Lemniscal and Extralemniscal Compartments in the VPM of the Rat

The ventral posteromedial thalamic nucleus (VPM) of the rat contains at least two major vibrissa-representing compartments: the dorsomedial (VPMdm), which belongs to the lemniscal afferent pathway, and the ventrolateral (VPMvl), which belongs to the extralemniscal afferent pathway. Although input–output projections and functional characteristics that distinguish these two compartments were recently clarified, a comprehensive structural analysis of these compartments and the border between them was lacking. This paper addresses structural and functional relationships between the VPMdm and VPMvl. We found that the size of the VPM is almost constant across individual rats. Next, we computed a canonical map of the VPM in the oblique plane, where structural borders are best visualized. Using the canonical map, and sequential slices cut in oblique and coronal planes, we determined the border between the VPMdm and VPMvl in the standard coronal plane, and verified it with in vivo extracellular recordings. The position of the border between these two vibrissal sub-nuclei changes along the rostrocaudal extent within the VPM due to the relative sizes of these sub-nuclei at any point. The border between the VPMdm and VPMvl, which was revealed by this technique, can now be included in atlases of the rat brain and should facilitate experimental correlation of tactile functions with thalamic regions.


INTRODUCTION
Since the original description of spatial organization of somesthetic regions within the rat thalamus (Davidson, 1965;Emmers, 1965), known as the ventrobasal complex (VB), the structure and function of thalamic relay stations have been described in detail (Groenewegen and Witter, 2004;Macchi, 1983;Price, 1995). In rat brain atlases (Paxinos and Watson, 1998;Swanson, 1992) and reviews of thalamic structure and function (Groenewegen and Witter, 2004;Price, 1995), the ventral posteromedial thalamic nucleus (VPM) is considered to be, and is mapped as, a separate thalamic anatomical structure that includes the gustatory sub-nucleus. Functionally, the VPM was classifi ed as a subcortical relay station of the lemniscal pathway (Sugitani et al., 1990;Vahle-Hinz and Gottschaldt, 1983;Waite, 1973) that also contains periodontal mechanoreceptive (Tabata et al., 2002), as well as taste, temperature, and tactile oral sensory representations (Cechetto and Saper, 1987;Emmers, 1965;Verhagen et al., 2003). Thus, the VPM was considered as an obligatory relay station in the sensory pathways mentioned above (Kosar et al., 1986;Price, 1995;Saper, 1995). Haidarliu et al. 2001;Land et al., 1995). In the rat, we found that barreloids are rod-shaped, with their long axes directed from dorsomedial to ventrolateral, and a length gradient that increases diagonally from barreloid A1 to barreloid E4 (Haidarliu and Ahissar, 2001). Individual barreloids are most easily seen in young animals, but are also distinguishable in adults.
In previously proposed three-dimensional models of barreloid arrangement in the VPM (Haidarliu and Ahissar, 2001;Land et al., 1995), barreloids reconstructed from cytochrome oxidase (CO)-stained sections do not occupy all the area assigned to the VPM in current rat brain atlases. Anterograde tracing with biotinylated dextran amine injected into the SpVi, and retrograde tracing with Fluoro-Gold injected into a single cortical barrel column, facilitated a three-dimensional reconstruction in which barreloids consisted of a core located in the VPMdm, and a tail that extended ventrolateral and caudally into the VPMvl (Pierret et al., 2000). In Nissl-stained slices, these subdivisions cannot be distinguished in the rat VPM. Staining for CO activity revealed homologous regions in the VPM of rodents, but the border between the VPMdm and VPMvl could not be visualized in traditional section planes (Land and Simons, 1985;Pierret et al., 2000). Although the transition from the core to tail regions of barreloids was assumed to occur at the VPMdm/ VPMvl border (Pierret et al., 2000), the exact position of the border and its extent was unclear. Recently, it was concluded that no cytoarchitectonic feature or immunohistochemical stain delineated the boundary of the VPMvl within the VPM (Bokor et al., 2008).
Previously, we showed that (1) the border between the two VPM compartments (VPMdm and VPMvl) can be clearly identifi ed in both young and adult rats by cutting brains at specifi c angles and staining for CO activity (Haidarliu and Ahissar, 2001), and (2) the neuronal populations of the two VPM compartments exhibit different electrophysiological characteristics during whisking and object touch: VPMvl neurons convey contact-time information whereas VPMdm neurons convey complex information related to both whisking and touch (Yu et al., 2006). We also described a method of normalization of anatomical VPM coordinates that enables translation of individual parameters of recording sites (lesions), visualized by CO-staining of coronal slices, into an oblique image, with the VPMdm clearly separated from the VPMvl (Yu et al., 2006). This procedure permits translation of lesions observed in thalamic coronal slices into an oblique canonical section of the VPM that facilitates viewing of recording sites in relevant compartments of the VB complex. Here, we modifi ed this method to project the anatomical border between the VPMdm and VPMvl, which can be identifi ed in consecutive oblique slices through the thalamus, onto consecutive coronal slices. Determination of segmentation of the VPM in the coronal plane should allow division of the vibrissal part of the VPM into two sub-nuclei, and inclusion of the border between the VPMdm and VPMvl in rodent brain atlases.

ANIMALS
Histological preparations of the brains of eight 6-day-old, three 9-day-old, and 28 adult Albino Wistar rats, weighing 11-13, 21-23, and 200-300 g, respectively, were subjected to morphological analysis, including mapping of complete sets of slices through the VPM in coronal and two non-traditional cutting planes. Morphological and physiological data from histological preparations, and neuronal recordings of another 40 adult rats (200-300 g) with thalamic lesions (Yu et al., 2006), were also used. All animals were obtained from The Animal Breeding Unit of this Institute. Procedures for animal maintenance, manipulations, and surgeries were approved by the Institute's Animal Care and Use Committee, and conform to the "Principles of Laboratory Animal Care" (NIH publication No. 86-23, revised 1985).

RECORDINGS
Recordings were conducted as previously described (Szwed et al., 2003). Briefl y, surgery was performed under general anesthesia (urethane; 1.5 g/kg, i.p.), with supplemental doses of anesthetic (10%) being administered when required. Atropine methyl nitrate (0.3 mg/kg, i.m.) was administered to prevent respiratory complications. Anesthetized animals were secured in a stereotaxic device (SR-6; Narishige, Japan), and their body temperature maintained at 37°C. An opening was made in the skull overlying the right thalamus, and tungsten microelectrodes (0.5-1 MΩ; Alpha Omega Engineering; Nazareth, Israel) were lowered, according to known stereotaxic coordinates of the POm and VPM, until units drivable by whisker stimulations were encountered. Up to four electrodes, spaced 0.33 mm from each other, were lowered in parallel in each recording session. Standard methods for singleunit recordings were used. Single-units were sorted by spike templates. Units were considered single only if they had homogenous spike shapes that did not overlap with other units or noise, and if they exhibited refractory periods of >1 ms in their autocorrelation histograms. Artifi cial whisking was induced as described in Szwed et al. (2003). Briefl y, the buccal branch of the facial nerve was cut, and its distal end mounted on a pair of silver electrodes. Bipolar, rectangular electrical pulses (0.5-4.0 V, 40 μs duration) were applied through an isolated pulse stimulator (Model 2100; A-M Systems, Sequim, WA, USA) at 83 Hz, the lowest frequency that still produces continuous whisker movement. Whisker movements were recorded at 1000 frames/s with a fast digital video camera (MotionScope PCI 1000; Redlake, San Diego, CA, USA). Artifacts produced by electrical stimulation were isolated by an online spike-sorter (MSD-3.21; Alpha-Omega Engineering) and removed from unit recordings.

HISTOLOGY
Rats were euthanized with Pental (0.1-0.5 ml pro capito, i.p.), perfused transcardially with 2.5% glutaraldehyde, 0.5% paraformaldehyde, and 5% sucrose in 0.1 M phosphate buffer, pH 7.4, and then decapitated. Their brains were excised and stored in postfi xation solution until sectioned, usually within 36 h. Tissue slices were prepared with a sliding microtome (SM 2000R; Leica Instruments, Germany) supplemented with a freezing unit (K400; Microm International, Germany). Histological procedures were identical to those previously employed (Haidarliu and Ahissar, 2001). Briefl y, brains were sliced into 60 μm thick slices, in a traditional coronal plane and in two planes that reveal barreloid arcs or entire barreloid fi elds. We found that the border between the two VPM compartments is most clearly seen in oblique sections, at 50° to the horizontal plane, from dorsomedial to ventrolateral. All slices were stained for CO activity as previously described (Haidarliu and Ahissar, 2001), coverslipped with Entellan, and subjected to light microscopy (Zeiss, Oberkochen, Germany). In a few cases, sections stained for CO activity were also stained with cresyl violet (Haidarliu et al., 1999) to visualize cell bodies. Brightfi eld images were captured by Adobe Premiere 5.0 software (Adobe Systems, Mountain View, CA, USA), and imported into Adobe Photoshop 4.0. During editing of the resulting images, only minimal adjustments in contrast and brightness were made.

PROCESSING OF CORONAL SLICES
In coronal slices of the thalamus, the most rostral barreloid row of the VPM (row E) appeared approximately −2.3 mm caudal to bregma, according to the atlas of Paxinos and Watson (1998). The most caudal row (row A) disappeared about −4.3 mm from bregma. In the rostrocaudal direction, the VPM was represented by 22-26 consecutive 60 μm thick sections when cut after postfi xation with 15-20% sucrose. In each section, the position of the "tip", i.e., the dorsolateral pole of the VPM, was determined, and its distance from the midline and bregma measured. For alignment of coronal sections, the distance from the VPM tip to bregma and to midline appeared suffi cient.

PREPARATION OF OBLIQUE SLICES AND OF AN OBLIQUE CANONICAL MAP OF THE VPM
After overnight postfi xation, entire rat brains were cut into two hemispheres, and left in the postfi xation solution for an additional 24 h. The dorsolateral and ventromedial poles of each hemisphere were then cutoff at an angle of 50° to the horizontal plane, as previously indicated (Haidarliu and Ahissar, 2001). When cut correctly, the two parts of the hippocampus (dorsomedial and ventrolateral) were visible in the sectioning plane, and were separated by a fi eld that stained intensively for CO and contained the corpora geniculata. Usually, the VPM started in slices 1 mm deeper than the beginning of the corpora geniculata, and continued in oblique slices for another 2.6-3.0 mm. In oblique sections, clear compartmentalization of the vibrissal part of the VPM was observed for about half of the VPM, starting from its dorsolateral pole, i.e., from the straddlers in the part represented by macrovibrissae, and was preserved until the parvicellular part of the ventral posterolateral thalamic nucleus (VPLpc) appeared in the slices adjacent to the most ventrocaudal sector of the VPM. In the rat brain atlas of Paxinos and Watson (1998), the VPM contour in the horizontal plane can be characterized by a simple curve. We found that the clearest and most representative images of the vibrissal part of the VPM correspond to the arcs 3-5 of the barreloid fi eld ( Figure 1A). In such oblique slices, the contours of the entire VPM, and of individual barreloids were manually outlined. The contours of the VPM thus obtained were superimposed, rotated, and aligned, and an average contour was computed for this set of curves ( Figure 1B, red lines). It can be seen that VPM has a simple outline, and its shape can be considered as an asymmetric ellipse, with the major axis (j) directed rostrocaudal, and the minor axis (n), directed from dorsomedial to ventrolateral ( Figure 1C).
This averaged VPM contour, with the border outlined between the VPMdm and VPMvl ( Figure 1C, solid black lines), was used as a canonical image that represents a valid portrayal of the VPM compartments for translation of functional sites from oblique to coronal sections. The correspondence of the canonical image to the real relationships between VPM compartments in the oblique plane was studied by its superimposition on consecutive oblique sections of the VPM. The canonical image satisfactory fi ts both the VPMdm and VPMvl compartments in the oblique slices, starting from arc 3 until the appearance of most of the thin barreloids. Thus, structural relationships between the VPMdm and VPMvl compartments, which were revealed and mapped in the canonical map, are maintained in oblique sections of the VPM for ∼1 mm along its oblique axis.

TRANSLATION OF THE BORDER BETWEEN THE VPMdm AND VPMvl FROM THE OBLIQUE TO THE CORONAL PLANE
Previously, we proposed a method for translation lesion coordinates from the coronal to oblique plane (Yu et al., 2006). Here, we propose a method of coordinate translation, from the oblique to coronal plane, that consists of consecutive determinations of the position of borderline fragments that correspond to each of the consecutive oblique slices of the dorsolateral part of the VPM. The vertical solid line b 1 (Figure 2A) corresponds to the 13th coronal slice of the VPM ( Figure 2B). For clarity, a magnifi ed contour of the VPM from the coronal slice 13 ( Figure 2B) is depicted in Figure 2C, and the position of the oblique slice relevant to canonical image (Figure 2A) is marked by the solid line b 2 . For coordinate translation, the border between the VPMdm and VPMvl in the 13th coronal slice at the level of arc 3 (x 1 in Figure 2C) must be located. The position of each of 24 consecutive coronal slices along the length of the rostrocaudal extent of the VPM is indicated by the x-axis in Figure 2A. The VPMdm extent (a 1 ) is measured as the distance from the VPM/POm border to the VPMdm/VPMvl border; b 1 is the diameter of the VPM in this oblique slice. The length of the core of the barreloids in coronal slice 13 is derived by a 2 = a 1 × b 2 /b 1 . The entire length of the border between the VPMdm and VPMvl in coronal slice 13 could be determined by performing this procedure on all, or a subset of, consecutive oblique slices of the vibrissal subdivision of the VPM. In each oblique slice, the distances from the VPM/POm border to the ventrolateral end of the barreloid core (denoted as a 1 ), and to the VPM/VPL border (denoted as b 1 ), were measured, and the value for the distance a 1 was marked on a relevant image of the VPM in the coronal plane. Since segregation of the vibrissal part of the VPM into the VPMdm and VPMvl can be clearly seen after oblique sectioning of the rat brain at an angle of ∼50° to the horizontal plane, from dorsomedial to ventrolateral, and histochemical staining for CO activity (Haidarliu and Ahissar, 2001;Yu et al., 2006), these two VPM compartments can be mapped for all oblique consecutive images through the vibrissal part of the VPM. In the rostrocaudal direction, the oval, and almost symmetric, shape of the VPM, with two clearly separated compartments in oblique slices, is conducive for translation of the position of the two compartments to the coronal plane.

APPEARANCE OF VPM COMPARTMENTS IN AN OBLIQUE CUTTING PLANE
In oblique rat brain slices, cut dorsomedial to ventrolateral at an angle of 50° to the horizontal plane, staining for CO activity visualized barreloids arranged in arcs. In such slices, the VPM is easily recognized, with the dorsolateral end of the VPM becoming visible as a structure strongly stained for CO activity, medial to the reticular nucleus (Rt) and VPL. A series of slices that includes 6 (nonconsecutive) of 34 consecutive oblique slices through the right VPM (ventral view) of an adult rat is shown in Figure 3A. In slice 1, representations of four straddlers, together with more laterocaudally located supraorbital (SO) vibrissa representations are seen. The barreloids that represent straddlers have similar orientations, with their short axes directed rostrocaudal and their long axes directed ventrolateral. In adult rats, the rostrocaudal diameter of the cores of straddler representing barreloids varied from 180 to 220 μm, and the mediolateral length varied from 400 to 500 μm (data not shown). The 4th arc of vibrissal barreloids is represented in slice 6. Slices 2-6 contained representations of the fi rst four arcs of mystacial vibrissae, with fi ve barreloids present in each arc. Row E in slices 2-6 is composed of the most curved and longest barreloids, which form the rostral, and part of the lateral, border of the VPM, and which determine the convexity of the rostral contour of the VPM. In this mystacial vibrissa representing part of the VPM, the outlines of individual barreloids arranged in arcs ( Figure 3B) can be determined, and the size gradient of barreloids, which were previously described (Haidarliu and Ahissar, 2001) is clearly seen. Slice 16 contains thin barreloids. These barreloids represent small hairs and hairy buccal pads rostral and ventral to mystacial vibrissae, respectively.
The cores of large barreloids (which represent macrovibrissae) and of thin barreloids (which represent microvibrissae and other face regions) occupy the dorsomedial part of the VPM. The laterocaudal part of the VPM contains the "tails" of the barreloids. Entire tails are not seen in individual oblique sections cut at 50° to the horizontal plane, because of their curvilinear confi guration, as shown by Pierret et al. (2000). In fact, only short fragments of tails that belong to barreloids seen in preceding slices are represented in these oblique slices. The VPMvl appears as a narrow strip at the level of the 1st barreloid arc in the fi rst few slices, and typically becomes wider in the next 14-16 (60 μm thick) slices, with a length up to ∼1.5 mm along the ventrolateral border of the VPM.
At the level of the VPM represented by slice 22, thin barreloids are seen, but only in the rostral part of the VPM, and do not seem to possess tails. Instead, the ventrolateral parts of structures extensively stained for CO activity are present in the VPLpc, which separates the VPM from the medial lemniscus (ml). Further ventromedially (e.g., slice 28), oblique slices contain the VPMpc and VPLpc, which stain homogenously for CO activity. The fi nal slices (see slice 34) contain only the VPMpc, which stains more extensively for CO activity than surrounding tissues. Contours of the VPM in relation to oblique slicing ( Figure 3A) are depicted in Figure 3B. Three vertical lines cross these contours at −2.56, −3.60, and −4.20 mm caudal to bregma, and correspond to the coronal positions of contours shown in Figure 3C. At −2.56 mm caudal to bregma, coronal slice 6 contains only core components of the VPM. At −3.60 mm caudal to bregma, coronal slice 14 also contains cores of barreloids, but its ventrolateral part is occupied by the tail compartment, the VPMvl. At −4.20 mm from bregma, more than half of the mediolateral length of the VPM in coronal slice 22 is occupied by the VPMvl. In oblique slices of young rat brains that were stained for CO activity (Figure 4A), and then stained with cresyl violet (Figure 4B), the border between the VPMdm and VPMvl, as well as the septa between barreloids in arcs, are clearly seen as areas poorly stained for CO and with low density of cell bodies. In corresponding and similarly stained oblique sections of adult rats, the cores of barreloids, as well as the border between the VPMdm and VPMvl, and the septa between the barreloids, are not as clear (Figures 4C,D). In the VPMvl, tails of barreloids can appear as small patches stained for CO activity, but with no regular pattern.

APPEARANCE OF THE VPMdm AND VPMvl IN CORONAL SLICES
In consecutively-cut coronal slices stained for CO activity, the VPM is distinguishable along its whole rostrocaudal length (see Figure 5A). For viewing progressive relationships between the VPMdm and VPMvl in the rostrocaudal direction, positions of coronal cuttings through the VPM (according to delineations by Paxinos and Watson, 1998) are shown in an oblique canonical image of the VPM (Figure 5C), along with corresponding coronal slices (Figure 5A), and enlarged contours of both the VPMdm and VPMvl (Figure 5B). In the most rostral slices, the VPM fi rst appeared as an oval dark-brown spot about −2.3 mm caudal to bregma (slice 1 in Figure 5A), and was surrounded by a less intensively stained VPL in the ventrolateral direction, and by the ventrolateral thalamic nucleus in the dorsomedial direction. In more caudal slices, the size of the VPM rapidly increased, becoming maximal between −3.3 and −3.6 mm caudal to bregma (slices 12-15 in Figure 5A). Note that the consecutive rostral slices (slices 1-6) contain only the cores of barreloids (VPMdm). The tails, i.e., VPMvl, fi rst appeared as a narrow strip at the border between the VPM and VPL (see slice 10), which continued to increase in more caudal slices ( Figure 5B).

MORPHOLOGICAL AND FUNCTIONAL CHARACTERISTICS OF THE VPMdm AND VPMvl
In the rostral part of the VPM (slices 1-6 of the VPM in Figure 5B), the mediolateral extent of the VPM belongs only to the VPMdm. However, in the caudal part of the VPM, more than half of the mediolateral extent of the VPM belongs to the VPMvl. Since cytoarchitectonic subdivisions of the VPM cannot be observed in Nissl-stained coronal slices or slices stained for CO activity alone (Haidarliu and Ahissar, 2001;Land and Simons, 1985;Pierret et al., 2000), it cannot be determined to which compartment (dm or vl) a lesion in the ventrolateral half of the VPM belongs (see slices 9 and 16 in Figures 6A,B, respectively). In these examples, each slice contains a lesion indicated by an arrow, and both lesions are closer to the border with the VPL than the border with the POm. The locations of lesions in these slices were translated to canonical images in the oblique cutting plane (Figures 6C,D). The lesion in Figure 6A appeared to be located in the core of a barreloid in row D. In fact, the principal whisker identifi ed for this recording site was D3. The location of the lesion in Figure 6B corresponded to the VPMvl, and the neurons recorded by that electrode responded to stimulation of two whiskers (C1 and C2). The contours of the VPM, and the lesion locations for Figures 6A,B are depicted in Figures 6E,F, respectively. Since the VPMvl compartment of Figure 6F extends more medially than that of Figure 6E, the  5 mm (A,B), and 1 mm (C,D).
A B C D lesion in it was localized in the VPMvl compartment, whereas that of Figure 6E, although a similar distance from the POm border, was localized in the VPMdm. The activities of the neurons recorded from these two VPM sites during artifi cial whisking (Szwed et al., 2003) are shown in Figures 6G,H, respectively. When extracellular recordings were performed from these sites during whisking in air and during object touch, neuron(s) from the site depicted in Figure 6A displayed a Whisking/Touch response pattern (W + T), characteristic of VPMdm neurons, while neuron(s) recorded from the site depicted in Figure 6B displayed a Touch response pattern (T), characteristic of VPMvl neurons (Yu et al., 2006).
Our results demonstrate that whether or not an electrode tip is in the VPMdm or VPMvl cannot be determined by the distance of a recording site from the border between POm and VPM. For example, the recording sites in Figure 6A (slice 9 from rostral) and Figure 6B (slice 16) are approximately the same distance from the POm/VPM border, but the characteristics of their responses were typical of two different VPM compartments: the VPMdm and VPMvl, respectively (Figures 6G,H).

DISCUSSION
We describe, for the fi rst time, the border between the VPMdm and VPMvl in consecutive coronal slices of rat brains. This border can now be included in standard rat brain atlases, and will facilitate analysis of physiological and anatomical data according to functional subdivisions of the rat somatosensory thalamus. Construction of the dm/vl border in the VPM was derived from non-standard oblique slices, in which the border was identifi ed anatomically, using a normalized linear coordinate transformation. In oblique, dorsomedial to ventrolateral slices of young rat VPM, septa that separate the core from the tails of macrobarreloids were revealed for the fi rst time. These septa exhibit weak CO activity, and contain sparse cell bodies (see Figure 4). Thus, the two compartments (dm, which contains cores of barreloids, and vl, which contains the tails) of the VPM can be easily differentiated in young rats. As rats mature, the septa in their VPM become less clear. In adult rats, the septa between the cores and tails of barreloids are narrow, and contain more axonal bundles than neighboring barreloid cores or tails. The septa contain myelinated fi bers that fulfi ll a conductive function. Other functions of septa in the VPM were discussed by Pierret et al. (2000) who specifi ed the region between the VPMdm and VPMvl as a transition zone that contains cells that may receive convergent inputs from both PrV and SpVi afferents. These authors concluded that the transition zone was "ill-defi ned" with regard to both the topographic distribution of trigeminal inputs and the dendroarchitecture of the relay cells. In oblique slices that revealed both barreloid arcs (see Figures 3A and 4) and entire barreloid fi elds (Figures 7A-F), septa between individual barreloids along the arcs, as well as along the rows, were clearly seen in both young and adult rats. Interbarreloid septa were fi rst described in the VPM of mice by Van der Loos (1976), who occasionally observed a septum of low cell density similar to, but thinner than, the septa that separate the large cortical barrels. In the VB of neonatal rats, discrete curvilinear arrays of cells that are separated from each other by narrow, cell-sparse zones were described by Ivy and Killackey (1982), using retrograde transport of horseradish peroxidase. In rat VPM stained for CO activity, a series of segregated oval patches of intense CO activity that are separated from each other by narrow zones in which CO activity is considerably lower was observed by Land and Simons (1985). Land et al. (1995) concluded that the distinctive appearance of barreloids in oblique planes is partly caused by the arrangement of fi ber bundles entering and leaving the nucleus via the trigeminal lemniscus and internal capsule, and passing between individual rows and arcs. The functional signifi cance of interbarreloid septa may be related to the fact that they contain neuronal projections from the SpVi. These projections were revealed by rhodamine dextran injections into the SpVi (Williams et al., 1994).
In the present study, staining for CO activity revealed different patterns of neuronal organization within the VPM. The ventromedial part of the VPM, which contains small neurons and is known as the parvicellular part of the VPM (VPMpc), appeared as a homogenously and strongly stained sub-structure in the coronal and both oblique planes used (see Figures 3A and 7E,F). The VPMpc extended from ∼0.3 mm to ∼1.5 mm laterally from the midline. Detailed analysis of consecutive oblique slices of the rest of the VPM revealed a highly organized, dorsomedial compartment of the VPM (VPMdm) that contained the cores of barreloids, and a ventrolateral compartment (VPMvl) that contained the tails of barreloids. In oblique slices, in the dorsolateral to ventromedial direction, the entire VPMdm (along the "long axis" of the VPM) can be divided into two specifi cally organized parts: (1) a dorsolateral part (up to 1 mm in length), which contains macrobarreloids with transversal diameters of ∼0.1 mm along rows, and ∼0.2 mm along arcs, and which can be referred to as the "macrovibrissal part"; and (2) a more ventromedial  (A,B), during steady-state for the VPMdm (G) and VPMvl (H), respectively, to whisking in air (black) and against an object (red), relative to the time of protraction onset (t = 0). For both neurons, a raster display of single spikes accumulated from three randomly selected cycles from cycles 5-10 is depicted by the top graph. Peristimulus time histograms (PSTHs) computed for the entire steady-state period (cycles 5-10) are depicted in the middle. The horizontal angle of the principal whisker during a single cycle is depicted at the bottom; the ordinate denotes whisker angle, with full scale = 50°; traces were low pass fi ltered at 160 Hz. Contact times during touch trials are indicated by arrows. DM, dorsomedial; M, medial; R, rostral; T, touch signals; V, ventral; W + T, additive whisking and touch signals. Scale bars are 1 mm. of the VPM. In young rats, tissue components that stained for CO activity, especially cell bodies, were evenly distributed within each of the barreloids in the core compartment. In adult rats, many unstained strips of axonal bundles passed through the core of barreloids and the septa. The ventrolateral (vl) and caudal parts of the VPM, which contain multiple axonal bundles, and are not considered to display a typical barreloid arrangement, exhibit less CO activity. However, the VPMvl does contain barreloid continuations ("tails"), which are curved along their long axes and are visualized when cut at specifi c angles or anterogradely labeled with biotinylated dextran amine injected into the SpVi (Pierret et al., 2000). The shape of the VPMvl revealed by our measurements is consistent with the observations of Pierret et al. (2000) that when SpVi terminal fi elds are visualized in coronal sections of the VPM with biotinylated dextran amine, the VPMvl is thicker caudally, and narrows rostrolaterally (see also Figures 3 and 5). Injection of biotinylated dextran amine in the infragranular layers of the rat S2 reveal corticothalamic terminals in consecutive coronal slices (Bokor et al., 2008), the distribution of which appears to be within the boundaries of the VPMvl determined in the present study.
Of the three VPM parts (dorsolateral, intermediate, and ventromedial), the intermediate one seems to be the most complicated structurally and functionally. The dorsolateral portion of the intermediate part contains thin barreloids, which represent microvibrissae and hairy buccal pads. More ventromedially, barreloids are observed only in the rostral part of the intermediate portion (Figure 3A, slice 22), which is separated from the part, 1.2-1.5 mm in length, that extends between the macrovibrissal part and VPMpc, and which contains many thin barreloids (with diameters ≤0.1 mm), and which can be referred to as the "intermediate part." The highly reproducible appearance of VPM compartments facilitated our proposal of a model of the compartmentalization of the rat VPM (Figure 8). Each compartment is illustrated with typical oblique sections (slices) that contain macrobarreloids (a and b), thin barreloids (c), or a homogenously-stained substrate (d). Structural peculiarities of the vibrissal and intermediate parts of the VPM were not usually visible in coronal slices, but were easily seen in oblique slices.
In this and our previous (Haidarliu and Ahissar, 2001) study, barreloids appear as rod-like structures, with almost constant values (∼100 × 200) μm for their two short axes, while that of the third is represented by a length gradient. The VPMdm, which contains the cores of barreloids, displays the most CO activity  (Figures 7C,D, arrows) that does not stain for CO activity. Such segregation may be related to the spatial separation of regions relaying different sensory modalities. Data about the exact location of these regions varies, depending on the sensory modality studied. For example, representations of periodontal mechanosensitive neurons occurred in the most ventral part of the intermediate portion of the VPM (Tabata et al., 2002), while oral nociceptive sensations were relayed mostly by the rostral half of the VPM Zhang et al., 2006). So the intermediate segment of the VPM differs from the other two VPM segments by relaying sensory pathways of different modalities.
In summary, mapping of the structural organization of the rat VPM was performed by cutting rat brains at different angles, staining brain slices for CO activity, and translating anatomical coordinates from one brain cutting plane to another. Extensive staining for CO activity was used to microscopically defi ne individual vibrissal representations and as to establish intrinsic organization of the VPM sub-nuclei. The present study revealed that the dorsolateral to ventromedial extent of the VPM consists of three specifi cally organized parts: (1) a macrovibrissal part that is composed of large barreloids that represent macrovibrissae of the mystacial pad; (2) an intermediate part that contains large number of thin barreloids that relay small vibrissae as well as head representations of different sensory modalities; and (3) a parvicellular part that is adjacent to the intermediate part of the VPM, and relays gustatory representations. In the vibrissal part of the VPM, we defi ned the border between the two sub-nuclei, the VPMdm and VPMvl, which was mapped onto images of coronal slices along the rostrocaudal extent of the VPM. Mapping of these sub-nuclei can augment rat brain atlases, facilitate target localization in relevant parts of the VPM, and enable association of neuronal function with its corresponding afferent pathway.