Glial cell line-derived neurotrophic factor-conjugated nanoparticles suppress acquisition of cocaine self-administration in rats

被引:58
作者
Green-Sadan, T
Kuttner, Y
Lublin-Tennenbaum, T
Kinor, N
Boguslavsky, Y
Margel, S
Yadid, G [1 ]
机构
[1] Bar Ilan Univ, Fac Life Sci, Neuropharmacol Lab, Ramat Gan, Israel
[2] Bar Ilan Univ, Susan Gonda Goldshmied Multidisciplinary Brain Re, Ramat Gan, Israel
[3] Bar Ilan Univ, Fac Exact Sci, Dept Chem, IL-52900 Ramat Gan, Israel
关键词
cocaine; self-administration; nanoparticles; neurotrophic factors;
D O I
10.1016/j.expneurol.2005.01.020
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The neurotrophic factor glial cell line-derived neurotrophic factor (GDNF) may have therapeutic potential for preventing and treating cocaine addiction. Previously, we found that transplantation of a GDNF-expressing astrocyte cell line into the striatum and nucleus accumbens attenuates cocaine-secking behavior in Sprague-Dawley rats. However, as a potential treatment for humans, cell transplantation presents several technical and ethical complications. Nanoparticulate systems are a safe and effective method for introducing exogenous compounds into the brain. Therefore, we examined the effect of GDNF-conjugated nanoparticles microinjected into the striatum and nucleus accumbens on cocaine self-administration in rats. GDNF-conjugated nanoparticles blocked the acquisition of cocaine self-administration compared to control treatments. Furthermore, a cocaine dose response demonstrated that decreased lever response in rats that received GDNF-conjugated nanoparticles persisted after substitution with different cocaine doses. This effect is not due to a non-specific disruption of locomotor or operant behavior, as seen following a water operant task. The current study is one of the first demonstrations that drug-conjugated nanoparticles may be effective in treating brain disorders. These findings suggest that GDNF-conjugated nanoparticles may serve as a novel potential treatment for drug addiction. (c) 2005 Published by Elsevier Inc.
引用
收藏
页码:97 / 105
页数:9
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