Preconditioning with plus Gz acceleration (head-to-foot inertial load) produces neuroprotection against transient focal cerebral ischemia in rats

被引:6
作者
Sang, Hanfei [1 ]
Li, Jinsheng [2 ]
Liu, Junle [1 ]
Wang, Zhou [2 ]
Huo, Tingting [1 ]
Sun, Jing [1 ]
Xiong, Lize [1 ]
机构
[1] Fourth Mil Med Univ, Dept Anesthesiol, Xijing Hosp, Xian 710032, Shaanxi, Peoples R China
[2] Fourth Mil Med Univ, Fac Aerosp Med, Dept Aerosp Hyg, Xian 710032, Shaanxi, Peoples R China
基金
中国国家自然科学基金;
关键词
Middle cerebral artery occlusion; Neuroprotection; +Gz acceleration; Heat shock protein 70;
D O I
10.1016/j.neulet.2008.08.067
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Ischemic preconditioning is considered to be the most robust endogenous neuroprotectant. However, the conventional ischemic preconditioning protocol is both invasive and impractical to apply. The aim of the present study was to evaluate whether preconditioning with +Gz centrifuge acceleration (head-to-foot inertial load) which could induce brief episodes of sublethal ischemia in brain had neuroprotection against focal cerebral ischemic injury. A total of 85 male Sprague-Dawley rats were randomly assigned to five groups (n = 17 in each). The 2 Gz, 4 Gz. 6 Gz and 8 Gz groups were subjected to 3 min exposures at +2 Gz, +4 Gz, +6 Gz and +8 Gz, respectively for consecutive three times in animal centrifuge, with a 30-min rest period between each centrifuge run. The control group had no exposure to +Gz acceleration. Twenty-four hours after the last pretreatment, 12 rats in each groups were subjected to focal cerebral ischemia for 120 min and the other five rats in each group were sacrificed to measure the expression of hear shock protein 70(HSP70) in hippocampus by Western blot analysis. The results indicated that the 6 Gz and 8 Gz groups showed smaller infarct volume and lower neurologic deficit scores than the control group. The expression of HSP70 was significantly increased in 6 Gz and 8 Gz groups than those in the control group. Therefore, preconditioning with +Gz acceleration produced delayed neuroprotection against focal cerebral ischemia and that the neuroprotection may be related to the induction of HSP70. (C) 2008 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:78 / 82
页数:5
相关论文
共 30 条
[1]   Ischemic preconditioning and brain tolerance - Temporal histological and functional outcomes, protein synthesis requirement, and interleukin-1 receptor antagonist and early gene expression [J].
Barone, FC ;
White, RF ;
Spera, PA ;
Ellison, J ;
Currie, RW ;
Wang, XK ;
Feuerstein, GZ .
STROKE, 1998, 29 (09) :1937-1950
[2]   Acceleration after-effects on learning and memory in rats: +10Gz or +6Gz for 3 min [J].
Cao, Xin-Sheng ;
Sun, Xi-Qing ;
Zhang, Shu ;
Wang, Bing ;
Wu, Yan-Hong ;
Liu, Ting-Song ;
Wu, Xing-Yu .
NEUROSCIENCE LETTERS, 2007, 413 (03) :245-248
[3]   Benign focal ischemic preconditioning induces neuronal Hsp70 and prolonged astrogliosis with expression of Hsp27 [J].
Currie, RW ;
Ellison, JA ;
White, RF ;
Feuerstein, GZ ;
Wang, XK ;
Barone, FC .
BRAIN RESEARCH, 2000, 863 (1-2) :169-181
[4]   RETRACTED: Cell biology - Non-thermal heat-shock response to microwaves (Retracted Article. See vol 440, pg 437, 2006) [J].
de Pomerai, D ;
Daniells, C ;
David, H ;
Allan, J ;
Duce, I ;
Mutwakil, M ;
Thomas, D ;
Sewell, P ;
Tattersall, J ;
Jones, D ;
Candido, P .
NATURE, 2000, 405 (6785) :417-418
[5]  
Green NDC, 2006, AVIAT SPACE ENVIR MD, V77, P619
[6]  
Guillaume AI, 2002, AVIAT SPACE ENVIR MD, V73, P171
[7]  
Han L, 1998, J CELL BIOCHEM, V71, P577, DOI 10.1002/(SICI)1097-4644(19981215)71:4<577::AID-JCB12>3.0.CO
[8]  
2-V
[9]   Ischemic tolerance [J].
Kirino, T .
JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 2002, 22 (11) :1283-1296
[10]   ISCHEMIC TOLERANCE PHENOMENON FOUND IN THE BRAIN [J].
KITAGAWA, K ;
MATSUMOTO, M ;
TAGAYA, M ;
HATA, R ;
UEDA, H ;
NIINOBE, M ;
HANDA, N ;
FUKUNAGA, R ;
KIMURA, K ;
MIKOSHIBA, K ;
KAMADA, T .
BRAIN RESEARCH, 1990, 528 (01) :21-24