Cabergoline stimulates synthesis and secretion of nerve growth factor, brain-derived neurotrophic factor and glial cell line-derived neurotrophic factor by mouse astrocytes in primary culture

被引:33
作者
Ohta, K
Fujinami, A
Kuno, S
Sakakimoto, A
Matsui, H
Kawahara, Y
Ohta, M [1 ]
机构
[1] Kobe Pharmaceut Univ, Dept Clin Chem, Kobe, Hyogo 6588558, Japan
[2] Natl Utano Hosp, Clin Res Ctr, Kyoto, Japan
关键词
cabergoline; nerve growth factor; brain-derived neurotrophic factor; glial cell line-derived neurotrophic factor; astrocytes; Parkinson's disease;
D O I
10.1159/000077451
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Neuroprotection is the primary concern in patients with newly diagnosed Parkinson's disease. The D-2/weak D-1 dopamine agonist cabergoline elicits neuroprotection by antioxidation and scavenging free radicals, and may protect neurons by up-regulating endogenous neurotrophic factors synthesis in the brain. In primary cultured mouse astrocytes, cabergoline 37 mumol/l immediately elevated concentrations of nerve growth factor, brain-derived neurotrophic factor, and glial cell line-derived neurotrophic factor ( GDNF) in culture medium, reaching 9.9-, 2.6- and 30-fold, respectively, of control levels at 16 h. Relative mRNA levels were 3.0-, 1.5- and 1.9-fold, respectively, of controls at 3 h. These effects may be mediated partly by the dopamine D-2 receptor. Cabergoline may be a good candidate for an inducer of GDNF, which may have neuroprotective and neurorestorative properties in dopaminergic nigral neurons. Copyright (C) 2004 S. Karger AG, Basel.
引用
收藏
页码:162 / 168
页数:7
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