Electroacupuncture pretreatment inhibits NADPH oxidase-mediated oxidative stress in diabetic mice with cerebral ischemia

被引:28
|
作者
Guo, Fan [1 ,2 ]
Song, Wenying [1 ]
Jiang, Tao [1 ]
Liu, Lixin [3 ]
Wang, Feng [1 ]
Zhong, Haixing [1 ]
Yin, Hong [2 ]
Wang, Qiang [1 ]
Xiong, Lize [1 ]
机构
[1] Forth Mil Med Univ, Xijing Hosp, Dept Anesthesiol, Xian, Peoples R China
[2] Forth Mil Med Univ, Xijing Hosp, Dept Radiol, Xian, Peoples R China
[3] SUNY Stony Brook, Sch Med, Dept Anesthesiol, Stony Brook, NY 11794 USA
基金
中国国家自然科学基金;
关键词
Diabetes mellitus; Cerebral ischemia-reperfusion injury; Electroacupuncture; Oxidative stress; NADPH oxidase; LIPID-PEROXIDATION; VASCULAR-DISEASE; RAPID TOLERANCE; INFARCT SIZE; RAT; ACUPUNCTURE; STROKE; HYPERGLYCEMIA; REPERFUSION; INJURY;
D O I
10.1016/j.brainres.2014.05.020
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
We investigated the protective effect of electroacupuncture (EA) on cerebral ischemic injury in diabetic mice, and explored the role of NADPH oxidase-mediated oxidative stress. Male C57BL/6 mice were injected streptozotocin to induce diabetes. The mice were pretreated with EA at acupoint "Baihui" for 30 min. Two hours after the end of EA pretreatment, focal cerebral ischemia was induced following 24 h reperfusion. The neurobehavioral scores and infarction volumes, malondialdehyde (MDA), reactive oxygen species (ROS), and activation of NADPH oxidase were determined in the presence or absence of the NADPH oxidase inhibitor apocynin or activator tetrabromocinnamic acid (TBCA). EA pretreatment reduced infarct size and improved neurological outcomes 24 h after reperfusion in the diabetic mice. EA also decreased cerebral MDA and ROS levels compared with the control group, and inhibited the NADPH oxidase activation. The beneficial effects were abolished by TBCA while pretreatment with apocynin mimicked the neuroprotective and anti-oxidative effects of EA. Our results demonstrated that EA attenuated cerebral ischemic injury by inhibiting NAPDH oxidase-mediated oxidative damage in diabetic mice. These results suggest a novel mechanism of EA pretreatment-induced tolerance in diabetic cerebral ischemia. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:84 / 91
页数:8
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