Corresponding author M. Martina: Department of Physiology, Northwestern University Feinberg School of Medicine, 303 E. Chicago Avenue, Chicago, IL 60611, USA. Email: email@example.com
In CA1 pyramidal neurons, burst firing is correlated with hippocampally dependent behaviours and modulation of synaptic strength. One of the mechanisms underlying burst firing in these cells is the afterdepolarization (ADP) that follows each action potential. Previous work has shown that the ADP results from the interaction of several depolarizing and hyperpolarizing conductances located in the soma and the dendrites. By using patch-clamp recordings from acute rat hippocampal slices we show that D-type potassium current modulates the size of the ADP and the bursting of CA1 pyramidal neurons. Sensitivity to α-dendrotoxin suggests that Kv1-containing potassium channels mediate this current. Dual somato-dendritic recording, outside-out dendritic recordings, and focal application of dendrotoxin together indicate that the channels mediating this current are located in the apical dendrites. Thus, our data present evidence for a dendritic segregation of Kv1-like channels in CA1 pyramidal neurons and identify a novel action for these channels, showing that they inhibit action potential bursting by restricting the size of the ADP.
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The dendritic contribution to the ADP is not only determined by inward currents but is also shaped by dendritic potassium currents. Magee & Carruth (1999) showed that application of the potassium channel antagonist 4-aminopyridine (4-AP) to the dendrites – but not to the soma – promotes bursting through potentiation of the ADP, and concluded that the effect was mediated by the block of A-type current. However, 4-AP also potently reduces the relatively non-inactivating, D-type potassium current (Storm, 1988; Grissmer et al. 1994), which is also present in CA1 pyramidal neuron dendrites (Hoffman et al. 1997; Chen & Johnston, 2004).
D-type potassium current was first described in CA1 pyramidal neurons and named for the delay it imposes on action potential firing in response to long current injections (Storm, 1988); however, neither the molecular determinants of D-type current, nor its specific role in modulating the ADP and bursting have been investigated in these neurons. Channels belonging to the Kv1 family, which are blocked by α-dendrotoxin (DTX; Storm, 1990; Grissmer et al. 1994), are potential candidates for mediating this current as they have been shown to enhance excitability and bursting in CA3 and neocortical pyramidal neurons (Bekkers & Delaney, 2001; Lopantsev et al. 2003). In CA1 pyramidal cells, DTX enhances initiation of dendritic spiking (Golding et al. 1999), another mechanism for producing bursting. The location of Kv1 channels in CA1 pyramidal cells is still unresolved. There is very little DTX-sensitive current in somatic nucleated patches from CA1 pyramidal cells (Martina et al. 1998), yet these cells express several Kv1 family mRNAs (Sheng et al. 1994; Martina et al. 1998). Moreover, the stratum radiatum – through which the apical dendrites of CA1 pyramidal cells extend – is immunopositive for Kv1.2 (Sheng et al. 1994), suggesting localization of these channels in the apical dendrites where they may be aptly situated to inhibit the ADP.
In this study we tested the joint hypotheses that inward voltage-gated currents in the apical dendritic tree, activated by the backpropagated action potential, have the capacity to contribute to the production of the ADP, yet the magnitude of the contribution is restricted by dendritic DTX-sensitive, D-type potassium currents. We used simultaneous somatic and dendritic current-clamp recordings, excised dendritic patches, and selective pharmacology to test these hypotheses. Using a novel recording configuration to functionally remove the contribution of the dendrite, we show that under control conditions the dendritic current provides a small contribution to the ADP, but when D-type currents are blocked the dendritic contribution is more than doubled. Focal application of DTX and voltage-clamp recordings in dendritic outside-out patches reveal that the D-type current is localized to the apical dendrite.
All animal procedures were approved by the Northwestern University Animal Care and Use Committee.
Male Wistar rats, 14–26 days old, were used for the preparation of transverse hippocampal slices following standard procedures. Animals were deeply anaesthetized with halothane or isofluorane inhalation (∼200 μl to 1 l container, vaporized) and killed by decapitation. The brain was removed and sliced in ice-cold artificial cerebral spinal fluid (ACSF; see ‘Solutions and drugs’ section). Slices were transferred to a suspended mesh within a chamber containing sucrose solution (see below), incubated at 35°C for 15–20 min, and subsequently stored at room temperature. For recording, individual slices were transferred to a small chamber continuously perfused with ACSF at 1–3 ml min−1, and visualized with an upright, fixed-stage microscope (Axioscop, Zeiss) using differential interference contrast infrared videomicroscopy at ×60–160 magnification.
Whole-cell recordings were performed at 33–35°C using either a BVC-700 amplifier (Dagan Products, Minneapolis, MN, USA) or an Axopatch 200B (Axon Instruments, Union City, CA, USA) employing series resistance and capacitance compensation. Patch electrodes (3–6 MΩ) were made from thick-walled borosilicate glass (Garner Glass, Claremont, CA, USA or Hilgenberg, Malsfeld, Germany) and filled with K-gluconate internal solution. Only cells with membrane potentials negative to −55 mV were used for experiments. Membrane potential was maintained at −67 mV with somatic DC current injection as needed (0 to −150 pA). Data were filtered at 10 kHz and sampled at 100 kHz.
For electronic-excision experiments, the voltage output of the somatic amplifier in current-clamp mode was appropriately scaled and used as the voltage command to the dendritic amplifier by passing it through a preamplifier (Warner Instruments, Hamden, CT, USA). Only recordings in which series resistance was less than 15 MΩ, stable, and at least 65% compensated (with 20 μs or less lag) were used for analysis.
Recordings were made in the presence of kynurenic acid (2 mm) and picrotoxin (100 μm) to block fast synaptic excitatory and inhibitory transmission, respectively.
Voltage-clamp recordings were performed in outside-out patches pulled from the apical dendrites of CA1 pyramidal cells 25–60 μm from the soma. Recordings were done at room temperature (22–24°C) using a patch-clamp amplifier (Axopatch 200B, Axon Instruments). Data were filtered at 2 kHz and sampled at 20 kHz. Patch pipettes of 2.5–4 MΩ contained KCl internal solution. Pipettes were wrapped in Parafilm (Pechiney, Chicago, IL, USA) to minimize capacitive transients, the remainders of which were cancelled using the fast compensation circuitry of the amplifier. The whole-cell configuration was first obtained and the pyramidal identity of cells was confirmed by presence of sag in the membrane potential in response to a hyperpolarizing current injection and spike frequency adaptation. In patch recordings, leakage and capacitive currents were subtracted using P/−4 protocols. Stimuli were repeated 5–15 times and results were averaged.
Solutions and drugs
Unless otherwise indicated, chemicals were obtained from Sigma (St Louis, MO, USA). ACSF contained (mm): 125 NaCl, 25 NaHCO3, 2.5 KCl, 1.25 NaH2PO4, 25 glucose, 2 CaCl2 and 1 MgCl2. Sucrose solution contained (mm): 87 NaCl, 25 NaHCO3, 25 glucose, 75 sucrose, 2.5 KCl, 1.25 NaH2PO4, 0.5 CaCl2, and 7 MgCl2. ACSF and sucrose solutions were bubbled with a 95% O2 and 5% CO2 gas mixture. K-gluconate internal solution contained (mm): 140 K-gluconate, 10 NaCl, 5 EGTA, 10 Hepes, 2 Mg-ATP, 0.3 Na-GTP. The KCl internal solution contained (mm): 140 KCl, 10 NaCl, 2 MgCl2, 2 Na2-ATP, 0.3 Na-GTP, 10 EGTA, 10 Hepes. We used K-gluconate solution because, using this internal solution, the ADP amplitude has been shown to remain very stable for at least 45 min (Kaczorowski et al. 2007), exceeding the duration of our recordings. In some recordings, 5 mm KF was substituted for 5 mm KCl. All internal solutions were adjusted to pH 7.3 (with KOH) and contained 0.1% biocytin for later histological staining. Voltage-clamp recordings were performed in Hepes-buffered ACSF containing (mm): 138 NaCl, 2.5 KCl, 10 Hepes, 25 glucose, 2 CaCl2, and 1 MgCl2 (pH 7.3 with NaOH). DTX (Alomone Laboratories, Jerusalem, Israel) was always co-applied with 0.05% BSA. For bath application experiments, DTX was included in the ACSF. For outside-out patch recordings and local application, DTX was in solution with Hepes-buffered ACSF. For outside-out recordings, drugs were applied to the patches by using a multibarrel system consisting of four glass capillaries (1.5 mm i.d.) glued together and connected to a syringe pump (WPI, Sarasota, FL, USA). The patch-pipette carrying the patch was inserted into each of the pipes, which contained Hepes-buffered ACSF (pH 7.4) plus the drugs of interest.
Local drug application in slices was achieved by applying light positive pressure to the back of a small-bore patch pipette. The location of the cloud of perfusate was confirmed, in a subset of recordings, via two-photon laser scanning fluorescent microscopy (see Fig. 1 in online Supplemental material); 200 μm Fluo4 and 10 μm Alexa 594 (Molecular Probes, Carlsbad, CA, USA) were included in the intracellular solution and 40 μm Alexa 594 was included in the perfusion pipette. The dyes were excited by laser scanning at 806 nm. Emission was detected with separate, tuned photomultiplier tubes. The cloud of fluorescence was limited to the applied region and washed away in the direction of the apical dendrites and above the plane of the cell. Pharmacological effects were measured at steady state. When DTX was bath applied to the slices, it could not be washed out, but reversibility was obtained in outside-out patches and with focal application.
Data acquisition and analysis
Data were transferred to a computer during experiments, by either an ITC-18 digital-analog converter (Instrutech, Port Washington, NY, USA) or a Digidata 1322A (Axon Instruments). Igor Pro (Wavemetrics, Lake Oswego, OR, USA) and pCLAMP (Axon Instruments) software were used for acquisition and analysis. Statistical tests were performed using Excel software (Microsoft, Redmond, WA, USA). All results are reported as mean ±s.e.m.; error bars in the figures also represent s.e.m. Statistical significance was assessed by paired two-tailed t tests, unless otherwise indicated.
Action potentials were evoked by brief current injections with amplitudes just above threshold for reliable firing. The ADP is reported as the average membrane potential, relative to the resting membrane potential (for 10 ms before the spike), in the first 10 ms following the fast phase of action potential repolarization (the point at which the change in voltage with time reached a minimum as detected in the derivative of the waveform). Traces used for analysis were from 10 to 15 averaged recordings. Input resistance was determined from the slope of the steady-state voltage versus current plot that resulted from giving 600 ms current injections ranging from −150 to 50 pA. The concentration–response curve of the enhancement of the ADP by DTX was determined by fitting the data with a Hill equation in the form of
where ADPDTX/ADPcontrol is the amplitude of the ADP in DTX relative to control, [DTX] is the concentration of DTX, Kd is the half-maximal concentration, and n is the Hill coefficient.
To construct activation curves, chord conductance (G) was calculated from the peak current within the first 25 ms of the pulse, assuming ohmic behaviour and a reversal potential of −105 mV – the equilibrium potential predicted by the Nernst equation for our experimental conditions. Activation curves were fitted with a Boltzmann function with the form
where V is the membrane potential, V1/2 is the voltage at which the activation is half-maximal, and k is the slope factor. The results reported in the text reflect the averages of the fits of data from individual patches.
In order to compare with literature values for heterologously expressed Kv1 channels, the time course of DTX-sensitive current activation was determined by fitting currents with an exponential equation:
where Imax is the peak current and t is time, yielding a time constant (τ); therefore, we also used this fit for the composite potassium current and DTX-resistant current.
Apical dendrite contribution to the ADP
To study the dendritic contribution to the ADP, we performed simultaneous current-clamp recordings from soma and apical dendrites. In order to observe the net effect of the entire apical dendritic tree on somatic ADPs, dendrites were patched proximal to the first large branch point; the membrane potential was very similar at the two locations, having a value of −62.4 ± 0.9 mV at the soma and −62.7 ± 1 mV at the dendrite (n= 19). Single action potentials were evoked by suprathreshold 2 ms current injections at the soma. The resulting ADPs measured in the dendrite were consistently larger than their somatic counterparts (13.5 ± 0.6 mV in the soma, versus 14.2 ± 0.7 mV in the dendrite, n= 23, P < 0.01, Fig. 1). Comparing the membrane potentials of the two recording sites by point-by-point subtraction of the dendritic from the somatic trace revealed that the dendrite is depolarized relative to the soma, beginning during the fast phase of action potential repolarization and throughout the ADP, with the maximum difference appearing ∼1 ms after the peak of the action potential (Fig. 1B and D).
The membrane potential gradient between the dendrite and the soma generates a driving force for a flow of depolarizing current to the soma, which underlies the dendritic contribution to the ADP. Removing this driving force, then, should reduce the amplitude of the ADP. To accomplish this we performed simultaneous somatic and dendritic recordings, and the two amplifiers were connected so that the output of one could be used as the input of the other. At the beginning of the experiment (Fig. 2A, top) both the somatic and the dendritic pipettes were in current-clamp mode. Subsequently, the dendritic amplifier was switched to voltage-clamp mode (Fig. 2A, bottom) and its input signal consisted of the output (scaled to obtain a command voltage of the same amplitude) of the somatic amplifier. This eliminated, in real time, any difference in membrane potential between the two sites, producing a virtual ‘electronic excision’ of the dendrite. Electronic excision of the dendrite resulted in an average 10.7 ± 2.1% reduction in the size of the somatic ADP (the amplitude of the ADP measured at the somatic location was 13.9 ± 0.7 mV in the standard configuration versus 12.4 ± 0.8 with electronic excision, n= 18, P < 0.01, Fig. 2C). Control experiments, in which the second pipette was also positioned on the soma, were performed in order to rule out artifacts due to imperfect voltage clamp. In these experiments no change was detected in the size of the ADP (9.4 ± 1.2 mV in standard configuration versus 9.9 ± 1.4 mV with electronic excision, n= 3, P > 0.05, data not shown).
DTX-sensitive current, the ADP and bursting
While consistent, the effect of electronic excision was relatively small (the reduction in the size of ADP was ∼1.5 mV). The apical dendrites of CA1 pyramidal neurons are rich with voltage-gated inward currents (Magee & Johnston, 1995a) which, when activated by the backpropagating action potential, could contribute to the ADP. This suggests that other conductances may act to actively dampen the dendritic contribution to the ADP. Several types of potassium channels are differentially located in CA1 pyramidal neuron dendrites where they may serve such a role. M-type potassium currents in the proximal apical dendrite can do so (Yue & Yaari, 2004, 2006). Magee & Carruth (1999) demonstrated that 4-AP-sensitive, fast-inactivating dendritic A-type potassium current also provides such a restriction. D-type potassium current, which is also blocked by 4-AP, is another candidate for this action. To test this hypothesis, we used DTX, a selective blocker of Kv1-mediated D-type current. Bath application of 2 μm DTX resulted in a 38.6 ± 4.5% increase in the size of the ADP (14.8 ± 0.6 mV in control versus 20.5 ± 1 mV in DTX, measured at the soma, n= 20, P < 0.01, Fig. 3A and D). This was accompanied by a trend toward membrane depolarization as evidenced by a slight increase in holding current required to maintain a membrane potential of −67 mV (−37.1 ± 12.5 pA versus−46 ± 13.7 pA, n= 19, P= 0.07 Fig. 3B) and by an increase in input resistance (117 ± 7 MΩ in DTX versus 103 ± 6 MΩ in control, n= 19, P < 0.01, Fig. 3C), both indicating that the toxin blocked a conductance active at rest. In keeping with an action on Kv1 channels, the effect of DTX on the ADP was concentration dependent, with a half-maximal effect at ∼5 nm, a concentration similar to that causing half-maximal block of Kv1.1 and Kv1.2 channels expressed in heterologous systems (Grissmer et al. 1994).
The enhancement of the ADP by DTX resulted in an increased propensity for action potential bursting in response to both simulated synaptic currents and sustained current injections. A simulated excitatory postsynaptic current (sEPSC) was injected in the soma during the ADP (Fig. 4A, lower panel), and its amplitude was increased until it evoked a second action potential. DTX decreased the amplitude of the sEPSC required to evoke the second spike (Fig. 4B); control measurements showed that in control conditions the amplitude of the ADP was unchanged during the same time span (not shown; see also Kaczorowski et al. 2007). To quantify this effect, we used the burst current index, a measure of the propensity to burst in response to such stimuli (Metz et al. 2005). In this index, the amplitude of the smallest sEPSC that evokes a second spike is expressed relative to the amplitude of the first 2 ms, suprathreshold current injection (which was unaffected: 387 ± 32 pA in control, 409 ± 38 in DTX, n= 19, P > 0.05). DTX reduced the burst current index from 0.75 ± 0.04 to 0.46 ± 0.8 (n= 19, P < 0.01, Fig. 4B). The ADP following the second action potential was essentially the same size as the ADP of a single spike (14.8 ± 0.6 mV after a single spike, 15.3 ± 5 mV after an evoked burst, P > 0.05), and was similarly affected by DTX (+30.8 ± 5.5%, n= 20, P < 0.05, data not shown).
In some cells DTX also caused a just suprathreshold, 600 ms current injection to evoke a burst instead of a single spike at the beginning of the response (Fig. 4C). The percentage of cells that demonstrated action potential bursting in response to a 600 ms-long current injections increased from 20% to 45% (Fig. 4D). In order to quantify bursting, we calculated the interspike interval ratio (ISI ratio) in which the shortest ISI in a cell is divided by the average ISI in the same cell. This is based on our previous results (Metz et al. 2005), showing that cells with an ISI ratio of less than 0.1 represent a distinct subpopulation of CA1 pyramidal neurons, and therefore that bursting represents a specific firing phenotype and not merely the extreme of a continuous range.
Localization and characteristics of DTX-sensitive currents
To this point, DTX was bath applied in order to maximize its effect. To test whether DTX-sensitive K+ channels are localized in the dendrites, as suggested by Sheng et al. (1994) and, very recently, by Raab-Graham et al. (2006), we next used focal application (Supplemental Fig. 1) of 500 nm DTX in three cellular regions: the soma, the proximal apical dendrite (50–200 μm from the soma), and the distal apical dendrite (250 μm and beyond). Only application to the proximal dendrite (Fig. 5A) resulted in a significant enhancement of the ADP (+1.0 ± 0.5 mV, n= 17, P < 0.05), although a trend was observable also for applications at larger distance (+0.5 ± 0.4 mV n= 13, P > 0.05, Fig. 5B). While the lack of a significant effect with application of DTX to the distal apical dendrite does not rule out the possibility that there are DTX-sensitive currents in the distal dendrites, it does suggest that channels expressed in the proximal dendrite exert particular control over the somatically recorded ADP. The effect of focal application of DTX to the proximal dendrites was rapid and reversible (Fig. 5C), supporting the notion that DTX exerts its action by block of Kv1 channels.
In order to ascertain the contribution of DTX-sensitive current to the total potassium current in this critical region of the dendrite, and to determine some of the characteristics of the current, we tested the effect of DTX on potassium currents in outside-out patches from the proximal dendrites of CA1 pyramidal neurons. DTX (500 nm) reduced the peak potassium current by 16.4 ± 4.9% (Fig. 6A-C, n= 12, P < 0.01). For further confirmation of the effect of DTX on a distinct channel type, we compared the voltage dependence of activation in two populations of patches: one recorded in control conditions and the other in the presence of DTX. The activation curve of the current shifted rightward in DTX compared to control conditions. The average voltage of half-maximal activation was −19.3 ± 7.3 mV in control and 1 ± 3.8 mV in DTX (n= 4 each, P < 0.05, Fig. 6D) indicating that the DTX-sensitive current activated at hyperpolarized potentials relative to the other potassium current components, similar to what has been described for Kv1 channels in medial nucleus of the trapezoid body (MNTB) neurons (Brew & Forsythe, 1995). The DTX-sensitive current also had a slower activation than the other dendritic potassium currents, in keeping with the properties described for Kv1 delayed rectifier channels (Stühmer et al. 1989). The time course of activation of the current (at +40 mV) was 2.48 ± 1 ms for the DTX-sensitive component, and 1.22 ± 0.2 ms and 1.1 ± 0.2 ms for the total current and DTX-resistant component, n= 4, 11 and 9, respectively, P < 0.05 by ANOVA, data not shown).
Electronic excision of the dendrite in DTX
We have shown that DTX-sensitive currents are present in the proximal region of the dendrite. Their block causes an enhancement of the ADP, suggesting that they are critical in regulating the dendritic contribution to the ADP. To test this prediction, we performed electronic excision experiments in the presence of bath-applied DTX (250 nm). In these experiments DTX enhanced the size of the ADP measured at the soma by 1.6 ± 0.7 mV. Subsequent dendritic excision reduced the amplitude of this enlarged ADP from 14.8 ± 1.8 mV to 11.8 ± 1.5 mV (n= 6, P= 0.01), an effect larger than that of electronic excision of the dendrite under control conditions: the ADP was reduced by 20.3 ± 4.3% in DTX compared to 10.7 ± 2.1% in control (Fig. 7B). Figure 7C also shows that the size of the ADP with electronic excision of the dendrite is approximately the same in both control and DTX, suggesting that the reduction of the ADP caused by electronic excision of the dendrite in the presence of DTX was larger because the block, by the toxin, of dendritic D-type potassium channels unmasks additional depolarizing current. These data support our hypothesis that DTX-sensitive, D-type potassium channels are localized in the apical dendrite and control the amplitude of the ADP of CA1 pyramidal neurons by limiting the contribution of the dendrite.
Spatial distribution of currents regulating the ADP
The results of our experiments indicate that active apical dendrites enhance the somatic ADP and that dendritic, DTX-sensitive, D-type potassium channels limit this action.
Current flow from the dendrite has been shown to contribute to production of the ADP in several cell types (Mainen & Sejnowski, 1996; Williams & Stuart, 1999; Lemon & Turner, 2000; Dorion et al. 2003); however, it has been shown that in CA1 pyramidal neurons, a somatic current mediates the ADP (Metz et al. 2005; Yue et al. 2005; Golomb et al. 2006) except under conditions of potassium channel block, modulation, or inactivation (Magee & Carruth, 1999; Yue & Yaari, 2004, 2006; Yue et al. 2005). We show here that early in the ADP – beginning ∼1 ms after the peak of the spike – the apical dendrites of CA1 pyramidal neurons are depolarized relative to the somata; as a consequence, current flow from the dendrite actively depolarizes the soma. The depolarization of the dendrite relative to the soma peaks during the fast phase of action potential repolarization and early in the ADP. Thus the dendritic contribution is synchronous with the fast, somatic, calcium tail current that underlies the ADP (Metz et al. 2005); this suggests that these two events are tuned to produce an ADP limited to a time window of just a few milliseconds. The remaining component of the ADP (>20 ms) may reflect near-passive decay of the active component of the ADP.
Potassium current in CA1 pyramidal neuron dendrites
Differential distribution of potassium channels in dendrites has previously been observed in several neuronal types. For instance, in the apical dendrites of CA1 pyramidal neurons, A-type current density increases with distance from the soma (Hoffman et al. 1997), while the IAHP has been suggested to be mostly located in proximal dendrites (Sah & Bekkers, 1996). The ratio of inactivating to sustained current increases with distance also in Purkinje neuron dendrites (Martina et al. 2003) and, although to a lesser degree, in layer 5 pyramidal neurons (Bekkers, 2000; but see also Korngreen & Sakmann, 2000) because of an increasing density of fast inactivating K+ current, just as in CA1 pyramidal neurons. Also G-protein-activated K+ current density is enriched in neocortical pyramidal neuron apical dendrites (Takigawa & Alzheimer, 1999).
Several dendritic potassium currents have been shown to minimize the dendritic contribution to the ADP (Magee & Carruth, 1999; Yue & Yaari, 2004, 2006). Hints of the presence in CA1 pyramidal cell dendrites of DTX-sensitive, D-type potassium currents and their potential roles can be found in the literature. First, DTX-sensitive currents have been recorded in the dendrites of other cell types (Bekkers & Delaney, 2001; McKay et al. 2005; Guan et al. 2005). Second, there was faint staining for Kv1 protein and mRNA in the stratum radiatum of the CA1 pyramidal region in immunohistochemistry and in in situ hybridization studies (Sheng et al. 1994; Monaghan et al. 2001). Third, single-cell reverse transcription polymerase chain reaction experiments in CA1 pyramidal neurons detected mRNAs for several members of the Kv1 family, yet DTX-sensitive current is virtually absent from the soma of CA1 pyramidal neurons (Martina et al. 1998). Some of the staining results from Kv1 channels in Schaffer collateral terminals, which synapse onto the dendrites of the pyramidal neurons (Monaghan et al. 2001), but there is also clear staining for the Kv1-associated β2 subunits in the soma and proximal dendrites of pyramidal neurons, suggesting the presence of Kv1-containing channels in these compartments (Rhodes et al. 1997). Fourth, very recent data show that Kv1 RNAs are detected in dendrites from hippocampal neurons (Raab-Graham et al. 2006). Finally, DTX also enhances dendritic calcium spikes, another mechanism for driving bursting in response to strong excitatory synaptic activation (Golding et al. 1999).
Our results confirm the presence of DTX-sensitive, D-type potassium current in the apical dendrites of CA1 pyramidal neurons. Furthermore, we show that DTX-sensitive channels directly influence the size of the ADP and regulate action potential firing mode. DTX-sensitive current inactivates considerably more slowly than A-type potassium current (Storm, 1990; Grissmer et al. 1994), so D-type potassium current would be able to continue to restrict the size of the ADP in the face of sustained depolarizing inputs as may happen during periods of high activity or seizures. In support of this, the ADP that followed the second spike in an evoked burst was enhanced by DTX to the same extent as the ADP following single spikes.
Local application of DTX to the proximal apical dendrite results in enhancement of the ADP, while distal application had a smaller, non-significant, effect. A possible interpretation of this result is that the density of DTX-sensitive channels is higher in the proximal than in the distal dendrite; however, another possibility is that DTX-sensitive channels are diffusely distributed throughout the dendrite but the increased depolarization resulting from local blockade in distal dendrites does not propagate to the soma because of the cable properties of the dendrites; the intervening, unblocked D-type K+ channels in the proximal dendrites may further limit the effect of blocking distal channels alone. The proximal apical dendrite may therefore represent a critical region where the DTX-sensitive current regulates the contribution of the distal dendrite to the ADP. Bath application of DTX increases the ADP by a factor of 1.4 ± 0.5, compared to 1.1 ± 0.3 for proximal application. While this may result from a lack of saturation at the site of local application because of dilution, another possibility is that DTX-sensitive channels are also present in other compartments such as the distal apical dendrites, basal dendrites, or axon. The presence of DTX-sensitive channels beyond the proximal dendrites is also suggested by the results obtained in two cells where the ADP was first enhanced by local application of DTX (500 nm) to the proximal dendrite; subsequent bath application of DTX to the same neurons (at the same concentration) further increased the ADP (7%, in both cells, not shown).
The authors are deeply grateful to Dr Bruce Bean for his contribution to the development of the idea of the electronic excision of the dendrite. This work was supported by departmental funds (M.M.) and by NIH grants to N.S. (NS-35180, MH-074866, and RR-015497). A.E.M. was supported by a National Research Service Award from the National Institutes of Health (NS044688).