Effects of Cerebrolysin® on in vitro primary microglial and astrocyte rat cell cultures

被引:29
作者
Lombardi, VRM
Windisch, M
García, M
Cacabelos, R
机构
[1] EuroEspes, Div Biotechnol, Basic & Clin Neurosci Res Ctr, Bergondo 15166, La Coruna, Spain
[2] Res Initiat Ebewe Pharmaceut, Graz, Austria
来源
METHODS AND FINDINGS IN EXPERIMENTAL AND CLINICAL PHARMACOLOGY | 1999年 / 21卷 / 05期
关键词
Cerebrolysin (R); microglia; IL-1; beta; BDNF; Alzheimer's disease;
D O I
10.1358/mf.1999.21.5.541910
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
In recent years the potential use of neurotrophic factors in the prevention and/or treatment of neurodegenerative diseases has received much attention. To determine whether Cerebrolysin(R), a porcine brain-derived peptide preparation, was able to modulate in vitro lipopolysaccharide (LPS)-induced microglial activation and to test the direct effect of Cerebrolysin(R) on astrocyte morphology, survival and proliferation, rat glial and astrocyte cell culture experiments were carried our. The morphology of microglia, ameboid/activated and flat/resting, was examined under contrast microscopy and cell counts obtained. In addition, the release of interleukin (IL)-1 beta and brain-derived neurotrophic factor (BDNF) wets measured from cell culture supernatant using an enzyme-linked-immunoassay (ELISA). The results obtained in this study clearly suggest a protective effect of Cerebrolysin(R) as revealed by downregulation of microglial activation after LPS treatment as well as by the control of IL-1 beta expression. No significant differences were observed on astrocyte morphology, survival or the production and/or release of BDNF. In conclusion, these in vitro studies indicate that Cerebrolysin(R) might exert a neuroimmunotrophic function which can in turn reduce the extent of inflammation and accelerate neuronal death under pathological conditions such as human neurodegenerative disorders, (C) 1999 Prous Science. All rights reserved.
引用
收藏
页码:331 / 338
页数:8
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