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Department of Anatomy and Neurobiology and the Program in Neuroscience, University of Maryland School of Medicine, Baltimore, Maryland 21201
Submitted 17 March 2004; accepted in final form 25 May 2004
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ABSTRACT |
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INTRODUCTION |
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). Similarly, in all species, there exist several discrete somatosensory and auditory cortical areas (Disbrow et al. 2003; Harel et al. 2000; Huang and Winer 2000; Welker and Sinha 1972; Woolsey 1967). The roles and relationships of these multiple sensory representations are controversial. In the visual system, there is evidence that different cortical regions process information hierarchically, such that visual information is processed serially from one cortical area to the next (Casagrande and Kaas 1994; Kennedy and Bullier 1985; Stone et al. 1979). However, there is also evidence that visual information is processed in parallel by multiple cortical areas (Herkenham 1980; Weyand and Swadlow 1986). A similar ambiguity characterizes somatosensory cortical regions, with evidence existing for both serial and parallel processing by different cortical areas (Burton 1991; Coleman et al. 1999; Dykes 1983; Pons et al. 1992; Turman et al. 1995; Zhang et al. 1996).
In rodents, stimulation of the mystacial vibrissae (whiskers) evokes responses both in the first somatosensory ("barrel") cortex (SI) and in the second somatosensory cortex (SII; so named because it was discovered later than SI; White 1987). However, apart from the fact that whisker-related neurons in SII have large receptive fields (Carvell and Simons 1986; Fabri and Burton 1991; Remple et al. 2003), relatively little is known about the functional organization of this cortical area. For example, whereas the response properties of SI neurons may be shaped primarily by inputs from the lemniscal pathway (Keller 1995), it is not known whether SII responses are mediated by inputs from SI or by direct subcortical inputs from the paralemniscal pathway.
Our aim was to take advantage of the extensive information on response properties of neurons in barrel cortex (SI) and the unique anatomical structure of the whisker system to compare response properties of whisker-related neurons in SI and SII. These comparisons provide strong support for the hypothesis that SII is part of the paralemniscal system that processes information in parallel with lemniscal pathways, including SI. Some of these results were reported previously in abstract form (Kwegyir-Afful and Keller 2002).
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METHODS |
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Twelve female Sprague-Dawley rats weighing 250–350 g were used in this study. All procedures strictly adhered to institutional and federal guidelines. Under halothane anesthesia (3%) and infusion of local anesthetics at surgical sites, a craniotomy was performed over the right primary and second somatosensory cortex. The dura was removed, and agarose (1.4% in buffered saline) was poured over the craniotomy to prevent drying. A venous catheter was inserted in the jugular vein for drug delivery, and a second catheter placed in the femoral artery for monitoring blood pressure and heart rate. Following the surgical procedures, administration of halothane was discontinued, and the rats were infused intravenously with fentanyl (10 µg/kg/h) for the rest of the experiment. The rats were then immobilized with pancuronium bromide (1.5 mg/kg/h) and artificially respired with a positive pressure respirator at 90 breaths/min. Blood pressure, heart rate, and electroencephalographs were monitored throughout the experiment to ensure that the animal was in no pain or distress. Body temperature was maintained at 37°C with a servo-controlled heating blanket.
A separate series of experiments was conducted with three additional rats, using approaches identical to the ones described above, except that urethane (1.5 g/kg) was used as an anesthetic for the duration of the experiments.
Recording and stimulation
Extracellular unit recordings were obtained with quartz-insulated platinum electrodes (2–4 M
). Electrodes were advanced perpendicular to the cortical surface, using either a stepper motor (Burleigh, Fishers, NY) or a seven-channel manipulator (Thomas Recording). Whiskers on the contralateral face were continually stimulated during electrode penetrations to detect units with low or no spontaneous activity. Waveforms recorded from well-isolated units were digitized through a Plexon data acquisition system (Dallas, TX) at 40 kHz. Units were isolated off-line with Plexon's Off-line Sorter, and auto-correlograms were generated with Neuroexplorer software (Littleton, MA) to confirm that recordings were obtained from single units.
At the end of the experiment, recording sites were marked with electrolytic lesions (5 µA for 10 s). The animals were deeply anesthetized with sodium pentobarbital (60 mg/kg) and perfused transcardially with buffered saline followed by 4% buffered paraformaldehyde. Recording sites were identified in Nissl-stained coronal sections.
Whisker stimulation
Receptive fields were initially determined by manually deflecting individual whiskers. Whiskers evoking detectable responses were then individually attached—10 mm from their base—to a computer-controlled piezoelectric stimulator that can be deflected in eight different directions. Ramp-and-hold stimuli, 200 ms in duration and having onset/offset velocity of 102 mm/s, were applied at 1 Hz. To reduce mechanical ringing, the trapezoid ramp-and-hold waveforms were filtered with a Bessel filter. The peak onset and offset velocity were measured as the slope of the linear portion of the deflection ramp. The stimulator was calibrated with a photodiode device. Individual whiskers were deflected in one of eight directions (in 45° increments), delivered randomly for a total of 50 stimuli per deflection angle. In experiments involving urethane-anesthetized rats, whiskers were manually deflected with a handheld probe.
Data analysis
Time stamps of well-isolated units and of stimulus triggers were exported to Matlab (MathWorks, Natick, MA) for analyses using custom written software. Peristimulus time histograms (PSTHs, 1-ms bins) were constructed from these time stamps. PSTHs were constructed from responses to stimulation of a whisker at the cell's preferred angle. Significant stimulus-evoked responses were defined as PSTH bins whose response magnitude significantly exceeded (99% CI) spontaneous activity levels, computed from a 200-ms period preceding the stimuli. Response onset latency was identified as the time of occurrence of two consecutive poststimulus bins displaying significant responses.
Statistical analyses were performed in SPSS and Microsoft Excel. Where appropriate, results are displayed using a boxplot to depict the median and distribution of the data (see Fig. 1B ). Between-group statistical comparisons were assessed with the nonparametric Kolmogorov-Smirnov (K-S) test, because it is sensitive to any type of distributional differences (i.e., central tendency, variability, skewness, and kurtosis) and makes no assumptions regarding normality or equivalence of variance. Multiple-group comparisons were assessed with ANOVA with nonparametric posthoc tests. Within-group (individual neuron) comparisons made use of one-tailed Student's t-tests. Categorized data were analyzed using a 
2 test. To fully describe data distributions, both means ± SD and medians are presented.
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RESULTS |
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Included in the following analyses are data from 140 well-isolated units, of which 124 units were recorded from 35 electrode penetrations in the SII. We compared these data with previously published findings on neurons in SI, recorded under identical conditions (Table 1). In addition, we include data from 16 units we recorded in layer IV of SI. This was done to ensure that, under our recording conditions, response properties of SI neurons are comparable to previously reported data. All recording sites were identified posthoc by histologically examining electrode tracks and lesion sites (see METHODS). SI units were all in layer IV of the granular posteromedial barrel subfield (Woolsey and Van der Loos 1970), the cortical area containing representations of the large whiskers (Welker and Woolsey 1974). We specifically targeted recording to neurons in barrel hollows by identifying neuronal clusters exhibiting a strong preference to stimulation of a single, principal whisker. All SII units were in the dysgranular cortical region immediately lateral to SI (Fabri and Burton 1991; Remple et al. 2003) and medial to primary auditory cortex (Fabri and Burton 1991; Remple et al. 2003). Laminar location was determined from microdrive readings and histological analyses. SII units in layers II/III (n = 44) were recorded at depths of 400–900 µm from the pial surface; units in layer V (n = 57) were at depths of 900–1,400 µm; units in layer VI (n = 23) were at depths of 1,400–1,900 µm. As previously reported (Carvell and Simons 1986; Fabri and Burton 1991), we did not observe a well-defined layer IV in SII.
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; Simons 1978). Fast spiking units (FSUs)—which correspond to GABAergic, parvalbumin-expressing inhibitory interneurons (Connors and Gutnick 1990)—have significantly shorter waveforms compared with regular spiking units (RSUs), most of which are excitatory neurons. We applied the criteria developed by Bruno and Simons (2002) to distinguish between these populations. RSUs were defined as units whose waveforms had an initial negativity (N1) lasting >180 µs, followed by a positivity (P1) lasting >400 µs (Fig. 1A). FSUs had an N1 component 
175 µs and a P1 component 350 µs (Fig. 1A). According to these criteria, 92% of SII neurons were classified as RSUs and 8% as FSUs. This ratio of RSUs and FSUs is similar to the one reported in studies of SI barrel cortex (Simons and Carvell 1989). Our sample includes RSUs recorded in layers II to VI of SII (40 units in layer II/III; 53 in layer V, and 22 in layer VI) and FSUs recorded in the same layers (4 units in layer II/III, 4 in layer V, and 1 in layer VI). All SI units in our study were RSUs recorded from layer IV barrels of SI. Spontaneous activity
RSUs in SII had spontaneous firing rates ranging from 0.05 to 25.15 Hz (median, 3.55 Hz; 5.20 ± 5.70 Hz), whereas spontaneous firing of SI RSUs ranged from 0.15 to 12.52 Hz (median, 1.63 Hz; 3.27 ± 3.99 Hz) similar to values previously reported for SI (<1–12 Hz) (Simons and Carvell 1989). This difference was not statistically significant (K-S test, P = 0.14). FSUs in SII tended to have higher spontaneous firing rates than RSUS, but this difference did not reach statistical significance (K-S test, P = 0.38), with FSUs ranging from 0.87 to 29.8 Hz (median, 5.3 Hz; 7.95 ± 8.74 Hz). This finding is in contrast to that reported for rat SI (Simons and Carvell 1989) and in SII of the rabbit (Swadlow 1991), where FSUs have significantly higher spontaneous activity than RSUs.
Response latency
We reasoned that if the responses of SII neurons are shaped by direct thalamic inputs, the onset latencies of SII neurons would be indistinguishable from those of SI cells. To test this, we compared the onset latency of SI and SII neurons to whisker deflections (at each cell's preferred direction). Figure 1, C and D, depicts PSTHs computed for representative units recorded from SI and SII, using 1-ms bins (identical results were obtained using 100-µs bins). The response onset latencies of these neurons were nearly identical (7 and 8 ms). The median response latency of all SII neurons was 9.0 ms (4–30 ms; 9.1 ± 3.6 ms), and for SI neurons, the median was 8.5 ms (5–16 ms; 9.3 ± 3.0 ms; K-S test, P = 0.95; Fig. 1B). Although our sample size of SI neurons is smaller than that of SII cells, the onset latencies of SI neurons we recorded is similar to that reported in previous studies (e.g., Brumberg et al. 1999). Thus SII neurons respond to whisker deflections with latencies that are similar to those of their counterparts in SI.
In SI barrel cortex, neurons in layer IV and some neurons in the deeper layers respond to whisker deflections earlier than cells in superficial layers (Brumberg et al. 1999). To determine if a similar difference in response latency characterizes SII neurons, we compared the onset latency of cells in different layers. We found no statistically significant differences in onset latency for units recorded from layer II/III (median, 9.0 ms; n = 44), layer V (median, 9.0 ms; n = 58), or layer VI (median, 8.0 ms; n = 23; ANOVA P = 0.97; Fig. 1B). Similarly, the onset latencies of RSUs and FSUs were indistinguishable (P = 0.65).
These results suggest that, unlike in SI, neurons in all layers of SII receive suprathreshold inputs from thalamic afferents and that the response properties of neurons in all layers of SII are shaped by these inputs. Therefore in the following analyses, we compared the response properties of SII neurons in all layers with those of neurons in layer IV of SI.
Response kinetics
Ramp-and-hold whisker deflections evoked phasic responses in most (90.3%) SII neurons, with cells responding vigorously to stimulus onset (ON) and offset (OFF), while evoking no significant activity during the hold phase of the stimulus (Fig. 2A ). We identified the beginning of ON and OFF responses as two consecutive, statistically significant PSTH bins (see METHODS) and the end of each ON and OFF response as three consecutive bins with no significant activity. The duration of the entire ON response ranged from 7 to 54 ms (median, 24 ms; 24.98 ± 10.61 ms). ON response durations of SI neurons were more variable, ranging from 18 to 99 ms. Using criteria introduced by Simons and Carvell (1989), we classified units whose responses (at their preferred direction) were 50 ms or longer as slowly adapting, and the remaining neurons as rapidly adapting. Of SI cells, 18.8% were slowly adapting, whereas all but four neurons (3%) recorded in SII were rapidly adapting. The duration of ON responses in rapidly adapting SI neurons ranged from 18 to 48 ms (median, 25 ms; 31.46 ± 11.21 ms), and in slowly adapting SI neurons, ranged from 84 to 99 ms (median, 91 ms; 91.33 ± 7.51 ms). There was no significant difference between ON response duration of SI rapidly adapting neurons and SII neurons (K-S test, P = 0.09). Additionally, there was no significant difference (K-S test, P = 0.93) in ON response duration between RSUs (median, 24 ms; range, 7–54 ms) and FSUs (median, 25 ms; range, 10–54 ms; Fig. 2E) in SII.
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Units recorded from SI and SII differ in their ON response magnitude (computed for the entire duration of the ON response; K-S test, P = 0.04; Fig. 2C). SI RSU responses ranged from 0.40 to 3.42 spikes/stimulus (median, 1.80 spikes/stimulus; 1.62 ± 0.97 spikes/stimulus). SII units response magnitudes were significantly smaller, ranging from 0.11 to 4.52 spikes/stimulus (median, 0.93 spikes/stimulus; 1.07 ± 0.8 spikes/stimulus). In contrast, SII RSUs and FSUs did not differ in response magnitudes (K-S test, P = 0.45; Fig. 2C).
In SI neurons, the magnitude of ON responses is usually larger than that of OFF responses (Kyriazi et al. 1994). We found a similar preference for ON responses in both SI and SII neurons, with OFF-ON response magnitude ratios of 0.66 ± 0.34 for SI cells and 0.49 ± 0.33 for SII neurons. In SII, OFF-ON ratios of RSUs (0.04–2.14; median, 0.46; 0.49 ± 0.33) were similar to those of FSUs (0.12–1.01; median, 0.43; 0.48 ± 0.32; K-S test, P = 1.0; Fig. 2D). Similarly, we found no significant differences (K-S test, P = 0.12) in OFF-ON ratios between SI and SII RSUs: RSUs in SI had ratios ranging from 0.07 to 1.19 (median, 0.68; 0.66 ± 0.34; similar to ratios reported by Kyriazi et al. 1994). Thus OFF-ON ratios of RSUs are similar in SI and SII neurons. However, whereas in SII, RSUs and FSUs have similar OFF-ON ratios, in SI, RSUs have a significantly smaller OFF-ON ratio compared with FSUs (Kyriazi et al. 1994).
Receptive field size
We defined receptive field size as the number of whiskers whose stimulation evokes a significant response, averaged across all eight angles, in SII neurons. In initial experiments (see METHODS), we recorded responses to manual deflection of individual whiskers in urethan-anesthetized rats. Under these conditions, SII neurons responded to stimulation of 5–13 whiskers (median, 9 whiskers; n = 30 neurons). Whiskers whose stimulation evoked responses in a particular neuron were always located contiguously along the whisker pad. In other experiments—under fentanyl analgesia—we recorded responses of individual neurons to piezoelectric stimulation of individual whiskers. Although this approach is advantageous in that stimulation parameters are better controlled, the time needed to fully characterize the responses of a neuron limits the number of whiskers that can be tested. As a result, values obtained with this approach underestimate the size of SII receptive fields. We included in this analysis only cases in which we recorded responses to stimulation of 
4 adjacent whiskers (n = 58 units). These cells responded to stimulation of 4 whiskers and as many as 12 whiskers (median, 6 whiskers). For 18 units, we were able to test responses to stimulation of eight or more individual whiskers. These units responded to stimulation of 5–12 whiskers (median, 10 whiskers). Thus the receptive field size of SII neurons does not appear to be affected significantly by the choice of anesthetic. Under both fentanyl analgesia and urethane anesthesia, the median receptive field size was 10 whiskers. This contrasts sharply with the receptive field size of SI neurons, the majority of which respond to stimulation of a single whisker (e.g., Bruno and Simons 2002).
Neurons in the SI barrel field that respond to stimulation of more than one whisker respond preferentially to stimulation of the whisker associated with their anatomically defined barrel. That whisker is termed the principal whisker (PW; Welker 1971). Stimulation of the PW evokes responses having larger magnitude and shorter onset latency compared with responses to adjacent whiskers (AW; Armstrong-James 1995; Simons 1995). We sought to determine whether a similar distinction between PW and AW responses characterized SII neurons. Figure 3A shows PSTHs constructed from responses of a representative layer V SII neuron to deflections of different whiskers. Robust responses were evoked in this cell by stimulation of each of nine different whiskers. Note that stimulation of different whiskers evoked responses having different magnitudes but similar onset latencies. We obtained similar results from each of the 58 neurons in which we tested responses to four or more whiskers. To quantitatively assess whether different whiskers evoke responses having significantly different onset latencies, we identified, for each neuron, the whisker evoking the shortest latency response (termed "W-1"). The onset latency of responses to the remaining whiskers, rank ordered by response latency (W-2, W-3...), were then normalized to the onset latency of W-1. Figure 3B shows the means (±99% CIs) of these normalized latencies, computed from responses recorded from the 58 neurons described above. Note that, although the mean difference in latency is somewhat variable, there are no significant differences in onset latency in response to stimulation of different whiskers. Thus individual SII neurons respond to stimulation of different whiskers with similar onset latency, and as a result, onset latency cannot be used to distinguish between PW and AW responses.
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Interestingly, although response latency proved an inadequate metric to define PWs, PWs—defined as the group of whiskers evoking significantly stronger responses—have onset latencies that were significantly shorter than responses to AWs (K-S test, P < 10–4; Fig. 3E).
Angular selectivity
Neurons throughout the lemniscal pathway of the rat whisker system are selective for the angle of whisker deflection (Hartings et al. 2000; Lee and Simons 2004; Minnery and Simons 2003; Simons 1978; Simons and Carvell 1989), eliciting larger magnitude responses to preferred angle deflections. To determine if this property also characterizes SII neurons, we recorded responses to whisker deflections in eight different angles. Figure 4A presents results from an SII neuron with strong angular preference, and Fig. 4B depicts results from a poorly tuned neuron. PSTHs were constructed from responses to deflections in the angles indicated, with 0° representing deflection in the caudal direction and 90° in the dorsal direction. ON response magnitudes to the different deflections were normalized to the maximum ON response and used to construct polar plots (Fig. 4, A and B, insets) showing the normalized response magnitudes against the direction of deflection.
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) representing the number of angles with responses that are statistically smaller than responses to the maximally activating angle. Category 0 represents the least-tuned cells (cells that respond equally to all deflection angles), and category 7 represents the best-tuned cells (cells that responds preferentially to one deflection angle). The polar plot in Fig. 4A depicts a category 6 neuron, whereas that in Fig. 4B depicts a category 0 neuron. Figure 4C shows the distribution of angular tuning for SII and SI neurons (the latter reproduced from Simons and Carvell 1989). Well-tuned cells (categories 5–7) constituted 33.9% of SII neurons, but only 15.7% of SI cells. Thus SII contains a larger proportion of neurons with strong angular selectivity.
We investigated the possibility that there is a laminar segregation of angular tuning of SII neurons. Neurons in layer II/III had angular tuning ranging from category 0 to 6 (median, 3.0), layer V neurons ranged from category 0 to 7 (median, 3.0), and layer VI neurons ranged from category 3 to 7 (median, 5.5). Although layer VI neurons tended to have a higher angular selectivity, this difference is not statistically significant (2 = 16.52; P > 0.05; df = 14).
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DISCUSSION |
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Response latency
Although neurons in layers II to VI of SI may receive direct thalamic inputs (White and Keller 1989), layer IV (barrel) neurons respond to whisker stimuli at latencies that are significantly shorter than those of neurons in supragranular layers, and most cells in infragranular layers (Armstrong-James et al. 1992; Wilent and Contreras 2004). Laminar comparisons of other response properties also suggest that direct thalamic inputs have a larger influence on the receptive fields of barrel neurons compared with those of cells in other layers of SI (Brumberg et al. 1999; Pinto et al. 2003). In contrast, neurons in all layers of SII respond to whisker stimuli at similar short latencies and have similar response properties. This suggests that, unlike SI, the receptive field properties of neurons in all layers of SII may be shaped, to a significant extent, by direct thalamic inputs.
Neurons in SII and in layer IV of SI (the latter displaying the shortest response latencies in the barrel cortex; Brumberg et al. 1999) respond to whisker deflections with indistinguishable onset latencies. This finding argues against the possibility that SII responses are dependent on inputs from SI, because the conduction time and synaptic delay of SI to SII inputs would result in longer latency responses in SII. Thus SII neurons are likely to receive direct driving inputs from the thalamus in parallel with their counterparts in SI.
Inactivating SI can more directly test the dependence of SII on SI inputs, but the close proximity of these cortical regions in the rat complicates such a manipulation. However, reversible inactivation of SI has been successfully performed in larger species, including cat (Turman et al. 1992, 1995), marmoset (Zhang et al. 1996), and possum (Coleman et al. 1999). In all species, this manipulation failed to abolish SII responses, although it did produce some reductions in both spontaneous and evoked activity of some SII neurons. These findings support the conclusion that SII receives driving inputs from thalamic afferents and suggests that SI inputs are modulatory.
In contrast, SI lesions in Rhesus monkeys have been reported to abolish activity in homotypical SII regions (Burton et al. 1990; Pons et al. 1992). These authors postulate an evolutionary shift from nonprimates and lower primates—in which tactile information is processed in parallel in SI and SII—to a new organization in higher primates in which the processing of tactile information proceeds serially from SI to SII. However, there is also evidence from human and other primates that SII receives direct ascending inputs and operates in parallel with SI (for review, see Burton 1991). It has also been shown that SII of higher primates contains two subdivisions: one that may be driven preferentially by thalamic inputs and the other whose responses depend on inputs from SI (Burton et al. 1995).
The origin of driving inputs to rat SII is currently unknown. Anatomical studies indicate that the ventrolateral portion of the ventral posterior medial thalamus (VPMvl) and the posterior nucleus of the thalamus (POm) project densely to SII (Pierret et al. 2000). These thalamic afferents ramify extensively and diverge in most layers of SII. This laminar divergence is consistent with our finding that the response latency of neurons throughout layers II to VI of SII is indistinguishable (Fig. 1B).
Receptive field size
The receptive field size of SII whisker-related neurons is substantially larger than that of SI cells (Fig. 3). This is in agreement with previous findings in rat and other mammals (Carvell and Simons 1986; Jones and Peters 1984; Swadlow 1991). The large receptive field of SII neurons is not likely the result of converging inputs from SI, for reasons discussed above. Furthermore, anatomical findings show limited convergence of inputs from different SI whisker representations onto SII neurons (Alloway and Burton 1985a; Fabri and Burton 1991). Alternatively, these large receptive fields may be due to convergence of inputs from multi-whisker thalamic neurons in VPM barreloids (Simons and Carvell 1989) or to inputs from thalamic neurons having large receptive fields in VPMvl or POm (Friedberg et al. 1999; Pierret et al. 2000). We favor the latter hypothesis, since VPMvl and POm neurons receive inputs from neurons in the spinal trigeminal nucleus interpolaris (SPVi), and these neurons have some of the largest receptive fields in the whisker-trigeminal system (Jacquin et al. 1986; Timofeeva et al. 2004; Veinante et al. 2000).
Neurons throughout the whisker-to-barrel lemniscal pathway respond preferentially to a well-defined PW. In contrast, most SII neurons respond to several whiskers with similar latency and response magnitude and thus have several PWs (Fig. 3). The difference between the number of PWs in SII and in neurons in the lemniscal system lends further support to the conclusion that SII neurons may be driven by inputs from the paralemniscal system. The large receptive fields and multiple PWs of SII neurons suggest that they are not optimized for single-whisker discrimination. Carvell and Simons (1987) suggested that the large receptive fields in SII imply that this region may have a more contextual role in stimulus detection.
Response kinetics
Response magnitudes of SII neurons to single whisker deflection are significantly lower than those in SI neurons (Fig. 2). This may reflect differences in the efficacies or number of thalamic inputs to SI versus SII neurons. It is possible that SII neurons respond preferentially to simultaneous activation of multiple whiskers, a possibility we are currently exploring. It has been proposed that the paralemniscal system may be essential in the operation of mobile sensory organs (e.g., whiskers; Friedberg et al. 1999; Veinante et al. 2000) and that paralemniscal neurons are preferentially active during voluntary movements. Thus if SII receives driving inputs from the paralemniscal pathway, it may be preferentially active during active whisking.
RSUs and FSUs in SI barrels respond differently to whisker-derived inputs. FSUs have significantly larger response magnitudes (Bruno and Simons 2002), reflecting the higher convergence and efficacy of thalamic inputs to these cells (Gibson et al. 1999; Keller 2001; Porter et al. 2001). As a result of this and other network properties, the barrel circuitry is described as a damping circuit in which inhibition is finely tuned to constrain the temporal responses and receptive field size of RSUs (see Pinto et al. 2003). In contrast, in SII, FSUs and RSUs display similar response magnitudes (Fig. 2), suggesting that there is less net intracortical inhibition in SII compared with SI due to the relatively lower firing rates of FSUs. The reduced efficacy of feed-forward inhibition in SII may contribute to the larger receptive fields of neurons in this region.
RSUs and FSUs in SI differ also in their OFF-ON response ratios, with the former displaying significantly smaller ratios (Kyriazi and Simons 1993). Experimental and modeling studies indicate that the smaller OFF-ON ratios of SI RSUs are also a consequence of the dominance of feed-forward inhibition in the layer IV damping circuit (Kyriazi et al. 1994; Pinto et al. 2003). Thus the similarity in OFF-ON ratios of SII RSUs and FSUs may also reflect reduced feed-forward inhibition in this cortical area.
As in other species (Alloway and Burton 1985b; Coleman et al. 1999; Jones and Peters 1984), the majority of SII neurons are rapidly adapting. Subsequent stations along the lemniscal pathway contain progressively smaller proportions of slowly adapting neurons: 93% in the principal trigeminal nucleus (PrV; Minnery and Simons 2003), 37% in VPM, and 15% in SI (Simons and Carvell 1989). The paralemniscal pathway begins with a smaller proportion of slowly adapting neurons, with 54% of the cells in SPVi described as slowly adapting type I and II neurons (Jacquin et al. 1986). This lends further support for the assumption that SII—having only 3% slowly adapting neurons—is part of the paralemniscal system.
Angular tuning
The relatively strong angular preference of neurons at subcortical levels of the whisker-to-barrel system is thought to reflect the receptor properties and their configuration at the base of the whisker follicle (Lichtenstein et al. 1990; Rice et al. 1986). The proportion of well-tuned cells decreases at subsequent levels of the whisker-to-barrel neuroaxis: 81% of the neurons in trigeminal ganglion are well tuned (Lichtenstein et al. 1990), 46% in PrV (Minnery and Simons 2003), 31.1% in VPm, and 15.7% in SI (Simons and Carvell 1989). This progressive decrease may be due to convergence of inputs from neurons with different and sometimes opposing angular preferences. Surprisingly, 34% of SII neurons are well tuned for whisker deflection angles (Fig. 4). Because the angular tuning properties of neurons in VPMvl and POm—the putative sources of thalamic inputs to SII—are unknown, we cannot speculate as to the mechanisms responsible for the higher angular tuning of SII neurons. Notably, neurons in septa between the layer IV barrels, which are also thought to receive inputs from POm (Lu and Lin 1993; Pierret et al. 2000), have a higher angular preference than their counterparts in the barrel hollows (Lee and Simons 2004).
FSUs in SI of rat and rabbit are reported to exhibit lower angular tuning compared with RSUs (Lee and Simons 2004; Swadlow 1989). Swadlow (1991) reported a similar difference in angular tuning between FSUs and RSUs in rabbit SII. In contrast, we found no significant difference in angular tuning between FSUs and RSUs in SII. Whether these results reflect a species difference, or methodological variability, remains unknown.
The differences between the response properties of SI and SII neurons suggest that these two regions may receive inputs from different subpopulations of thalamic cells. The differences in input transformation in these cortical areas may be a reflection of unique circuit dynamics essential for parallel processing of different, but complementary somatosensory information.
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GRANTS |
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ACKNOWLEDGMENTS |
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FOOTNOTES |
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Address for reprint requests and other correspondence: A. Keller, Dept. of Anatomy and Neurobiology, Univ. of Maryland School of Medicine, 685 W. Baltimore St., Baltimore, MD 21201 (E-mail: akeller{at}umaryland.edu).
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