Attenuation of morphine withdrawal signs by muscimol in the locus coeruleus of rats

被引:18
|
作者
Mirzaii-Dizgah, Iraj [2 ]
Karimian, Seyed Morteza [1 ]
Hajimashhadi, Zahra [1 ]
Riahi, Esmail [1 ]
Ghasemi, Tayeb [1 ]
机构
[1] Univ Tehran Med Sci, Sch Med, Dept Physiol, Tehran, Iran
[2] Qom Univ Med Sci, Sch Med, Dept Physiol, Qom, Iran
来源
BEHAVIOURAL PHARMACOLOGY | 2008年 / 19卷 / 03期
关键词
gamma-amino-butyric acid; locus coeruleus; morphine; muscimol; naloxone; rat; withdrawal;
D O I
10.1097/FBP.0b013e3282fe8849
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
This study examined the effects of intra-locus coeruleus injection of a gamma-amino-butyric acid type A (GABA(A)) receptor agonist on naloxone-induced withdrawal signs of morphine-dependent rats. Twenty different withdrawal signs were assessed. The total withdrawal score was calculated and used as an index of withdrawal intensity. The gamma-amino-butyric acid agonist and antagonists were injected 15 and 30 min before naloxone injection, respectively. Muscimol, a GABAA agonist (25, 50, and 100 ng/site), decreased the total withdrawal score in a dose-independent manner, whereas bicuculline (0.367, 3.67, and 36.7ng/site), a GABAA antagonist, and CGP35348 (48.6 ng/site), a gamma-amino-butyric acid type B antagonist, alone had no effects. On the other hand, muscimol effects were reversed by CG P35348 (48.6 ng/site) but not by bicuculline (36.7 ng/site). It may be concluded that the effects of muscimol were antagonized by gamma-amino-butyric acid type B but not by GABAA receptor antagonists. The mechanism involved seems to be intricate and needs further study.
引用
收藏
页码:171 / 175
页数:5
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