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
相关论文
共 32 条
[1]  
Barnard EA, 1998, PHARMACOL REV, V50, P291
[2]   CATECHOLAMINERGIC AND GABAERGIC ANATOMICAL RELATIONSHIP IN THE RAT SUBSTANTIA NIGRA, LOCUS COERULEUS, AND HYPOTHALAMIC MEDIAN-EMINENCE - IMMUNOCYTOCHEMICAL VISUALIZATION OF BIOSYNTHETIC-ENZYMES ON SERIAL SEMITHIN PLASTIC-EMBEDDED SECTIONS [J].
BEROD, A ;
CHAT, M ;
PAUT, L ;
TAPPAZ, M .
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, 1984, 32 (12) :1331-1338
[3]   θ, a novel γ-aminobutyric acid type A receptor subunit [J].
Bonnert, TP ;
McKernan, RM ;
Farrar, S ;
le Bourdellès, B ;
Heavens, RP ;
Smith, DW ;
Hewson, L ;
Rigby, MR ;
Sirinathsinghji, DJS ;
Brown, N ;
Wafford, KA ;
Whiting, PJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (17) :9891-9896
[4]   ELECTROPHYSIOLOGY OF GABAA AND GABAB RECEPTOR SUBTYPES [J].
BORMANN, J .
TRENDS IN NEUROSCIENCES, 1988, 11 (03) :112-116
[5]   SEROTONIN DIFFERENTIALLY MODULATES RESPONSES MEDIATED BY SPECIFIC EXCITATORY AMINO-ACID RECEPTORS IN THE RAT LOCUS-CERULEUS [J].
CHARLETY, PJ ;
CHERGUI, K ;
AKAOKA, H ;
SAUNIER, CF ;
BUDA, M ;
ASTONJONES, G ;
CHOUVET, G .
EUROPEAN JOURNAL OF NEUROSCIENCE, 1993, 5 (08) :1024-1028
[6]   GABA-activated ligand gated ion channels: Medicinal chemistry and molecular biology [J].
Chebib, M ;
Johnston, GAR .
JOURNAL OF MEDICINAL CHEMISTRY, 2000, 43 (08) :1427-1447
[7]   GABAERGIC PROCESSES INVOLVED IN CONTROL OF DOPAMINE RELEASE FROM NIGROSTRIATAL DOPAMINERGIC-NEURONS IN CAT [J].
CHERAMY, A ;
NIEOULLON, A ;
GLOWINSKI, J .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1978, 48 (03) :281-295
[8]   GABA-ERGIC ANALGESIA - A NALOXONE-INSENSITIVE SYSTEM [J].
DEFEUDIS, FV .
PHARMACOLOGICAL RESEARCH COMMUNICATIONS, 1982, 14 (05) :383-390
[9]   Attenuation of morphine withdrawal signs by a D1 receptor agonist in the locus coeruleus of rats [J].
Dizgah, IM ;
Karimian, SM ;
Zarrindast, MR ;
Sohanaki, H .
NEUROREPORT, 2005, 16 (15) :1683-1686
[10]   BICUCULLINE-INSENSITIVE GABA RECEPTORS - STUDIES ON THE BINDING OF (-)-BACLOFEN TO RAT CEREBELLAR MEMBRANES [J].
DREW, CA ;
JOHNSTON, GAR ;
WEATHERBY, RP .
NEUROSCIENCE LETTERS, 1984, 52 (03) :317-321