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Organization of corticostriatal projections from the vibrissal representations in the primary motor and somatosensory cortical areas of rodents.

To characterize corticostriatal projections from rodent sensorimotor cortex, the anterograde tracers biotinylated dextran amine (BDA) and fluororuby (FR) were injected into the whisker representations of the primary motor (MI) and somatosensory (SI) cortices. Reconstructions of labeled terminals and their beaded varicosities in the neostriatum and thalamus were analyzed quantitatively to determine the degree of labeled overlap in both of these subcortical structures. Corticostriatal projections from the vibrissal representation in MI were more extensive than corresponding projections from SI. Both cortical areas sent dense projections to the dorsolateral neostriatum, but the MI vibrissal representation also projected to regions located more rostrally and medially. Despite these differences, both MI and SI projected to overlapping parts of the dorsolateral neostriatum. Tracer injections in both cortical areas also produced dense anterograde and retrograde labeling in the medial sector of the posterior complex of the thalamus (POm). Because POm is somatotopically organized and has reciprocal connections with both SI and MI cortices, the amount of labeled overlap in POm was used to indicate whether the tracers were injected into corresponding whisker representations of MI and SI. We found that the proportion of labeled overlap in the neostriatum was highly correlated with the amount of labeled overlap in POm. These results indicate that the rodent neostriatum receives convergent projections from corresponding regions in MI and SI cortex. Furthermore, the thalamocortical projections of the POm indicate that it may modulate corticostriatal outputs from corresponding representations in MI and SI.

Animals↗

Organization of connectivity of the rat presubiculum: I. Efferent projections to the medial entorhinal cortex.

The organization of the laminar and topographical projections from the presubiculum to the entorhinal area was studied in the rat by anterograde labeling with Phaseolus vulgaris leucoagglutinin and retrograde labeling with horseradish peroxidase conjugated to wheat germ agglutinin. We found that the pattern of presubiculo-entorhinal projections differs between the superficial and deep layers of the presubiculum. The superficial layers (layers II and III) of the presubiculum gave rise to bilateral projections to layers I-VI of the medial entorhinal area (MEA). Many terminals were distributed in layer III, fewer in layer II and the deep portion of layer I, and many fewer terminals in the deep layers (layers V and VI) of MEA. In contrast, the deep layers (layers V and VI) of the presubiculum gave rise to ipsilateral projections to the entorhinal area. Many axon terminals were distributed in layers V and VI of MEA and the most superficial portion of layer I of MEA, but very few in layers II and III. In addition, the ramifications in layer I extended to the lateral entorhinal area (LEA). Using two-dimensional unfolded maps of parahippocampal cortices, we elucidated the distinct topographical relationship in the presubiculo-entorhinal projection: 1) The septotemporal or longitudinal axis of the presubiculum corresponded to the axis on the MEA/LEA boundary, where the septal presubiculum projected toward the rhinal fissure and the temporal presubiculum projected away from the fissure. 2) The proximodistal axis of the presubiculum corresponded to the axis from the MEA/LEA boundary to the MEA/parasubiculum boundary that was virtually perpendicular to the MEA/LEA boundary, where the proximal portion of the presubiculum (close to the subiculum) projected to the region near the MEA/LEA boundary.

Animals↗

Defining projections from the caudal pressor area of the caudal ventrolateral medulla.

We previously defined a functional area in the caudal medulla oblongata that elicits an increase in arterial pressure when stimulated (Sun and Panneton [2002] Am. J. Physiol. 283:R768-R778). In the present study, anterograde and retrograde tracing techniques were used to investigate the projections of this caudal pressor area (CPA) to the medulla and pons. Injections of biotinylated dextran amine into the CPA resulted in numerous labeled fibers with varicosities in the ipsilateral subnucleus reticularis dorsalis, commissural subnucleus of the nucleus tractus solitarii, lateral medulla, medial facial nucleus, A5 area, lateral vestibular nucleus, and internal lateral subnucleus of the parabrachial complex. Sparser projections were found ipsilaterally in the pressor and depressor areas of the medulla and the spinal trigeminal nucleus and contralaterally in the CPA. Injections of the retrograde tracer Fluoro-Gold into these areas labeled neurons in the CPA as well as the nearby medullary dorsal horn and reticular formation. However, we conclude that the CPA projects preferentially to the subnucleus reticularis dorsalis, commissural nucleus tractus solitarii, lateral medulla, A5 area, and internal lateral parabrachial nucleus. Weaker projections were seen to the CVLM and RVLM and to the contralateral CPA. The projection to the facial nucleus arises from nearby reticular neurons, whereas projections to the vestibular nucleus arise from the lateral reticular nucleus. Labeled neurons in the CPA consisted mostly of small bipolar and some triangular neurons. The projection to the CVLM, or to A5 area, may provide for the increase in arterial pressure with CPA stimulation. However, most of the projections described herein are to nuclei implicated in the processing of noxious information. This implies a unique role for the CPA in somatoautonomic regulation.

Animals↗

Prefrontal cortex in the rat: projections to subcortical autonomic, motor, and limbic centers.

This paper describes the quantitative areal and laminar distribution of identified neuron populations projecting from areas of prefrontal cortex (PFC) to subcortical autonomic, motor, and limbic sites in the rat. Injections of the retrograde pathway tracer wheat germ agglutinin conjugated with horseradish peroxidase (WGA-HRP) were made into dorsal/ventral striatum (DS/VS), basolateral amygdala (BLA), mediodorsal thalamus (MD), lateral hypothalamus (LH), mediolateral septum, dorsolateral periaqueductal gray, dorsal raphe, ventral tegmental area, parabrachial nucleus, nucleus tractus solitarius, rostral/caudal ventrolateral medulla, or thoracic spinal cord (SC). High-resolution flat-map density distributions of retrogradely labelled neurons indicated that specific PFC regions were differentially involved in the projections studied, with medial (m)PFC divided into dorsal and ventral sectors. The percentages that WGA-HRP retrogradely labelled neurons composed of the projection neurons in individual layers of infralimbic (IL; area 25) prelimbic (PL; area 32), and dorsal anterior cingulate (ACd; area 24b) cortices were calculated. Among layer 5 pyramidal cells, approximately 27.4% in IL/PL/ACd cortices projected to LH, 22.9% in IL/ventral PL to VS, 18.3% in ACd/dorsal PL to DS, and 8.1% in areas IL/PL to BLA; and 37% of layer 6 pyramidal cells in IL/PL/ACd projected to MD. Data for other projection pathways are given. Multiple dual retrograde fluorescent tracing studies indicated that moderate populations (<9%) of layer 5 mPFC neurons projected to LH/VS, LH/SC, or VS/BLA. The data provide new quantitative information concerning the density and distribution of neurons involved in identified projection pathways from defined areas of the rat PFC to specific subcortical targets involved in dynamic goal-directed behavior.

Animals↗

The patterns of projection of cortical areas 17, 18, and 19 onto the laminae of the dorsal lateral geniculate nucleus in the cat.

The projection of cortical areas 17, 18, and 19 onto the laminar part of the dorsal lateral geniculate nucleus was investigated with degeneration methods and with the autoradiographic axon tracing method. In agreement with previous accounts, degenerating cortical axons stained by the Nauta method were restricted to laminae A, A1, C and to the interlaminar zones. In contrast, adjacent sections stained with the Fink-Heimer method showed fine dust like degeneration throughout all of the laminae of the nucleus. Comparisons of Fink-Heimer degeneration resulting from lesions of area 17 with that resulting from lesions of areas 18 and 19 further suggested that the area ) projection is heavier and more uniform than the projections from areas 18 and 19. Autoradiographic tracing of axons after intracortical injections of 3H-proline provided detailed demonstrations of the cortical projection patterns that confirmed the Fink-Heimer results. Following restricted injections of areas 17 or 18 the termination zones in the dorsal lateral geniculate nucleus consisted of columns of labeled tissue oriented perpendicular to the laminae of the nucleus. Area 17 was found to project heavily and uniformly throughout all of the laminae of the nucleus. The projection from area 18 also extended throughout all of the laminae of the nucleus, but was sparser and less uniformly distributed than that from area 17. Projections from area 18 distributed more heavily to the interlaminar zones and to lamina C than to laminae A, A1 C1, C2 or C3. A projection from area 19 to laminae C1, C2 and C3 was also demonstrated autoradiographically.

Animals↗

The anatomical organization of the cerebello-olivary projection in the cat.

The cerebello-olivary pathway in the cat has been examined using orthograde and retrograde neuroanatomical tracing techniques. The orthograde transport of 3H-leucine from injection sites in the deep cerebellar nuclei labeled dentate and interpositus projections to the rostral two-thirds of the contralateral inferior olivary complex. These projections are topographically organized, with the dentate nucleus projecting to the principal olivary nucleus and the posterior and anterior interpositus nuclei projecting to the medial and dorsal accessory olives respectively. Fibers from the ventral half of the dentate nucleus terminate in the lateral bend and ventral lamina of the principal olive, whereas the medial and lateral parts of the dorsal half of the nucleus project to the medial and lateral regions of the dorsal lamina respectively. It is apparent that the more caudal parts of the interpositus nuclei project to areas of the medial and dorsal accessory olives near the caudal end of the principal olivary nucleus, whereas neurons in the more rostral parts of the interpositus nuclei project to the more rostral areas of the accessory olivary nuclei. A connection between the fastigial ncleus and the inferior olive could not be demonstrated. The retrograde transport of horseradish peroxidase (HRP) from injections sites in the inferior olive labeled cells throughout the contralateral dentate and interpositus nuclei. The labeled cells were especially numerous in the ventral parts of the dentate and posterior interpositus nlclei. These HRP-positive neurons were consistently small (10--15 mu) ovoid or spindle-shaped cells, with relatively large nuclei and light-staining Nissl substance. This evidence strongly suggests that the cerebello-olivary pathway originates from a population of small neurons in the dentate and interpositus nuclei and projects to specific, topographically defined areas in the contralateral inferior olive.

Animals↗

Efferent projections of the subthalamic nucleus: an autoradiographic study in monkey and cat.

The efferent projections of the subthalamic nucleus were studied with the autoradiographic tracing technique in Rhesus monkey and cat. From the data it appears that the major efferent projections of the nucleus are to the pallidal complex and the substantia nigra. In both monkey and cat, the projection to the pallidal complex is truly massive and is directed at both pallidal segments. The projection field includes an infracommissural part of the pallidal complex bordering on the substantia innominata. In the monkey the termination in the pallidal complex is organized in several characteristic bands oriented parallel to the medullary laminae. The subthalamo-pallidal projection in monkey further appears to be topographically organized. The projections to the substantia nigra is prominent in both cat and monkey though not as massive as that to the pallidal complex. The distribution of termination in the substantia nigra favors the more ventral strata near the cerebral peduncle. In the monkey the terminal distribution appears to avoid regions of the substantia nigra containing pigmented neurons and it is suggested that the subthalamo-nigral pathway may prefer non-dopaminergic neurons. In addition to the above major projections, sparse projections were noted to the thalamic nuclei ventralis lateralis and ventralis anterior, to the putamen, and to the mesencephalic nucleus tegmenti pedunculopontinus, pars compacta. The findings are discussed.

Animals↗

Anatomical and physiological properties of ipsilaterally projecting spinothalamic neurons in the second cervical segment of the cat's spinal cord.

Anatomical and electrophysiological methods were used to investigate the projections and response properties of neurons in the second cervical (C2) spinal segment of the cat giving origin to a previously undescribed projection to the ipsilateral thalamus. The method of retrograde axonal transport of horseradish peroxidase (HRP) was used to identify neurons in C2 giving rise to thalamic projections. Following large (3.0 microliter) thalamic HRP injections, a large number of labeled neurons was observed in lateral laminae VII-VIII of C2 ipsilateral to the injections. They occurred as small clusters of cells along the longitudinal axis of C2. Labeled neurons were also observed contralaterally in the lateral cervical nucleus, dorsal horn (especially medial lamina VI), and loosely distributed in the ventral horn. The ipsilaterally projecting neurons were also labeled following small (0.2--0.5 microliter) HRP injections restricted to individual spinothalamic terminal zones (intralaminar nuclei, ventrobasal complex-nucleus ventralis lateralis border zone, medial division of the posterior nuclei), indicating that as a group they project widely throughout the thalamus. Single unit recording methods were used to obtain complementary information on the functional properties of these neurons. The antidromic stimulation method was applied to identify units in C2 projecting to the ipsilateral thalamus in anesthetized, paralyzed cats. Three categories of ipsilaterally projecting C2 units were identified: (1) units not driven by any type of natural stimulation; (2) units having large cutaneous receptive fields (RFs) and wide dynamic response ranges ("widefield"), and (3) units with smaller RFs and varied properties ("other"). Widefield units with bilaterally symmetrical and asymmetrical RFs were observed. Co-stimulation of different portions of an excitatory RF produced summation of the unit response. Inhibitory RF components were identified in one-third of the widefield units. Unit recordings after spinal tract lesions revealed that the afferent input passed via the ipsilateral lateral and/or ventral funiculi. Widefield unit responses to somatosensory stimuli could be inhibited by dorsal column conditioning stimulation. Several "other" units resembled widefield units, while a second group had small RFs restricted to the C2 dermatome. Possible functional roles of the projecting C2 neurons in somatosensory and non-specific systems are discussed.

Animals↗

An HRP and autoradiographic study of the projection from the cerebellar cortex to the nucleus interpositus anterior and nucleus interpositus posterior of the cat.

The recently developed anatomical techniques of retrograde transport of the enzyme horseradish peroxidase (HRP), anterograde transport of tritiated amino acid, and intracellular injections of HRP were used to study the organization of the corticonuclear projection to the nucleus interpositus anterior (NIA) and the nucleus interpositus posterior (NIP) of the cat. Injections of HRP into the NIA and the NIP revealed that the major areas of the cortex which provided afferents to these two nuclei were the intermediate cortex of the anterior lobe (IAL) and the paramedian lobule (PML). There were, however, significant differences in the distribution of Purkinje (Pk) cells which projected to each nucleus. The NIA received afferents from all areas of the IAL while the NIP projection area was restricted to a band located at the medi-almost aspect of the lobe. All areas of the PML, in particular the intermediate folia, projected to the NIP, while the Pk cells which sent axons to the NIA were restricted to the rostral and caudal folia of this lobule. The projection from each area was somatotopically organized. The axons of intracellularly stained Pk cells were followed to their termination in the NIA and NIP confirming the results obtained with the two extracellular techniques. An attempt was made to examine the organization of the corticonuclear projection at the single cell level in the PML. Pk cells located in the same sagittal plane appeared to terminate in the same area of the same nucleus while Pk cells located not more than 500 micrometers medial or lateral to each other terminated in different nuclei. Basically, the organization of the corticonuclear projection from the IAL is longitudinally organized while the PML has a much more complex arrangement in which the Pk cells projecting to the NIA and NIP are interspersed.

Amino Acids↗

The retinal projection to the superior colliculus in the cat: a quantitative study with HRP.

The projections of cat retinal ganglion cells to the superior colliculus (SC) were examined using the method of retrograde axonal transport of horseradish peroxidase (HRP). Several injections of HRP were made in a single SC after the visual projection to the injection sites had been established physiologically. The HRP injections resulted in a homogeneous distribution of labelled ganglion cells in whole mount preparations of the retinae of both eyes. In the eye contralateral to the injected colliculus, ganglion cells with a crossed projection were labelled in both nasal and temporal retina; in the ipsilateral eye, ganglion cells with uncrossed projection were labelled only in the temporal retina. Analysis of the counterstained retinal whole mounts indicated that at least 50% of all ganglion cells in the nasal retina and 26% in the temporal retina have crossed projection to SC, and that 24% of all ganglion cells of the temporal retina have an uncrossed projection to the SC. The morphological classes of retinal ganglion cells have different patterns of crossed/uncrossed decussation and they participate in varying proportions in the retino-tectal projection. Almost all Alpha cells in the retina send axon collaterals to the SC. Probably only about 10% of the Beta cells project to the SC and at least 80% of all Gamma cells send axons to the SC.

Animals↗

Anomalous uncrossed retinal projections fail to activate superior colliculus neurons in rabbits unilaterally enucleated by fetal surgery.

Previous studies have shown that unilateral enucleation of rabbit pups produces an aberrant uncrossed retinotectal projection. These fibers failed to drive collicular units when stimulated with either light or electric shock. The present study attempts to assess the possibility that enucleation at earlier stages of development would lead to a greater degree of morphological and physiological reorganization in the uncrossed retinotectal projection. Rabbit fetuses were unilaterally enucleated at day 20 or 25 of gestation. Birth is at day 31. After 3 months, the degree of reorganization of the uncrossed retinotectal projection was assessed using the following techniques: (1) autoradiographic demonstration of the projection from the remaining eye, (2) electrophysiological recording of collicular unit activity, and (3) a combination of these methods. Autoradiographic data indicated a much greater expansion of the anomalous uncrossed projection in fetally enucleated animals than in those enucleated at birth. Labelled terminals were found to occupy more than the anterior third of the ipsilateral colliculus and were distributed to the entire depth of the stratum griseum superficiale and stratum opticum. Electrode penetrations within the boundaries of the expanded projection failed to locate collicular units which could be driven by either light stimulation of the eye or electric shock of the optic nerve. Only a few cells encountered in the lateral border area, receiving the normal uncrossed retinal projection, could be driven by light stimulation. These negative findings are in contrast to the data reported for the rat and hamster where anomalous retinal projections are capable of forming functional connections. Further comparative studies of reorganization are needed.

Animals↗

Spinocerebellar projections to lobules I and II of the anterior lobe in the cat, as studied by retrograde transport of horseradish peroxidase.

Spinocerebellar tract (SCT) neurons projecting to lobules I and II of the cerebellar anterior lobe were identified by the retrograde horseradish peroxidase technique in the cat. Instead of a conventional stereotaxic approach, we removed ventral parts of the vermis of the posterior lobe and approached the posterior aspect of lobule I through the fourth ventricle. Under direct visual guidance, discrete injections were made into lobule I or II with a glass micropipette. Neurons projecting to lobule I were located mainly in the central cervical nucleus (CCN), the medial part of lamina VII of L6 to the causal segments, and in lamina VIII of S2 to the caudal segments (with crossed ascending axons). The latter two groups correspond to medial lamina VII group of the lumbar to the caudal segments and the ventral horn group of the sacral-caudal segments of our previous studies. A small number of Clarke column neurons (with uncrossed ascending axons) also projected to lobule I. All of these neuronal groups projected to lobule II. In addition, large neurons in lamina V and the border between laminae IV and V from S2 to the caudal segments projected to sublobule IIA, and more numerously to sublobule IIB (with crossed ascending axons). They belong to the dorsal horn group of the sacral-caudal segments of our previous studies. Spinal border cells (with crossed ascending axons) projected to sublobule IIB, and a small number, to sublobule IIA. It was suggested that the CCN neurons project more densely to the median region whereas Clark column neurons project to the lateral part of these lobules.

Afferent Pathways↗

Projections from visual areas of the middle suprasylvian sulcus onto the lateral posterior complex and adjacent thalamic nuclei in cat.

The distribution of corticothalamic projections from lateral suprasylvian areas AMLS, PMLS, ALLS, and PLLS was investigated with the autoradiographic method. Areas AMLS and PMLS were both found to project retinotopically upon the medial interlaminar nucleus and the lateral and pulvinar zones of the lateral posterior complex, as well as to the ventral lateral geniculate nucleus, intralaminar nuclei, and thalamic reticular complex. Retinotopic projections to the dorsal lateral geniculate nucleus were demonstrated from PMLS but not AMLS, and projections to zona incerta were demonstrated from AMLS but not PMLS. Areas PLLS and ALLS were both found to project retinotopically upon the interjacent zone of the lateral posterior complex, as well as to the intermediate and suprageniculate divisions of the posterior nuclear group, the magnocellular division of the medial geniculate complex, the thalamic reticular complex, and central lateral nucleus. Area ALLS was also found to project onto the dorsal division of the medial geniculate complex and lateral division of the posterior nuclear group. Differences between the four cortical areas in the pattern and density of their thalamic projections supports the parcellation of these areas as proposed by Palmer et al. ('78). The projection patterns of areas PMLS, AMLS, PLLS, and ALLS were found to respect the boundaries of the zones of the lateral posterior complex, which had been identified and defined previously (Updyke, '77), and the results thus support the hypothesis that these zones are the functional units of organization of visual traffic between the cat's extrastriate visual areas.

Animals↗

Amygdalopetal projections in the cat. I. Cortical afferent connections. A study with retrograde and anterograde tracing techniques.

The cortical afferent connections of the amygdaloid complex of the cat have been studied by means of retrograde tracing of horseradish peroxidase and the fluorescent substances bisbenzimid and nuclear yellow. Subsequently, anterograde tracing experiments were carried out in order to define more precisely the termination areas of the corticoamygdaloid fibers. The results of the present study indicate that the main and accessory olfactory bulbs, the anterior olfactory nucleus, the prepiriform cortex and discrete regions of the medial frontal lobe, the insular and temporal cortices, as well as the perirhinal and entorhinal cortices and the ventral subiculum project to the amygdaloid complex. The main termination sites of these projections are the central, basolateral, and lateral amygdaloid nuclei. Neocortical regions project to the lateral nucleus and the lateral division of the lateral central nucleus. The mesocortical regions project predominantly to the basolateral nucleus and a medial division of the lateral central nucleus. In addition, area 35 distributes fibers to the lateral nucleus and the entorhinal cortex projects to the cortical nuclei of the amygdaloid complex. Fibers from the infralimbic area only reach the region of the medial central nucleus. Of the allocortical regions the prepiriform cortex distributes its fibers to the lateral, basolateral, and cortical nuclei, whereas the ventral subiculum projects to the medial division of the lateral central nucleus and the cortical nuclei. In the neocortical and most of the mesocortical regions the cells which project to the lateral and basolateral amygdaloid nuclei lie in layer III, whereas the cells which project to the central nucleus are located in layer V.

Afferent Pathways↗

Afferent projections to the oral motor nuclei in the rat.

Projections to the trigeminal, facial, ambiguus, and hypoglossal motor nuclei were determined by using horseradish peroxidase histochemistry. Most of the afferent projections to these motor nuclei were from the brainstem reticular formation, frequently in areas adjacent to other synergetic motor nuclei. The reticular formation lateral to the hypoglossal nucleus and reticular structures surrounding the trigeminal motor nucleus projected to each of these other brainstem motor nuclei involved in oral-facial function. Afferent projections to these motor nuclei also were organized along the rostrocaudal axis. Within the reticular formation most of the afferent projections to the trigeminal motor nucleus originated rostral to the majority of neurons projecting to the hypoglossal and ambiguus nuclei, which in turn were rostral to the primary source of reticular afferents to the facial nucleus. In comparison, projections from the sensory trigeminal nuclei and nucleus of the solitary tract were sparse. The interneuron pools that project to the orofacial motoneurons provide one further link in understanding the brainstem substrates for integrating oral and ingestive behaviors.

Afferent Pathways↗

Postnatal development of the inferior olivary complex in the rat. II. Topographic organization of the immature olivocerebellar projection.

The state of organization of the olivocerebellar projection in newborn and 5-day-old rats has been analyzed by autoradiography of anterogradely transported 3H-leucine, as well as by retrograde transport of horseradish peroxidase. The efferent axons of the inferior olivary neurons are already present and already highly organized in the cerebellum of newborn rats. Most of the autoradiographic labelling subsequent to the injection of 3H-leucine into the inferior olive is seen in the subcortical medullary zone. Labelled axons only partially invade the gray matter, where they reach the zone occupied by randomly distributed Purkinje cells. At this immature stage, olivocerebellar projections are already entirely crossed and distributed according to a pattern which is similar to the adult. At the fifth postnatal day olivocerebellar projections have moved from the medullary zone toward the interface between the molecular and the granular layers where Purkinje cells have arranged in a monolayer. Evidence for translocation of climbing fibers from their perisomatic to their peridendritic position is already distinct in these young cerebella. Combination of anterograde and retrograde fiber system tracing experiments discloses the following crossed topography of olivocerebellar projections: The caudal half of the medial accessory olive projects mainly to the vermis of the posterior lobe, whereas its rostral half projects to the flocculus, paraflocculus, and the intermediate cortex. The principal olive, ventral and dorsal lamellae, supplies climbing fiber inputs to the hemispheric cortex. The caudal half of the dorsal accessory olive projects to the lateral portion of the vermis of the anterior lobe, whereas neurons in its rostral half send their axons toward the intermediate cortex. This topographic arrangement is, therefore, similar to that reported for adult mammals. The present results, alone or when compared with those obtained during other studies on the synaptogenesis between climbing fibers and Purkinje cells, allow the following conclusions: The climbing fibers enter the cerebellar cortex before Purkinje cells have reached the developmental phase compatible with synaptogenesis. They wait in the medullary white matter until appropriate maturation of their cellular targets. Olivocerebellar topography is roughly similar in newborn, 5-day -old, and adult rats. Synaptogenesis between climbing fibers and Purkinje cells, which is known not to start before the second postnatal day, is not necessary for the establishment of the topographic organization of the olivocerebellar projection.

Animals↗

Localizing spinal-cord-projecting neurons in adult albino rats.

Following horseradish peroxidase injection into the cervical and lumbosacral cords of adult albino rats, labeled neurons were seen in the first cervical segment, brain stem, and cerebellar and diencephalic nuclei. A new pathway, the faciospinal projection, originating in the medial portion of the rostral part of the facial nucleus, was traced. Another new pathway, the olivospinal pathway, is probably also present. Our results for neurons projecting to the spinal cord (spinal-projecting neurons) from the nucleus ambiuus, dorsal motor nucleus of the vagus, superior vestibular nucleus and nucleus f, nucleus Darshevch, nucleus Rolleri, nucleus prepositus hypoglossi, and nucleus of the posterior commissure have been reported before in other mammals but not in rats. Projections from the following regions are in general agreement with previous results in rats, but show significant topographical differences: the first cervical segment; nuclei gracilis, cuneatus, and cuneatus lateralis; the midline and lateral reticular nuclear complex; the trigeminal nuclear complex (spinal, principal, and mesencephalic); nucleus of the tractus solitarius; the medial, lateral, and descending vestibular nuclei, nuclei coeruleus and subcoeruleus; superior colliculus; interstitial nucleus of Cajal, and the deep cerebellar nuclei. The distribution of labeled neurons in the nucleus parabrachialis, nucleus tegmentolaterodorsalis, nucleus Kölliker-Fuse, nucleus Edinger-Westphal, and the hypothalamic nuclear complex confirmed that of previous reports in rats. With the exception of a few nuclear groups which project primarily to either lumbosacral (e.g., the paraventricular nucleus of the hypothalamus) or cervical segments (e.g., the facial motor nucleus and the superior colliculus) most of the other nuclear groups project to both the lumbar and cervical levels. There is no distinct somatotopy in the neuronal groups projecting to both cervical and lumbosacral levels. With only a few exceptions (e.g., the superior vestibular nucleus) most of the spinal-projecting neurons are bilaterally distributed, some with contralateral and others with ipsilateral predominance.

Animals↗

Cerebellar efferents in the lizard Varanus exanthematicus. I. Corticonuclear projections.

The organization of the cerebellar corticonuclear projections, i.e., the projections from the Purkinje cell layer to the cerebellar nuclei and the vestibular nuclear complex, was investigated with the horseradish peroxidase (HRP) technique in the lizard Varanus exanthematicus. After HRP slow-release gels were implanted in the cerebellar nuclei or various parts of the vestibular nuclear complex, the following longitudinally oriented zones of labeled Purkinje cells could be distinguished: a medial zone projecting to the medial cerebellar nucleus; an intermediate zone projecting to the vestibular nuclear complex, especially the ventrolateral vestibular nucleus, but probably also the dorsolateral vestibular nucleus; a caudolaterally located area of the cerebellar cortex projecting to the lateral cerebellar nucleus; and the flocculus and the adjacent lateral part of the Purkinje cell layer with projections to the middle and caudal parts of the vestibular nuclear complex, i.e., the descending and ventromedial vestibular nuclei. All projections of the Purkinje cells appeared to be strictly ipsilateral. It can be concluded that in reptiles a longitudinal organization of cerebellar corticonuclear projections exists, which may be basic for terrestrial vertebrates.

Animals↗