Neuroprotective effect of calycosin on cerebral ischemia and reperfusion injury in rats

被引:166
作者
Guo, Chao [1 ]
Tong, Li [2 ]
Xi, Miaomaio [1 ]
Yang, Haifan [2 ]
Dong, Hailong [2 ]
Wen, Aidong [1 ]
机构
[1] Fourth Mil Med Univ, Dept Pharm, Xijing Hosp, Xian 710032, Peoples R China
[2] Fourth Mil Med Univ, Dept Anesthesiol, Xijing Hosp, Xian 710032, Peoples R China
基金
中国国家自然科学基金;
关键词
Calycosin; Antioxidant; Neuroprotective; Ischemia/Reperfusion; Reactive oxygen species; SPINAL-CORD ISCHEMIA; OXIDATIVE STRESS; IN-VITRO; STROKE; ISCHEMIA/REPERFUSION; PROTECTION; ISOFLAVONE; APOPTOSIS; OXYGEN;
D O I
10.1016/j.jep.2012.09.056
中图分类号
Q94 [植物学];
学科分类号
071001 [植物学];
摘要
Ethnopharmacological relevance: Radix Astragali has been commonly used as traditional herbal medicine in China for reinforcing vital energy, strengthening superficial resistance and promoting the discharge of pus and the growth of new tissue. Aim of the study: The present study was to investigate the neuroprotective effect of calycosin isolated from the roots of Radix Astragali on cerebral ischemic/reperfusion injury. Materials and methods: After 24 h of reperfusion following ischemia for 2 h induced by middle cerebral artery occlusion (MCAO), Sprague-Dawley rats were intragastrically administered different doses of calycosin (7.5, 15, 30 mg/kg, respectively). Neurological deficit, infarct volume, histopathology changes and some oxidative stress markers were evaluated after 24 h of reperfusion. Results: Treatment with calycosin significantly ameliorated neurologic deficit and infarct volume after cerebral ischemia reperfusion. Calycosin also reduced the content of malondialdehyde (MDA), protein carbonyl and reactive oxygen species (ROS), and up-regulated the activities of superoxide dismutase (SOD), catalase and glutathione peroxidase (GSH-Px) in a dose-dependent manner. Moreover, calycosin can also inhibit the expression of 4-Hydroxy-2-nonenal (4-HNE). Conclusion: These results suggest that calycosin has a neuroprotective effect against cerebral ischemia/reperfusion injury. The mechanism might be attributed to its antioxidant effects. (C) 2012 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:768 / 774
页数:7
相关论文
共 33 条
[1]
Dual effect of HBO on cerebral infarction in MCAO rats [J].
Badr, AE ;
Yin, W ;
Mychaskiw, G ;
Zhang, JH .
AMERICAN JOURNAL OF PHYSIOLOGY-REGULATORY INTEGRATIVE AND COMPARATIVE PHYSIOLOGY, 2001, 280 (03) :R766-R770
[2]
Neuroprotective effect of SolCD39, a novel platelet aggregation inhibitor, on transient middle cerebral artery occlusion in rats [J].
Belayev, L ;
Khoutorova, L ;
Deisher, TA ;
Belayev, A ;
Busto, R ;
Zhang, YB ;
Zhao, WZ ;
Ginsberg, MD .
STROKE, 2003, 34 (03) :758-763
[3]
Chirino Yolanda I., 2004, BMC Pharmacology, V4, P20, DOI 10.1186/1471-2210-4-20
[4]
Mitochondria: A target for neuroprotective interventions in cerebral ischemia-reperfusion [J].
Chtistophe, M ;
Nicolas, S .
CURRENT PHARMACEUTICAL DESIGN, 2006, 12 (06) :739-757
[5]
Cindric M., 2012, TOXICOLOGY IN VITRO
[6]
Protein carbonylation, cellular dysfunction, and disease progression [J].
Dalle-Donne, Isabella ;
Aldini, Giancarlo ;
Carini, Marina ;
Colombo, Roberto ;
Rossi, Ranieri ;
Milzani, Aldo .
JOURNAL OF CELLULAR AND MOLECULAR MEDICINE, 2006, 10 (02) :389-406
[7]
Preconditioning with hyperbaric oxygen and hyperoxia induces tolerance against spinal cord ischemia in rabbits [J].
Dong, HL ;
Xiong, L ;
Zhu, ZH ;
Chen, SY ;
Hou, L ;
Sakabe, T .
ANESTHESIOLOGY, 2002, 96 (04) :907-912
[8]
Formation of 4-hydroxy-2-nonenal-modified proteins in ischemic rat heart [J].
Eaton, P ;
Li, JM ;
Hearse, DJ ;
Shattock, MJ .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 1999, 276 (03) :H935-H943
[9]
Protection by metal complexes with SOD-mimetic activity against oxidative gastric injury induced by indometacin and ethanol in rats [J].
El-Missiry, MA ;
El-Sayed, IH ;
Othman, AI .
ANNALS OF CLINICAL BIOCHEMISTRY, 2001, 38 :694-700
[10]
Effects of calycosin on the impairment of barrier function induced by hypoxia in human umbilical vein endothelial cells [J].
Fan, Y ;
Wu, DZ ;
Gong, YQ ;
Zhou, RY ;
Hu, ZB .
EUROPEAN JOURNAL OF PHARMACOLOGY, 2003, 481 (01) :33-40