Osthole improves chronic cerebral hypoperfusion induced cognitive deficits and neuronal damage in hippocampus

被引:99
作者
Ji, Hai-Jie [1 ,2 ]
Hu, Jin-Feng [1 ,2 ]
Wang, Yong-Hui [3 ]
Chen, Xiao-Yu [1 ,2 ]
Zhou, Ran [3 ]
Chen, Nai-Hong [1 ,2 ]
机构
[1] Chinese Acad Med Sci, Inst Mat Med, Beijing 100050, Peoples R China
[2] Peking Union Med Coll, Beijing 100050, Peoples R China
[3] Shanxi Coll Tradit Chinese Med, Taiyuan 030024, Peoples R China
关键词
Osthole; Chronic cerebral hypoperfusion; Cognition; Oxidative stress; Apoptosis; OXIDATIVE STRESS; CNIDIUM-MONNIERI; OVARIECTOMIZED RATS; IN-VITRO; BRAIN; IMPAIRMENT; TRANSIENT; CELLS; DYSFUNCTION; APOPTOSIS;
D O I
10.1016/j.ejphar.2010.03.038
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
This study is to investigate the effects of osthole on cognitive impairment and neuronal degeneration in hippocampus induced by chronic cerebral hypoperfusion in rats, as well as the potential mechanism. Permanent occlusion of bilateral common carotid arteries (2VO) induced severe cognitive deficits tested by the water maze task, along with oxidative stress and neuronal loss in hippocampus. Oral administration of osthole for 3 weeks markedly attenuated cognitive deficits and neuronal damage. Biochemical experiments revealed that osthole decreased the production of malondialdehyde (MDA) and significantly increased the activities of Glutathione Peroxidase (GPx) and Catalase. Western blot analyses indicated that osthole prevented the downregulation of bcl-2 expression and upregulation of bax expression, which resulted in decreasing bax/bcl-2 ratio in hippocampus of 2VO rats. Additionally, osthole effectively alleviated the activation of caspase-3 induced by permanent occlusion of bilateral common carotid arteries. The observed results in present study suggest that osthole exhibits therapeutic potential for vascular dementia, which is most likely related, at least in part, to its antioxidation and anti-apoptotic actions. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:96 / 101
页数:6
相关论文
共 40 条
[1]   The effect of ethanol on lipid peroxidation and glutathione level in the brain stem of rat [J].
Agar, E ;
Bosnak, M ;
Amanvermez, R ;
Demír, S ;
Ayyildiz, M ;
Çelík, C .
NEUROREPORT, 1999, 10 (08) :1799-1801
[2]   THE 3-DIMENSIONAL ORGANIZATION OF THE HIPPOCAMPAL-FORMATION - A REVIEW OF ANATOMICAL DATA [J].
AMARAL, DG ;
WITTER, MP .
NEUROSCIENCE, 1989, 31 (03) :571-591
[3]  
ARMSTRONG D, 1994, ADV EXP MED BIOL, V366, P43
[4]  
Bennett SAL, 1998, NEUROREPORT, V9, P161
[5]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[6]   Protective effice of chronic ethyl docosahexaenoate administration on brain injury in ischemic gerbils [J].
Cao, DH ;
Xu, HF ;
Xue, RH ;
Zheng, WF ;
Liu, ZL .
PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 2004, 79 (04) :651-659
[7]  
Chiu Pu-Rong, 2008, Pediatrics and Neonatology, V49, P135, DOI 10.1016/S1875-9572(08)60028-5
[8]   Oxidative stress in the brain: Novel cellular targets that govern survival during neurodegenerative disease [J].
Chong, ZZ ;
Li, FQ ;
Maiese, K .
PROGRESS IN NEUROBIOLOGY, 2005, 75 (03) :207-246
[9]   Antitumor effects of osthol from Cnidium monnieri:: An in vitro and in vivo study [J].
Chou, Szu-Yuan ;
Hsu, Chun-Sen ;
Wang, Kun-Teng ;
Wang, Min-Chieh ;
Wang, Ching-Chiung .
PHYTOTHERAPY RESEARCH, 2007, 21 (03) :226-230
[10]   The BCL2 family: Regulators of the cellular life-or-death switch [J].
Cory, S ;
Adams, JM .
NATURE REVIEWS CANCER, 2002, 2 (09) :647-656