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Muscimol has been regarded as a universal agonist for all γ-aminobutyric acid type A receptor (GABAA-R) subtypes. However, brain regional distribution of muscimol's high-affinity binding sites greatly differs from those of other binding sites of the GABAA-R. To test whether behavioral effects of muscimol correlated with the density of high-affinity [3H]muscimol binding, we examined several GABAA-R subunit gene-modified mouse lines: α1, α4, or δ-knockouts (KO), α4+δ-double KO, and Thy1.2 promoter-driven α6 transgenic mice (Thy1α6). We determined the high-affinity [3H]muscimol binding in brain sections by quantitative autoradiography and sedative/ataxic effects induced in vivo by muscimol using a constant speed rotarod. α4-KO mice had reduced [3H]muscimol binding in the caudate-putamen, thalamus, and hippocampus, and were less sensitive to the behavioral impairment by muscimol. Similarly, δ-KO mice also had reduced binding to forebrain regions and a lower behavioral sensitivity to muscimol than their wild-type controls. In contrast, α1-KO mice had unaltered behavioral sensitivity to muscimol and unaltered [3H]muscimol binding, even though previous studies have demonstrated dramatically reduced binding to various other GABAA-R sites in these mice. Finally, Thy1α6 mice exhibited increased behavioral sensitivity to muscimol, and to another direct GABA-site agonist gaboxadol, and increased [3H]muscimol binding in the cerebral cortex and hippocampus. Thus, the differences in sedative and motor-impairing actions of muscimol in various mouse models correlated with the level of forebrain high-affinity [3H]muscimol binding. These data suggest that a small special population of GABAA-Rs, most likely extrasynaptic non-α1-containing receptors, strongly contributes to the in vivo pharmacological effects of muscimol.
γ-Aminobutyric acid (GABA) is the major inhibitory neurotransmitter in the mammalian central nervous system and it acts primarily through the GABA type A receptor (GABAA-R). GABAA-Rs are pentameric complexes that function as ligand-gated anion channels. They can be modulated by a number of clinically used sedative, hypnotic, and anesthetic drugs. There are a variety of subunit families that make up GABAA-Rs; a total of 19 distinct subunit genes have been cloned, α1–6, β1–3, γ1–3, δ, , π, θ, and ρ1–3 (Barnard et al, 1998). The subunit stoichiometry is usually two α-subunits+two β-subunits+one γ- or δ-subunit (Backus et al, 1993; Boileau et al, 2005). The diversity in GABAA-R subunit composition results in substantial, anatomical, functional, and pharmacological heterogeneity. For example, GABAA-Rs containing α1, α2, or α3, with β and γ2 are typically found at subsynaptic sites, where they mediate fast synaptic inhibition by synaptically released GABA and show potentiation by benzodiazepines, as these drugs bind to α/γ2 subunit interface (Sigel and Buhr, 1997). In contrast, GABAA-Rs containing α4 or α6, with β and δ are typically found at extrasynaptic or perisynaptic locations, where they mediate a tonic form of inhibition by virtue of their ability to respond to low concentrations of spill-over GABA and show insensitivity to classical benzodiazepines. Thus, receptors containing γ2 along with α1, α2, α3, or α5 are potentiated by benzodiazepines, whereas those containing α4 or α6 are not, but all receptor subtypes respond to GABA (Luddens and Wisden, 1991; Sieghart, 1995).
Muscimol, a constituent and psychoactive ingredient of the mushroom Amanita muscaria, is regarded as a compound that activates all GABAA-R subtypes (Krogsgaard-Larsen et al, 1979), and it is described as the prototypic exogenous agonist for GABAA-Rs in current textbooks (Meyer and Quenzer, 2005; Brunton et al, 2006). Thus, its effects on behavior and brain metabolism should be similar or at least comprise all those effects that allosteric benzodiazepines produce. In agreement, muscimol differs from benzodiazepines in its more global actions on brain metabolism; eg, muscimol reduces cerebral glucose metabolism more strongly than the benzodiazepine clonazepam that actually shows a ceiling effect at higher receptor occupancy (Ito et al, 1994). However, muscimol and benzodiazepines affect glucose metabolism in different brain regions (Brett and Pratt, 1991; Kelly et al, 1986; Kelly and McCulloch, 1982), and behavioral effects of muscimol and benzodiazepines are often different, even up to the level that benzodiazepines have been concluded to act through some other mechanism than facilitation of GABAA-R function (Mendelson and Monti, 1993). Spatial distribution of high-affinity [3H]muscimol binding at low nanomolar concentrations differs from that of benzodiazepine site ligands throughout the rodent brain (Korpi et al, 2002a; Mans et al, 1992; Olsen et al, 1990; Palacios et al, 1981). [3H]Muscimol and [3H]GABA bind to two kinds of agonist binding sites on the GABAA-Rs with three- to twenty-fold difference in affinity (Browner et al, 1981; Burch et al, 1983; Wang et al, 1979), with the binding site being formed at α/β-interfaces (Sigel and Buhr, 1997).
Biochemical and pharmacological experiments have suggested that high- and low-affinity conformations might be interchangeable forms of the same GABAA-R complex (see for discussion, Agey and Dunn, 1989; Maksay, 1996; Sieghart, 1995). Interestingly, in most studies, functional responses to GABA have been observed only at micromolar concentrations, as opposed to nanomolar concentrations that are needed to occupy the high-affinity binding sites, and, therefore, the high-affinity sites have been interpreted to represent a desensitized form of GABAA-R or otherwise non-functional binding sites (DeLorey and Brown, 1992; Dunn and Thuynsma, 1994; Edgar and Schwartz, 1992; Maconochie et al, 1994; Maloteaux et al, 1987; Mennini and Gobbi, 1990; Uusi-Oukari and Korpi, 1992; but see Birnir and Korpi, 2007). Recently, the high-affinity [3H]muscimol binding has been associated with α6- and δ-subunits of GABAA-R in the cerebellum and with δ-subunits in the forebrain (Korpi et al, 2002b; Mihalek et al, 1999; Quirk et al, 1995); ie, this pharmacological fingerprint might be specific to subtype(s) of GABAA-R not containing γ2-subunit.
To understand the possible behavioral significance of GABAA-Rs forming high-affinity [3H]muscimol binding sites, we used novel genetic mouse lines with known or predicted differences in forebrain high-affinity [3H]muscimol binding, and tested them for sedative/ataxic behavioral effects of muscimol. The mice either lack GABAA-R α1, α4, δ or α4 and δ-subunits (knockout models) or they ectopically overexpress the cerebellar α6-subunit in the forebrain (a transgenic model). Behavior was measured by fixed-speed rotarod test with muscimol, and brain regional high-affinity binding of [3H]muscimol was assessed by quantitative ligand autoradiography.
Five different GABAA-R subunit mutant mouse strains were used: (1) α1-subunit knockout (KO) (Vicini et al, 2001), (2) α4-subunit KO (Chandra et al, 2006), (3) δ-subunit KO (Mihalek et al, 1999), (4) α4+δ-double KO, and (5) Thy1.2 promoter-driven α6-subunit transgenic mice (Wisden et al, 2002). Thy1α6 mice express ectopically extrasynaptic α6β±γ2 GABAA-R in the forebrain, especially in the hippocampus (Sinkkonen et al, 2004; Wisden et al, 2002), which results in increased tonic GABAA-R current in their hippocampal CA1 principal neurons. All KO mice were compared with their wild-type littermate controls and were created by heterozygous interbreeding. Genetic backgrounds of the single KO lines are as follows: α4-KO (mixed C57BL/6J and Strain 129S1/X1, F2-F6 generations), δ-KO (mixed C57BL/6J and Strain 129S1/X1, >F20 generations), and α1-KO (mixed C57BL/6J, FvB, and Strain 129S1/X1 from >F15 generations). α4+δ-double KOs were produced by mating the aforementioned α4-KO and δ-KO mice and interbreeding their double heterozygous offspring. Thy1α6 transgenic mice were on a C57BL/6 background (>10 generations; Saarelainen et al, 2008). Mice were produced for experiments by mating within a homozygous line, and compared with C57BL/6NHsd controls (Harlan Netherland, Horst, Netherlands), which were purchased at the age of 5 weeks and housed in the same facility until experiments took place.
At weaning, mice were genotyped using Southern blot analysis of tail DNA. Mice were group housed, given free access to standard rodent chow and water, and maintained on a 12-h alternating light/dark schedule with lights on at 0700 hours, with the temperature of 20–22°C. Autoradiographic experiments used mice at the age between 2 and 3 months. Behavioral experiments used both male and female drug-naive mice that were age matched and between 2 and 6 months old. Gender differences were observed in some cases (noted below). Wherever no gender differences were observed, data were pooled across gender.
The animal care and use committees of the Universities of Pittsburgh and Helsinki approved all experimental procedures.
In the first set of autoradiography experiments, we compared the GABAA-R α4-KOs (n=3), δ-KOs (n=3), α4+δ-KOs (n=5), and their common wild-type controls (n=4); in the second set, the α1-KOs (n=5) and their wild-type littermate controls (n=6). In the last set, we compared the Thy1α6 (n=6) mice to their wild-type controls (n=6). Mice were decapitated, the brains were carefully dissected out, rinsed in ice-cold saline and frozen on dry ice. The frozen brains were wrapped airtight in plastic, and then stored at −80°C.
The autoradiographic procedures for GABA-sensitive high-affinity [3H]muscimol binding were as previously described in detail (Korpi et al, 2002a). Fourteen-μm-thick horizontal sections were cut with a Leica CM 3050 S cryostat, thaw-mounted onto gelatine-coated object glasses (Menzel GmbH, Braunsweig, Germany) and stored at −80°C until used in the experiments. For autoradiography, the sections were preincubated in an ice–water bath for 15min in 0.17M Tris-HCl (pH 7.4). Final incubations in the same buffer were performed with 15nM [3H]muscimol (Perkin-Elmer, Boston, MA) at 0–4°C for 30min. All binding signal was sensitive to 100μM GABA (Sigma, St Louis, MO; data not shown). After incubation, the sections were quickly washed in ice-cold incubation buffer twice for 30s. Sections were then dipped into distilled water, air-dried at room temperature, and exposed with plastic 3H-microscales standards (GE Healthcare, Little Chalfont, Buckinghamshire, UK) to Kodak Biomax MR films (Eastman Kodak, Rochester, NY) for 4 months.
Representative images from autoradiography films were scanned using an EPSON Expression 1680 Pro scanner and EPSON Scan v. 1.11e program and finalized in CorelDraw X3 (Corel Corporation, Ottawa, Canada). For quantification of binding densities, the films were first scanned with the standards and then analyzed with Scion Image analysis program (Scion Corporation, Frederick, Maryland). Binding densities for each brain area were referenced to the standards, converted to radioactivity levels estimated for gray matter areas (nCi/mg), and given as means±SE.
For each experimental set, one-way analysis of variance (ANOVA) and/or Bonferroni corrected t-test were used to assess the statistical significance of the differences using SPSS program (version 15.0; SPSS, Chicago, IL, USA).
α1, α4, and δ-KO mice were tested using the Ugo Basile 7650 (Varese, Italy) apparatus with a rod diameter of 6cm, rotating at a fixed speed of 6r.p.m. Thy1α6 transgenic mice were tested on a Rotamex 4/8 (Columbus Instruments, Ohio, USA) with a rod diameter of 4cm, rotating at 15r.p.m. Mice were acclimated to the apparatus by pretraining them on the rotarod 1–3 times on the day before testing muscimol or gaboxadol. Only mice that were capable of walking on the rotarod for 180s were used for drug-induced ataxia experiments. No difference in rotarod performance between mutant mice and their wild-type controls were observed during this training. Mice were evaluated once again before drug injection. Muscimol (Tocris-Cookson, Avonmouth, UK or Ellisville, MO, USA) or gaboxadol hydrochloride (4,5,6,7-tetrahydroisoazolo(5,4-c)pyridin-3-ol; THIP; H. Lundbeck A/S, Copenhagen, Denmark) was diluted in saline and administered into the intraperitoneal (i.p.) cavity in a volume of 10ml per kg of body weight. Mice were then placed on the rotarod every 30min before injection. The time a mouse was able to stay on the rotarod was recorded. Data were analyzed by repeated measures ANOVA.
To test the effect of muscimol (0.75mg/kg, i.p.) on exploratory locomotor activity, the mice were individually placed 30min after drug administration on a novel arena (box with a 50 × 50-cm white floor and 50-cm-high gray walls) for 5min. The animal was monitored and its movements were analyzed using a CCD video camera above the arena and EthoVision Color-Pro 3.0 software (Noldus Information Technology, Wageningen, The Netherlands).
Distribution of high-affinity [3H]muscimol binding in various brain regions in all control mouse lines using the autoradiographic assay preferentially followed the expression pattern of GABAA-R δ- and α6-subunits (Korpi et al, 2002b; Makela et al, 1997; Quirk et al, 1995; Wisden et al, 1992), being abundant in the cerebellar granule cell layer and thalamus, but absent, eg, in the brainstem (Figure 1, Table 1).
The wild-type brains differed from the α4, δ, and α4+δ-KO brains (F3,11=7.9, p<0.005 for the cerebral cortex; F3,11=126.3, p<0.001 for the caudate-putamen, F3,11=59.0, p<0.001 for the thalamus; F3,11=4.4, p<0.05 for the hippocampus, and F3,11=6.1, p<0.05 for the granule cell layer of cerebellum), except for the olfactory bulb (F3,9=0.3, p>0.05). In keeping with Korpi et al (2002b), we confirmed the reduced binding in the δ-KO brains, especially in the caudate-putamen and thalamus (Figure 1, Table 1). The binding levels in the caudate-putamen, thalamus, and hippocampus were also reduced in the α4-KO brains, and the greatest reductions were found in the double α4+δ-KO brains. Conversely, the binding in the cerebellar granule cell layer was significantly reduced only in the double KO brains, suggesting that the main differences in the high-affinity [3H]muscimol binding took place in the forebrain regions.
GABAA-R α1-subunit does not seem to be important for the high-affinity [3H]muscimol binding, as there was no significant reduction of the binding in the α1 KO brains as compared with the control brains in any brain region (F1,9 <0.8, p>0.05; Figure 1, Table 1). This contrasts strongly with the great reduction in ligand binding to the ion channel and benzodiazepine sites of GABAA-R of the α1-KO brains (Halonen et al, 2009; Kralic et al, 2002).
Transgenic Thy1α6 mice express the cerebellar granule cell-specific α6-subunit gene under pan-neuronal Thy1.2 promoter, especially in the cerebral cortex and hippocampus (Wisden et al, 2002). [3H]Muscimol binding appears to be markedly increased in these areas of the transgenic mice (Figure 1, Table 1), increasing to 155 and 256% of the values for the wild-type mice in the cerebral cortex (F1,10=14.7, p<0.005) and hippocampus (F1,10=19.3, p<0.005), respectively. This change in the binding contrasts to the unaltered binding of an ion channel ligand in the Thy1α6 mice (Saarelainen et al, 2008).
Recovery from ataxia induced by 1.5, 2.0, and 3.0mg/kg muscimol was measured in α4-KO and control mice by fixed speed rotarod (Figure 2). α4-KO mice were significantly less sensitive to 1.5mg/kg (Figure 2a; repeated measures ANOVA (F1,64=4.6, p<0.05)), 2.0mg/kg (Figure 2b; F1,100=8.3, p<.05), and 3.0mg/kg (Figure 2c; F1,100=6.1, p<0.05). There were no significant effects of gender (p>0.05) at any of the three doses and, therefore, the data from males and females were collapsed in the analysis. However, at 2.0mg/kg, there was a trend toward a gender effect (F1,100=2.8, 0.05 < p<0.10), with females possibly being more sensitive to muscimol than males.
In the analysis of the δ-KO mice, there was a significant gender effect at the muscimol dose of 1.5mg/kg (F1,45=4.9, p<0.05). Analysis of data split between genders revealed a significant effect of genotype in female mice (Figure 3a; p<0.01) but not in male mice (Figure 3b). Neither δ-KO nor wild-type males were affected by 1.5mg/kg muscimol. At 2.0 and 3.0mg/kg, no gender effect was observed. δ-KO mice recovered faster than the wild-type mice, following 2.0mg/kg (Figure 3c; F1,104=17.8, p<0.001) and 3.0mg/kg (Figure 3d; F1,104=21.5, p<0.0001).
These data demonstrate that both α4-KO and δ-KO mice are less sensitive to the ataxic effects of muscimol than the wild-type mice.
Muscimol-induced ataxia was assessed in α1-KO mice and their wild-type littermate controls. Recovery from ataxia induced by 2.0 (Figure 4a) and 3.0mg/kg (Figure 4b) muscimol was not different between α1-KO and wild-type mice.
Ataxia induced by 1.0 or 1.5mg/kg muscimol was compared between Thy1α6 transgenic mice and C57BL/6 wild-type control mice (Figure 5). There were significant effects of gender at both 1.0mg/kg (F2,117=17.69, p<0.001) and 1.5mg/kg (F2,117=2.67, p<0.05). Therefore, analysis of data was split by gender. At both doses and between both genders, Thy1α6 mice were more sensitive to muscimol than the control mice (Figure 5c: 1.0mg/kg, females, F1,58=25.76, p<0.001; Figure 5d: 1.0mg/kg, males, F1,58=10.51, p<0.001; Figure 5e: 1.5mg/kg, females, F1,58=2.79, p<0.05; Figure 5f: 1.5mg/kg, males, F1,58=3.72, p<0.05).
To test a lower dose, which had no significant effect on rotarod performance (Figure 5a and b), we used an open field test and determined exploratory locomotor activity after 0.75mg/kg muscimol (Figure 6). Thy1α6 mice were more sensitive to muscimol than the control mice, as muscimol increased their total movements (Figure 6a, genotype × drug interaction F1,36=12.62, p<0.01) and the time they spent in the periphery (10-cm zone from the wall) (Figure 6b, interaction F1,36=24.86, p<0.001), and reduced the number of rears (Figure 6c, interaction F1,36=7.49, p<0.05).
To test whether Thy1α6 mice are more sensitive to gaboxadol in the fixed-speed rotarod test, we administered a slightly sedating dose of gaboxadol (6mg/kg) and determined the latency of falling from the rod (Figure 7). The transgenic mice were significantly more sensitive to gaboxadol than the wild-type controls (genotype effect F1,117=58.55, p<0.001).
The present data using novel mouse models suggest that the prototypic direct GABAA-R agonist muscimol preferentially acts through high-affinity GABA sites. Ataxic/sedative responses to muscimol were measured using the rotarod. We observed that α4 or δ-KO mice, but not α1-KO mice, were less sensitive to muscimol-induced impairment, and in Thy1α6 mice, the sedative/ataxic and locomotor stimulating responses of muscimol were significantly increased compared with the wild-type mice. Importantly, these bidirectional behavioral differences from the corresponding wild-type mice could be correlated with the bidirectional alterations in density of high-affinity [3H]muscimol binding sites in the forebrain regions, such as the cerebral cortex, hippocampus, caudate-putamen, and thalamus of the gene-modified mice. Importantly, we did not find any consistent alterations in the cerebellar high-affinity [3H]muscimol binding in the mouse models, although the rotarod performance can be affected by selective modulation of the cerebellar circuits (Wulff et al, 2007).
Our finding is striking particularly if we consider that the α1-KO mice with unchanged high-affinity [3H]muscimol binding in brain sections have dramatic overall changes in their GABAA-Rs: (1) a 55% reduction in total GABAA-Rs, (2) a 35% reduction in muscimol-stimulated chloride uptake in cortical neurosynaptosomes, and (3) a 55% reduction in [3H]muscimol binding in cerebellar homogenates (Kralic et al, 2002). α1-subunit-containing GABAA-Rs are widely expressed throughout the brain, in far greater number than GABAA-Rs containing α4- or δ-subunits (Bencsits et al, 1999; Fritschy et al, 1992; Pirker et al, 2000; Quirk et al, 1995). It should be also noted that autoradiography showed no differences in high-affinity [3H]muscimol binding in a conditional α1-knockout mouse model (Sonner et al, 2005). Therefore, the behavioral differences we observed in other mouse models in response to muscimol very likely implicate the high-affinity non-α1 subunit-containing GABAA-Rs.
Reduced sensitivity to muscimol in α4-KO and δ-KO mice is consistent with in vitro studies of GABAA-Rs and molecular pharmacological studies using these KO lines. Muscimol has a 40% greater maximal effect on extrasynaptic GABAA-Rs than on synaptic GABAA-Rs (Ebert et al, 1997; Storustovu and Ebert, 2006). In addition, δ-KO mice have a greatly reduced number of high-affinity [3H]muscimol sites as measured by ligand autoradiography (Mihalek et al, 1999; this study). A similar reduction in the forebrain was also observed in α4-KO mice (this study). Therefore, reduced behavioral sensitivity of α4-KO and δ-KO mice may be because of the loss of the high-affinity [3H]muscimol binding sites.
Muscimol is structurally similar to GABA and has been used extensively as a lead compound for the design of several other GABA analogs, such as gaboxadol (Krogsgaard-Larsen et al, 2004). It is important to notice that changes in sensitivity to muscimol of transgenic mouse lines resemble closely the changes seen in sensitivity to gaboxadol, which mediates its action mainly directly on GABA sites of extrasynaptic receptors (Belelli et al, 2005; Jia et al, 2005). α4 and δ-KO mice are significantly less sensitive to gaboxadol (Boehm et al, 2006; Chandra et al, 2006), α1-KO mice have unaltered response to it (Herd et al, 2009) and Thy1α6 mice display increased sensitivity to it (Saarelainen et al, 2008). The regional distribution of high-affinity [3H]gaboxadol binding in the rat brain recapitulates that of [3H]muscimol binding (Friemel et al, 2007), both of them being very different from low-affinity GABAA-Rs detected, eg, by GABA-stimulation of benzodiazepine agonist binding (Mennini and Gobbi, 1990). This is consistent with gaboxadol and benzodiazepine agonists acting on behavior by different mechanisms and showing little cross-tolerance (Michelsen et al, 2007; Voss et al, 2003). Interestingly, the present findings suggest that at least some of the gaboxadol-induced behavioral effects may not be specific for that compound, but may be general properties of directly acting GABAA-R agonists. This idea was supported in this study by enhanced sensitivity to ataxic/sedative effects of both muscimol and gaboxadol in Thy1α6 mice (Figures 5 and and7).7). However, even if muscimol seems to show preferential behavioral activity through its high-affinity binding sites, our data demonstrate that residual effectiveness can be observed in our ataxia/sedation test by higher muscimol doses even in mouse lines with reduced high-affinity binding. This suggests that muscimol is a prototypic GABAA-R agonist with preferential efficacy and selectivity, but not specificity, to high-affinity receptor subtypes.
No pharmacokinetic data on muscimol are available at present for mice. In rats, it has been estimated using intravenous administration of [3H]muscimol (1mg/kg) that, although it is quickly metabolized, the drug passes into the brain, resulting in a peak brain concentration of about 200nmol/kg 30min after administration (Baraldi et al, 1979; Moroni et al, 1982). Therefore, it is conceivable that in this study the concentrations achieved after i.p. dosing of 0.75–3.0mg/kg muscimol would be remaining only at nanomolar levels. Thus, also the brain levels would be consistent with preferential action on high-affinity extrasynaptic vs low-affinity synaptic GABAA-Rs.
The exact subunit composition of GABAA-Rs mediating the high-affinity [3H]muscimol binding in autoradiography and the ataxic/sedative effect of muscimol remains to be solved in later studies. Biochemically, low- and high-affinity binding sites can be selectively and independently interconversed by chaotropic agents or chemicals modifying histidine or tyrosine residues (Browner et al, 1981; Burch et al, 1983; Maksay and Ticku, 1984). Presently, it is not known whether the sites recognized by [3H]muscimol in brain sections could be transformed to low-affinity binding sites. In recombinant α1β2γ2 GABAA-Rs, there are two agonist binding sites in one GABAA-R, both having different agonist binding properties (Baumann et al, 2003; Baur and Sigel, 2003). Specific amino-acid residues in the N-terminal extracellular domains of various α (and β) subunits are responsible for agonist binding and for differences in binding affinity and functional sensitivity between recombinant receptor subtypes (Amin and Weiss, 1993; Baur and Sigel, 2003; Bohme et al, 2004; Boileau et al, 1999, 2002). The agonist binding sites are most likely between α- and β-subunits. Because of the pentameric structure of GABAA-Rs, these two agonist binding sites are not symmetrically positioned, which forms basis to their functional difference. The fact, that a significant proportion of GABAA-Rs contain two different α-subunits (Benke et al, 2004) makes the number of possible agonist binding sites with different properties even larger. However, all recombinant GABAA-Rs display high-affinity agonist binding, and the difference in agonist binding affinity even between αβδ and αβγ2-subunit-containing GABAA-Rs has been modest (Hevers and Luddens, 1998; You and Dunn, 2007). It has been suggested that also the δ-subunit participates in the formation of agonist binding site (Kaur et al, 2009), eg, a domain containing the transmembrane regions 1 and 2 of the δ-subunit explains at least partly the high efficacy of various agonists, such as gaboxadol, in αβδ GABAA-Rs (You and Dunn, 2007). These molecular structural and functional data together with the data on mouse models (see above) make it very likely that the amino-acid compositions of various subunits, rather than posttranslational modifications, have the most important role in defining the agonist sensitivity. There still remains the mismatch between the autoradiographic signal for nanomolar [3H]muscimol binding and the rather similar agonist binding affinities of various recombinant ‘synaptic' and ‘extrasynaptic' GABAA-Rs. Part of that difference might be explained, eg, by the effects of auxiliary proteins in neurons (Everitt et al, 2004; see for review, Birnir and Korpi, 2007).
In conclusion, the present results point to a correlation between high-affinity agonist binding sites of the GABAA-R in the forebrain and behavioral sensitivity to muscimol, and thus suggest that the behavioral effects of muscimol are preferentially mediated through high-affinity agonist binding sites of the forebrain GABAA-Rs. Most likely these receptors are non-α1 extrasynaptic GABAA-Rs containing δ and α4-subunits. It should be noted that muscimol is not a specific agonist for these receptor subtypes, as at higher doses it was effective even in the absence of δ or α4-subunits. Importantly, the experimental transgenic model on ectopic upregulation of extrasynaptic α6-subunit-containing GABAA-Rs in the forebrain provided evidence for a correlation between increased high-affinity binding and increased behavioral effects of GABA-site agonists. Further dissection of GABAA-Rs to synaptic and extrasynaptic receptors mediating phasic and tonic inhibition, respectively, might enable pharmacological manipulation of different components of inhibitory circuits. In addition to molecular and pharmacological profiling of these specific GABAA-R populations, their physiological roles and behavioral effects caused by their manipulation need to be further studied.
This work was supported by NIH Grants AA10422 (GEH) and DE14184 (DC) and by the Academy of Finland (ERK, AML) and the Sigrid Juselius Foundation (ERK). We thank Bjarke Ebert for a donation of gaboxadol.
The authors declare no conflict of interest.