Gastrodin Alleviates Cerebral Ischemic Damage in Mice by Improving Anti-oxidant and Anti-inflammation Activities and Inhibiting Apoptosis Pathway

被引:179
作者
Peng, Zhengwu [1 ,2 ]
Wang, Shiquan [3 ]
Chen, Guanjie [2 ]
Cai, Min [2 ]
Liu, Rui [1 ]
Deng, Jiao [3 ]
Liu, Jiangzheng [1 ]
Zhang, Tao [1 ]
Tan, Qingrong [2 ]
Hai, Chunxu [1 ]
机构
[1] Fourth Mil Med Univ, Shaanxi Key Lab Free Radical Biol & Med, Key Lab Hazard Assessment & Control Special Opera, Dept Toxicol,Minist Educ,Sch Publ Hlth, Xian 710032, Peoples R China
[2] Fourth Mil Med Univ, Xijing Hosp, Dept Psychiat, Xian 710032, Peoples R China
[3] Fourth Mil Med Univ, Xijing Hosp, Dept Anesthesiol, Xian 710032, Peoples R China
基金
中国国家自然科学基金;
关键词
Gastrodin; Cerebral ischemia/reperfusion; Akt; Nrf2; EXTENDED THERAPEUTIC WINDOW; P-HYDROXYBENZYL ALCOHOL; NF-KAPPA-B; OXIDATIVE STRESS; DELAYED TREATMENT; FOCAL ISCHEMIA; ETHER FRACTION; INFARCT SIZE; NRF2; PATHWAY; BRAIN-INJURY;
D O I
10.1007/s11064-015-1513-5
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Gastrodin (GAS), an active constituent of the Chinese herbal medicine Tianma, has anti-oxidant and anti-inflammation activities but its protective effect to the prevention of neurotoxicity induced by ischemic stroke is unclear. In the present study, middle cerebral artery occlusion (MCAO) was used to establish a mice ischemic stroke model. Infarct volume ratio and neurobehavioral score were evaluated, Nissl staining was performed and the expression of cleaved Caspase 3, Bax and B cell lymphoma 2 (Bcl-2) were assessed at 24 h or 7 days after reperfusion. In addition, the total superoxide dismutase (SOD) activity and malondialdehyde (MDA) content, as well as the expression of Nuclear factor erythroid 2-related factor 2 (Nrf2), heme oxygenase-1 (HO-1), SOD1, phospho-Akt and total Akt and TNF-alpha and IL-1 beta in the ischemic hemispheres were also observed at 6 h after reperfusion to assess oxidative stress and inflammatory changes after GAS treatment. It was found that GAS, especially at high dose (100 mg/kg) reduced tested neuronal injury and neurobehavioral deficient in MCAO mice. Enhanced expression of cleaved Caspase 3 and Bax and decreased expression of Bcl-2 by MCAO were also reversed by GAS. Moreover, GAS treatment decreased the MDA content and the expression of TNF-alpha and IL-1 beta, and increased amount of SOD activity and the expression of HO-1 and SOD1 in GAS-treated ischemic brain. Furthermore, GAS significantly increased Akt phosphorylation and Nrf2 expression. These results support the neuroprotective effects of GAS, and the activation of Akt/Nrf2 pathway may play a critical role in the pharmacological action of GAS.
引用
收藏
页码:661 / 673
页数:13
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