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4 subunit by GABA and pentobarbital
Department of Anaesthesiology, Campus Box 8054, 660 South Euclid Ave, Washington University, St Louis, MO 63110, USA
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4ß2
2 and 4ß2
subunits were examined in the presence of GABA or pentobarbital. The receptors were expressed transiently in HEK 293 cells, and the electrophysiological experiments were carried out using cell-attached single-channel patch clamp or whole-cell macroscopic recordings. The data show that GABA is a stronger activator of 4ß22 receptors than 4ß2 receptors. Single-channel clusters were recorded from 4ß22 receptors in the presence of 10–5000 µM GABA. The maximal intracluster open probability was 0.35, with a half-maximal response elicited by 32 µM GABA. Simultaneous kinetic analysis of single-channel currents obtained at various GABA concentrations yields a channel opening rate constant of 250 s–1, and a KD of 20 µM. In contrast, only isolated openings were observed in the presence of GABA for the 4ß2 receptor. Pentobarbital was a strong activator of both 4ß22 and 4ß2 receptors. The maximal cluster open probability, recorded in the presence of 100 µM pentobarbital, was 0.7. At higher pentobarbital concentrations, the cluster open probability was reduced, probably due to channel block. The results from single-channel experiments were confirmed by macroscopic recordings from HEK cells in the presence of GABA or pentobarbital.
(Received 17 November 2003;
accepted after revision 13 February 2004;
first published online 13 February 2004)
Corresponding author G. Akk: Department of Anaesthesiology, Washington University in St Louis, Campus Box 8054, 660 S. Euclid Ave, St Louis, MO 63110, USA. Email: akk{at}morpheus.wustl.edu
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Introduction |
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ß or ß subunits where the ratio of subunits is normally 2 : 2ß : 1 or subunit (Chang et al. 1996; Baumann et al. 2001).
The expression of the 4 subunit is concentrated in the hippocampus and thalamus where it colocalizes mostly with the ß2 or ß3, and 2 or subunits (Wisden et al. 1992). There seems to be a preference for the subunit, with which twice as many 4 subunits assemble compared to the 2 subunit (Sur et al. 1999). While the general expression levels for the 4 subunit, and hence the total number of receptors containing this subunit, are relatively low, the functional significance of such receptors may be disproportionally great. A case has been made that the receptors containing the 4 subunit localize mainly to the extrasynaptic regions where they participate in generating tonic current (Nusser & Mody, 2002), thereby controlling the passive membrane properties of the cell (Hausser & Clark, 1997). A high apparent affinity to GABA is a characteristic feature of extrasynaptic receptors, with a concentration producing a half-maximal evoked response of <3 µM (Yeung et al. 2003).
Studies of receptors formed after expression of recombinant proteins have demonstrated that the 4 subunit confers distinct pharmacological properties. Such receptors are generally more sensitive to GABA than ones containing the more common 1 subunit (Brown et al. 2002). Partial agonists, such as THIP and P4S, are more efficacious on 4 containing receptors, while the receptors containing both the 4 and the subunit have been found to be more sensitive to these agonists than ones containing the 2 subunit (Adkins et al. 2001; Brown et al. 2002). The presence of the 4 subunit does not significantly affect receptor modulation by neuroactive steroids, barbiturates or other anaesthetics (ibid.). However, it has been reported that pentobarbital and propofol are unable to directly activate the 4ß12 GABAA receptor (Wafford et al. 1996). Although receptors containing the 4 subunit have distinctive pharmacological properties, there have been only limited quantitative studies of activation of the receptors by GABA or other agonists (Wafford et al. 1996; Brown et al. 2002). Accordingly, to provide a more precise quantitative description of the activation of these receptors by GABA and pentobarbital, we examined single-channel currents. These studies are the initial steps to define the functional differences between the receptors likely to underlie rapid, synaptic inhibitory transmission and those likely to be associated with tonic GABAergic inhibition.
Single-channel kinetic analysis has been used previously to study the biophysical and pharmacological properties of a number of native or recombinant GABAA receptor subtypes (Twyman et al. 1990; Newland et al. 1991; Fisher & Macdonald, 1997; Steinbach & Akk, 2001). This approach is particularly well-suited for studies where receptors with known subunit compositions are available, such as in transfection systems. The method allows one to examine the receptor activation properties in detail, and separate a general dose–response curve into components of ligand binding, channel gating and desensitization. The receptors were expressed transiently in HEK 293 cells, and the data were obtained using the cell-attached single-channel patch clamp and whole-cell recording techniques. The results demonstrate that 4 containing receptors are strongly activated by pentobarbital, the efficacy of which is greater at these receptors than that of GABA.
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4), D. Weiss (rat ß1, ß2, 2L) and R. Olsen (rat ). The cDNA was subcloned into a CMV promoter-based vector, pcDNAIII (Invitrogen, San Diego, CA, USA), and used to transfect HEK 293 cells.
Transient transfection of HEK 293 cells using calcium phosphate precipitation was carried out as described earlier (Akk, 2002). In brief, 3.5 µg of cDNA per 35 mm culture dish was used in the ratio of 2 : 2 : 1 ( : ß : or ). The cells were exposed to the precipitate for 14–18 h, after which the medium in the culture dish was replaced. The electrophysiological experiments commenced 24 h after changing the bath medium.
The single-channel currents were recorded using a patch clamp technique in the cell-attached configuration (Hamill et al. 1981). The bath solution contained (mM): 140 NaCl, 5 KCl, 1 MgCl2, 2 CaCl2, 10 glucose and 10 Hepes; pH 7.4. The pipette solution contained (mM): 120 NaCl, 5 KCl, 10 MgCl2, 0.1 CaCl2, 20 tetraethylammonium, 5 4-aminopyridine, 10 glucose, 10 Hepes; pH 7.4. Agonists (GABA or pentobarbital) were added to the pipette solution at concentrations indicated in the text. The pipette potential was normally held at +60 to +80 mV. Based on our experience (data not shown), the HEK cell membrane potential is typically –40 mV. Thus, the total potential difference across the patch membrane was between –120 and –100 mV. The channel activity was recorded with an Axopatch 200B amplifier, low-pass filtered at 10 kHz and acquired with a Digidata 1322 Series Interface at 50 kHz using pCLAMP 8 software (Axon Instruments, Foster City, CA, USA). The data were stored on a PC hard drive for further analysis.
In most cases, the kinetic analysis of single-channel currents was restricted to single-channel clusters. A cluster is defined as an episode of intense channel activity which originates from the activation of a single ion channel. A cluster starts when a receptor returns from a long-lived desensitized state and is terminated once the receptor re-enters the long-lived desensitized state. The procedure for identification of GABAA receptor clusters has been previously described (Steinbach & Akk, 2001). In brief, series of openings isolated from each other by silent periods of at least 250 ms were extracted from the rest of the recording. Episodes containing overlapping currents indicating the activity of two or more receptors were excluded from the analysis. In general, episodes shorter than 250 ms were not included in cluster analysis.
The single-channel clusters were low-pass filtered at 2–4 kHz, and the data were idealized using the segmented-k-means algorithm (Qin et al. 1996). The intracluster open and closed times were estimated from histogram fitting using maximum likelihood methods which incorporated a correction for missed events (Qin et al. 1996). The open interval duration histograms were initially analysed by fitting a simple C 
O model. The number of open states was then increased progressively as long as the increase in the log-likelihood justified the addition of the extra state (Horn, 1987). The open states were connected directly to the closed state, and unconnected to each other. The closed interval duration histograms were analysed in a similar fashion, starting with an O C model and adding closed states until the addition of more closed states did not significantly improve the fit. Error limits were estimated from the curvature of the likelihood surface as previously described (Qin et al. 1997). Cluster open probability, calculated as the fraction of time the receptor spends in the open states within a cluster, and plotted as a function of agonist concentration, is used as the variable in the single-channel concentration–response curve.
In certain cases, receptor activation did not result in single-channel clusters (e.g. 4ß2 activated with GABA). Then, 0.5–2 s episodes of single-channel activity were isolated from the recording, and the current open times were analysed as described above. However, no studies on the current closed times were undertaken for these patches.
The currents arising from the ß and ß receptors were distinguished from activity of receptors containing just ß subunits according to single-channel conductance, which is approximately 50% greater in the ß/ß configuration (Puia et al. 1990; Fisher & Macdonald, 1997; G. Akk, unpublished data). During visual inspection, the majority of currents belonged to the high-conductance class, suggesting that ß receptors did not contribute significantly to the electrophysiological responses (data not shown).
The pipette solution in whole-cell macroscopic recordings contained (mM): 140 CsCl, 4 NaCl, 4 MgCl2, 0.5 CaCl2, 5 EGTA, 10 Hepes; pH 7.3. Agonists were applied using a gravity-fed delivery system consisting of seven lines entering a single manifold (Fletcher & Steinbach, 1996). The cells were clamped at –50 mV. No compensation for series resistance was carried out. The currents were filtered at 5 kHz and digitized at 100 µs per point. The analysis was carried out using Clampfit 8 (Axon Instruments) software.
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4ß22 receptors by GABA
Receptors containing the 4, ß2 and 2 subunits are activated in the presence of GABA. Single-channel clusters were observed at GABA concentrations as low as 10 µM. As the agonist concentration was raised, the cluster open probability (Po) increased. Shown in Fig. 1 are sample clusters elicited by 20 and 1000 µM GABA. The 50-fold increase in GABA concentration results in a notably higher Po of a cluster.
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The CTß state has been associated with dwells in the mono- and unliganded states due to its dependence on the nature and concentration of the agonist (Steinbach & Akk, 2001). The inverse of CTß at different agonist concentrations, defined as an effective opening rate (ß'), is shown in Fig. 2C. The curve was fitted using a Hill equation, yielding a maximal effective opening rate (ß) of 399 ± 127 s–1, an EC50 of 204 ± 155 µM, and a Hill slope of 1.3 ± 0.3. The effective opening rate curve saturates at the value corresponding to the true opening rate constant of the ion channel. Hence, using this approach, the channel opening rate constant of the 4ß22 subunit-containing receptor, in the presence of GABA, is estimated as 
400 s–1. The Hill slope value of more than 1 indicates that the binding of more than one agonist molecule is required for activation.
The durations or fractions of CT1, CT2 and CTSD are not affected by the concentration of GABA. While the true molecular origin of these states is unknown, it is not likely that they form part of the activation pathway, i.e. dwells in the monoliganded or unliganded states. Similar non-conducting states have been observed previously for the recombinant 1ß2 receptor (ß1, Haas & Macdonald, 1999; ß2, Steinbach & Akk, 2001) and in native GABAA receptors from mouse spinal cord neurones (Twyman et al. 1990) or cultured hippocampal neurones (Jones & Westbrook, 1995).
In the absence of a generally accepted GABAA receptor activation model, another approach to determine the channel opening rate constant, and to get an estimate for the receptor affinity, is to fit a model in which a single open state is connected with closed states associated with agonist binding and the three agonist-independent closed states to the single-channel data obtained at several GABA concentrations:
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In this model, the transitions between the open state (A2O) and CT1, CT2 or CTSD are independent of GABA concentration. The pathway from C (unliganded, closed state) to A2O corresponds to the CTß component in the closed time histograms. This pathway consists of two agonist binding steps, and a step corresponding to the conformational change of the diliganded, closed receptor (marked with ß). The conformational change is unaffected by the agonist concentration, being the limiting value for the CTß component at saturating GABA concentrations. It should be mentioned that no assumptions regarding the true activation model have been made here other than that (i) two agonist binding steps are required for channel opening, (ii) all three open states observed in the recordings behave essentially similarly to the single composite open state shown in Model 1, and (iii) states corresponding to closed time components CT1, CT2 and CTSD are not part of the activation pathway. Some or all of these closed states may actually originate from the A2C state.
We used the QuB suite (http://www.qub.buffalo.edu) to fit Model 1 to the single-channel data obtained in the presence of 20, 100 and 5000 µM GABA (one patch at each concentration containing 5624, 11716 and 3506 events, and 13, 28 and 10 clusters, respectively). The dead time was set at 72 µs. The GABA concentrations were chosen to fully cover the low and high ends of the concentration–response curves (Fig. 2C and D). In the simultaneous fitting of the three files, the only constraint was to assume that the two agonist binding sites have equivalent affinities to GABA. It should be mentioned that there are no data suggesting that the GABA binding sites have equal KD values; this constraint was used simply to reduce the number of free parameters. The results of the fit are as follows. The agonist association rate constant (k+) is 5 ± 1 µM–1 s–1, the agonist dissociation rate constant (k–) is 100 ± 26 s–1, yielding a KD of 20 µM. The channel opening rate constant (ß), estimated from Model 1, is 250 ± 32 s–1, and the channel closing rate constant () is 218 ± 69 s–1. The rates of entry into and return from the blocked/desensitized states are: for CT1, k+CT1= 224 ± 83 s–1 and k–CT1= 3894 ± 387 s–1, for CT2, k+CT2= 526 ± 40 s–1 and k–CT2= 666 ± 49 s–1, and for CTSD, k+S.D.= 16 ± 4 s–1 and k–S.D.= 39 ± 5 s–1. Figure 3 shows the closed interval duration histograms for the three patches used in the analysis, and the interval duration distributions as predicted from the rate constants estimated using Model 1.
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The intracluster open and closed times determine the cluster open probability. The intracluster open probability versus GABA concentration relationship is given in Fig. 2D. The curve was fitted with the Hill equation, yielding a maximal open probability of 0.35 ± 0.04, an EC50 of 32 ± 16 µM and a Hill coefficient of 0.9 ± 0.4.
Activation of 4ß22 receptors by pentobarbital
We next studied receptor activation by pentobarbital (PB). Within the concentration range 10–1000 µM PB, activation of 4ß22 receptors occurred in single-channel clusters. Sample clusters obtained in the presence of 200 and 1000 µM PB are shown in Fig. 4A and B. Comparison of the two clusters demonstrates a typical characteristic of PB-mediated activation – a decrease in the channel open probability at high PB concentrations due to channel block. A similar effect of high concentrations of PB has been previously described for the 1ß22 receptor (Akk & Steinbach, 2000). Figure 4C gives the intracluster open probability obtained at various PB concentrations. The data demonstrate a decline in cluster open probability at PB concentrations above 200 µM caused by a decline in the open time durations (Fig. 4D) and an increase in the mean intracluster closed interval duration (Fig. 4E). The cluster open probability at 30–200 µM PB is higher than the maximal open probability in the presence of GABA (Fig. 2D), indicating that PB is a higher efficacy agonist at the 4ß22 receptor.
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The intracluster closed time durations increased when the PB concentration is raised above 200 µM. The mean closed time was 2.5 ± 0.04 ms at 200 µM, 6.4 ± 0.1 ms (5643 events) at 500 µM and 8.9 ± 0.2 ms (4115 events) at 1 mM PB. The trends observed in the open and closed times are similar to what was observed previously for the 1ß22 subunit-containing receptor where the increase in the channel closed time durations and the decrease in the channel open time durations were associated with PB-mediated channel block (Akk & Steinbach, 2000).
Figure 4D shows the relationship between the mean open duration and the concentration of PB. As PB concentration is increased, the mean open duration is decreased. The continuous line was fitted to: OT = 1/(+k+B[PB]), where is the true channel closing rate constant and k+B is the channel blocking rate constant. According to the fit, k+B= 0.59 ± 0.27 µM–1 s–1 and = 134 ± 24 s–1. In this fit, no consideration was given to the presence of the multiple open time components. The value for k+B is similar to one obtained previously for the 1ß22 receptor (0.56 µM–1 s–1; Akk and Steinbach, 2000) suggesting that the site involved in the PB blocking mechanism remains intact when the 1 subunit is replaced by the 4 subunit.
The calculated mean closed time in a cluster decreased with increasing PB concentrations from 10 to 100 µM, as would be expected for an agonist. The observation that the mean closed time increased with PB concentration above 100 µM suggests that more than one PB molecule can be involved in block, as was suggested previously for the 1ß22 receptor (Akk & Steinbach, 2000) and the 1ß2 receptor (Serafini et al. 2000).
Macroscopic currents from 4ß22 receptors activated by GABA and pentobarbital
We also studied the activation of 4ß22 receptors using whole-cell voltage clamp. The reason for doing these experiments was to confirm receptor activation by PB under non-equilibrium conditions, such as during a pulse of agonist application. It has been proposed that different kinetic states are occupied during different phases of macroscopic currents (Haas & Macdonald, 1999). The steady-state single-channel currents may be related to the residual currents in the end of a prolonged pulse of agonist application. Therefore, we were interested in comparing the amplitudes of peak currents under non-equilibrium conditions during receptor activation by GABA or PB.
The results from the whole-cell experiments demonstrate that PB is a strong activator of the 4ß22 receptor. The peak currents obtained in response to applications of 100 µM PB were higher than those recorded in the presence of 1 mM GABA (Fig. 5A and B). Both agonist concentrations represent the conditions under which maximal responses were elicited during steady-state single-channel patch clamp. Thus, the macroscopic peak currents qualitatively agree with the findings from the single-channel experiments demonstrating that PB is a higher efficacy agonist than GABA on the 4ß22 receptor. The whole-cell currents elicited by 1 mM GABA compared to that elicited by 100 µM PB (85%) were somewhat larger than expected based on cluster open probability (0.4/0.7 = 56%).
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Residual current levels were estimated during an agonist application 5 s after the peak. These values were used to evaluate receptor desensitization in the presence of PB or GABA. Figure 5C gives the residual current levels in the presence of 100 or 1000 µM PB, or 1 mM GABA. The results indicate only relatively minor desensitization (< 40%) taking place within 5 s. It should be noted, however, that steady-state levels were not reached within 5 s for receptors activated by 100 µM PB.
We have compared the current levels in the presence of 10– 2000 µM PB as estimated from the single-channel and whole-cell experiments. The parameter used for single-channel currents was cluster open probability (see above), while for whole-cell currents, the amplitude of the peak current was used. In both cases, the values for current levels were normalized to that observed in the presence of 100 µM PB. Shown in Fig. 5D are the relative current levels as estimated from single-channel and whole-cell experiments. With both methods, a bell-shaped relationship between the relative current and the concentration of PB is detected, with maximal current levels observed at 50–100 µM PB.
Single-channel and macroscopic currents from 4ß2 receptors elicited by GABA and pentobarbital
Finally, we also studied the activation of 4ß2 receptors by GABA and PB. In the presence of GABA, the activity of 4ß2 receptors takes place as isolated openings with no apparent desensitization-delimited single-channel clusters. Shown in Fig. 6A are sample currents elicited by 1000 µM GABA. The channel open events were fitted with a sum of two exponentials (to a total of 1406 events), with the time constants of 0.12 ± 0.03 ms and 3.2 ± 0.1 ms. The longer-duration openings were four times as prevalent as the shorter duration openings. Due to the absence of single-channel clusters, no further analysis was carried out on 4ß2 receptors activated by GABA.
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4ß2 receptors by 10–200 µM pentobarbital (PB). In contrast to what was observed in the presence of GABA, PB was a strong activator of the 4ß2 receptor. Groups of channel openings with high open probability were observed at PB concentrationsof 40 µM (Fig. 6B). The open time histograms from such groups obtained in the presence of 40 µM PB contained three components. The mean durations (relative frequencies) of the components were (3913 events): for OT1, 0.11 ± 0.02 ms (10 ± 1%); for OT2, 1.5 ± 0.4 ms (13 ± 2%); for OT3, 11.1 ± 0.4 ms (77 ± 4%). Therefore, similarly to the 4ß22 receptor, the channel open times are prolonged in the presence of low concentrations of PB compared to GABA. PB at higher concentrations appeared to block the channel openings. This resulted in the loss of the longest-lived component, OT3 from the open time histograms at PB concentrations of 100 µM and above, and the subsequent reduction in the duration of OT2. The calculated mean open time durations were 9.2 ms with 40 µM PB, 4.6 ms with 100 µM PB and 3.3 ms with 200 µM PB.
The analysis of the channel closed times was complicated by the number of components in the closed time histograms and the simultaneous, competing actions of PB on the receptor activation – a decrease in the mean closed time duration due to an increased effective opening rate, and an increase in the mean closed time duration due to channel block by PB. Hence, the identification of single-channel clusters in the records was hindered. The overall closed time histograms were best-fitted with the sum of four exponentials. We calculated the mean closed times for 4ß2 currents elicited by PB using the three shorter-lived closed time components and ignoring the longest-lived component which has a mean duration of >100 ms. The mean closed times were 5.2 ms with 40 µM PB, 3.3 ms with 100 µM PB and 4.3 ms with 200 µM PB. The initial reduction in the closed time duration probably results from an increase in the effective opening rate. The subsequent increase in the closed time duration is likely to be due to increased channel block, as shown above for the 4ß22 receptor activation by PB.
The effect of 40 µM PB on the activation of 4ß2 receptors by 10–5000 µM GABA was also examined. Sample currents elicited by 1000 µM GABA in the absence and presence of 40 µM PB are shown in Fig. 6. To our surprise, the addition of GABA did not lead to an enhancement of receptor function. The open time histograms contained three components whose mean durations and relative weights were unaffected by changes in the concentration of GABA. The mean durations (relative frequencies) of the components at 10–5000 µM GABA, in the presence of 40 µM PB, were: for OT1, 0.18 ± 0.08 ms (17 ± 7%); for OT2, 2.4 ± 1.5 ms (28 ± 21%); for OT3, 10.8 ± 1.7 ms (54 ± 23%). The open times were averaged from six patches, with a total number of events 20550. These values are similar to the open time parameters obtained at 40 µM PB, in the absence of GABA (see above). The data indicate that GABA and PB do not positively interact on the 4ß2 receptor to prolong open times. This is in clear contrast to results found for 1ß22 receptors, for which the combination of PB (50 µM) and GABA (10–1000 µM) resulted in a prolongation of the mean duration of the OT3 component from 3.3 ms (PB alone) or 6.3 ms (GABA alone) to 13.3 ms.
Upon examining the channel closed times, we also failed to see an effect of GABA on currents elicited by 40 µM PB. The channel mean closed times were 4.8 ms with 10 µM GABA, 8.9 ms with 50 µM GABA, 5.9 ms with 100 µM GABA, 6.0 ms with 500 µM GABA, 4.5 ms with 1000 µM GABA, 4.2 ms with 2000 µM GABA and 4.1 ms with 5000 µM GABA. In all cases, 40 µM PB was coapplied with the specified concentration of GABA. Similarly to the analysis of currents elicited by PB alone (see above), we excluded the long-lived closed time component (
> 100 ms) from this analysis.
Macroscopic currents from 4ß2 receptors were examined in the presence of 1 mM GABA, or 100 or 1000 µM PB. Sample macroscopic responses, comparison of peak currents and residual currents (current levels at 5 s after peak, compared to peak value) are presented in Fig. 7. The results demonstrate that the peak amplitude in the presence of 100 µM PB is 3-fold greater than the amplitude of responses elicited by 1 mM GABA. The responses to 100 µM PB decayed quickly due to desensitization in the sustained presence of PB. The residual current at 5 s was only 10% of the peak current. In comparison, the residual currents in the presence of 1 mM PB or 1 mM GABA were 40–60%. The results from whole-cell recordings agree with the single-channel studies demonstrating that PB is a more efficacious agonist than GABA on the 4ß2 receptors, and that GABA-activated receptors desensitize more slowly than those activated by PB.
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subunit, and the 6 or 4 subunit are located in the extrasynaptic regions, and preferentially associated with tonic inhibition (Nusser et al. 1998). In contrast, the rapidly desensitizing synaptic currents are likely to be mediated by receptors containing 1 and 2 subunits (Nusser & Mody, 2002). It should be mentioned that the number of GABA-activated conductance classes is greater for extrasynaptic than synaptic GABAA receptors in cerebellar granule cells suggesting of higher degree of heterogeneity in receptor subunit composition (Brickley et al. 1999). The currents associated with tonic (extrasynaptic) and phasic (synaptic) inhibition may have different roles. It has been proposed that the activation of extrasynaptic receptors controls the passive membrane properties, such as the cell input resistance affecting the time window for synaptic integration (Hausser & Clark, 1997). In rat cerebellar granule cells, the activation of synaptic GABAA receptors leads to an increased synchronicity in firing while tonic inhibition has the opposite effect (De Schutter, 2002). An increase in the concentrations of ambient GABA by tiagabine or vigabatrin potentiates tonic inhibition but reduces miniature and evoked IPSCs (Overstreet & Westbrook, 2001). Both these compounds have anticonvulsant properties, suggesting that activation and/or potentiation of extrasynaptic but not synaptic GABAA receptors underlie the treatment of certain types of seizures. Hence, discovery of site-specific pharmacological agents would be particularly useful.
Because of the differences in the subunit composition, it comes as no great surprise that the biophysical and pharmacological properties of synaptic and extrasynaptic receptors differ. In rat CA1 pyramidal neurones, extrasynaptic receptors demonstrate slower deactivation, compared to synaptic receptors, and the responses from extrasynaptic receptors are modulated by cytoplasmic calcium (Banks & Pearce, 2000). In hippocampal neurones, gabazine and penicillin inhibit mIPSCs but not the tonic current (Bai et al. 2001; Yeung et al. 2003). Also, midazolam and propofol, at clinical concentrations, have a greater effect on charge transfer during tonic current than mIPSCs (ibid.). On the other hand, in dentate gyrus granule cells, zolpidem potentiated synaptic receptors without affecting tonic inhibition (Nusser & Mody, 2002). Work on recombinant receptors containing the 4 subunit has shown them to be insensitive to benzodiazepines such as diazepam or flunitrazepam, setting such receptors apart from those containing the 1 subunit (Wieland et al. 1992; Brown et al. 2002). Receptors containing the 4 and subunits exhibit reduced desensitization (Brown et al. 2002), making them suitable for maintaining tonic inhibition. Recently, the ability of ethanol to potentiate GABA-elicited currents from 4ß2 receptors was demonstrated (Sundstrom-Poromaa et al. 2002).
Here, we have studied the activation of 4 subunit-containing receptors by GABA and pentobarbital. The 4 subunit was coexpressed with the ß2, and 2 or subunits. Both subunit combinations expressed receptors activatable by GABA and PB. The results from kinetic modelling demonstrate that GABA is a high affinity but a relatively low efficacy agonist for the 4ß22 receptor. The microscopic affinity of the resting 4ß22 receptor to GABA is about 20 µM. This value is similar to the estimates for the affinity of GABAA receptors containing the 1 subunit (Haas & Macdonald, 1999; Li & Pearce, 2000). The channel opening rate constant is 250 s–1. Hence, the substitution of the 1 by the 4 subunit reduces the channel opening rate constant by almost 10-fold (Steinbach & Akk, 2001). This effect was not accompanied by changes in the general pattern of receptor activation, as the number of open and closed states in the records and their overall properties were unaffected (ibid.).
The EC50 of the 4ß22 receptor cluster Po curve (32 µM) is approximately 10-fold higher than EC50 values for whole-cell dose–response curves estimated for recombinant 4ß32 receptors (Brown et al. 2002) or native receptors responsible for tonic currents in mouse hippocampal neurones (Yeung et al. 2003). The disagreement may arise from differences in subunit composition or expression system. We have not pursued this issue further.
In contrast, the activation of 4ß2 receptors by GABA was not characterized by single-channel clusters. Instead, persisting, non-desensitizing currents (isolated openings and short bursts) were seen at GABA concentrations up to 1 mM. Changes in GABA concentration did not affect noticeably the channel closed durations. In the whole-cell recordings, currents from 4ß3 receptors are also characterized by slow desensitization (Brown et al. 2002). This pattern of behaviour is similar to currents from receptors containing 1ß subunits (1ß2, G. Akk, unpublished observations; 1ß3, Haas & Macdonald, 1999). We speculate that reduced desensitization of receptors containing the subunit leads to such persisting currents while a dominating, long-lived closed state in the single-channel records masks the agonist-dependent CTß component. The origin of the long-lived closed state is unclear but a prominent, frequently visited closed state which rapidly equilibrates with the open states would agree with the experimental findings.
Our results show that PB is a strong activator of 4 containing receptors. In the single-channel recordings, the maximal open probability of receptors containing the 4 and ß2 subunits, and either the 2 or the subunit was greater in the presence of PB than GABA. The open probability was greatest at 100–200 µM, while at higher concentrations of PB the open probability was reduced due to channel block. Channel block was manifested as both a reduction in the mean open duration as well as an increase in the mean closed time duration. In the 4ß22 receptor, the rate of entry into the blocked state, determined from the reduction in the mean open time durations, was similar to the blocking rate in the 1ß22 receptor (Akk & Steinbach, 2000).
Interestingly, in 4ß2 receptors, the addition of GABA had no effect on currents (open or closed time durations) elicited by 40 µM PB. Earlier studies on the recombinant 1ß22 receptor have shown that the coapplication of GABA and PB results in an increase in the mean open time duration over that seen in the presence of either GABA or PB alone (Akk & Steinbach, 2000; Steinbach & Akk, 2001). In the present case, the channel open times were fully determined by PB, and the addition of GABA had no further effect. It is not immediately clear how to account for this finding. It is possible that the channel activation was saturated by 40 µM PB. However, the observation that the mean closed time within clusters decreased between 40 µM and 100 µM PB suggests that this is not the case. Alternatively, it is possible that channel block could obscure potentiation.
It is generally accepted that the agonistic properties of GABA and PB are mediated via separate sites (Amin & Weiss, 1993; Ueno et al. 1997). Our findings are clearly consistent with GABA and PB binding to distinct domains as PB-mediated activation was not inhibited by GABA acting as a low-efficacy agonist, even at 5 mM. Further studies will have to be carried out to investigate the modulatory properties of barbiturates. The concentration of pentobarbital used in these experiments is similar to the concentrations measured in brains of anaesthetized animals (100 µM, Saubermann et al. 1974). Hence, if pentobarbital-mediated anaesthetic effects are due to interactions with the 4ß2 receptor, such interactions would probably be mediated via direct activation of the receptor by pentobarbital, not by potentiation of GABA-activated currents.
Strong direct activation of 4-containing receptors by PB was unexpected as a previous study had demonstrated a lack of direct activation of 4ß12 receptors by PB (Wafford et al. 1996). We do not have an explanation for this discrepancy between our data and the results obtained previously. To test the unlikely possibility that the difference among the ß subunits used in these two studies is responsible for the inconsistency, we examined the activation of 4ß12 receptors by GABA and PB. In this combination, the open probability of receptors was 0.33 when activated by 1 mM GABA, and 0.66 in the presence of 100 µM PB (data not shown). Similarly to ß2 subunit-containing receptors, the cluster open probability decreased when the concentration of PB was further increased to 1 mM. Therefore, the nature of the ß subunit did not affect the activation (or block) by PB. We also examined whether differences in the expression system may affect responses to PB (oocytes were used by Wafford et al. 1996versus HEK cells in the present study). Our results indicate that 4ß12 receptors expressed in Xenopus oocytes are responsive to PB (data not shown). Finally, the species difference may be responsible for the lack of direct activation by PB in Wafford et al. (1996), who used fully human receptors. In the present study, the human 4 subunit was used along with rat ß and 2 or subunits.
In conclusion, the results presented in this manuscript demonstrate that 4ß22 and 4ß2 receptors are activated by GABA and PB. The strong responses seen in the presence of PB suggest a role for 4 subunit-containing receptors in PB-mediated effects in the mammalian nervous system. The presumed extrasynaptic location of the 4ß2 receptors makes these receptors an attractive target of barbiturates in controlling tonic inhibitory conductance.
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