The novel catecholaminergic and serotoninergic activity enhancer R-(-)-1-(benzofuran-2-yl)-2-propylaminopentane up-regulates neurotrophic factor synthesis in mouse astrocytes

被引:23
作者
Ohta, K [1 ]
Ohta, M
Mizuta, I
Fujinami, A
Shimazu, S
Sato, N
Yoneda, F
Hayashi, K
Kuno, S
机构
[1] Natl Utano Hosp, Clin Res Ctr, Kyoto 6168255, Japan
[2] Kobe Pharmaceut Univ, Kobe, Hyogo 6588558, Japan
[3] Fujisawa Pharmaceut Co Ltd, Matsubara, Osaka 5800011, Japan
[4] Gifu Pharmaceut Univ, Gifu 5028585, Japan
关键词
nerve growth factor; brain-derived neurotrophic factor; glial cell line-derived neurotrophic factor; R-(-)-1-(benzofuran-2-yl)2-propylaminopentane; astrocyte; Parkinson's disease; selegiline;
D O I
10.1016/S0304-3940(02)00461-5
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
We investigated the effects of the novel catecholaminergic and serotoninergic activity enhancer R-(-)-1-(benzofuran-2-yl)-2-propylaminopentane ((-)-BPAP) on the synthesis and secretion of neurotrophins, nerve growth factor (NGF), brain-derived neurotrophic factor (BDNF), and glial cell line-derived neurotrophic factor (GDNF), in cultured mouse astrocytes. The protein and mRNA levels of the neurotrophic factors were measured using the enzyme-linked immuno-sorbent assay and reverse transcription-polymerase chain reaction methods, respectively. The amounts of NGF, BDNF, and GDNF secreted from astrocytes into the culture medium increased by up to 120, two, and seven times higher than those of the control, respectively, by treatment with 0.35 mM (-)-BPAP for 24 h. The increases in NGF and GDNF induced by the treatment with (-)-BPAP was inhibited by concomitant treatment with actinomycin D for transcriptional blockade. Furthermore, the treatment with (-)-BPAP for 6 In increased the mRNA expression of NGF, BDNF, and GDNF. These results suggest that (-)-BPAP up-regulated neurotrophic factor synthesis in cultured astrocytes. (C) 2002 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:205 / 208
页数:4
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