Increase in expression of the GABAA receptor α4 subunit gene induced by withdrawal of, but not by long-term treatment with, benzodiazepine full or partial agonists

被引:47
作者
Follesa, P [1 ]
Cagetti, E
Mancuso, L
Biggio, F
Manca, A
Maciocco, E
Massa, F
Desole, MS
Carta, M
Busonero, F
Sanna, E
Biggio, G
机构
[1] Univ Cagliari, Dept Expt Biol Bernardo Loddo, CNR, Ctr Neuropharmacol, I-09123 Cagliari, Italy
[2] Univ Sassari, Dept Pharmacol, I-07100 Sassari, Italy
来源
MOLECULAR BRAIN RESEARCH | 2001年 / 92卷 / 1-2期
关键词
neuronal cell culture; GABA(A) receptor; gene expression; withdrawal; tolerance; dependence;
D O I
10.1016/S0169-328X(01)00164-4
中图分类号
Q189 [神经科学];
学科分类号
071006 [神经生物学];
摘要
The effects of long-term exposure to, and subsequent withdrawal of, diazepam or imidazenil (full and partial agonists of the benzodiazepine receptor, respectively) on the abundance of GABA, receptor subunit mRNAs and peptides were investigated in rat cerebellar granule cells in culture. Exposure of cells to 10 muM diazepam for 5 days significantly reduced the amounts of alpha (1) and gamma (2) subunit mRNAs, and had no effect on the amount of alpha (4) mRNA. These effects were accompanied by a decrease in the levels of alpha (1) and gamma (2) protein and by a reduction in the efficacy of diazepam with regard to potentiation of GABA-evoked Cl- current. Similar long-term treatment with 10 muM imidazenil significantly reduced the abundance of only the gamma S-2 subunit mRNA and had no effect on GABA(A) receptor function. Withdrawal of diazepam or imidazenil induced a marked increase in the amount of a, mRNA; withdrawal of imidazenil also reduced the amounts of alpha (1) and gamma (2) mRNAs. In addition, withdrawal of diazepam or imidazenil was associated with a reduced ability of diazepam to potentiate GABA action. These data give new insights into the different molecular events related to GABA, receptor gene expression and function produced by chronic treatment and withdrawal of benzodiazepines with full or partial agonist properties. (C) 2001 Elsevier Science BY All rights reserved.
引用
收藏
页码:138 / 148
页数:11
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