EGb 761 enhances adult hippocampal neurogenesis and phosphorylation of CREB in transgenic mouse model of Alzheimer's disease

被引:166
作者
Tchantchou, Flaubert
Xu, Yanan
Wu, Yanjue
Christen, Yves
Luo, Yuan [1 ]
机构
[1] Univ Maryland, Sch Pharm, Dept Pharmaceut Sci, Baltimore, MD 21201 USA
[2] Univ Maryland, Sch Med, Ctr Integrat Med, Baltimore, MD USA
[3] Ipsen, Paris, France
关键词
AD; dementia; neuronal cells; memory;
D O I
10.1096/fj.06-7649com
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Standardized Ginkgo biloba extract EGb 761 exhibits beneficial effects to patients with Alzheimer's disease ( AD). It was previously demonstrated that EGb 761 inhibits amyloid beta ( A beta) oligomerization in vitro, protects neuronal cells against A beta toxicity, and improves cognitive defects in a mouse model of AD ( Tg 2576). In this study, the neurogenic potential of EGb 761 and its effect on cAMP response element binding protein ( CREB) were examined in a double transgenic mouse model ( TgAPP/ PS1). EGb 761 significantly increases cell proliferation in the hippocampus of both young ( 6 months) and old ( 22 months) TgAPP/ PS1 mice, and the total number of neuronal precursor cells in vitro in a dose-dependent manner. Furthermore, A beta oligomers inhibit phosphorylation of CREB and cell proliferation in the hippocampus of TgAPP/ PS1 mice. Administration of EGb 761 reduces A beta oligomers and restores CREB phosphorylation in the hippocampus of these mice. The present findings suggest that 1) enhanced neurogenesis by EGb 761 may be mediated by activation of CREB, 2) stimulation of neurogenesis by EGb 761 may contribute to its beneficial effects in AD patients and improved cognitive functions in the mouse model of AD, and 3) EGb 761 has therapeutic potential for the prevention and improved treatment of AD.
引用
收藏
页码:2400 / 2408
页数:9
相关论文
共 58 条
[1]   AUTORADIOGRAPHIC AND HISTOLOGICAL EVIDENCE OF POSTNATAL HIPPOCAMPAL NEUROGENESIS IN RATS [J].
ALTMAN, J ;
DAS, GD .
JOURNAL OF COMPARATIVE NEUROLOGY, 1965, 124 (03) :319-&
[2]  
Barker N, 2000, ADV CANCER RES, V77, P1
[3]   The Ginkgo biloba extract (EGb 761) protects and rescues hippocampal cells against nitric oxide-induced toxicity:: Involvement of its flavonoid constituents and protein kinase C [J].
Bastianetto, S ;
Zheng, WH ;
Quirion, R .
JOURNAL OF NEUROCHEMISTRY, 2000, 74 (06) :2268-2277
[4]   Regulation of CRE-dependent transcription by presenilins: prospects for therapy of Alzheimer's disease [J].
Beglopoulos, V ;
Shen, J .
TRENDS IN PHARMACOLOGICAL SCIENCES, 2006, 27 (01) :33-40
[5]   Enhanced CREB phosphorylation in immature dentate gyrus granule cells precedes neurotrophin expression and indicates a specific role of CREB in granule cell differentiation [J].
Bender, RA ;
Lauterborn, JC ;
Gall, CM ;
Cariaga, W ;
Baram, TZ .
EUROPEAN JOURNAL OF NEUROSCIENCE, 2001, 13 (04) :679-686
[6]   Amyloid β-protein (Aβ) assembly:: Aβ40 and Aβ42 oligomerize through distinct pathways [J].
Bitan, G ;
Kirkitadze, MD ;
Lomakin, A ;
Vollers, SS ;
Benedek, GB ;
Teplow, DB .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (01) :330-335
[7]   Familial Alzheimer's disease-linked presenilin 1 variants elevate A beta 1-42/1-40 ratio in vitro and in vivo [J].
Borchelt, DR ;
Thinakaran, G ;
Eckman, CB ;
Lee, MK ;
Davenport, F ;
Ratovitsky, T ;
Prada, CM ;
Kim, G ;
Seekins, S ;
Yager, D ;
Slunt, HH ;
Wang, R ;
Seeger, M ;
Levey, AI ;
Gandy, SE ;
Copeland, NG ;
Jenkins, NA ;
Price, DL ;
Younkin, SG .
NEURON, 1996, 17 (05) :1005-1013
[8]  
Brinton Roberta Diaz, 2006, Current Alzheimer Research, V3, P185
[9]   Self-assembly of Aβ1-42 into globular neurotoxins [J].
Chromy, BA ;
Nowak, RJ ;
Lambert, MP ;
Viola, KL ;
Chang, L ;
Velasco, PT ;
Jones, BW ;
Fernandez, SJ ;
Lacor, PN ;
Horowitz, P ;
Finch, CE ;
Krafft, GA ;
Klein, WL .
BIOCHEMISTRY, 2003, 42 (44) :12749-12760
[10]   Amyloid precursor protein metabolism is regulated toward alpha-secretase pathway by Ginkgo biloba extracts [J].
Colciaghi, F ;
Borroni, B ;
Zimmermann, M ;
Bellone, C ;
Longhi, A ;
Padovani, A ;
Cattabeni, F ;
Christen, Y ;
Di Luca, M .
NEUROBIOLOGY OF DISEASE, 2004, 16 (02) :454-460