Anti-apoptotic and neuroprotective effects of Tetramethylpyrazine following subarachnoid hemorrhage in rats

被引:39
作者
Gao, Cheng [1 ]
Liu, Xiangzhen [1 ]
Liu, Wei [2 ]
Shi, Huaizhang [1 ]
Zhao, Zhenhuan [1 ]
Chen, Huirong [1 ]
Zhao, Shiguang [1 ]
机构
[1] HARBIN Med Univ, Affiliated Hosp 1, Dept Neurosurg, Harbin 150001, Heilongjiang, Peoples R China
[2] HARBIN Med Univ, Affiliated Hosp 1, Dept Cardiol, Harbin 150001, Heilongjiang, Peoples R China
来源
AUTONOMIC NEUROSCIENCE-BASIC & CLINICAL | 2008年 / 141卷 / 1-2期
关键词
tetramethylpyrazine; early brain injury; subarachnoid hemorrhage; cerebral vasospasm; caspase-3;
D O I
10.1016/j.autneu.2008.04.007
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
This study was designed to explore the effects of Tetramethylpyrazine on cerebral vasospasm and early brain injury and its underlying mechanisms after experimental SAH in rats. Male Sprague-Dawley rats (n = 164) were allocated randomly to SAH + TMP, SAE + vehicle (sodium chloride), or sham-operated group. The SAH model was induced through perforating internal carotid artery. TMP (30 mg/kg) or the vehicle was injected via vena caudalis 60 min before the perforation. Mortality, neurological scores, water content of brain and cerebral vasospasm were recorded at 24 h after SAH. Apoptosis of cerebral cortex was determined by TUNEL staining; caspase-3, bax and bcl-2 by Western blotting; P53 expression by immunohistochemical staining. TMP administrated in advance improved neurological scores, ameliorated cerebral edema and cerebral vasospasm. TUNEL-positive cells were reduced significantly in TMP-treated group. P53 was not found significantly different between TMP-treated and vehicle-treated group, while P53 positive cells were markedly higher in SAH group than that in sham-operated group. Cleaved caspase-3 protein was decreased significantly in TMP-treated group, while bax, bcl-2 protein expression did not differ statistically among the three groups. In conclusion, TMP ameliorated cerebral vasospasm and early brain injury after experimental SAH in rats. The underlying mechanisms may be partly related to inhibition of caspase-3 dependent proapoptosis pathway. Crown Copyright (c) 2008 Published by Elsevier B.V All rights reserved.
引用
收藏
页码:22 / 30
页数:9
相关论文
共 24 条
[1]   Therapeutic effect of caspase inhibitors in the prevention of apoptosis and reversal of chronic cerebral vasospasm [J].
Aoki, K ;
Zubkov, AY ;
Ross, IB ;
Zhang, JH .
JOURNAL OF CLINICAL NEUROSCIENCE, 2002, 9 (06) :672-677
[2]   Tetramethylpyrazine suppresses HIF-1α, TNF-α, and activated caspase-3 expression in middle cerebral artery occlusion-induced brain ischemia in rats [J].
Chang, Yi ;
Hsiao, George ;
Chen, Seu-hwa ;
chen, Yi-g Chen ;
Lin, Jiing-han ;
Lin, Kuang-hung ;
Chou, Duen-suey ;
Sheu, Joen-rong .
ACTA PHARMACOLOGICA SINICA, 2007, 28 (03) :327-333
[3]   Anti-apoptotic and neuroprotective effects of Tetramethylpyrazine following spinal cord ischemia in rabbits [J].
Fan, Li-Hong ;
Wang, Kun-Zheng ;
Cheng, Bin ;
Wang, Chun-Sheng ;
Dang, Xiao-Qian .
BMC NEUROSCIENCE, 2006, 7 (1)
[4]   Effect of ligustrazine on ischemia-reperfusion injury in murine kidney [J].
Feng, L ;
Xiong, Y ;
Cheng, F ;
Zhang, L ;
Li, S ;
Li, Y .
TRANSPLANTATION PROCEEDINGS, 2004, 36 (07) :1949-1951
[5]  
GAHILL J, 2006, J CEREB BLOOD FLOW M, V26, P1341
[6]   NEUROLOGICAL DEFICIT AND EXTENT OF NEURONAL NECROSIS ATTRIBUTABLE TO MIDDLE CEREBRAL-ARTERY OCCLUSION IN RATS - STATISTICAL VALIDATION [J].
GARCIA, JH ;
WAGNER, S ;
LIU, KF ;
HU, XJ .
STROKE, 1995, 26 (04) :627-634
[7]   Comparison of three rat models of cerebral vasospasm [J].
Gules, I ;
Satoh, M ;
Clower, BR ;
Nanda, A ;
Zhang, JH .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 2002, 283 (06) :H2551-H2559
[8]  
Hara A, 1998, NEUROL RES, V20, P127
[9]   Inhibitory mechanisms of tetra methylpyrazine in middle cerebral artery occlusion (MCAO)-induced focal cerebral ischemia in rats [J].
Hsiao, G ;
Chen, YC ;
Lin, JH ;
Lin, KH ;
Chou, DS ;
Lin, CH ;
Sheu, JR .
PLANTA MEDICA, 2006, 72 (05) :411-417
[10]   Neuroprotection by tetramethylpyrazine against ischemic brain injury in rats [J].
Kao, TK ;
Ou, YC ;
Kuo, JS ;
Chen, WY ;
Liao, SL ;
Wu, CW ;
Chen, CJ ;
Ling, NN ;
Zhang, YH ;
Peng, WH .
NEUROCHEMISTRY INTERNATIONAL, 2006, 48 (03) :166-176