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The Journal of Neuroscience, February 15, 2000, 20(4):1348-1357

Modulation of Transmission during Trains at a Cerebellar Synapse

Anatol C. Kreitzer and Wade G. Regehr

Department of Neurobiology, Harvard Medical School, Boston, Massachusetts 02115


    ABSTRACT
TOP
ABSTRACT
INTRODUCTION
MATERIALS AND METHODS
RESULTS
DISCUSSION
REFERENCES

Activity-dependent processes dynamically regulate synapses on the time scale of milliseconds to seconds. Here, we examine the factors governing synaptic strength during repetitive stimulation, both in control conditions and during presynaptic inhibition. Field recordings of presynaptic volleys, optical measurements of presynaptic calcium, and voltage-clamp recordings of postsynaptic currents were used to examine parallel fiber to Purkinje cell synapses in cerebellar brain slices at 34°C. In control conditions, regular stimulus trains (1-50 Hz) evoked up to a 250% peak synaptic enhancement, whereas during irregular stimulation, a threefold variability in EPSC amplitude was observed. When initial EPSC amplitudes were reduced by 50%, either by lowering external calcium or by activating adenosine A1 or GABAB receptors, the peak enhancement during regular trains was 500%, and synaptic variability during irregular trains was nearly sixfold. By contrast, changes in fiber excitability and calcium influx per pulse were small during trains. Presynaptic calcium measurements indicated that by pulse 10, stimulus-evoked calcium influx had increased by ~15%, which on the basis of the measured relationship between calcium influx and release corresponds to an EPSC enhancement of 50%. This enhancement was the same in all experimental conditions, even in the presence of N6-cyclopentyladenosine or baclofen, suggesting that repetitive stimulation does not relieve the G-protein inhibition of calcium channels by these modulators. Therefore, for our experimental conditions, changes in synaptic strength during trains are primarily attributable to residual calcium (Cares)-dependent short-term plasticities, and the actions of neuromodulators during repetitive stimulation result from their inhibition of initial calcium influx and the resulting effects on Cares and calcium-driven processes.

Key words: GABAB receptor; adenosine A1 receptor; presynaptic inhibition; short-term plasticity; residual calcium; cerebellar granule cell; cerebellar Purkinje cell


    INTRODUCTION
TOP
ABSTRACT
INTRODUCTION
MATERIALS AND METHODS
RESULTS
DISCUSSION
REFERENCES

Neurons in vivo fire both regularly and irregularly, often at rates of up to several hundred Hertz. The amount of neurotransmitter released in response to an action potential depends on the type of synapse, its history of activity, and the presence of neuromodulators (Magleby, 1987; Zucker, 1989; Wu and Saggau, 1997; Zucker, 1999). High-frequency stimulation enhances some synapses, depresses others, and can often produce transient enhancement followed by depression (Feng, 1941; Liley and North, 1953; Del Castillo and Katz, 1954). Furthermore, complex activity patterns similar to those observed in vivo can lead to highly variable synaptic responses (Tsodyks and Markram, 1997; Varela et al., 1997; Dobrunz and Stevens, 1999), and this variability is thought to play an important role in nervous system function (Buonomano and Merzenich, 1995; Abbott et al., 1997; Lisman, 1997; Tsodyks and Markram, 1997).

Many temporally overlapping processes could contribute to changes in synaptic strength during repetitive activity. (1) Changes in the presynaptic action potential waveform could alter the activation of voltage-dependent calcium channels driving neurotransmitter release (Dunlap and Fischbach, 1978; Klein and Kandel, 1980; Augustine, 1990; Sabatini and Regehr, 1997). (2) Both facilitation and inactivation of presynaptic calcium currents have been observed during stimulus trains (Borst and Sakmann, 1998; Cuttle et al., 1998; Forsythe et al., 1998; Patil et al., 1998). (3) Tonic G-protein inhibition of calcium channels may be relieved during repetitive stimulation (Bean, 1989; Elmslie et al., 1990; Herlitze et al., 1996; Ikeda, 1996; Brody et al., 1997), also leading to increased calcium influx during a train. (4) Neuromodulators can accumulate and act presynaptically to inhibit release, often through an inhibition of calcium channels (Isaacson et al., 1993; Yawo and Chuhma, 1993; Dittman and Regehr, 1997; Scanziani et al., 1997). (5) A transient decrease in the probability of release or a decrease in the number of readily releasable vesicles could depress synaptic strength during a train (Takeuchi, 1958; Elmqvist and Quastel, 1965; Betz, 1970; Silver et al., 1998). (6) High rates of presynaptic activity also increase presynaptic Cares, which can facilitate transmission (Katz and Miledi, 1968; Kamiya and Zucker, 1994; Atluri and Regehr, 1996) and accelerate recovery from depression (Dittman and Regehr, 1998; Stevens and Wesseling, 1998; Wang and Kaczmarek, 1998).

The presence of neuromodulators can significantly alter the responses of synapses during trains (Varela et al., 1997; Brenowitz et al., 1998; Pananceau et al., 1998; Selig et al., 1999). Most mechanistic studies of modulators have characterized their effects during low-frequency stimulation. In these conditions, modulators change the probability of release either by modulating presynaptic calcium channels or by changing release probability downstream from calcium influx. However, the actions of neuromodulators in vivo occur against a background of continuous neural activity, and their effects in these conditions may be more complex (Qian and Delaney, 1997; Vyshedskiy et al., 1998). Modulators could alter the rate of calcium extrusion from the presynaptic terminal after an action potential, thereby changing the residual calcium signal for facilitation and recovery from depression. Additionally, processes involved in short-term plasticity could be targeted directly.

Here, we test the effects of agonists of adenosine A1 and GABAB receptors on synaptic transmission during repetitive stimulation at the parallel fiber to Purkinje cell synapse. It was found previously that for low-frequency stimulation, synaptic inhibition by these receptors is primarily a consequence of presynaptic calcium channel inhibition, although 10-30% of the EPSC inhibition by GABAB receptors was presynaptic downstream of calcium influx (Dittman and Regehr, 1996). During trains of stimuli, the actions of these neuromodulators appear no different from those of low external calcium, and contributions from additional mechanisms, such as relief of G-protein inhibition of calcium channels, are not apparent.


    MATERIALS AND METHODS
TOP
ABSTRACT
INTRODUCTION
MATERIALS AND METHODS
RESULTS
DISCUSSION
REFERENCES

Slice preparation and solutions. Transverse slices (300 µm thick) were cut from the cerebellar vermis of 11- to 14-d-old Sprague Dawley rats. Slices were superfused with an external saline solution containing (in mM): 125 NaCl, 2.5 KCl, 1.5 CaCl2, 1 MgCl2, 26 NaHCO3, 1.25 NaH2PO4, and 25 glucose, bubbled with 95% O2/5% CO2. Divalent ion concentrations were matched near reported values for rat CSF (Manthei et al., 1973), and experiments were conducted at 34 ± 1°C to better simulate physiological conditions. Bicuculline (20 µM) was added to the external solution to suppress synaptic currents mediated by GABAA receptors. To minimize changes in fiber excitability when switching between external solutions, divalent ion concentrations were optimized as follows: 1 Cae contained 1 mM CaCl2 and 1.75 mM MgCl2; 2 Cae saline contained 2 mM CaCl2 and 0.25 mM MgCl2.

To preclude endogenous G-protein-mediated modulation during trains of stimuli, the GABAB receptor antagonist CGP55845a (2 µM) (Davies et al., 1993), the adenosine A1 receptor antagonist 8-cyclopentyl-1,3-dipropylxanthine (DPCPX) (5 µM) (Haleen et al., 1987), and the mGluRIII antagonist (RS)-alpha -cyclopropyl-4-phosphonophenylglycine (CPPG) (30 µM) (Jane et al., 1996) were included in the external saline. These antagonists had no effect on EPSC amplitudes during low-frequency stimulation (<0.1 Hz) (n = 3; data not shown). During modulation experiments in which the adenosine A1 agonist N6-cyclopentyladenosine (CPA) (2 µM) was added to the external saline, the concentration of DPCPX was reduced to 50 nM. In experiments with the GABAB receptor agonist baclofen (8 µM), the concentration of CGP55845a was reduced to 100 nM. By retaining a small amount of antagonist in the saline, a higher concentration of agonist could be used in these experiments. The higher concentration of agonist effectively buffered against small amounts of endogenous ligand that could accumulate and differentially depress later stimuli in a train.

Electrophysiology. Whole-cell recordings of Purkinje cells were obtained as described previously (Llano et al., 1991; Regehr and Mintz, 1994). Glass electrodes (1-1.4 MOmega ) were filled with an internal solution containing (in mM): 35 CsF, 100 CsCl, 10 EGTA, 10 HEPES, and 0.2 D600, adjusted to pH 7.3 with CsOH. Synaptic currents were monitored with a holding potential of -40 mV to inactivate voltage-gated sodium channels, and D600 was added to block L-type voltage-gated calcium channels. Synaptic currents did not decay completely between pulses at stimulation frequencies higher than 50 Hz, and a significant shift of the baseline current developed. This introduced series resistance errors, and it might also have signaled the prolonged presence of glutamate in the synaptic cleft, which could lead to postsynaptic receptor desensitization (Trussell and Fischbach, 1989; Trussell et al., 1993). Therefore, we did not stimulate at frequencies higher than 50 Hz. Between trains of stimuli, single EPSCs were monitored throughout experiments to ensure that no long-term changes in synaptic strength were occurring. Because of the trial-to-trial variability in EPSC size at this synapse, the initial EPSC amplitude (EPSC1) in a train of stimuli was calculated by averaging together the initial EPSC of a train with the three preceding single EPSCs. The access resistance, leak current (-20 to -200 pA, holding at -40 mV), and EPSC decay time constant (2-4 msec at 34°C) were monitored continuously. Experiments were rejected if these parameters increased significantly during recording. Parallel fibers were stimulated with two glass electrodes (tip diameter, 10-12 µm) filled with external saline solution placed in the molecular layer ~15 µm apart. Brief pulses (200 µsec) of current (5-15 µA) were passed between the two stimulating electrodes. This configuration greatly reduced the size of the stimulus artifact and allowed for a clear resolution of the EPSC onset. The interstimulus interval was 10 sec for single stimuli, 2 min for trains of <= 10 stimuli, and 4 min for trains of >10 stimuli. Low stimulus intensities were used to keep synaptic currents small (-100 to -200 pA) and the resulting series resistance errors to a minimum.

Detecting presynaptic volleys. Presynaptic volleys were measured as described previously (Sabatini and Regehr, 1997). In brief, a glass electrode (tip diameter, 2-3 µm; resistance, 1 MOmega when filled with 3 M NaCl) was placed 200-400 µm away from the stimulation site in the molecular layer near the Purkinje cell layer. Voltage records were amplified with a gain of 100 using an operational amplifier (356N) mounted onto the micromanipulator. When the two stimulus electrodes were placed near the Purkinje cell layer, no significant change in either the waveform or the amplitude of the presynaptic volleys was detected during a train in 75% of fiber tracts. In 25% of tracts, the volley amplitude increased during a train, and the waveform became narrower. This effect became more pronounced and occurred more frequently when the stimulus electrodes were placed in the middle of the molecular layer. Whole-cell recordings were only established when presynaptic volley amplitudes differed by <10% for the 1st and 10th stimulus of a 50 Hz train. Presynaptic fiber volleys were monitored simultaneously throughout experiments to ensure that no changes in fiber excitability occurred.

Detecting presynaptic calcium transients. Parallel fibers, made up of granule cell axons and presynaptic terminals, were labeled with a high-pressure stream of the low-affinity calcium indicator magnesium green-AM (Zhao et al., 1996) (Molecular Probes, Eugene, OR) using techniques developed previously (Regehr and Tank, 1991; Regehr and Atluri, 1995; Atluri and Regehr, 1996). The loading time for magnesium green-AM was 8-10 min, and recordings commenced 2 hr after dye loading. Parallel fiber tracts were stimulated extracellularly, and epifluorescence was measured with a photodiode from a spot several hundred micrometers from the loading site, where the vast majority of the fluorescence signal arises from parallel fiber presynaptic boutons that synapse onto Purkinje cells. The peak Delta F/F change produced by a single stimulus was used as a linear measure of presynaptic calcium influx, as established previously. The filter set for magnesium green was 470DF20 (Zeiss) for excitation, 510DRLP dichroic, and OG530 for emission (Omega Optical, Brattleboro, VT).

Data acquisition and analysis. Field recordings were filtered at 5 kHz with a model 900C9L8L eight-pole Bessel filter (Frequency Devices, Haverhill, MA). EPSCs were filtered at 1 kHz with a four-pole Bessel filter. Fluorescence transients were filtered digitally off-line with an eight-pole filter. All signals were digitized at 20 kHz with a 16 bit D/A converter (Instrutech, Great Neck, NY), with Pulse Control software (Herrington and Bookman, 1995). Analysis was performed using Igor Pro software (Wavemetrics, Lake Oswego, OR).


    RESULTS
TOP
ABSTRACT
INTRODUCTION
MATERIALS AND METHODS
RESULTS
DISCUSSION
REFERENCES

The parallel fiber to Purkinje cell synapse has a number of advantages for this study. First, there is no recurrent excitation in this circuit that could contribute to later responses during a train of stimuli (Palay and Chan-Palay, 1974; Ito, 1984). Second, previous work has already examined the mechanisms by which agonists of the adenosine A1 and GABAB receptor modulate initial release probability (Dittman and Regehr, 1996). Activation of these receptors has been shown to inhibit presynaptic N-type and P/Q-type calcium channels. Third, it is possible to measure fiber excitability, presynaptic calcium transients, and postsynaptic currents at this synapse (Konnerth et al., 1990; Regehr and Atluri, 1995; Sabatini and Regehr, 1997).

Experimental conditions were chosen to approximate physiological conditions. Stimulation consisted of regular and irregular trains. Experiments were conducted at 34°C and divalent ion concentrations in the external saline (1 mM Mg2+, 1.5 mM Ca2+ in control conditions) were near reported values for rat CSF (Manthei et al., 1973).

Use-dependent plasticity during trains

In control conditions, parallel fibers were stimulated with an irregular spike train whose interspike intervals followed a Poisson distribution. The amplitudes of the evoked EPSCs in Purkinje cells varied nearly threefold during stimulation (Fig. 1A). Although there were small trial-to-trial differences in EPSC amplitudes, most of the variation was stereotyped over multiple trials using this same stimulus pattern (Fig. 1B). Application of the adenosine A1 receptor agonist CPA (2 µM), along with the A1 receptor antagonist DPCPX (50 nM) (see Materials and Methods), reduced the EPSC amplitude to 49 ± 4% of control. In these conditions, an irregular stimulus train evoked responses that varied nearly sixfold, and this variability was reproducible over multiple trials. Therefore, in addition to changing initial release probability, presynaptic modulators of neurotransmitter release can alter synaptic responses to a pattern of presynaptic spikes.



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  		Figure 1.   Parallel fiber responses to irregular stimulus trains. A, Evoked currents recorded in response to an irregular stimulus train (stimulus pattern shown at top; mean frequency, 20 Hz) in control conditions and during bath application of 2 µM CPA. Amplitudes were normalized to the initial EPSC in each trace. Traces represent averages of three trials. Before normalization, initial EPSC amplitudes were 100-200 pA in all experiments. B, Relative enhancement of evoked currents in control conditions (open circle ) and during application of CPA (). Plots are derived from data shown in A. Error bars are SD.

To investigate the factors controlling synaptic strength during repetitive stimulation, both in control conditions and in the presence of neuromodulators, parallel fibers were stimulated with regular trains over a range of frequencies. We limited the trains to 10-20 pulses to minimize the contribution of post-tetanic potentiation (Magleby, 1987), long-term potentiation (Salin et al., 1996), and a slow form of synaptic depression (Dittman and Regehr, 1998; Galarreta and Hestrin, 1998). The parallel fiber responses exhibited sustained facilitation of neurotransmitter release in response to trains of 10 stimuli (Fig. 2A). This facilitation built up over the first five to six pulses and reached a steady state that was maintained for 150-200 pulses (data not shown). The magnitude of this facilitation varied with stimulation frequency, with a maximal enhancement at 50 Hz of 350 ± 30% of control (Fig. 2B).



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  		Figure 2.   Frequency responses of parallel fiber synaptic currents. A, Representative traces in response to regular trains of 10 pulses at 10, 20, and 50 Hz. Traces represent averages of three to four trials. B, Mean relative enhancement of evoked currents at 1, 3, 10, 20, and 50 Hz (n = 5 cells). EPSC8-10 represents the average of the peak EPSC amplitudes of pulses 8, 9, and 10. Error bars are SEM.

A number of use-dependent processes could contribute to the variation observed in evoked responses during sustained stimulation. (1) High stimulation rates have been demonstrated to increase the excitability of presynaptic fibers (Kocsis et al., 1983). (2) The width of the presynaptic action potential waveform could change. (3) The calcium influx in response to an action potential could facilitate or decrease during a train. (4) Endogenous ligands such as adenosine, GABA, and glutamate may accumulate and depress the release of neurotransmitter. (5) Increases in Cares, which typically last several hundred milliseconds after elevated presynaptic activity, could increase the magnitude of facilitation and speed recovery from depression. To understand the changes in synaptic strength we observe during a train, we next evaluated the contributions from each of these mechanisms.

We used an extracellular electrode to monitor the presynaptic volley, which is produced by the current flow associated with propagating action potentials. The magnitude of the presynaptic volley is proportional to the number of fibers stimulated, and its shape can be used to detect changes in the presynaptic waveform (Sabatini and Regehr, 1997). We simultaneously monitored field potentials during all whole-cell recording and optical imaging. Figure 3A shows a representative field potential recording during a 50 Hz stimulus train. The changes in the amplitude and the waveform of the presynaptic volley between pulses 1 and 10 were small. This suggests that in control conditions, the presynaptic action potential stays approximately the same size and the same number of fibers is activated for each stimulus in the train.



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  		Figure 3.   Presynaptic volley and calcium influx during a train of stimuli. A, Presynaptic volleys recorded in 1.5 Cae in response to 50 Hz stimulation. Stimulus artifacts have been blanked for clarity. Inset, No major changes occur in either the waveform or amplitude of the volley between pulse 1 (solid line) and pulse 10 (dotted line). Traces represent averages of 10 trials. B, Presynaptic calcium transients measured with the low-affinity indicator magnesium green in response to a 50 Hz train of stimuli. Inset, There is little change in calcium influx per pulse between pulse 1 (solid line) and pulse 10 (dotted line). On average, pulse 10 was enhanced by 14 ± 5% (n = 4) in control conditions. Traces are the averages of 20 trials.

Optical methods were used to detect changes in presynaptic calcium influx (Regehr and Atluri, 1995). To monitor Cares, we loaded granule cell terminals with the low-affinity calcium-sensitive fluorophore magnesium green (Atluri and Regehr, 1996; Zhao et al., 1996). Because granule cell presynaptic boutons are small (<1 µm in diameter) (Palay and Chan-Palay, 1974), calcium gradients dissipate rapidly. Therefore several milliseconds after stimulation, the normalized changes in magnesium green fluorescence (Delta F/F) provide a good estimate of Cares dynamics (Atluri and Regehr, 1996, 1998; Sabatini and Regehr, 1998). In control conditions, a train of 10 stimuli at 50 Hz elicited only a slight increase in Delta F/F per stimulus between pulses 1 and 10 (pulse 10 was 114 ± 5% of pulse 1, n = 4) (Fig. 3B). For magnesium green, which is a low-affinity indicator, there is a linear relationship between the change in Delta F/F and Cares. These results therefore indicate that changes in calcium influx per pulse during a train are small (see Discussion).

To test the hypothesis that an accumulation of metabotropic receptor ligands inhibit transmitter release during repetitive stimulation, we added to the external saline high-affinity antagonists to adenosine A1 receptors (DPCPX: 5 µM), GABAB receptors (CGP55845a: 2 µM), and type II/III mGluR receptors (CPPG: 30 µM). These drugs did not affect baseline synaptic strength (n = 3; data not shown), nor did they appear to impact the amount of facilitation observed during short trains of pulses (n = 4; data not shown). Nevertheless, in subsequent experiments, antagonists were used to preclude any possible contributions of these receptors (5 µM DPCPX, 2 µM CGP55845, 30 µM CPPG).

In control conditions, we have found little contribution from mechanisms (1)-(4) (outlined above). Therefore, the variation in synaptic responses that we observe is likely attributable to short-term plasticities such as facilitation and recovery from depression, which are driven by Cares (Kamiya and Zucker, 1994; Atluri and Regehr, 1996; Dittman and Regehr, 1998). It is apparent in Figure 3 that Cares levels are significantly elevated during a train of action potentials. Therefore, we hypothesize that the interaction between these calcium-dependent processes shapes the amount of transmitter released during sustained activity.

The effects of external calcium during regular trains

We next examined the effect of changing calcium entry by changing the calcium concentration in the external solution. This manipulation affects both the high local calcium signal driving neurotransmitter release as well as the residual calcium signal driving facilitation and recovery from depression.

Before characterizing the effects of external calcium (Cae) during a train, it was first necessary to examine the dependence of single stimuli on Cae. Shown in Figure 4 are examples of an external solution change from 1.5 to 2 Cae. In the experiments shown, changing to 2 Cae increased calcium influx to 131% of control and increased the EPSC to 177% of control (Fig. 4A). The effect of lowering Cae to 1 mM was also assessed. On the basis of a number of such experiments we can approximate the relationship between calcium influx and EPSC amplitude to be a power law (Dodge and Rahamimoff, 1967), EPSC = k (Cainflux)n, where k is a constant, Cainflux represents the total presynaptic calcium influx during an action potential, and n = 2.9 (Fig. 4B) at 34°C. This compares with previous estimates at 24°C of n = 2.5 (Mintz et al., 1995) and n = 3.1 (Sabatini and Regehr, 1997).



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  		Figure 4.   Relationship between presynaptic calcium influx and synaptic strength. A, Increase in peak fluorescence transients () and peak EPSC amplitudes (open circle ) during a change from 1.5 to 2 Cae. Peak EPSC amplitudes each represent the average of two trials. Insets, Averaged traces in 1.5 and 2 Cae. B, Peak EPSC amplitude for 1 Cae (n = 4 cells) and 2 Cae (n = 4 cells) plotted as a function of peak Delta F/F per stimulus (n = 4, 1 Cae; n = 4, 2 Cae). Peak values are normalized to values in 1.5 Cae (mean inhibition in 1 Cae, 49 ± 2% of control; mean enhancement in 2 Cae, 186 ± 5% of control). Data points are well fit to a power law function with n = 2.91.

Changes in external calcium concentration not only modified the amplitude of single EPSCs but also dramatically affected the degree of enhancement during trains (Fig. 5). Relative enhancement, defined as the average response to pulses 8-10 normalized to the synaptic response evoked by the first stimulus, was less in 2 Cae than in 1 Cae. The enhancement in 2 Cae appeared to saturate quickly during the train, but in 1 Cae continued to build up until approximately the seventh pulse (Fig. 5A). The relative enhancements observed in different values of Cae for a range of frequencies (Fig. 5B) provide an indication of the dynamic range of this synapse in various conditions.



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  		Figure 5.   Frequency responses in different external calcium concentrations. A, Representative traces recorded in 1, 1.5, and 2 Cae in response to 50 Hz stimulation. Amplitudes are normalized to the initial EPSC. Traces represent averages of three to four trials. B, Mean relative enhancement of evoked currents in 1 (dotted line, n = 5 cells), 1.5 (solid line, n = 5 cells), and 2 Cae (dashed line, n = 5 cells) at stimulation frequencies of 1, 3, 10, 20, and 50 Hz. C, Mean absolute enhancement in 1, 1.5, and 2 Cae plotted as a function of stimulation frequency. Absolute values in 1 and 2 Cae have been derived by scaling relative values according to data shown in Figure 4. D, Absolute enhancement of EPSC amplitudes during trains in 1 and 2 Cae as a percentage of control values. Error bars are SEM.

Another way of comparing the effect of external calcium on synaptic plasticity is to consider absolute enhancement (Fig. 5C), which we define as the average of the responses to pulses 8-10, normalized to the synaptic response evoked by the first stimulus in control conditions. The absolute values were derived by scaling the relative enhancement in 1 and 2 Cae by 49 and 186%, respectively; these scaling factors represent the changes in single EPSC amplitudes produced by changing Cae, as summarized in Figure 4. During high-frequency stimulation, steady-state EPSC amplitudes approach a similar absolute value in 1, 1.5, and 2 Cae (Fig. 5C). Because the effect of Cae on synaptic strength was less pronounced at 50 Hz (Fig. 5D), this suggests that faster firing rates can relieve the effects of calcium-dependent modulation at this synapse.

Synaptic modulation during regular trains

We next examined the effects of neuromodulators on synaptic transmission during repetitive stimulation. On the basis of what is known about the calcium dependence of synaptic plasticity, and what we have shown here for low versus high Cae, such changes in calcium entry will clearly contribute to changes in the behavior of synapses during trains. Whether additional mechanisms contribute significantly to the effects of neuromodulators during repetitive stimulation is an open question.

We tested the effects of presynaptic inhibition on synaptic transmission during trains. Periods of high-frequency activity can lead to the buildup of extracellular levels of GABA and adenosine, which are then detected by receptors on the presynaptic terminals and ultimately inhibit synaptic transmission. At the granule cell to Purkinje cell synapse, activation of adenosine A1 and GABAB receptors has been shown to reduce the amplitude of single pulses primarily through an inhibition of presynaptic calcium channels (Dittman and Regehr, 1996). Our basic strategy was to compare the effects of A1 and GABAB receptor inhibition with low Cae on synaptic transmission during trains. We used different concentrations of Cae to determine how synaptic strength changes during trains when only calcium influx has been altered. If modulation of transmission by GABAB receptors and A1 receptors uses additional mechanisms, these modulators might affect the train differently from low Cae.

Our first step in these experiments was to choose concentrations of neuromodulators that reduced single EPSC amplitudes by a degree similar to that of 1 Cae (Fig. 6A). Reducing Cae to 1 mM decreased the EPSC to 49 ± 2% of control (n = 4). A combination of a receptor agonist and antagonist was used to inhibit transmission (see Materials and Methods). For the adenosine A1 receptor, 2 µM of the agonist CPA and 50 nM of the antagonist DPCPX reduced the EPSC to 49 ± 4% of control (n = 4). For the GABAB receptor, 8 µM of the agonist baclofen and 100 nM of the antagonist CGP55845a decreased the EPSC to 52 ± 4% of control (n = 5).



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  		Figure 6.   Modulation of synaptic strength with 1 Cae, CPA, and baclofen. A, Reduction in peak single EPSC amplitude during exposure to 1 Cae, CPA, and baclofen (see Materials and Methods). Control solution contained 1.5 Cae. The dashed line below the data for baclofen indicates the times at which steady-state responses were measured. Insets, Averaged traces in control conditions and after modulation. B, Representative EPSC and Delta F/F traces during 50 Hz stimulation in 1 Cae, CPA, and baclofen. Traces represent averages of three to four trials (EPSC) and 15-20 trials (Delta F/F).

For baclofen, inhibition was maximal immediately after drug application, and a steady-state value was reached in ~3-5 min. This effect was reliably observed, and we restricted our analysis of baclofen inhibition to times in which a clear steady state had been reached. Because we used a combination of an agonist and antagonist (see Materials and Methods), this effect may have arisen from a slow equilibration of these molecules with receptor binding sites. This effect is not prominent when baclofen is washed in alone (Dittman and Regehr, 1996).

We next assessed the effects of these manipulations on presynaptic calcium transients and EPSCs during trains. Shown in Figure 6B are normalized representative traces of 10 stimuli at 50 Hz in each condition. During trains, no differences were observed in the presynaptic calcium transients or EPSC amplitudes between low Cae, CPA, and baclofen.

Because relative synaptic enhancement was maximal during high-frequency stimulation, we examined the effect of 50 Hz stimulation on the EPSC, Delta F/F, and presynaptic volley more closely for low Cae, baclofen, and CPA in Figure 7. During these manipulations, the EPSC amplitude during the train was greatly enhanced, whereas by comparison, the calcium influx and the fiber excitability exhibited only small changes, which were no different from control conditions. A comparison of the effects of the modulators and 1 Cae reveals that all manipulations produced a five- to sixfold enhancement of EPSC amplitude (Fig. 7A), which is significantly more than the threefold enhancement in control conditions. Plotting the Delta F/F signals and the presynaptic volley amplitude (Fig. 7B) on a greatly expanded scale reveals the changes in Delta F/F per pulse and in the presynaptic volley amplitude during the train. The extent of the increase in Delta F/F per pulse is similar in control conditions, 1 Cae, and in the presence of the neuromodulators. Compared with the 1st pulse, the 10th pulse evokes 10-15% more calcium influx. For all conditions tested, the presynaptic volley evoked by the second stimulus in the train declined by 12-18%. The amplitude of subsequent volleys then gradually increased during the train, so that by the 10th pulse the presynaptic volley amplitude was comparable to that evoked by the first pulse. These small changes in fiber excitability and calcium influx could not account for the very large synaptic enhancement observed during the train (see Discussion).



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  		Figure 7.   Mean enhancement during repetitive stimulation in 1 Cae, CPA, and baclofen. A, Mean relative changes in EPSC (black with error bars), Delta F/F (black), and presynaptic volley (white) amplitudes during 50 Hz stimulation in 1 Cae (circles), CPA (triangles), and baclofen (diamonds). B, Mean relative changes in EPSC, Delta F/F, and presynaptic volley, on an expanded scale, in 1 Cae (circles, solid line, n = 5 cells), CPA (triangles, dotted line, n = 6 cells), and baclofen (diamonds, dashed line, n = 5 cells). Control (1.5 Cae) traces (squares, solid line, n = 5 cells) are shown for comparison. Error bars are SEM.

At all frequencies tested, the effects of low Cae, CPA, and baclofen on synaptic plasticity were similar to each other and significantly different from control conditions. This is apparent in plots of both the relative steady-state enhancement (Fig. 8A) and the absolute steady-state enhancement (Fig. 8B) as a function of stimulus frequency. This result suggests that despite the differences in the power law dependencies of these modulators on presynaptic calcium influx, changes in initial release probability were most important in shaping synaptic responses during trains.



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  		Figure 8.   Frequency responses in CPA and baclofen. A, Mean relative enhancement at 1, 3, 10, 20, and 50 Hz after application of CPA (triangles, dotted line, n = 6 cells) and baclofen (diamonds, dashed line, n = 5 cells). Shown for comparison are 1 Cae (filled circles, solid line, n = 5 cells) and 1.5 Cae (open circles, solid line, n = 5 cells). B, Absolute enhancement derived by scaling relative values by data shown in Figure 6. Error bars are SEM.

Synaptic modulation during irregular trains

We also examined the behavior of synapses during irregular stimulus trains for various experimental conditions (Fig. 9A). Compared with control conditions, there was more enhancement and greater variability in the presence of adenosine A1 and GABAB receptor agonists and in low Cae. Bursts of stimuli resulted in a greater relative enhancement of transmitter release in the presence of neuromodulators. This is apparent in examining the responses to pulses 2-3, pulses 4-6, and pulses 7-10. Therefore, even during more realistic spike trains, the effects of these neuromodulators are no different than the effect of low Cae (Fig. 9B).



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  		Figure 9.   Responses to irregular stimuli in 1.5 Cae, CPA, baclofen, and 1 Cae. A, Left, Average evoked currents in response to a 20 Hz irregular stimulus train (stimulus pattern shown above). Right, Mean enhancement in 1.5 Cae (open circles, n = 3 cells), 1 Cae (filled circles, n = 4 cells), baclofen (diamonds, n = 3 cells), and CPA (triangles, n = 3 cells). Error bars are SEM. B, Mean enhancement in 1.5 Cae, CPA, baclofen, and 1 Cae (same symbols as in A).


    DISCUSSION
TOP
ABSTRACT
INTRODUCTION
MATERIALS AND METHODS
RESULTS
DISCUSSION
REFERENCES

We found that during repetitive stimulation, parallel fiber synapses show significant enhancement that becomes more profound when transmission is inhibited by activating presynaptic metabotropic receptors. In all conditions, changes in fiber excitability and calcium influx during the train cannot account for the bulk of this enhancement, which is likely a consequence of facilitation of the release apparatus. Measurements of the EPSC amplitude, presynaptic volley, and calcium influx during trains in various experimental conditions constrain the mechanism responsible for synaptic enhancement.

Do changes in fiber excitability or calcium influx contribute to synaptic plasticity during trains?

For all conditions tested, presynaptic volley amplitudes declined by 12-18% for the second stimulus, and then gradually returned to original values by the 10th stimulus. Changes in the number of fibers stimulated and alterations in the current flow in individual fibers can both contribute to changes in the presynaptic volley amplitude. Previous results with voltage-sensitive dyes at this synapse suggest that the peak of the action potential changes very little during short high-frequency trains, whereas the baseline voltage is substantially elevated because of a long-lasting afterdepolarization of fibers after the first pulse in a train (Sabatini and Regehr, 1997). The decrease in the presynaptic volley amplitude that we observe on the second pulse is consistent with a smaller baseline-to-peak action potential in these fibers. The gradual increase in volley amplitude between pulses 2 and 10 is likely attributable to an increase in the number of fibers stimulated. Because there is a linear relationship between the number of fibers excited and synaptic strength, we can conclude that changes in fiber excitability are small relative to the EPSC enhancement that we observe and therefore do not contribute significantly to synaptic plasticity during trains.

Measurements of Delta F/F for the calcium-indicator magnesium green provide an upper limit for the changes in calcium influx per pulse during repetitive activation. The change in Delta F/F per stimulus gradually increased during the train, and by the 10th pulse was ~15% larger in all conditions. If the change in Delta F/F per spike reflects an increase in calcium entry, it is possible to estimate its contribution to the enhancement during the train. Considering the observed power law relating influx and release with n = 2.9, a 15% increase in calcium influx would result in an EPSC enhancement of 50%. This is an upper bound, because calcium cooperativity declines during facilitation (Stanley, 1986). If, on the other hand, the increase in Delta F/F represents an increased number of excited fibers, as suggested by the presynaptic volley measurements, then a 15% increase in the number of stimulated fibers would result in a maximal EPSC enhancement of only 15% by the 10th pulse. By comparison, the EPSC enhancement ranges from 250% for control conditions to >500% for other conditions.

The increase in Delta F/F per spike could arise in several ways. It may represent a small facilitation of the calcium current associated with faster channel opening during a train of action potentials (Borst and Sakmann, 1998; Cuttle et al., 1998). Saturation of the endogenous calcium buffer could also contribute. It may also arise from changes in the number of activated fibers. Relief of G-protein-mediated calcium channel inhibition by a train of action potentials (Brody et al., 1997) does not likely contribute significantly, because the increase in Delta F/F per spike was the same in control conditions, and in the presence of either antagonists or agonists of presynaptic A1 or GABAB receptors. Whatever the mechanism responsible for the increase in Delta F/F per spike, these findings establish that changes in calcium influx are small and could not account for most of the synaptic enhancement.

Enhancement during regular trains

Previous studies of paired-pulse facilitation at this synapse showed that the enhancement of the EPSC evoked by the second of two closely spaced stimuli is caused by enhanced transmitter release driven by Cares (Atluri and Regehr, 1996). It is likely that most of the enhancement during trains is a result of this calcium-driven process. Although there are many potential modulatory targets that would impact transmission during trains, we found that the effects of activating presynaptic A1 receptors and GABAB receptors during trains can be explained in terms of calcium channel inhibition. The effects of baclofen, CPA, and low Cae on synaptic strength during trains are indistinguishable. The inhibition of calcium channels is therefore the most important site of action for these modulators. Changing calcium influx has complex actions because it alters the initial release probability and Cares, thereby affecting calcium-driven processes such as facilitation and recovery from depression.

These findings do not preclude the contribution of additional mechanisms, but they indicate that such mechanisms are not the primary determinants of the behavior of these synapses during high-frequency trains. For example, we know that there are subtle differences in inhibition at this synapse by A1 receptors and GABAB receptors. Activation of A1 receptors inhibits N-type calcium channels to a greater extent than P/Q-type channels. Activation of GABAB receptors inhibits P/Q-type calcium channels to a greater extent than N-type channels, and a small fraction of the inhibition also appears to be mediated by effects downstream from calcium influx (Dittman and Regehr, 1996). Despite such mechanistic differences, the dominant behavior during trains, when either of these metabotropic receptors is activated, is well approximated by lowering Cae.

Effects of modulation on synaptic filtering properties

Manipulations that alter calcium entry affect plasticity during trains in interesting ways. Activation of A1 or GABAB receptors, or lowering Cae, decreased synaptic strength by nearly one-half at low firing rates, whereas it nearly doubled steady-state enhancement at high firing rates. In contrast, high Cae nearly doubled synaptic strength at low frequencies, but at faster firing rates reduced enhancement by one-half. At this synapse, altering presynaptic calcium influx preferentially affects low-frequency activity (Fig. 5). Presynaptic inhibition via A1 or GABAB receptors, or low Cae, also accentuated synaptic variability during irregular trains (Fig. 9).

These alterations in the frequency dependence of enhancement, and in synaptic variability, indicate that changing calcium influx affects the synaptic filtering properties of synapses. Presynaptic inhibition by neuromodulators reduces release probability while simultaneously increasing the amount of relative facilitation. By reducing the sensitivity of the synapse to isolated stimuli, presynaptic inhibition effectively increases the signal-to-noise ratio of synapses, were information to be encoded in bursts (Lisman, 1997).

Comparisons to other synapses

Virtually all synapses display use-dependent plasticity and synaptic variability for patterns of activity similar to those used here. At most synapses, it has been difficult to determine the mechanisms responsible for such changes in synaptic strength, because it is hard to assess spike invasion of presynaptic terminals and to measure presynaptic calcium transients. For these reasons, most mechanistic studies during repetitive stimulation have focused primarily on synapses such as the squid giant synapse or the calyx of Held, where it is possible to record electrically from the presynaptic terminal. At the squid giant synapse, changes in the presynaptic action potential waveform or calcium influx do not contribute to facilitation (Charlton and Bittner, 1978; Charlton et al., 1982). At the calyx of Held, repetitive activity depresses transmission in most experimental conditions yet enhances calcium influx per spike (Borst and Sakmann, 1998; Cuttle et al., 1998). The enhancement of calcium influx is a result of accelerated calcium channel activation kinetics and can be as much as twofold during a short train.

Here, we measure presynaptic calcium influx and EPSCs at a fast central synapse that displays prominent synaptic facilitation. The increases in calcium influx that we observe are much smaller than at the calyx of Held. In granule cell terminals, calcium influx increases only ~15% during brief high-frequency stimulation. Such changes in calcium entry cannot account for the very large synaptic enhancement at parallel fiber synapses, especially in conditions of low release probability.

Our experiments have important implications for the study of synapses during trains. We confirm that changes in fiber excitability are potentially a significant complication in such studies. Here, we needed to measure the presynaptic volley during trains to select fiber tracts where the presynaptic volley remained relatively constant throughout the train (see Materials and Methods). For other synapses this may not be possible.

We studied two modulators that were known to have large effects on calcium influx, and this mechanism turned out to be the primary means by which they affected transmission during trains. Although activation of A1 or GABAB receptors does not appear to differentially affect short-term plasticity at this synapse, we do not exclude the possibility that during trains, other modulators might have more diverse actions.


    FOOTNOTES

Received Sept. 27, 1999; revised Nov. 22, 1999; accepted Nov. 30, 1999.

This work was supported by National Institutes of Health Grants R01-NS32405-01 and MH/NS20017-02. We thank Adam Carter, Chinfei Chen, Jeremy Dittman, Matthew Xu-Friedman, and Kaspar Vogt for comments on this manuscript.

Correspondence should be addressed to Dr. Wade G. Regehr, Department of Neurobiology, Harvard Medical School, 220 Longwood Avenue, Boston MA 02115. E-mail: wade_regehr{at}hms.harvard.edu.


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GABA Spillover from Single Inhibitory Axons Suppresses Low-Frequency Excitatory Transmission at the Cerebellar Glomerulus
J. Neurosci., December 1, 2000; 20(23): 8651 - 8658.
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V. Matveev and X.-J. Wang
Differential Short-term Synaptic Plasticity and Transmission of Complex Spike Trains: to Depress or to Facilitate?
Cereb Cortex, November 1, 2000; 10(11): 1143 - 1153.
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E. S. Fortune and G. J. Rose
Short-Term Synaptic Plasticity Contributes to the Temporal Filtering of Electrosensory Information
J. Neurosci., September 15, 2000; 20(18): 7122 - 7130.
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