Attenuating brain edema, hippocampal oxidative stress, and cognitive dysfunction in rats using hyperbaric oxygen preconditioning during simulated high-altitude exposure

被引:20
|
作者
Lin, Hung [2 ]
Chang, Ching-Ping [4 ]
Lin, Hung-Jung [2 ,4 ]
Lin, Mao-Tsun [3 ]
Tsai, Cheng-Chia [1 ]
机构
[1] Mackay Mem Hosp, Dept Surg, Taipei, Taiwan
[2] Chi Mei Med Ctr, Dept Surg, Dept Emergency Med, Tainan, Taiwan
[3] Chi Mei Med Ctr, Dept Med Res, Tainan, Taiwan
[4] So Taiwan Univ, Dept Biotechnol, Tainan, Taiwan
来源
关键词
High-altitude cerebral edema; hyperbaric oxygen preconditioning; hippocampus; cognition; oxidative stress; ACUTE MOUNTAIN-SICKNESS; UP-REGULATING HEAT-SHOCK-PROTEIN-70; THIOBARBITURIC ACID REACTION; HYPOBARIC HYPOXIA; CEREBRAL-ISCHEMIA; GLUTATHIONE; INJURY; TOLERANCE; NEURONS; TISSUES;
D O I
10.1097/TA.0b013e318246ee70
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
BACKGROUND: We assessed whether hyperbaric oxygen preconditioning (HBO2P) in rats induced heat shock protein (HSP)-70 and whether HSP-70 antibody (Ab) preconditioning attenuates high altitude exposure (HAE)-induced brain edema, hippocampal oxidative stress, and cognitive dysfunction. METHODS: Rats were randomly divided into five groups: the non-HBO2P + non-HAE group, the HBO2P + non-HAE group, the non-HBO2P + HAE group, the HBO2P + HAE group, and the HBO2P + HSP-70 Abs + HAE group. The HBO2P groups were given 100% O-2 at 2.0 absolute atmospheres for 1 hour per day for 5 consecutive days. The HAE groups were exposed to simulated HAE (9.7% O-2 at 0.47 absolute atmospheres of 6,000 m) in a hypobaric chamber for 3 days. Polyclonal rabbit anti-mouse HSP-70-neutralizing Abs were intravenously injected 24 hours before the HAE experiments. Immediately after returning to normal atmosphere, the rats were given cognitive performance tests, overdosed with a general anesthetic, and then their brains were excised en bloc for water content measurements and biochemical evaluation and analysis. RESULTS: Non-HBO2P group rats displayed cognitive deficits, brain edema, and hippocampal oxidative stress (evidenced by increased toxic oxidizing radicals [e. g., nitric oxide metabolites and hydroxyl radicals], increased pro-oxidant enzymes [e. g., malondialdehyde and oxidized glutathione] but decreased antioxidant enzymes [e. g., reduced glutathione, glutathione peroxide, glutathione reductase, and superoxide dismutase]) in HAE. HBO2P induced HSP-70 overexpression in the hippocampus and significantly attenuated HAE-induced brain edema, cognitive deficits, and hippocampal oxidative stress. The beneficial effects of HBO2P were significantly reduced by HSP-70 Ab preconditioning. CONCLUSION: Our results suggest that high-altitude cerebral edema, cognitive deficit, and hippocampal oxidative stress can be prevented by HSP-70-mediated HBO2P in rats. (J Trauma. 2012; 72: 1220-1227. Copyright (C) 2012 by Lippincott Williams & Wilkins)
引用
收藏
页码:1220 / 1227
页数:8
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