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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:
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.
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页码:171 / 175
页数:5
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