- Research article
- Open Access
Synchrony between orientation-selective neurons is modulated during adaptation-induced plasticity in cat visual cortex
© Ghisovan et al; licensee BioMed Central Ltd. 2008
- Received: 01 February 2008
- Accepted: 03 July 2008
- Published: 03 July 2008
Visual neurons respond essentially to luminance variations occurring within their receptive fields. In primary visual cortex, each neuron is a filter for stimulus features such as orientation, motion direction and velocity, with the appropriate combination of features eliciting maximal firing rate. Temporal correlation of spike trains was proposed as a potential code for linking the neuronal responses evoked by various features of a same object. In the present study, synchrony strength was measured between cells following an adaptation protocol (prolonged exposure to a non-preferred stimulus) which induce plasticity of neurons' orientation preference.
Multi-unit activity from area 17 of anesthetized adult cats was recorded. Single cells were sorted out and (1) orientation tuning curves were measured before and following 12 min adaptation and 60 min after adaptation (2) pairwise synchrony was measured by an index that was normalized in relation to the cells' firing rate. We first observed that the prolonged presentation of a non-preferred stimulus produces attractive (58%) and repulsive (42%) shifts of cell's tuning curves. It follows that the adaptation-induced plasticity leads to changes in preferred orientation difference, i.e. increase or decrease in tuning properties between neurons. We report here that, after adaptation, the neuron pairs that shared closer tuning properties display a significant increase of synchronization. Recovery from adaptation was accompanied by a return to the initial synchrony level.
We conclude that synchrony reflects the similarity in neurons' response properties, and varies accordingly when these properties change.
- Firing Rate
- Tuning Curve
- Tuning Property
- Synchronization Index
- Orientation Tuning
From the primary visual cortex (area 17; V1), neurons acquire sensitivity and selectivity for orientation, motion direction and other visual features as emergent properties [1–3]. In the cat, more than 90% of V1 neurons are well tuned to stimulus orientation . Such orientation selectivity is generally considered a fairly "hard-wired" property acquired before or at the time of eye opening and maintained by patterned visual experience . However, it was reported in the adult cat that V1 neurons could temporarily shift their preferred orientation following prolonged exposure (adaptation) to a non-preferred orientation [6–8] – but see . Plasticity in cat V1 was also reported for adaptation to spatial and temporal frequency [10–12] suggesting that it might be a general property at this level of sensory information processing. In mammalian cortex, tuning properties were also shown to change following adaptation to speed [13, 14] and motion direction in MT  and V4 . In the present study, we took advantage of this phenomenon to examine how orientation tuning plasticity is related to time-correlated activity in V1 neuron pairs.
Relatively small receptive fields make cells respond to an object's local features, and these individual responses require spatial binding across cortical and visual space as well as binding across types of features . This issue is of particular importance for contour integration, a process that is thought to be mediated by neuronal synchrony  – but see . Theoretical studies suggest that the precise synchronization of action potentials represents a potential mechanism for binding [19–21]. Consistent with these theoretical considerations, a body of experimental studies showed that synchronous neural activity is correlated with stimulus properties like coherent motion and similarity [17, 22–27]. Furthermore, synchrony was reported to be strong between cells with similar feature selectivity [23, 28, 29], due in part to specific horizontal connections between cortical domains having similar tuning properties [30, 31].
The experiments we report here examine the issue of neural synchrony and its relationship to neurons' tuning properties. To obtain a dynamic view of this relationship, adaptation-induced plasticity was used as a means of producing transient changes of preferred orientation difference among V1 neuron pairs. Precise synchronization between neurons has been expected to dynamically reflect functional similarity of neuronal responses, that is, the closer the tuning properties become following adaptation, the stronger the synchrony. We first examined the result of our adaptation protocol. We then looked at how pairwise synchronization is modulated during adaptation-induced plasticity of orientation tuning.
We carried out pairwise recordings of multi-unit activity in the anesthetized cat's area 17 (V1). An adaptation protocol consisting in the prolonged presentation of a non-preferred stimulus was applied in order to induce a transient plasticity of the neurons' orientation tuning properties. First, we measured the orientation tuning curve of 89 neurons before and following adaptation, and after a 60-minute period of recovery from adaptation. We then formed neuron pairs and measured the temporal correlation between their spike trains prior to and after adaptation-induced plasticity.
In order to determine the plasticity of orientation tuning in our cell population (n = 89 neurons), curve fits were generated for all cells. The sample size (n = 78) corresponds to the 89 cells that were recorded minus 11 neurons for which we could not obtain a satisfactory curve fit before and after adaptation. In our sample fits accounted for 90% of the variance in the data across conditions.
Synchrony modulation through adaptation
To examine the effect of adaptation on pairwise correlated activity, the synchronization index (SI; see Methods for definition) was measured before and following adaptation, and after a 60-minute period of recovery from adaptation. Because the experiments were aimed at measuring the modulation of synchrony in relation to the preferred orientation difference, neuron pairs were selected with respect to two criteria. A pair was kept for analysis if (i) it had a significant SI in at least one condition, and (ii) at least one cell of the pair displayed an adaptation-induced shift in orientation preference on the raw tuning curves. Consequently, from the 103 pairs (89 cells) that were recorded, we selected 52 pairs (60 cells) for further analyses. Among those 52 pairs, 30 comprised cells having different initial preferred orientations for which SIs were computed for each cell's preferred orientation (that is, 60 SI values). The remaining 22 pairs had identical orientation preference, yielding 22 SI values. Altogether, our population amounted to 82 values of SI for the initial preferred orientation, and 52 for the adapting orientation.
Figures 3B, C and 3D display examples of CCHs for 3 neuron pairs showing preferred orientation differences of 0°, 45° and 90°, respectively, prior to adaptation (precise orientation differences calculated from curves fits were 4.0°, 40.0° and 84.1°, respectively). Cells sharing identical orientation preference displayed a large zero lag peak (events in the central bin, see Materials and Methods) in the CCH, and the SI value reached 0.041 (Fig. 3B). In a second example, the preferred orientation difference between the two cells was approximately 45° (Fig. 3C). In that case, the CCH zero lag peak was smaller, and the SI value was 0.027. The CCH of a pair whose preferred orientation difference was large yielded a non-significant zero lag peak, and the SI value was 0.004 (Fig. 3D). In addition, we verified that preferred orientation differences obtained from curve fits approximations agreed with the direct measurements from raw tuning curves prior to and after adaptation. Overall, there is only a weak discrepancy in mean preferred orientation differences using one method or the other (differences less than 2° across conditions, paired sample two-tailed t-test, p > 0.05). Thus, orientation differences between raw tuning curves are purposely illustrated in the CCHs examples.
Preferred orientation difference and synchrony
The low level of synchronization would be associated to the initial preferred orientation difference, and the higher one would be associated to the newly acquired, smaller preferred orientation difference. In the absence of recovery, the high level of pairwise synchrony that was observed after adaptation was expected to persist. In Figure 8, this would correspond to a first group (white bars) with both controls (recovery and no recovery) and the 60 min when recovery occurred, and a second group (black bars) with both adaptations (recovery and no recovery) and the 60 min after adaptation when recovery failed to occur. To verify our hypotheses, we tested with a nested ANOVA (1) the difference of the means between the 2 groups (F = 14.90, p < 0.001), and (2) the difference of the means within each group (F = 0.37, p = 0.69). Our results show that when the pairs displayed a full recovery, the mean SI showed a strong and significant increase after adaptation, and returned to control level. On the other hand, when pairs failed to recover their initial preferred orientation difference, their synchrony increased after adaptation as well but remained high 60 minutes afterwards. We conclude that there is a strong relationship between synchrony level and preferred orientation difference in neuron pairs, and that such a relationship is reflected by the effect of adaptation on both measures.
In the present study, we investigated how the synchronization strength among cortical cell pairs is modified by an adaptation protocol aimed at changing the pairwise preferred orientation difference. In a majority of cells, prolonged presentation of a non-preferred stimulus induced attractive shifts. We also find that synchronization can be dynamically modulated by adaptation-induced plasticity of tuning properties. Indeed, our results show that synchronization between cells becomes stronger when pairwise preferred orientation difference diminishes. In contrast, synchrony is not modulated by adaptation in the cases where the difference between preferred orientations increases.
Plasticity of orientation tuning
In our sample, most cells displayed a shift in orientation preference following adaptation. Among those cells, attractive shifts were observed more frequently than repulsive shifts (58% vs. 42%, respectively). This proportion is rather different from the ones reported in previous studies in V1. Whereas two groups described mainly repulsive shifts [6, 8, 36, 37], Kohn and Movshon  failed to induce shifts of preferred orientation in V1, while the same protocol applied in MT induced attractive shifts. These differences in the adaptation outcome, attractive vs. repulsive shifts, are rather intriguing, although an explanation can be found in the various adaptation protocols. First, if we consider the adaptation time, 40 seconds are apparently not sufficient to induce orientation preference shifts in V1 , while 2-min adaptation induced mostly repulsive shifts , and 12-min adaptation caused a majority of attractive shifts in the present study. Dragoi et al.  also studied the time course of adaptation and recovery. In their experiments, 3 out of 7 cells in a representative example (see their Fig. 3B and 3C) showed repulsive shifts that were followed during recovery by attractive shifts. These reported 'rebound' attractive shifts had about the same amplitude as the initial repulsive shifts. The time course of these 'rebound' shifts is consistent with the time course of adaptation in our experiments. Thus, an explanation that takes all results into account is that the first effect of adaptation in V1 consists in short-term repulsive shifts and that attractive shifts build up in time. Indeed, recent results showed that adaptation duration from three to twelve minutes reverses the shifts of neurons form repulsive to attractive . Given its duration (adaptation and recovery), our protocol is probably more susceptible to detect attractive shifts in orientation preference. Two other factors may contribute to explain the differences in our results in relation to previous studies in V1: (1) the use by most groups of a "topping-up" protocol, in which the adapting stimulus is presented as a reminder before each test stimulus (2) a possible effect of cortical location and layer . Finally, adaptation to motion direction was shown to induce attractive shifts in area MT. A simple populational model suggests that attractive shifts in MT neurons are consistent with the repulsive shifts in perceived direction observed in psychophysical experiments . Since V1 provides substantial input to MT , one interesting question would be to know how tuning shifts in V1 potentially affect or cause shifts in area MT. Overall, our results corroborate the new view of adaptation as an active process including both response depression and enhancement.
Convergence of orientation tuning properties enhances synchrony
We observed a general increase of pairwise synchrony after adaptation, independently of the preferred orientation difference (Fig. 4A). This effect of adaptation may be related to orientation discrimination. Indeed, cooperation (i.e. the advantage gained from the synchronous activity) between V1 neurons is considered as a supplementary channel of information that is crucial for fine discrimination of orientation [40, 41].
Adaptation-induced plasticity gave us the opportunity to examine the modulation of cells pairwise synchronization for various preferred orientation differences, by allowing experimental manipulation of such differences. Adaptation (prolonged exposure to a stimulus) can considerably reorganize the boundaries of cortical orientation maps as demonstrated by optical imaging. In adult cats revealed that during adaptation-induced plasticity, orientation preference maps undergo transient changes in the millimeter-order . In the distance range we used, it is likely that cells shifting their preferred orientations toward the adapting orientation also experienced a reorganization of the iso-orientation domains to which they belong. In the case of a cell pair with both cells having the same preferred orientation after adaptation, the two cells might be transiently part of the same iso-orientation domain. Interestingly, our data indicate that time-correlated activity of neurons forced to respond preferentially to the same orientation strongly increases. To a certain extent, that is comparable to the synchronization displayed by neurons belonging to columns with like-orientation preference. Indeed, following adaptation, the synchrony between cells initially belonging to different orientation columns in the control condition seems to emulate the high inter-columnar correlated activity observed between cells with similar tuning properties [23, 28, 29]. In general, we observed recovery of pairwise synchronization within sixty minutes, as well as recovery of the pre-adaptation tuning properties. However, after a sixty-minute period, some cells were still responding preferentially to the adapting orientation, and were probably still in the same iso-orientation domain, their synchronization thus remaining high. Our results therefore indicate that adaptation-induced plasticity is a reversible process, with variable recovery dynamics from cell to cell.
The mechanisms underlying orientation selectivity in the primary visual cortex are still debated [42–44]. The earlier models (feedforward) suggested that the selectivity of cortical cells originates primarily from the convergence of lateral geniculate nucleus (LGN) afferences [45, 46]. More recent models (recurrent) suggest that the LGN input is broadly tuned and that a sharpening due to lateral inhibitory connections takes place in V1 [47–49]. Although the recurrent models seem to provide the best description of V1 data, both feedforward and recurrent models explain some of V1 neurons properties . Excitatory feedback from higher visual areas like area 21a may also play a role. Chemical activation or inactivation of area 21a was indeed reported to cause major plasticity of area 17 neurons' orientation preference . In adult cortices, plasticity and cortical remodeling mostly originate from higher stages outside of layer IV, the LGN recipient layer [51–54]. Possible loci for plasticity would be layers II and III that involve vertical connections from layer IV, recurrent inputs from other pyramidal cells and/or intrinsic horizontal connections . It was demonstrated that in visual and barrel cortices, long-term potentiation (LTP) of neurons in layers II/III persist beyond puberty [54, 55]. Interestingly, in this investigation recordings were performed essentially in supragranular layers (< 1000 μm deep; mean 580 μm ± 70 μm). Adaptation-induced modifications of orientation tuning in mature cortex could thus implicate thalamo-cortical as well as local and long-range cortico-cortical networks connecting neighbouring orientation columns.
Moreover, intracellular studies indicate that, depending on the recorded cell, orientation tuning properties stem from a variety of combinations of excitatory and inhibitory inputs [42, 56, 57]. The latter could be related to a study by Dragoi et al.  where adaptation-induced plasticity of orientation tuning was shown to be loci-dependant: the closer a cell is to a 'pinwheel center' (convergence point of several iso-orientation domains), the more it is susceptible to plasticity .
It is likely, although not certain, that the mechanisms involved in adaptation-induced plasticity of orientation preference are the same as the mechanisms causing the pairwise synchrony modulation. Usrey and Reid  distinguish 3 categories of cortical synchronous activity: (i) synchrony from anatomical divergence, (ii) stimulus-dependent synchrony, and (iii) emergent synchrony (oscillations). The first category of synchrony is caused by a single source that projects a strong input (feedforward or feedback) onto multiple targets. The constant application of a non-preferred orientation could reinforce thalamo-cortical synapses, and thus synchrony from thalamo-cortical anatomical divergence. However, these connections are weak and need to be synchronized to efficiently drive cortical neurons . Experimental recordings of thalamo-cotical neurons demonstrate the presence of spike patterns suggesting that synchronous spike volleys occur at the population level . If synchronous activity extends across many thalamo-cortical neurons, time-correlated output spikes appear between spiny stellate cells in layer IV . Synchrony in the LGN can also occur via cortico-thalamic projections  that may relay the 30–60 Hz rhythm (emergent synchrony) generated by intracortical mechanisms . Even then, thalamo-cortical synapses, which represent ≈ 10% of a cortical cell's total inputs, are unlikely to generate the large changes in orientation preference that were reported in the present investigation. Stimulus-dependent synchrony is what was measured, although some of its components (stimulus coordination) were suppressed in the shift-corrected cross-correlation histograms . Indeed, the shuffling and subtraction procedure (shift-correction) allow the measurement of synchrony of neuronal origin. It was suggested that correlation of V1 single neuron's responses arises for the most part from an orientation-tuned input that causes sharp synchronization . In this investigation, shifts in orientation selectivity and synchrony modulation appear to be related particularly when cells were compelled to share identical orientation properties (see Fig. 7). An intuitive explanation for these findings would imply that adaptation-induced plasticity affects the ascending inputs from layer IV and the horizontal connections which link clusters of neurons displaying identical preferred orientations. Early in life, synapses are extremely plastic and the development of horizontal connections may depend on time-correlated activity triggered by visual experience. In the adult primary visual cortex, synchronous activation selectively stabilizes neuronal connections within and among iso-oriented columns that fine-tune modularity [23, 28, 29]. Following a prolonged adaptation, pyramidal neurons that displayed closer tuning properties are more coactivated most probably through recurrent reinforcement of their local horizontal excitatory synapses. This supplementary coactivation would enhance the synchrony between clusters of cells as long as they exhibited closer orientation tunings (see Fig. 8). Considering that synchrony and both orientation selectivity and plasticity are thought to occur from intracortical interactions, mechanism involving specific horizontal connections in supragranular layers seems the more suited to explain the simultaneous changes in orientation preference and pairwise zero-lag synchronization.
We found that in cat V1 orientation-selective neurons, the prolonged (>10 min) presentation of a non-preferred stimulus induces mainly response facilitation for the non-preferred stimulus and depression for the preferred one. This predominance of attractive shifts contrasts with previous similar studies. We propose that the adaptation duration is the major explaining factor: short-term adaptation causes repulsive shifts in V1, but if adaptation is maintained longer, the repulsive shifts are reversed to attractive shifts.
We have also shown that synchrony reflects similarity of tuning properties, specifically orientation preference, and is modulated accordingly when these properties change following adaptation. This novel result suggests a role for neural synchronization in dynamically linking cortical regions with similar functional properties in the presence of their optimal stimulus. Stimulus-dependent synchronization was shown to provide a positive information contribution  and might represent a crucial mechanism for efficiently conveying the relevant information to latter stages of visual processing [67, 68].
Fifteen adult cats (2.5–3.5 kg) were prepared for electrophysiological recordings from area 17 (superficial layers) as described in a previous report . Experimental procedures followed the regulations of the Canadian Council on Animal Care as well as the US National Institutes of Health guidelines for the care and use of animals in research, and were approved by the Institutional Animal Care and Use Committee of the University of Montreal.
Preparation, anesthesia and surgical procedures
Animals sedated with acepromazine maleate (Atravet, Wyeth-Ayerst, Guelph, ON, Canada; 1 mg·kg-1, intramuscular) and atropine sulfate (ATRO-SA, Rafter, Calgary, AB, Canada; 0.04 mg·kg-1, intramuscular) were anesthetized with ketamine hydrochloride (Rogarsetic, Pfizer, Kirkland, QC, Canada; 25 mg·kg-1, intramuscular). Lidocaine hydrochloride (Xylocaine, AstraZeneca, Mississauga, ON, Canada; 2%) was injected subcutaneously as a local anesthetic during surgery. A tracheotomy was performed for artificial ventilation, and one forelimb vein was cannulated. Animals were then placed in a stereotaxic apparatus. Xylocaine gel (Astra Pharma, Mississauga, ON, Canada; 5%) was applied on the pressure points. For the remaining preparations and recording, paralysis was induced with 40 mg and maintained with 10 mg·kg-1·h-1 gallamine triethiodide (Flaxedil, Sigma Chemical, St. Louis, MO, USA; intravenous) administered in 5% dextrose lactated Ringer's nutritive solution. General anesthesia was maintained by artificial ventilation with a mixture of N2O/O2 (70:30) supplemented with 0.5% isoflurane (AErrane, Baxter, Toronto, ON, Canada) for the duration of the experiment. Electroencephalogram, electrocardiogram and expired CO2 were monitored continuously to ensure an adequate level of anesthesia. The end-tidal CO2 partial pressure was kept constant between 25–30 mmHg. A heated pad was used to maintain a body temperature of 37.5°C. Tribrissen (Schering-Plough, Pointe-Claire, QC, Canada; 30 mg·kg-1 per day, subcutaneous) and Duplocillin (Intervet, Withby, ON, Canada; 0.1 mL·kg-1, intramuscular) were administered to the animals to prevent bacterial infection. The pupils were dilated with atropine sulfate (Isopto-Atropine, Alcon, Mississauga, ON, Canada; 1%) and the nictitating membranes were retracted with phenylephrine hydrochloride (Mydfrin, Alcon, Mississauga, ON, Canada; 2.5%). Plano contact lenses with artificial pupils (5 mm diameter) were placed on the cat's eyes to prevent the cornea from drying.
A craniotomy (6 × 6 mm) was performed over the primary visual cortex (including parts of both A17 and A18, Horsley-Clarke coordinates P0–P6; L0–L6). The underlying dura was removed, and once the electrodes were positioned in area 17, the hole was covered with warm agar (3–4% in saline). Melted wax was poured over the agar to provide stability and to prevent it from drying.
Multi-unit activity in the visual cortex was recorded by two sets of tungsten microelectrodes (Frederick Haer & Co, Bowdoinham, ME, USA; 10 M at 1 kHz). Each set, consisting of a 4-microelectrode linear array (inter-electrode spacing of 400 μm) enclosed in stainless steel tubing, was controlled by a separate micromanipulator. The signal from the microelectrodes was amplified, band-pass filtered (300 Hz – 3 kHz), digitized and recorded with a 0.05 ms temporal resolution (DataWave Technologies, Longmont, CO, USA). Action potentials were sorted out using window discriminator for further off-line analyses. Multi-unit recordings from one electrode usually included 2 (up to 3) well-isolated single units. The spike sorting method was based on cluster classification in reduced space (Autocut 3.0, DataWave Technologies). Z-scores were computed to quantify the difference between clusters. The stability of each cell's activity across conditions was verified qualitatively by visual control of the clusters disposition and of the waveforms shape (see Fig. 1C and 1D). The signal-to-noise (S/N) ratio was measured as the mean of the waveforms amplitude divided by the noise in the last bin of the temporal window (range: 1.9 to 3.4 ms).
Stimulation was monocular (dominant eye). After clearly detectable activity was obtained for 2 microelectrodes on one of the arrays, the multi-unit receptive fields (RF) were mapped as the minimum response fields  by using a hand-held ophthalmoscope. Eye-screen distance was 57 cm. RF edges were determined by moving a light bar from the periphery toward the center until a response was elicited. These preliminary tests revealed qualitative properties such as dimensions, velocity preference, orientation and directional selectivity. To ensure that both electrodes did not record spikes generated by the same cells, only microelectrodes from the same array were used for the analysis, because precise inter-electrode distances could not be guaranteed between the two electrode arrays. In our study, the interelectrode distance (400 to 1200 μm) was within the range of receptive fields overlapping for area 17 in cats (5mm2) . Accordingly the majority of recorded neurons had overlapping receptive fields. Visual stimuli were generated with a VSG 2/5 graphic board (Cambridge Research Systems, Rochester, England) and displayed on a 21-in. monitor (Sony GDM-F520 Trinitron, Tokyo, Japan) placed 57 cm from the cat's eyes, with 1024 × 768 pixels, running at 100-Hz frame refresh. Stimuli were sine-wave drifting gratings covering both RFs [72, 73]. Contrast was set at 80%. Mean luminance was 40 Cd.m-2. Optimal spatial and temporal frequencies were set within the 0.2–0.4 cycles·deg-1 and 1.0–2.0 Hz range respectively, where V1 neurons are known to respond well to sine-wave drifting gratings . In the first step, orientation tuning curves (16 equidistant points covering 360°, i.e. by steps of 22.5°) were determined using a single grating covering both RFs. Nine orientations covering 180° and centered on the preferred orientation (and direction) of one site were then used for the rest of the experiment. Each orientation was presented in blocks of 25 trials, with each trial lasting 4.1 s and a random inter-trial interval (1.0–3.0 s). Thus, recording sessions lasted for 25–30 min (25 trials*(4.1s + 2s) for each of 9 oriented-stimulus). Orientations were presented in random order. Peri-stimulus time histograms were recorded simultaneously for both sites. It should be noted that these tuning curves were obtained for moving stimuli, so it is strictly speaking incorrect to describe them as orientation tuning curves. Indeed, orientation is by definition cyclic over the interval 0°–180°, while direction is cyclic over the interval 0°–360° . In other words, for any given orientation, there are 2 possible perpendicular directions for a moving stimulus. Considering that most cells in the cat visual cortex show some degree of direction selectivity [1, 76], a proper description of their responses would rather be a directional tuning curve. However, this distinction will be ignored, as it has been in almost all other studies of orientation tuning in V1 .
Following the tuning properties characterization, an adapting stimulus was presented continuously for 12 minutes. The stimulus was a drifting grating whose orientation was generally set 22.5 to 45.0° off the preferred orientations of both sites (see arrows in Fig. 1A and 1B). No tests were conducted during this adaptation period. Immediately after adaptation, the orientation tuning curves of both sites were determined once again. In order to exclude effects which may arise from different randomization sequences during the post-adaptation recordings, responses to the adapting stimulus were always measured first followed by 3–4 semi-random orientations around control preferred stimuli. Hence, the most critical tested orientations were measured within 10–15 min following adaptation. Other orientations were further tested in random order. This procedure was adopted for all cells in order to insure robust effect of the long-term adaptation on near flanks of cells' preferred orientation. In addition, it should be mentioned that responses at far flank orientations (baseline) remained constant during recordings (see Fig. 2C). A last recording was performed 60 minutes post-adaptation to assess the stability of the tuning properties, i.e. the recovery time course. A recording session lasted 3 hours on average.
Preliminary tests with various adaptation and recovery times were conducted (data not shown). In our experimental conditions, an adaptation period of 12 minutes appeared sufficient to induce a shift in orientation selectivity. Longer time intervals were tested for recovery. A 60-minute period seemed a good compromise since the neurons' activity could be lost over the course of the experiment for longer durations. Within this time window, recovery of the initial properties was observed for about one half of the sites. No significant difference was observed in the recovery course whether the animals were left unstimulated or stimulated with randomly-oriented drifting gratings.
Once single cells were sorted out off-line from multi-unit spike trains accumulated during data acquisition, the cells from both electrodes were paired, and cross-correlation histograms (CCHs) were constructed (1-ms binwidth). To examine synchronization of neural origin, stimulus-induced coordination (i.e. time-locked responses) and rate covariation had to be removed. To that effect, shift-predictors were computed by correlating spike recordings shuffled by two stimulus presentations, and these were subtracted from the raw CCHs . All subsequent analyses were performed on the shift-corrected CCHs. Repeated shuffling allowed us to calculate the 99.9% confidence limits, which correspond to 3.3 standard deviations in a normalized distribution. Only peaks exceeding the confidence limits were considered statistically significant . Synchronization strength was computed as a correlation coefficient [78–80]. This correlation coefficient, or synchronization index (SI), reflects the strength of time-correlated activity in a neural CCH as a function of the number of simultaneous events normalized in relation to the firing rate of each neuron. As a consequence, the synchronization strength is considered independent of the response levels, i.e. the mean firing rates.
where A is the value of the function at the preferred orientation, c, and b is a width parameter. An additional parameter, d, represents the spontaneous firing rate of the cell [9, 75]. A fit was considered satisfactory if it accounted for at least 80% of the variance in the data. To ensure that our cells were properly tuned for orientation, we used an orientation selectivity index (OSI). It was measured using the fitted tuning curves, by dividing the firing rate at the baseline (orthogonal orientations) by the firing rate for the preferred orientation, and subtracting the result from one [81, 82]. The closer the OSI is to 1, the stronger the orientation selectivity. To test the significance of tuning shifts curve fits using von Mises function were generated on cells responses for every presentation (n = 25, see details above). Then, we compared between trial by trial the preferred orientation obtained prior to and after adaptation. A t-test revealed the significance level . Cells showing shifts in preferred orientation larger than 5° were statistically significant (paired sample two-tailed t-test, p < 0.01). The curve fitting method is the appropriate way of estimating the preferred orientation in a tuning curve and thus shifts in orientation selectivity . However, notwithstanding the gain in precision in comparison to raw tuning curves, the resulting optimal orientation would be located between the actual data points, a location for which there are no spike trains recorded. Although interpolation is an option, there is to our knowledge no indication of its physiological pertinence. Consequently, raw spike counts were used for all analyses involving synchrony calculations.
This research was supported by grants from the Natural Sciences and Engineering Research Council of Canada (NSERC). We thank Michael Brosch, Igor Timofeev, Maxim Volgushev, Adnane Nemri and Steve Itaya for their useful comments on the manuscript, and Guillaume Blanchet for help with data analysis.
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