Posterior Nuclear Complex Research Articles

Widespread thalamic terminations of fibers arising in the superficial medullary dorsal horn of monkeys and their relation to calbindin immunoreactivity.

The relay of pain fibers from the spinal and medullary dorsal horn in the thalamus has become a controversial issue. This study analyzed the relationship of fibers arising in lamina I to nuclei in and around the caudal pole of the ventral posterior nuclear complex and especially to a zone of calbindin-dense immunoreactivity (VMpo) identified by some authors as the sole thalamic relay for these fibers. We show that the densest zone of calbindin immunoreactivity is part of a more extensive, calbindin-immunoreactive region that lies well within the medial tip of the ventral posterior medial nucleus (VPM), as delineated by other staining methods, and prove that the use of different anti-calbindin antibodies cannot account for differences in interpretations of the organization of the posterior thalamic region. By combining immunocytochemical staining with anterograde tracing from injections involving lamina I, we demonstrate widespread fiber terminations that are not restricted to the calbindin-rich medial tip of VPM and show that the lamina I arising fibers are not themselves calbindin immunoreactive. This study disproves the existence of VMpo as an independent thalamic pain nucleus or as a specific relay in the ascending pain system.

Trigeminal projections to thalamus and subthalamus in the hedgehog tenrec

The objective of the present study was the identification and characterization of the trigemino-diencephalic target areas in the Madagascan lesser hedgehog tenrec in order to get a more comprehensive view on the mammalian somatosensory thalamus, its evolution and representation in different species. Such an analysis has been considered important because in lower mammals the head and face are relatively well represented, but their ascending trigeminal projections have scarcely been analysed. Following injections of different tracer substances into the rostral and caudal portions of the trigeminal nuclear complex the most prominent area of termination was found in the medial ventroposterior nucleus. These projections were patchy and scarcely overlapped the region previously shown to receive spinal and dorsal column nuclear afferents. On the basis of the laterality and the intensity of the projections, two subdivisions were distinguished, the principal portion and the accessory portion receiving a dense contralateral and a weak bilateral input, respectively. They were considered equivalents to the magnocellular and parvocellular subdivisions of the medial ventroposterior nucleus in more differentiated mammals. In the latter species, however, the overlap between trigeminal and parabrachial fibres appears less extensive than in the tenrec. In addition, a weak bilateral projection was shown from the caudal trigeminal nucleus to the caudal and dorsal subdivision of the nucleus submedius. There was little, if any evidence for a trigeminal projection to the intralaminar nuclei and we failed to identify a correlate to the posterior nuclear complex of higher mammals. On the other hand, there was a distinct contralateral projection to the ventral portion of the zona incerta. This projection was of similar strength as the projection to the medial ventroposterior nucleus; it supports the notion that the zona incerta may play a crucial role in relaying trigeminal information.

Functional anatomy of the thalamus in the blind mole rat Spalax ehrenbergi: an architectonic and electrophysiologically controlled tracing study.

The occipital cortex of the naturally blind mole rat, Spalax ehrenbergi, is occupied by an area of somatosensory representation. To date, no visual cortex has been identified electrophysiologically. In order to determine whether there are corresponding modifications in the thalamus, thalamocortical connections were studied with neuroanatomical tracing methods. Three different fluorescent tracers were injected under electrophysiological control into distinct cortical areas. Injections into the somatosensory head/face and hindlimb/trunk areas of representation revealed a posteromedial ventral nucleus and a posterolateral ventral nucleus, respectively. Additional somatotopic labeling was found in an area dorsomedial to the two ventral nuclei. This structure may be equivalent to the posterior nuclear complex in the laboratory rat. Injections into the auditory cortex of the mole rat resulted in labeling of the medial geniculate body. In contrast to the situation in the laboratory rat, in which a prominent dorsolateral geniculate body and a ventrolateral geniculate body assume dorsolateral positions, the somatosensory thalamus of the mole rat almost reaches the dorsolateral surface. This finding is corroborated by the results of the architectonic study, which failed to reveal a differentiated lateral geniculate body. Our observations suggest that the thalamocortical visual system in the mole rat is minute, whereas the somatosensory system is expanded. This situation fits the mode of life of this subterranean animal, for which touch is more important than vision.

Somatovisceral projections from spinal cord and dorsal column nuclei to the thalamus in hedgehog tenrecs.

In order first to overcome the difficulties in understanding the increasing amount of information available regarding the mammalian somatosensory thalamus, and then to correlate the findings among different species and integrate them into a general concept of thalamic organization, the present study investigated the spinothalamic and medial lemniscal projections in Madagascan hedgehog tenrecs (Echinops telfairi and Setifer setosus). Tracer substances were injected into the dorsal column nuclei and into spinal segments at various levels; additional injections were made into the inferior colliculus. The ascending somesthetic projections were to predominantly contralateral posterolateral target areas, and were almost mirror-like on both sides to intralaminar and medial thalamic nuclei. The densest and most extensive projections, originating mainly from the high cervical spinal cord and the dorsal column nuclei, reached the posterolateral thalamus caudal to the lateral geniculate nucleus. This region was difficult to subdivide cytoarchitecturally; nevertheless, on the basis of its labeling pattern, several subdivisions could be described and preliminary named. Some of them compared tentatively with the internal portion of the medial geniculate nucleus (GM) and the ventral posterior nuclear complex (VPC) in more differentiated mammals. The most prominent subdivision, however, located subjacent to the lateral surface of the brainstem, was shown to receive additional fibers from the inferior colliculus. This region might be considered a further subdivision of GM, VPC, a perigeniculate area, and/or a region of its own not comparable at present, with thalamic regions in other mammals. On the other hand, it may also be a remnant of the hypothetical, diffuse multimodal region from which GM and VPC have possibly evolved.(ABSTRACT TRUNCATED AT 250 WORDS)

Spinothalamocortical projections to the secondary somatosensory cortex (SII) in squirrel monkey

Anterograde labeling of the cervical spinothalamic tract was combined with retrograde labeling of thalamocortical cells projecting to the hand region of the second somatosensory cortex (hSII) to identify likely sites in the thalamus for processing and transmitting nociceptive information to hSII. Anterograde labeling of terminals was done with 2% WGA-HRP injections in the cervical enlargement; thalamocortical cells were retrogradely labeled with fluorescent tracers. In one experiment, the contralateral primary somatosensory cortex hand region (hSI) was injected to provide a direct comparison with hSII thalamic label. Both labeled cells and terminal-like structures were visualized in single thalamic sections and their numbers and positions quantitatively analyzed. The number of labeled cells within 100 microns from the STT terminals were counted as overlapping cells. Four thalamic nuclei, ventroposterior inferior (VPI), ventroposterior lateral (VPL), posterior nucleus (PO) and centrolateral nucleus (CL) combined to contain 86.5% of all hSII-projecting overlapping cells. Of all hSII-projecting thalamic overlapping cells, VPI contained the largest number (36.4% of the total) followed by the anterior portion of the posterior nuclear complex (POa; 20.4%), VPL (18.3%) and CL (11.4%). Results of the hSI injection show a different pattern of overlap in agreement with our earlier study. The relative distribution of overlapping cells was dependent on the antero-posterior position of the SII injections. The most anterior injections resulted in small numbers of labeled cells, with the majority of overlapping cells located in PO and CL. The more posterior injections resulted in overlapping cells mainly in VPI and VPL. The results indicate that, in the squirrel monkey, VPI, VPL, POa and CL relay nociceptive information from the spinal cord to the second somatosensory cortex.

Projections of cholinergic and non-cholinergic neurons of the brainstem core to relay and associational thalamic nuclei in the cat and macaque monkey

The projections of brainstem core neurons to relay and associational thalamic nuclei were studied in the cat and macaque monkey by combining the retrograde transport of wheat germ agglulinin conjugated with horseradish peroxidase with choline acetyltransferase immunohistochemistry.All major sensory (medial geniculate. lateral geniculate, ventrobasal). motor (venlroanterior. ventrolateral. ventromedial), associational (mediodorsal, pulvinar, lateral posterior) and limbic (anteromedial.,interoventral) thalamic nuclei of the cat were found to receive projections from cholinergic neurons located in the peribrachial area of the pedunculopontine nucleus and in the laterodorsal tegmental nucleus as well as from non-cholinergic neurons in the rostral (perirubral) part of the central tegmental mesencephalic field. Specific relay nuclei receive less than 10%) of their brainstem afferents from non-cholinergic neurons located at rostral midbrain levels and receive 85 96% of their brainstem innervation from a region at midbrain pontinc junction where the cholinergic perihrachial area and laterodorsal tegmental nucleus are maximally developed. of the total number of horseradish peroxidase-positive brainstem neurons seen after injections in various specific relay nuclei, the double-labeled (horseradish peroxidase + choline acetyltransferase) neurons represent approximately 70 85%. Three to eight times more numerous horseradish peroxidase-labeled brainstem cells were found after injections in associational (mediodorsal and pulvinar lateral posterior complex) and diffusely cortically projecting (ventromedial) thalamic nuclei of cat than after injections in specific relay nuclei. The striking retrograde cell labeling observed after injections in nuclei with associative functions and widespread cortical projections was due to massive afferentation from non-cholinergic parts of the midbrain and pontine reticular formation, on both ipsi- and contralateral sides.After wheat germ agglutinin horseradish peroxidase injections in the associative pulvinar lateral posterior complex and mediodorsal nucleus of Macaca sylvana.. 45 50% of horseradish peroxidase-positive brainstem peribrachial neurons were also choline acetyltransferase-positive. While cells in the medial part of the cholinergic peribrachial area were found to project especially towards the pulvinar lateral posterior nuclear complex in monkey, the retrograde cell labeling seen after the mediodorsal injection was mostly confined to the lateral part of both dorsal and ventral aspects of the peribrachial area.These findings support the role played by cholinergic and non-cholinergic hrainstem thalamic projections in various tonic and phasic events of behavioral slates of vigilance.

Retinal projections in two Australian polyprotodont marsupials: kowari, Dasyuroides byrnei, and fat-tailed dunnart, Sminthopsis crassicaudata (Dasyuridae).

Retinal projections were examined in two small dasyurids, the kowari and the fat-tailed dunnart, following injections of 3H-proline into one eye. In both animals retinal fibres terminate in the dorsal and ventral lateral geniculate nuclei (LGd, LGv), the lateral posterior nuclear complex, the pretectum, the superior colliculus, the suprachiasmatic nucleus of the hypothalamus and the nuclei of the accessory optic system. The lateroposterior thalamic complex and the accessory optic nuclei receive projections from the contralateral eye only; the remaining centres receive bilateral inputs. Both LGd contain an undifferentiated beta or medial segment and an alpha or lateral segment that comprises further cellular sublaminae, 4 in the kowari and 3 in the dunnart. There is substantial overlap of crossed and uncrossed terminals in both segments, though in each animal a narrow cell lamina next to the optic tract receives only crossed projections and the lateral part of the beta segment receives only uncrossed projections. There is a cell-sparse zone within the alpha segment that receives a predominately uncrossed projection in the kowari and a crossed projection in the dunnart. In both marsupials the density of crossed and uncrossed terminals is equal, a feature of dasyurid quolls but not of another dasyurid, the Tasmanian devil. Additionally, retinal terminals do not form dense clusters within the LGd neuropil. This feature is characteristic of quolls, but not of other mammals, marsupial or placental, all of which display LGd terminal clusters. These findings suggest that the functional organisation of the LGd in these dasyurids may differ from that found in other marsupials.

SII-projecting neurons in the rat thalamus: a single- and double-retrograde-tracing study.

Experiments were performed on adult albino rats, using single-labeling (free horseradish peroxidase [HRP] or wheatgerm agglutinin conjugated to HRP [WGA:HRP]) and double-labeling (fluorescent dyes) techniques to investigate the thalamic projections to the secondary somatosensory cortex (SII) and to demonstrate the presence and location of thalamic neurons projecting to both the primary somatosensory cortex (SI) and SII by way of branching axons. In single-labeling experiments, the tracer was injected in SI or SII with or without electrophysiological control; in double-labeling experiments, fast blue and diamidino yellow were injected into the electrophysiologically identified forelimb areas of SI and SII. Single-tracer experiments showed that after injections in SI, focused in the forelimb representation area, retrogradely labeled neurons were present mainly in the ventral third of the nucleus ventralis posterolateralis (VPL) and in the anterior part of the posterior nuclear complex (PO); labeled neurons were also present consistently in the caudal portion of PO. Injection of tracers in the forelimb or forelimb and hindlimb representation areas of SII resulted in labeling of neurons in the posterior part of PO and in the caudal part of VPL. Double-labeling experiments confirmed the distribution of neurons projecting to SI or to SII, as observed in single-labeling experiments. Some neurons labeled with both tracers were also present. These neurons are interpreted as projecting to both SI and SII by means of axon collaterals and were observed in areas of overlap of the two single-labeled population of neurons--that is, at the border between PO and the ventroposterior complex, and in the medial part of caudal PO. Comparison of these data with those obtained after injections of tracers in SI and SII of cats (Spreafico et al., 1981b) suggests that in both species thalamic neurons projecting to these two areas are largely segregated, though partially overlapping; and that thalamic neurons projecting simultaneously to SI and SII, modest in number in cats, are even sparser in rats.

Cytoarchitecture of the dorsal thalamus of the rat

Although several neuroanatomical studies have previously described various subdivisions of the rat thalamus, no comprehensive description of the entire thalamus accompanied by photomicrographs has been available. To provide such a description, the Cytoarchitecture of the normal rat thalamus was studied in the coronal plane using a series of celloidin embedded, Nissl-stained 33 μm sections spaced 400 μm apart. Using the criteria of cell packing density, relative cell size, and the presence or absence of fibers, the thalamus can be subdivided into a ventral nuclear complex which includes the ventrolateral, ventromedial, and ventrobasal nuclei; the intralaminar nuclei which include central medial, central lateral, paracentral and parafascicular nuclei; the midline nuclei which include the medioventral, paratenial, rhomboid, paraventricular, and submedial nuclei; the anterior nuclear group which include the anterodorsal, anteroventral, and anteromedial nuclei; the mediodorsal nucleus; the lateral nuclear complex including both lateral posterior and lateral dorsal; the posterior nuclear complex; the reticular nucleus; and the diencephalic-mesencephalic junction. The terminology used is based on previous studies.

Ascending projections from the nucleus of the brachium of the inferior colliculus in the cat.

Ascending projections from the nucleus of the brachium of the inferior colliculus (NBIC) in the cat were studied by the autoradiographic tracing method. Many fibers from the NBIC ascend ipsilaterally in the lateral tegmentum along the medial border of the brachium of the inferior colliculus. At midbrain levels, fibers from the NBIC end in the superior colliculus, the pretectum, the central gray and the peripeduncular tegmental region bilaterally with ipsilateral predominance. NBIC fibers to the superior colliculus are distributed densely to laminae VI and III throughout the whole rostrocaudal extent of the colliculus. In the pretectum, NBIC fibers terminate in the anterior and medial nuclei and the nucleus of the posterior commissure. NBIC fibers to the dorsal thalamus are distributed largely ipsilaterally. Many NBIC fibers end in the dorsal and medial divisions of the medial geniculate body, but few in the ventral division. The NBIC also sends fibers to the suprageniculate, limitans and lateralis posterior nuclei and the lateral portion of the posterior nuclear complex; these regions of termination of NBIC fibers constitute, as a whole, a single NBIC recipient sector. Additionally, the NBIC sends fibers to the centralis lateralis, medialis dorsalis, paraventricular and subparafascicular nuclei of the thalamus.

The thalamostriatal projection in the cat.

The organization of the projections from the intralaminar and other thalamic nuclei to the caudate nucleus (CD), putamen (PU), nucleus accumbens (Acc), and olfactory tubercle (TO) were examined in the cat by autoradiography after deposits of 3H-amino acids in individual thalamic nuclei and by retrograde cell labeling after intrastriatal deposits of wheat-germ-conjugated horseradish peroxidase. All of the rostral intralaminar nuclei, here considered to include the central lateral (CL), paracentral (PC), central medial (CeM), and rhomboid nuclei (Rh), project to the striatum. Projections closely associated with those of the rostral intralaminar group arise from cells of the paraventricular nucleus (PV) and a region lateral to the stria medullaris. These nuclei, which roughly form a ring around the mediodorsal nucleus, project in a highly particular, but loosely arranged topographic pattern to all parts of the striatum. The medially located cells in Rh, PV, and those alongside the stria medullaris project mainly to medial parts of Acc and CD; the dorsolaterally located cells of CL project mainly to the dorsolateral parts of CD and PU; cells in PC and CeM project to progressively more ventral and medial parts of CD and PU, and the lateral part of Acc. Superimposed on this projection from the rostral intralaminar region is the projection from the caudal intralaminar group including the centromedian (CM), parafascicular (PF), and subparafascicular nuclei (subPF). Together these nuclei project in a loosely but specifically organized topography to the entire striatum. The lateral and dorsal parts of CD and PU receive fibers mainly from CM. Ventral and medial parts of CD and PU and Acc receive fibers mainly from PF; TO receives fibers from subPF and the ventral part of PF. Several nuclei in the lateral nuclear mass of the thalamus also project to particular parts of the striatum. Thus, cells in the rostromedial part of the ventral anterior nucleus project to the head of CD and some cells in the rostral part of the ventromedial nucleus project to the head of CD and to PU. Several cells scattered in the lateral posterior complex project to lateral parts of the head of CD, and cells in the rostral extension of the medial subdivision of the posterior nuclear complex project to lateral parts of the head and body of CD. Finally, several cells of the paratenial nucleus project selectively to Acc. These data provide a detailed map of the total thalamostriatal projection in the cat and, hence, form a basis for more specific functional questions about this poorly understood system.

Afferents to the cortical pupillo-constrictor areas of the cat, traced with HRP.

Afferents of the cortical pupillo-constrictor areas (PCAs) of the cat were studied using the horseradish peroxidase method. PCAs receive heavy cortical inputs from areas 7, 19, 21, the lateral suprasylvian area, the splenial visual area, and subcortically from the claustrum, the intralaminar nuclei, the pulvinar-lateral posterior nuclear complex.

Contralateral corticofugal projections to cat visual thalamus.

Contralateral corticofugal projections from visual cortical areas to thalamic nuclei were demonstrated in the cat using anterograde transport of tritiated proline. Thalamic nuclei receiving projections from contralateral visual cortex include both subdivisions of the lateral-posterior nucleus, the posterior nucleus of Rioch, and the posterior nuclear complex.

The cells of origin of the incertofugal projections to the tectum, thalamus, tegmentum and spinal cord in the rat: A study using the autoradiographic and horseradish peroxidase methods

Efferent projections of the zona incerta were examined in the rat using the autoradiographic and horseradish peroxidase methods, with special reference to the cytoarchitectonic structure of the zona incerta. Autoradiographic experiments showed that the incertofugal fiber systems reach ipsilaterally to the thalamus (lateral dorsal, central lateral, ventral lateral geniculate, parafascicular, subparafascicular and reuniens nuclei, and posterior nuclear complex), to the hypothalamus (dorsal, lateral and posterior hypothalamic areas), to the tectum (medial pretectal area, deep pretectal and pretectal nuclei, superior colliculus and periaqueductal gray) and to the midbrain tegmentum, pons and medulla oblongata (subcuneiform, cuneiform and red nuclei, nuclei of the posterior commissure and Darkschewitsch, interstitial nucleus of Cajal, pedunculopontine tegmental nucleus, oral and caudal pontine reticular nuclei, nucleus raphe magnus, gigantocellular reticular nucleus, pontine gray and inferior olivary complex). Contralaterally, incertal efferent fibers reach to the zona incerta. Cells of origin of the incertofugal fiber systems to the tectum, thalamus, tegmentum and spinal cord were examined using the retrograde horseradish peroxidase method. Cells of origin of the incertotectal pathway are located mainly in the ventral and caudal parts of the zona incerta and partly in the antero-polar, dorsal and postero-polar parts. Cells projecting to the thalamus (at least to the lateral dorsal and central lateral nuclei) are situated in the ventral and caudal parts of the zona incerta, but they are rare in the other incertal structures. Cells of origin of the incertotegmental system are located mainly in the dorsal, magnocellular and caudal parts and partly in the antero- and postero-polar parts, but they are not situated in the ventral part. Cells of the magnocellular part project more caudally to the medulla oblongata and spinal cord than those of the other parts of the zona incerta. Forel's field contains many cells projecting to the tegmentum. The results provide good evidence that the cells of origin of efferent projections are topographically organized and are related to cytoarchitectonic areas within the zona incerta.

The organization of thalamic projections to the parietal cortex of the Virginia opossum.

The thalamic projections to somatic sensory-motor (SSM) cortex and adjacent cortical areas of the Virginia opossum were studied using anterograde and retrograde axoplasmic transport techniques. Large injections of horseradish peroxidase and/or tritiated amino acids were made in the parietal cortex to identify all of the thalamic nuclei that are interconnected with this large cortical area. Very restricted injections were then made in physiologically identified subdivisions of SSM cortex, in the remaining posterior portion of parietal cortex, and in the anteriorly adjacent postorbital cortex. The results show that the parietal cortex is reciprocally connected with a number of thalamic nuclei. Different combinations of these thalamic areas project to specific subregions within the parietal field. All parts of the SSM cortex, which occupies the anterior four-fifths of parietal cortex, receive input from the ventrobasal complex (VB), the ventrolateral complex (VL), the central intralaminar nucleus (CIN), the central lateral nucleus (CL), and the ventromedial nucleus (VM). We could detect no segregation of VL and VB inputs in any part of SSM cortex. Projections from all of these thalamic nuclei, except VM, show at least some degree of topographic organization. Anterior-posterior strips of SSM cortex receive input from clusters of thalamic neurons that extend dorsoventrally and rostrocaudally through VB and VL. The posterior one-fifth of the parietal cortex (the posterior parietal area) receives input from VL, the posterior nuclear complex, and the lateral complex, as well as input from CL, CIN, and VM. Postorbital cortex receives input mainly from intralaminar, midline, and medial thalamic nuclei. We conclude that the projection field of VB in the parietal cortex coincides precisely with the first somatic sensory area (SI) as defined by single unit studies (Pubols et al., '76). The VB projection field also delineates the area of the first motor (MI) representation. Thus, there is no separation of SI and MI cortex in the opossum. The posterior parietal area lies outside of SSM cortex and has thalamic connections similar to the posterior parts of parietal cortex in other mammals.

Functional organization of the tectothalamic section of the transcollicular visual afferent channel

On the basis of the results of electrical stimulation of the optic tract and upper layers of the superior colliculus in cats anesthetized with pentobarbital maps were compiled of the distribution of evoked potentials of the posterior thalamic nuclear complex, including the pulvinar and n. lateralis posterior, posterior, suprageniculatus, and lateralis dorsalis. Functional projections of the superior colliculus and optic tract to the posterior thalamus were shown to differ from each other. In response to stimulation of the superior colliculus the distribution of projections was more regular than to stimulation of the tract. Fibers running from the optic tract occupy a smaller territory than fibers from the superior colliculus. It is suggested that the transcollicular afferent channel of the visual system is not reduced in the course of evolution but, on the contrary, it acquires connections with the younger thalamic formations of the brain and assume more complex functions.

The termination of the spinothalamic tract in the cat an experimental study with silver impregnation methods

The termination of the spinothalamic tract (STT) in the cat has been studied light microscopically in Fink-Heimer and Nauta impregnated sections. Following lesions of the STT at various rostrocaudal levels of the spinal cord the degenerating fibres in the thalamus and subthalamus were mapped, mainly in transverse sections. The cervicothalamic tract was not injured by the lesions. The spinothalamic fibres enter the diencephalon through the mesencephalic reticular formation and terminate in the following regions: the medial portion of the magnocellular part of the medial geniculate body (MGmc), the ventrolateral portion of the medial part of the posterior nuclear complex (POm), the caudolateral and medial parts of the zona incerta (ZI), the nucleus centralis medialis (CeM), the nucleus parafascicularis (Pf), the lateral part of the nucleus centralis lateralis (CL), the medial and rostrolateral parts of the nucleus ventralis lateralis (VL). To reach these regions the fibres pass through the nucleus centrum medianum (CM), the nucleus subparafascicularis (SPf) and the nucleus paracentralis (Pc). The fibres that terminate in the VL pass through Forel's field H1 and the external medullated lamina (EML). Conclusive results were not obtained concerning a termination in the CM. The spinothalamic fibres do not pass through nor terminate in the nucleus ventralis posterolateralis (VPL) and the nucleus reticularis (R). The VPL, defined as that portion of the ventral thalamus that receives terminal fibres from the dorsal column nuclei, has been found to extend rostrally only as far as Horsley-Clarke level anterior 10.5. The results strongly support the view that all the spinothalamic fibres terminate ipsilateral to their course in the ventral quadrant of the spinal cord. No signs of a somatotopical organization of the termination of the STT were found.

The thalamic projection of hypoglossal afferents in the rhesus monkey

The present experiments were designed to determine the location within the thalamus of the hypoglossal nerve afferent projection. Electrolytic lesions were placed within the ventral posterior nuclear complex of ten rhesus monkeys, all under barbiturate anesthesia, and the effects of the lesions on the cortical potentials evoked by stimulation of the contralateral lingual and hypoglossal nerves were observed. In addition, activity in response to hypoglossal and lingual nerve volleys was recorded from the ventral posterior nuclear complex. Both sets of data were consistent in indicating that hypoglossal afferents project to a restricted region of the nucleus ventralis posteromedialis which is confined to the anterodorsal portion of the nucleus. In contrast, the lingual nerve representation, as has been shown in other studies, occupies a much greater volume of VPM. The relationship between the lingual and hypoglossal nerve projections in VPM was discussed with respect to the relation shown to exist between superficial and deep modality projections in the nucleus ventralis posterolateralis.