Protective effect of astaxanthin on acute cerebral infarction in rats

被引:80
作者
Nai, Yu [1 ]
Liu, Hong [1 ]
Bi, Xizhuang [1 ]
Gao, Hongyu [2 ]
Ren, Chao [1 ]
机构
[1] Qingdao Univ, Dept Neurol, Affiliated Yantai Yuhuangding Hosp, 20 Yuhuangding East Rd, Yantai, Shandong, Peoples R China
[2] Qingdao Univ, Coll Med, Qingdao, Peoples R China
基金
中国国家自然科学基金;
关键词
Astaxanthin; acute cerebral infarction; oxidative stress; neurological factors; OXIDATIVE STRESS; ARTERY OCCLUSION; BRAIN-DAMAGE; ISCHEMIA; INJURY; ISCHEMIA/REPERFUSION; COMBINATION; ACTIVATION; EXERCISE; AGENT;
D O I
10.1177/0960327117745693
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
The aim of the study was to investigate the effect of astaxanthin and its possible mechanisms on acute cerebral infarction (ACI) in rat model. Male Sprague Dawley rats were randomly divided into sham group, model group, and astaxanthin-treated groups (20, 40, and 80 mg/kg). Neurological examination, the ratio of cerebral edema, and histopathology changes were assessed. Moreover, some oxidative stress markers were obtained for biochemical analysis, and the expression of neurotrophic factors gene was detected by real-time polymerase chain reaction (RT-PCR) method. The results showed that treatment with astaxanthin notably reduced neurological deficit scores and the ratio of cerebral edema compared with the model group. Meanwhile, astaxanthin increased the activity of catalase, superoxide dismutase, and glutathioneperoxidase as well as decreased the content of malondialdehyde in brain tissue. RT-PCR results showed that the expression of brain-derived neurotrophic factor (BDNF) and nerve growth factor (NGF) mRNA were increased with astaxanthin treatment. The results indicated that astaxanthin could ameliorate ACI followed by suppressing oxidative stress and upregulating the expression of BDNF and NGF mRNA.
引用
收藏
页码:929 / 936
页数:8
相关论文
共 30 条
[1]   Neuroprotection by Sildenafil: Neuronal Networks Potentiation in Acute Experimental Stroke [J].
Chen, Xue-Mei ;
Wang, Nan-Nan ;
Zhang, Tian-Yu ;
Wang, Fang ;
Wu, Chun-Fu ;
Yang, Jing-Yu .
CNS NEUROSCIENCE & THERAPEUTICS, 2014, 20 (01) :40-49
[2]  
Chen YH, 2000, ACTA PHARMACOL SIN, V21, P463
[3]   The neuroprotective effect of glial cell line-derived neurotrophic factor in fibrin glue against chronic focal cerebral ischemia in conscious rats [J].
Cheng, H ;
Huang, SS ;
Lin, SM ;
Lin, MJ ;
Chu, YC ;
Chih, CL ;
Tsai, MJ ;
Lin, HC ;
Huang, WC ;
Tsai, SK .
BRAIN RESEARCH, 2005, 1033 (01) :28-33
[4]   Combination therapy with intranasal NGF and electroacupuncture enhanced cell proliferation and survival in rats after stroke [J].
Cheng, Songming ;
Ma, Minmin ;
Ma, Yuping ;
Wang, Zhaolu ;
Xu, Gelin ;
Liu, Xinfeng .
NEUROLOGICAL RESEARCH, 2009, 31 (07) :753-758
[5]   Exercise pre-conditioning reduces brain damage in ischemic rats that may be associated with regional angiogenesis and cellular overexpression of neurotrophin [J].
Ding, Y ;
Li, J ;
Luan, X ;
Ding, YH ;
Lai, Q ;
Rafols, JA ;
Phillis, JW ;
Clark, JC ;
Diaz, FG .
NEUROSCIENCE, 2004, 124 (03) :583-591
[6]   Comparison of administration routes for adipose-derived stem cells in the treatment of middle cerebral artery occlusion in rats [J].
Du, Guojia ;
Liu, Yao ;
Dang, Muren ;
Zhu, Guohua ;
Su, Riqing ;
Fan, Yandong ;
Tan, Zeming ;
Wang, Li Xin ;
Fang, Jiasheng .
ACTA HISTOCHEMICA, 2014, 116 (06) :1075-1084
[7]  
Duan XH, 2015, J TRADIT CHIN MED, V35, P671
[8]   Astaxanthin: A Potential Therapeutic Agent in Cardiovascular Disease [J].
Fassett, Robert G. ;
Coombes, Jeff S. .
MARINE DRUGS, 2011, 9 (03) :447-465
[9]   Protective Effect of Glycyrrhizin, a Direct HMGB1 Inhibitor, on Focal Cerebral Ischemia/Reperfusion-Induced Inflammation, Oxidative Stress, and Apoptosis in Rats [J].
Gong, Gu ;
Xiang, Lei ;
Yuan, Libang ;
Hu, Ling ;
Wu, Wei ;
Cai, Lin ;
Yin, Liang ;
Dong, Hailong .
PLOS ONE, 2014, 9 (03)
[10]   Combination of Ligusticum chuanxiong and Radix Paeoniae ameliorate focal cerebral ischemic in MCAO rats via endoplasmic reticulum stress-dependent apoptotic signaling pathway [J].
Gu, Junfei ;
Chen, Juan ;
Yang, Nan ;
Hou, Xuefeng ;
Wang, Jing ;
Tan, Xiaobin ;
Feng, Liang ;
Jia, Xiaobin .
JOURNAL OF ETHNOPHARMACOLOGY, 2016, 187 :313-324