Topographical projections from the cerebral cortex to the nucleus of the solitary tract in the cat

Summary The distribution of cerebral cortical neurons sending projection fibers to the nucleus of the solitary tract (NST), and the topographical distribution of axon terminals of cortico-NST fibers within the NST were examined in the cat by two sets of experiments with horseradish peroxidase (HRP) and HRP conjugated with wheat germ agglutinin (WGA-HRP). First, HRP was injected into the NST. In the cerebral cortex of these cats, neuronal cell bodies were labeled retrogradely in the deep pyramidal cell layer (layer V): After HRP injection centered on the rostral or middle part of the NST, HRP-labeled neuronal cell bodies were distributed mainly in the orbital gyrus and caudal part of the infralimbic cortex, and additionally in the rostral part of the anterior sylvian gyrus. After HRP injection centered on the caudal part of the NST, labeled neuronal cell bodies were seen mainly in the caudoventral part of the infralimbic cortex, and additionally in the orbital gyrus, posterior sigmoid gyrus and rostral part of the anterior sylvian gyrus. The labeling in the infralimbic cortex, orbital gyrus and anterior sylvian gyrus was bilateral with a predominantly ipsilateral distribution, while that in the posterior sigmoid gyrus was bilateral with a clear-cut contralateral dominance. In the second set of experiments, WGA-HRP was injected into the cerebral cortical regions where neuronal cell bodies had been retrogradely labeled with HRP injected into the NST: After WGA-HRP injection into the orbital gyrus, presumed axon terminals in the NST were labeled in the rostral two thirds of the nucleus bilaterally with an ipsilateral predominance. After WGA-HRP injection into the rostral part of the anterior sylvian gyrus, a moderate number of presumed axon terminals were labeled throughout the whole rostrocaudal extent of the NST bilaterally with a slight ipsilateral dominance. After WGA-HRP injection into the middle and caudal parts of the anterior sylvian gyrus, no labeling was found in the NST. After WGA-HRP injection into the caudal part of the infralimbic cortex, presumed terminal labeling in the NST was seen throughout the whole rostrocaudal extent of the nucleus bilaterally with a dominant ipsilateral distribution. After WGA-HRP injection into the posterior sigmoid gyrus, however, no terminal labeling was found in the NST. The results indicate that cortico-NST fibers from the orbital gyrus terminate in the rostral two thirds of the NST, while those from the infralimbic cortex and the rostral part of the anterior sylvian gyrus project to the whole rostrocaudal extent of the NST.     

A horseradish peroxidase study of the projections from the lateral reticular nucleus to the cerebellum in the rat

Summary The projection from the lateral reticular nucleus (LRN) to the cerebellar cortex was studied in the rat by utilizing the retrograde transport of horseradish peroxidase (HRP). In order to study the topographic features of this projection, small amounts of HRP were injected into various sites in the cerebellar cortex. The results demonstrated that the caudal lobules of the anterior lobe vermis tend to receive afferents from the medial LRN and the rostral lobules of the vermis receive afferents from more laterally situated cells. Lobules IV and V receive inputs primarily from the magnocellular division of the LRN of both the ventromedial and dorsolateral parts of the LRN, while lobules II and III receive inputs mainly from cells which lie in the border area between the parvocellular and magnocellular division of the ventromedial part. Following injections within various areas of the posterior lobe vermis, the results indicated that lobule VIII receives the most abundant projection from the LRN and that the cells of origin are present within the parvocellular and the adjacent part of the magnocellular division throughout the rostrocaudal extent of the LRN. Following injections within lobules VI and VII, few labelled cells were found and they tended to lie within the rostral two-thirds of the magnocellular division. Little or no projection from the LRN to lobule IX was evident. The hemispheres were found to receive a modest projection from the dorsal aspect of the LRN. The projection to lobulus simplex originates mainly from the caudal two-thirds of the magnocellular division, while the projection to the ansiform and paramedian lobules originates mainly from the dorsal aspect of the rostral two-thirds of the magnocellular division. Finally, there appears to be extensive overlapping of the orgins of all three projections to the cerebellar cortex studied, and this occurs within the central area of the magnocellular division throughout the rostrocaudal extent of the LRN.     

Topographical organization of the thalamic projections to the cortex of the anterior ectosylvian sulcus in the cat

Experimental Brain Research - The thalamic afferents of the anterior ectosylvian sulcal region were studied in the cat using retrograde axonal transport of horseradish peroxidase. Following...     

Cortical projections to the periaqueductal grey in the cat: a retrograde horseradish peroxidase study

Stereotaxic fluid microinjections of horseradish peroxidase into different parts of the rostral and caudal periaqueductal grey (PAG) in cats have provided substantial retrograde evidence that the somatosensory cortex (I and II), frontal cortex, insular and cingular cortex are the principal sources of cortical-PAG projections. The somatosensory cortex II projects to all the regions of the rostral and caudal PAG. The frontal cortex projects to dorso-lateral quadrant of the PAG. The same projections were determined from insular and cingular cortex to PAG. The findings revealed a morphological substratum of corticofugal effects on PAG.     

Subcortical crossed axonal projections to the caudate nucleus of the cat: a double-labelling study

The anatomical organization of the interhemispheric projections of subcortical caudate nucleus (Cd) input neurons in the cat was assessed by the retrograde axonal transport of multiple marker substances. These double-labelling methods indicated the existence of two types of subcortical afferents to the Cd. (1) Uncrossed projections terminating in the ipsilateral Cd (but not the contralateral Cd) originated from the globus pallidus, thalamus, substantia nigra and midbrain raphe nuclei. The uncrossed axons provided the vast bulk of the subcortical Cd inputs. (2) Crossed projections terminating in the contralateral Cd (but not the ipsilateral Cd) originated from the substantia nigra and raphe nuclei. The crossed projections from the midbrain provided a very small Cd input compared to the crossed and divergent corticocaudate projections. Therefore, interhemispheric connections of the Cds may be subserved primarily by arrangement of corticocaudate projections. Monosynaptic interhemispheric subcortical inputs to the Cds are minor. Multisynaptic pathways could provide alternative, but less tightly coupled, interhemispheric linkages of the Cds.     

Topographical organization of the cerebellar cortical projection to nucleus interpositus anterior in the cat.

1. A new methodological approach for detailed study of the organization of the cerebellar corticonuclear projection was evaluated in barbiturate-anaesthetized cats. Extracellular field potentials were simultaneously recorded in nucleus interpositus anterior and in the forelimb area of the C3 zone, at the cerebellar surface. On electrical and natural stimulation of the forelimb skin, the evoked positive field potentials in the nucleus and the climbing fibre field potentials in the cerebellar cortex had similar characteristics, indicating that the nuclear potentials were related to climbing fibre activity. 2. Application of a local anaesthetic to the cerebellar surface reversibly diminished the positive field potentials in the nucleus, demonstrating that the potentials were dependent on cerebellar cortical activity. It was thus concluded that the positive field potentials were mainly generated by climbing fibre-activated Purkinje cells and reflected synaptic inhibitory potentials in nuclear neurones. Accordingly, the positive field potentials in the nucleus could be used to reveal the termination area of Purkinje cells activated by a specific climbing fibre input evoked on peripheral stimulation. 3. The topographical organization of the cerebellar cortical projection to the forelimb part of nucleus interpositus anterior was then investigated by systematically mapping the cutaneous tactile and nociceptive 'receptive fields' of the positive field potentials at different sites in the nucleus. Five groups of receptive fields were distinguished and tentatively divided into a total of nineteen subgroups. 4. Each group of receptive fields corresponded to one or two of the previously described receptive field classes of climbing fibres to the C1, C3 and Y zones and was represented in a single area of the nucleus. Within each area there was an orderly representation of different receptive fields. The results suggest that microzones in the C1, C3 and Y zones with similar climbing fibre input project to a common set of neurones in nucleus interpositus anterior. 5. We propose a modular organization for the cerebellar control of forelimb movements through the rubrospinal tract. Each module would consist of a set of neurones in nucleus interpositus anterior and their afferent microzones in the C1, C3 and Y zones. A module would control a specific group of muscles and receive a homogeneous climbing fibre input related to the movement controlled.     

Cerebellar corticovestibular projections from lobule IX to the descending vestibular nucleus in the cat. A retrograde wheat germ agglutinin-horseradish peroxidase study

The distribution of Purkinje cells projecting to the descending vestibular nucleus was studied in lobule IX (uvula) of the cat by the retrograde wheat germ agglutinin-horseradish peroxidase method. In the transverse plane labeled Purkinje cells were seen diffusely within 1.0 mm from the midline and densely for 250-500 microns at around 1.0 mm lateral to the midline. Reconstruction of the distribution in the horizontal plane revealed that they were distributed in longitudinal areas extending in the apicobasal extent of lobule IX.     

Topographical projections from the thalamus to the putamen in the cat

Thalamic projections to the putamen (Put) in the cat were studied by the retrograde horseradish peroxidase method. Major thalamic projections to the Put originate from the midline and intralaminar nuclear regions including the centre médian-parafascicular complex (CM-Pf). The other thalamic projections to the Put arise mainly from the suprageniculate nucleus (Sg), magnocellular division of the medial geniculate nucleus (MGm), caudomedial part of the lateroposterior nucleus (LP) and ventrolateral part of the ventromedial nucleus (VM). The VM projects to the rostral Put, while the posterior thalamic regions (Sg, MGm, LP) project to the caudal Put.     

Cortical afferents to the prefrontal cortex of the cat: a study with the horseradish peroxidase technique.

Following horseradish peroxidase (HRP) injections into different areas within the prefrontal cortex (PFC) of the cat, labeled neurons were found in the cingulate and insular cortex. These results demonstrate that the cat's prefrontal cortex is reached directly from these cortical regions, and that the observed cortical projections are similar to those detected in the monkey's prefrontal cortex.     

Topographical organization of the projections from physiologically identified areas of the motor cortex to the striatum in the rat.

The present study was undertaken to determine in the rat the topography of the neostriatal projections originating from the motor cortex. For that purpose, anterograde tracers (Phaseolus vulgaris leucoagglutinin: PHA-L; wheat germ agglutinin conjugated to horseradish peroxidase: WGA-HRP) were deposited in discrete cortical sites physiologically identified by microstimulation. Five major motor areas were considered in this study: the rostral (RFL) and caudal (CFL) forelimb areas, the hindlimb (HL) area, the vibrissae motor-frontal eye field (V-FEF) region and the jaw, lips and tongue (JLT) area (according to the nomenclature of Neafsey et al.). The results indicate that functionally different regions of the motor cortex project to different sectors of the caudate putamen (CPU). All 3 distinct limb areas RFL, CFL and HL project to the dorsolateral quarter of the CPU, V-FEF area projects to the dorsomedial quarter, whereas the JLT area projects to the ventrolateral quarter. The pattern of terminal labeling is relatively consistent, whatever the cortical area in which the tracer is deposited. This pattern is characterized by the presence of two or more labeled bands which are obliquely oriented along a ventrolateral-dorsomedial axis. Control experiments were also undertaken in which a retrograde tracer (WGA-HRP) was deposited in various neostriatal loci. The results are congruent with the findings of the anterograde study and further indicate that a given neostriatal sector receives projections from cytoarchitectonically different but functionally related regions of the neocortex. The somatotopic features of both motor and somatosensory corticostriatal projections appear to be in register. In addition, the striatal distribution of motor cortical fibers was compared in 6 experimental cases to the compartmental subdivision of the striatum in patches and matrix, following immunohistochemical localization of calbindin 28 kDa. The calbindin-immunoreactivity is extremely weak in the dorsolateral sector but is higher in the central and ventrolateral parts of the CPU. In these deep striatal regions receiving fibers from V-FEF, JLT and, to a lesser extent, from the limb areas, the cortical fibers are mostly directed to the matrix. The band-like organization of the projection from the motor cortex is correlated to the patch-matrix organization. The patches correspond to the bands of low density of terminal fibers and the matrix to the bands of high terminal density. The present results provide an anatomical basis to both electrophysiological and behavioral observations suggesting that functional distinctions can be established between subregions of the striatum.     

Anatomical re-evaluation of the corticostriatal projections to the caudate nucleus: a retrograde labeling study in the cat

The distribution of cortical neurons projecting to the cat caudate nucleus (CN) was examined using retrograde labeling methods. Single injections of either horseradish peroxidase conjugated with wheat germ agglutinin (HRP-WGA), or the fluorescent tracers Fast Blue (FB) or Diamidino Yellow (DY) were made into different regions of the CN. This study confirms the following previous findings. (1) Labeled neurons were observed in the frontal and parieto-temporal cortices. (2) The corticocaudate cells were mainly located in layer V, although some cells were also observed in layer III and occasionally in layers II and VI. (3) Dorsal injections into the rostral CN yielded more dorsal labeling in the cerebral cortex. However, ventral cortical areas such as the ventral part of the prelimbic (PL) cortical area and the insular cortex (sylvian anterior (SA), agranular and disgranular insular areas) presented retrograde labeling after both dorsal and ventral injections into the CN. (4) Dorsal injections into the CN labeled all subdivisions of areas 4 and 6 whereas the ventral ones labeled only the areas 4delta, 6alphabeta, 6aalpha, 6iffu. The novel findings of this study are as follows. (1) The cortical area 6betabeta and the dorsolateral prefrontal area (PfDl) were labeled in all our cases. In addition, PL, anterior limbic, SA and rostral part of cingulate (Cg) cortical areas were also labeled in most of our cases. (2) Ventral injections into the CN elicited a higher number of retrogradely labeled neurons in the ventral prefrontal area than dorsal injections. (3) A topographical relationship was found between the caudal CN and the dorsomedial prefrontal area so that dorsal injections in the caudal CN elicited retrograde labeling in the rostral PfDl, whereas ventral injections labeled the caudal PfDl. (4) A topography from dorsal to rostral and ventral to caudal was also observed between injections into the CN and PL and Cg. (5) A mediolateral topography was observed in the presylvian, cruciate and splenial sulci.     

Corticocortical projections to the prefrontal cortex in the rhesus monkey investigated with horseradish peroxidase techniques

The corticocortical afferents innervating the prefrontal cortex in the monkey were studied by means of the retrograde axonal transport of horseradish peroxidase. After injection of small amounts (0.3-0.5 microliter) of this enzyme into various parts of the prefrontal cortex, many labeled neurons (mostly pyramids of 15-25 microns in diameter) were found in various cortical regions of the ipsilateral hemisphere. A small part of the prefrontal cortex received fibers from other parts of the same cortex. For example, area 8 receives many fibers from both the rostral part of area 9 and a small area adjacent to the inferior branch of the arcuate sulcus. On the other hand, area 9 in the inferior prefrontal convexity receives fibers from localized parts of areas 8 and 9 in the dorsolateral convexity as well as from area 6. It is also apparent that association connections from the dorsolateral to the inferior convexity are stronger than those going in the opposite direction. The prefrontal afferents from other cortical regions include many fibers originating from the posterior association cortex as well as some fibers arising in the cingulate and orbital gyri. The prefrontal cortex does not receive direct corticocortical fibers from the motor and "primary" sensory cortices. There is a topographic pattern in the prefrontal projections from the cortical walls (STs area) surrounding the superior temporal sulcus. Thus, the caudal half of the STs area projects to area 8 and a small adjacent part of area 9. The dorsal wall of the rostral half of the STs area projects to areas 9-12, the fundus to the inferior convexity, and the ventral wall only to the caudal part of the convexity. Projections from the circumjacent association cortex of the STs area to the prefrontal cortex as well as to the STs area are likewise found to be topographically organized. This suggests that certain parts of the posterior association cortex projecting to particular areas of the prefrontal cortex, also send fibers to those parts of the STs area which project to the same prefrontal areas.     

Three-dimensional organization of the striosomal compartment and patchy distribution of striatonigral projections in the matrix of the cat caudate nucleus

Acetylcholinesterase staining on successive frontal or sagittal sections was used to determine the three-dimensional organization of the striosomal and matrix compartments in the adult cat caudate nucleus. Reconstruction drawings of the acetylcholinesterase-poor zones (striosomes) indicated that the striosomal compartment is a labyrinthine network organized in the rostrocaudal and mediolateral axis which is reproducible from one animal to another. Four main anteroposterior channels converging in the mediorostral pole of the caudate nucleus were distinguished. Seven to eight diagonally oriented channels crossing the previous ones were seen also in the mediolateral axis on the central core of the caudate nucleus. The pattern of organization of the numerous and tortuous striosomal channels was more complicated medially, while the lateral part of the caudate nucleus was represented mainly by the matrix compartment. In addition, a sub-compartmentation of the matrix was demonstrated by retrograde tracing studies made by injecting either horseradish peroxidase-wheat germ agglutinin, [14C]amino acids or a mixture of horseradish peroxidase-wheat germ agglutinin and [14C]amino acids in several areas of the substantia nigra pars reticulata. Labelled patches were seen with both tracers, their topographical localization depended on the nigral injection site but reconstruction analysis indicated that the populations of cells which innervate the substantia nigra pars reticulata originate in the two third lateral parts of the caudate nucleus all along its rostrocaudal extension. Examination of horseradish peroxidase-wheat germ agglutinin labelled cells indicated that not all cells were labelled in patches suggesting a further sub-compartmentation of these patches. Finally, a comparison of the topographical distributions of labelled patches and of striosomes revealed that most patches were located in the extrastriosomal matrix.     

The cerebellar projections to the superior colliculus and pretectum in the cat: An autoradiographic and horseradish peroxidase study

Efferent projections from the cerebellar nuclei to the superior colliculus and the pretectum have been studied using both retrograde and orthograde labeling techniques in the cat. In order to identify what parts of the cerebellar nuclei project to the superior colliculus and the pretectum, the retrograde horseradish labeling technique was employed. In another set of experiments, tritiated amino acids were injected into each of the cerebellar regions from which the cerebello-tectal and cerebellopretectal projections arise, and the laminar and spatial distributions of orthograde labeling in the superior colliculus and the pretectum were compared.The results showed that the cerebello-tectal projections arise from two different regions of the cerebellar nuclei: the caudal half of the medial nucleus and the ventrolateral part of the posterior interposed nucleus. Fibers arising from the medial nucleus distribute bilaterally in the superficial zone of the intermediate gray layer in the superior colliculus, while those originating from the posterior interposed nucleus terminate contralaterally in the deeper aspect of the intermediate gray layer and in the deep gray and white layers. Although the lateral nucleus does not contribute to the cerebello-tectal projection, it projects profusely to the pretectum contralaterally. The origin of the cerebello-pretectal projection lies in the parvicellular part of the lateral nucleus. Among several pretectal nuclei, the posterior pretectal, the medial pretectal nucleus and the reticular part of the anterior pretectal nucleus receive the cerebellar afferents.The findings of the differential projections from the cerebellum to the superior colliculus and the pretectum suggest that the cerebellum exerts a regulatory influence on visuo-motor and somato-motor transfer in these midbrain structures by differential circuits.     

Vestibular projections to the nucleus intercalatus of Staderini mapped by retrograde transport of horseradish peroxidase

Medullary afferent projections to the nucleus intercalatus of Staderini have been studied by retrograde transport of horseradish peroxidase (HRP) from highly localized injections. This nucleus receives afferent projections particularly from the medial and descending vestibular nuclei as well as from the nucleus praepositus hypoglossi of both sides. The nucleus intercalatus of Staderini represents therefore an area of integration for the vestibular systems of both sides.