Prenatal exposure of rats to Ginkgo biloba extract (EGb 761) increases neuronal survival/growth and alters gene expression in the developing fetal hippocampus

被引:23
作者
Li, WP
Trovero, F
Cordier, J
Wang, Y
Drieu, K
Papadopoulos, V
机构
[1] Georgetown Univ, Med Ctr, Div Hormone Res, Dept Cell Biol, Washington, DC 20057 USA
[2] Key Obs SA, F-45100 Orleans, France
[3] Coll France, INSERM, U114, F-75231 Paris, France
[4] Beaufour IPSEN Pharma, F-75116 Paris, France
[5] Georgetown Univ, Med Ctr, Dept Pharmacol, Washington, DC 20057 USA
[6] Georgetown Univ, Med Ctr, Dept Neurosci, Washington, DC 20057 USA
来源
DEVELOPMENTAL BRAIN RESEARCH | 2003年 / 144卷 / 02期
关键词
gene expression; Ginkgo biloba; hippocampus; neurogenesis; neuroprotection; microarray;
D O I
10.1016/S0165-3806(03)00168-8
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Hippocampal neuron survival/growth and gene expression have been examined after prenatal (in utero) exposure of rats to EGb 761, a leaf extract of Ginkgo biloba. Oral administration of EGb 761 (100 or 300 mg/kg/day) to pregnant dams for 5 days increased the number of hippocampal neurons (maintained in culture) of their fetuses, indicating a neurotrophic effect of the extract. Using large-scale oligonucleotide microarrays containing over 8000 combined rat genes and expressed sequence tag clusters, it was shown that treatment of pregnant dams with EGb 761 (25, 50 or 100 mg/kg/day for 5 days) altered the expression of 187 genes in the hippocampi of male fetuses and 160 genes in those of female fetuses. Using gene-cluster analysis, these genes were grouped into 18 distinct clusters for mates and 17 distinct clusters for females. Among these clusters, 35 genes shared a common expression pattern in male and female hippocampal development. Of these genes, the changes observed in insulin growth factor 11, insulin growth factor binding protein 2, testosterone repressed prostate message-2, glutathione-dependent dehydroascorbate reductase, lipoprotein lipase, guanylate cyclase and DNA binding protein Brn-2 were confirmed by real-time quantitative polymerase chain reaction. These findings, which have provided the first genetic profile of the effects of EGb 761 on the developing rat hippocampus, increase our understanding of the molecular and genetic programs that are activated by the extract. These effects of EGb 761 may underlie its neuroprotective properties. (C) 2003 Elsevier B.V. All rights reserved.
引用
收藏
页码:169 / 180
页数:12
相关论文
共 71 条
[1]   Inhibition of serum deprivation- and staurosporine-induced neuronal apoptosis by Ginkgo biloba extract and some of its constituents [J].
Ahlemeyer, B ;
Möwes, A ;
Krieglstein, J .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1999, 367 (2-3) :423-430
[2]   Ex vivo regulation of adrenal cortical cell steroid and protein synthesis, in response to adrenocorticotropic hormone stimulation, by the Ginkgo biloba extract EGb 761 and isolated ginkgolide B [J].
Amri, H ;
Drieu, K ;
Papadopoulos, V .
ENDOCRINOLOGY, 1997, 138 (12) :5415-5426
[3]   In vivo regulation of peripheral-type benzodiazepine receptor and glucocorticoid synthesis by Ginkgo biloba extract EGb 761 and isolated ginkgolides [J].
Amri, H ;
Ogwuegbu, SO ;
Boujrad, N ;
Drieu, K ;
Papadopoulos, V .
ENDOCRINOLOGY, 1996, 137 (12) :5707-5718
[4]  
[Anonymous], 1999, WHO MONOGRAPHS SELEC
[5]  
[Anonymous], 1998, GINKGO BILOBA EXTRAC
[6]   Interactions between Bcl-2 and the IGF system control apoptosis in the developing mouse brain [J].
Baker, NL ;
Russo, VC ;
Bernard, O ;
D'Ercole, AJ ;
Werther, GA .
DEVELOPMENTAL BRAIN RESEARCH, 1999, 118 (1-2) :109-118
[7]  
Bastianetto S, 2002, CELL MOL BIOL, V48, P693
[8]  
Baum L, 2000, MICROSC RES TECHNIQ, V50, P291, DOI 10.1002/1097-0029(20000815)50:4<291::AID-JEMT8>3.0.CO
[9]  
2-L
[10]  
Chandrasekaran K, 2002, CELL MOL BIOL, V48, P663