1)Sieghart W, Sperk G:Subunit composition, distribution and function of GABA(A)receptor subtypes. Curr Top Med Chem 2:795-816, 2002
2)Jacob TC, Moss SJ, Jurd R:GABA(A)receptor trafficking and its role in the dynamic modulation of neuronal inhibition. Nat Rev Neurosci 9:331-343, 2008
3)Fritschy JM, Mohler H:GABAA-receptor heterogeneity in the adult rat brain;differential regional and cellular distribution of seven major subunits. J Comp Neurol 359:154-194, 1995
4)Sieghart W:GABAA receptors;ligand-gated Cl-ion channels modulated by multiple drug-binding sites. Trends Pharmacol Sci 13:446-450, 1992
5)Study RE, Barker JL:Diazepam and pentobarbital:fluctuation analysis reveals different mechanisms for potentiation of gamma-aminobutyric acid responses in cultured central neurons. Proc Natl Acad Sci U S A 78:7180-7184, 1981
6)Cheng T, Wallace DM, Ponteri B, et al:Valium without dependence? Individual GABAA receptor subtype contribution toward benzodiazepine addiction, tolerance, and therapeutic effects. Neuropsychiatr Dis Treat 14:1351-1361, 2018
7)McKernan RM, Rosahl TW, Reynolds DS, et al:Sedative but not anxiolytic properties of benzodiazepines are mediated by the GABA(A)receptor alpha1 subtype. Nat Neurosci 3:587-592, 2000
8)Knabl J, Witschi R, Höslk, et al:Reversal of pathological pain through specific spinal GABAA receptor subtypes. Nature 451:330-334, 2008
9)Atack JR:GABA(A)receptor subtype-selective efficacy;TPA023, an alpha2/alpha3 selective non-sedating anxiolytic and alpha5IA, an alpha5 selective cognition enhancer. CNS Neurosci Ther 14:25-35, 2008
10)Roehrs T, Merlotti L, Zorick F, et al:Sedative, memory, and performance effects of hypnotics. Psychopharmacology(Berl)116:130-134, 1994
11)Crestani F, Martin JR, Mohler H, et al:Mechanism of action of the hypnotic zolpidem in vivo. Br J Pharmacol 131:1251-1254, 2000
12)Tan KR, Brown M, Labouébe G, et al:Neural bases for addictive properties of benzodiazepines. Nature 463:769-774, 2010
13)Engin E, Bakhurm KI, Smith KS, et al:Neural basis of benzodiazepine reward:requirement for alpha2 containing GABAA receptors in the nucleus accumbens. Neuropsychopharmacology 39:1805-1815, 2014
14)Shinday NM, Sawyer EK, Fischer BD, et al:Reinforcing effects of compounds lacking intrinsic efficacy at alpha1 subunit-containing GABAA receptor subtypes in midazolam-but not cocaine-experienced rhesus monkeys. Neuropsychopharmacology 38:1006-1014, 2013
15)Helms CM, Rogers LS, Waters CA, et al:Zolpidem generalization and antagonism in male and female cynomolgus monkeys trained to discriminate 1.0 or 2.0g/kg ethanol. Alcohol Clin Exp Res 32:1197-1206, 2008
16)Licata SC, Platt DM, Rüedi-Bettschen D, et al:Discriminative stimulus effects of L-838, 417(7-tert-butyl-3-(2, 5-difluoro-phenyl)-6-(2-methyl-2H-[1, 2, 4]triazol-3-ylmethoxy)-[1, 2, 4]triazolo[4, 3-b]pyridazine);role of GABA(A)receptor subtypes. Neuropharmacology 58:357-364, 2010
17)Invernizzi R, Pozzi L, Samanin R:Release of dopamine is reduced by diazepam more in the nucleus accumbens than in the caudate nucleus of conscious rats. Neuropharmacology 30:575-578, 1991
18)Finlay JM, Damsma G, Fibiger HC:Benzodiazepine-induced decreases in extracellular concentrations of dopamine in the nucleus accumbens after acute and repeated administration. Psychopharmacology(Berl)106:202-208, 1992
19)Zetterstrom T, Fillenz M:Local administration of flurazepam has different effects on dopamine release in striatum and nucleus accumbens;a microdialysis study. Neuropharmacology 29:129-134, 1990
20)Horger BA, Elsworth JD, Roth RH:Selective increase in dopamine utilization in the shell subdivision of the nucleus accumbens by the benzodiazepine inverse agonist FG 7142. J Neurochem 65:770-774, 1995
21)Heikkinen AE, Moykkynen TP, Korpi ER:Long-lasting modulation of glutamatergic transmission in VTA dopamine neurons after a single dose of benzodiazepine agonists. Neuropsychopharmacology 34:290-298, 2009
22)Elliot EE, White JM:Precipitated and spontaneous withdrawal following administration of lorazepam but not zolpidem. Pharmacol Biochem Behav 66:361-369, 2000
23)Mirza NR, Nielsen EO:Do subtype-selective gamma-aminobutyric acid A receptor modulators have a reduced propensity to induce physical dependence in mice? J Pharmacol Exp Ther 316:1378-1385, 2006
24)Atack JR, Wafford KA, Tye SJ, et al:TPA023[7-(1, 1-dimethylethyl)-6-(2-ethyl-2H-1, 2, 4-triazol-3-ylmethoxy)-3-(2-fluor ophenyl)-1, 2, 4-triazolo[4, 3-b]pyridazine], an agonist selective for alpha2-and alpha3-containing GABAA receptors, is a nonsedating anxiolytic in rodents and primates. J Pharmacol Exp Ther 316:410-422, 2006