The α2-adrenoceptor antagonist yohimbine reduces glial fibrillary acidic protein upregulation induced by chronic morphine administration

被引:24
作者
Garrido, E [1 ]
Pérez-García, C [1 ]
Alguacil, LF [1 ]
Díez-Fernández, C [1 ]
机构
[1] Univ San Pablo CEU, Fac Farm, Lab Pharmacol & Toxicol, Madrid 28668, Spain
关键词
morphine; yohimbine; glial fibrillary acidic protein; neurotoxicity;
D O I
10.1016/j.neulet.2005.04.002
中图分类号
Q189 [神经科学];
学科分类号
071006 [神经生物学];
摘要
Previous literature data show prominent interactions between alpha(2)-adrenoceptor ligands and opioid drugs, however, the nature of such interactions is still largely unknown. In the present study, we aimed to examine the potential protective effect of yohimbine, a alpha(2)-adrenoceptor antagonist, against glial fibrillary acidic protein (GFAP) alterations elicited by chronic morphine treatment. Increased astrogliosis, as indicated by increased GFAP immunohistochemical staining, was observed in the ventral tegmental area, nucleus accumbens shell, and frontal cortex of chronic morphine-treated (10 mg kg(-1), i.p., every 12 h for 13 days) rats compared with those treated with saline. Pretreatment with yohimbine (2 mg kg(-1), i.p., 30 min before each morphine injection) provided protection against morphine-induced GFAP upregulation. The present study demonstrates that yohimbine pretreatment reduces long-term morphine exposure-induced alterations in the astroglial reaction, suggesting that alpha(2)-adrenergic mechanisms may play an important role in mediating morphine-induced pathological effects in the brain. (c) 2005 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:141 / 144
页数:4
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