90021-2
[5]  
Crowder RJ, 1998, J NEUROSCI, V18, P2933
[6]   NMDA receptor subunits: diversity, development and disease [J].
Cull-Candy, S ;
Brickley, S ;
Farrant, M .
CURRENT OPINION IN NEUROBIOLOGY, 2001, 11 (03) :327-335
[7]   Clenbuterol induces growth factor mRNA, activates astrocytes, and protects rat brain tissue against ischemic damage [J].
Culmsee, C ;
Stumm, RK ;
Schäfer, MKH ;
Weihe, E ;
Krieglstein, J .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1999, 379 (01) :33-45
[8]   Focal cerebral ischemia causes two temporal waves of Akt activation [J].
Friguls, B ;
Justicia, C ;
Pallàs, M ;
Planas, AM .
NEUROREPORT, 2001, 12 (15) :3381-3384
[9]   BDNF protects the neonatal brain from hypoxic-ischemic injury in vivo via the ERK pathway [J].
Han, BH ;
Holtzman, DM .
JOURNAL OF NEUROSCIENCE, 2000, 20 (15) :5775-5781
[10]   Neuroprotection by brain-derived neurotrophic factor is mediated by extracellular signal-regulated kinase and phosphatidylinositol 3-kinase [J].
Hetman, M ;
Kanning, K ;
Cavanaugh, JE ;
Xia, ZG .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (32) :22569-22580