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PubMed1983

The inferior olive of a prosimian primate, Galago senegalensis. II. Olivocerebellar projections to the vestibulocerebellum.

Olivocerebellar projections to the vestibulocerebellum of Galago senegalensis, a prosimian primate, were studied by using a horseradish peroxidase (HRP) method. Following implants of HRP into the flocculus, labeled cells are found in subgroup d of contralateral medial accessory olive (MAO), while labeled somata are present throughout subgroups c and d after injections of HRP into the nodulus and adjacent parts of the uvula. Labeled cells are also located throughout the dorsomedial cell column (DMCC) and a small contingent of HRP-filled cells are seen in dorsomedial areas of the ventral lamellae of the principal olivary nucleus (PO) after HRP placements in nodulus and uvula. Subsequent to injections of paraflocculus, labeled cells are found in subgroup a of MAO, in the lateral bend of PO, and in its ventral lamella (VLPO). Collectively these data indicate a topographically organized projection of olivocerebellar fibers to the flocculonodular lobe and adjacent areas of paraflocculus and uvula. The paraflocculus receives input from subgroup a of MAO, the lateral bend of PO, and VLPO. Subgroup d of MAO projects to the flocculus and nodulus with a relatively minor contribution to uvula. Neurons in subgroups c and DMCC of MAO project to specific portions of nodulus and adjacent uvula. These data are in general agreement with those from other species. In contrast to earlier reports, however, this study describes a projection from VLPO to lateral areas of the contralateral nodulus and uvula. A zonal organization of olivocerebellar terminations in the nodulus and ventral portions of uvula is suggested. A medial zone is subdivided into medial and lateral parts which receive projections from subgroups c and d of MAO, and from cells in DMCC, respectively. A more lateral area receives axons from cells in VLPO.

Animals↗
PubMed1983

Long descending projections of the hypothalamus in the pigeon, Columba livia.

An autoradiographic analysis was performed on the descending projections of nucleus periventricularis magnocellularis (PVM) of the hypothalamus in the pigeon. A PVM-medullospinal pathway was observed coursing posteriorly through the lateral hypothalamus, ventrolateral midbrain tegmentum, and into the spinal lemniscus (ls) in the ventrolateral pons and medulla. In the pons, some fibers course dorsomedially from ls and terminate at the lateral border of the locus coeruleus. At medullary levels, fibers from ls sweep dorsomedially in the plexus of Horsley and project to certain regions of the nucleus of the solitary tract (NTS) and the dorsal motor nucleus of the vagus (NX). Specifically, PVM fibers project heavily into NTS subnuclei medialis superficialis, medialis ventralis, and lateralis (sulcalis) dorsalis as well as into the ventral parvocellular subnucleus of NX. Fibers in ls were traced caudally into the lateral funiculus as far as upper cervical levels of the spinal cord. Although autoradiographs of lower cervical or thoracic spinal cord sections were not available, PVM fibers do descend to thoracic spinal cord levels, as evidenced by the retrograde transport of horseradish peroxidase. In addition to the medullospinal pathway, the autoradiographs demonstrated PVM projections to septum, diencephalon, and midbrain. Labeled PVM fibers are found in the lateral septal nucleus, nucleus of the anterior pallial commisure, dorsomedial thalamic nucleus, dorsolateral anterior thalamic nucleus (pars ventralis), median eminence, medial and lateral hypothalamus, medial mammillary area, and nucleus intercollicularis and central gray of the midbrain. The projection of fibers to medullospinal regions and median eminence suggests that PVM is homologous to the mammalian paraventricular nucleus. These projections to specific subnuclei of NTS and NX denote hypothalamic control over certain autonomic functions.

Animals↗
PubMed1984

Projections of the amygdala to the thalamus in the cynomolgus monkey.

The projections of the amygdala to the thalamus in cynomolgus monkeys (Macaca fascicularis) were studied with both anterograde and retrograde axonal tracing techniques. Horseradish peroxidase (HRP) was injected into medial and midline thalamic sites in five animals, and tritiated amino acids were injected into selected amygdaloid regions in a total of 13 hemispheres in ten animals. The findings from the two types of tracer experiments demonstrated the origins, course, and terminal pattern of amygdaloid projections to two thalamic nuclei--medialis dorsalis (MD) and reuniens. Almost all of the amygdaloid nuclei contribute projections to MD, though the greatest proportion arise from the basal group and terminate in discrete, interlocking patches within the medial, magnocellular portion of MD. In addition to this major projection, the central and medial amygdaloid nuclei send a lighter projection to the lateral portion of nucleus reuniens. The amygdalothalamic projections took a variety of routes out of the amygdala before the large majority joined the inferior thalamic peduncle and entered the rostral head of the thalamus where they turned caudally toward their targets. A small number of amygdalothalamic fibers may also run in the stria terminalis.

Amygdala↗
PubMed1984

Topography of spinal, dorsal column nuclear, and spinal trigeminal projections to the pontine gray in rats.

Several studies using a variety of animals have reported conflicting evidence concerning the distribution, laterally, and indeed the presence of ascending projections to the pontine nuclei. In an attempt to clarify this issue, projections to the pontine nuclei from the spinal cord, dorsal column nuclei, and spinal trigeminal nucleus were investigated with anterograde methods, i.e., the Fink-Heimer technique and/or autoradiography, in Long-Evans black-hooded rats. Results revealed that dorsal column nuclear projections to the contralateral pontine gray terminate predominantly in two regions--one in the caudal aspect of the medial pontine subdivision and another overlapping the ventral and lateral subdivisions. Within the medial and ventral lateral nuclear regions, fibers from nucleus cuneatus primarily terminated more rostrally to afferents from the nucleus gracilis. Spinal trigeminal projections terminated most heavily within the contralateral pontine gray at midpontine levels. Similar to the dorsal column nuclear projections, trigeminal afferents were observed in the medial and ventrolateral subdivisions, although these terminations were rostral and dorsal to areas receiving cuneatus input. Additional projections from the spinal trigeminal nuclei to the contralateral ventral peduncular nucleus were also observed. In comparison to the above-mentioned pontine afferents, both high cervical and midthoracic spinal cord lesions produced a similar pattern of axonal degeneration in the ipsilateral pontine gray which overlapped substantially with gracilis inputs. The observed topographic distribution pattern of ascending afferents to pontine gray confirm and extend previous findings which in general have only briefly described these pathways.

Afferent Pathways↗
PubMed1984

Projections to the frontal cortex from the posterior parietal region in the rhesus monkey.

The projections to the frontal cortex from the various subdivisions of the posterior parietal region in the rhesus monkey were studied by means of autoradiographic technique. The rostral superior parietal lobule (area PE) projects to the dorsal areas 4 and 6 on the lateral surface of the frontal lobe as well as to the supplementary motor area (MII) on its medial surface. The caudal area PE sends its connections to dorsal area 6 and MII. The projections from the medial parietal cortex (areas PEc and PGm) are similar to those of the superior parietal lobule but they tend to concentrate in the more rostral part of dorsal area 6, MII, and in the cingulate gyrus (area 24). The most caudal part of the medial parietal cortex also projects to area 8. The anteriormost part of the inferior parietal lobule (area PF) projects to the ventral area 6, including the caudal bank of the lower branch of the arcuate sulcus, to the ventral area 46 below the sulcus principalis, and to the frontal and pericentral opercular cortex. The middle inferior parietal lobule (areas PFG and PG) projects to the ventral part of area 46 and area 8, whilst the posteriormost inferior parietal lobule (caudal PG and area Opt) is connected with both dorsal and ventral area 46, dorsal area 8, as well as the anteriormost dorsal area 6, and the cingulate gyrus (area 24).

Animals↗
PubMed1985

Primary afferent projections of the major splanchnic nerve to the spinal cord and gracile nucleus of the cat.

Splanchnic afferent projections to the spinal cord and gracile nucleus were labeled following the application of HRP to the central cut end of the major splanchnic nerve. Labeled afferent fibers were detected in the ipsilateral dorsal column, in Lissauer's tract (LT), in laminae 1, 5, 7, and 10, and in the dorsal gray commissure at T1-T13 levels of the spinal cord. Afferent projections were not identified in laminae 2-4. Collaterals from LT projected ventrally along the lateral and medial margins of the dorsal horn (called lateral and medial pathways, respectively). Afferents in the lateral pathway formed small bundles, spaced rostrocaudally at intervals of 300-1,000 microns, which passed medially at the base of the dorsal horn into laminae 5, 7, and 10 and to the contralateral spinal cord. Some afferents in the lateral pathway projected to the intermediolateral nucleus where labeled sympathetic preganglionic neurons were located. Afferents in the medial pathway entered the lateral aspect of the dorsal column and projected as a group near the midline rostrally to the medulla. The dorsal column pathway terminated in the ventral gracile nucleus in four or five clusters, each occupying a region ranging in size from 0.01-0.1 mm3 and separated in the rostrocaudal axis by distances of 400-800 microns. These clusters were concentrated in the middle and caudal portions of the nucleus below the obex. A comparison of the present results with those from earlier experiments on the central projections of afferent fibers from the heart, kidney, and pelvic organs demonstrates a consistent pattern of visceral afferent termination in the thoracolumbar and sacral segments of the spinal cord. This is not unexpected, since visceral afferent pathways to different organs perform similar functions, such as the transmission of nociceptive information and the initiation of autonomic reflexes.

Afferent Pathways↗
PubMed1985

Cortical projections of the dorsolateral visual area in owl monkeys: the prestriate relay to inferior temporal cortex.

The dorsolateral visual area (DL) is one of a number of visual areas that have been defined by electrophysiological mapping procedures and cortical architecture in the extrastriate cortex of owl monkeys. The projections of DL were determined by the intra-axonal transport of 3H-proline, 3H-acetyl-wheat germ agglutinin, and horseradish peroxidase after cortical injections. The major ipsilateral projection of DL defined a new subdivision of the visual cortex in owl monkeys, the caudal inferior temporal cortex. Single injections in DL sometimes produced label in two separate regions in the caudal inferior temporal cortex, suggesting that functional subdivisions exist in this projection zone. Other targets of DL included the region of the frontal eye fields, the dorsomedial visual area, the dorsointermediate visual area (DI), a region of the cortex rostral to DI which we call the temporoparietal cortex, and possibly the ventral (V) and posterior parietal areas. A major feedback projection of DL was to V-II. Projections from DL to V-II and the dorsomedial visual area were roughly retinotopic. Projections from DL to the contralateral cerebral hemisphere were to DL and the inferior temporal cortex. Overall, the results support the concept that a major relay of visual information proceeds from V-I to V-II to DL and then to the inferior temporal cortex. In addition, similarities in connection patterns of DL in owl monkeys and V4 in macaque monkeys suggest that DL and much or all of V4 are homologous.

Animals↗
PubMed1985

Organization of cerebral cortical afferent systems in the rat. II. Hypothalamocortical projections.

The organization of hypothalamic projections to the cerebral cortex in the rat has been studied using retrograde and anterograde tracer methods. Four separate populations of hypothalamic neurons, which constitute a major source of diffuse cortical innervation, were identified: Tuberal lateral hypothalamic (LHAt) neurons which innervate the cerebral cortex tend to cluster in the perifornical region, in the zona incerta, and along the medial edge of the cerebral peduncle, at levels roughly coextensive with the ventromedial hypothalamic nucleus. Most of these neurons project to the ipsilateral cortex; a small percentage innervate the contralateral cortex, but this varies among cortical terminal fields. The perifornical neurons are organized in a roughly topographic medial-to-lateral relationship with respect to their cortical terminal fields. Field of Forel (FF) neurons, which project primarily to the frontal cortex of the ipsilateral hemisphere, are located just ventral to the medial edge of the medial lemniscus, at the level of the ventromedial basal thalamic nucleus. The more laterally placed neurons innervate the lateral frontal, insular and perirhinal cortex; the more medial neurons, around the mammillothalamic tract, innervate the medial frontopolar, prelimbic, infralimbic, and anterior cingulate cortex. Posterior lateral hypothalamic (LHAp) neurons form a dense cluster spanning the lateral hypothalamus, from the cerebral peduncle to the posterior hypothalamic area at premammillary levels, and extending into the supramammillary nucleus and the adjacent ventral tegmental area. LHAp neurons innervate the entire cerebral cortex, predominantly on the ipsilateral side. Populations of LHAp neurons projecting to different cortical target areas show considerable spatial overlap, but computer plots of the centers of these populations demonstrate a strict topographic relationship with respect to the cerebral cortex. Tuberomammillary (TMN) neurons form a sheet along the ventrolateral surface of the premammillary hypothalamus. About twice as many TMN neurons innervate the ipsilateral, as compared to the contralateral hemisphere; it is not known whether single neurons project to both hemispheres. No topographic organization of the TMN cortical projection is apparent. Injections of different-colored fluorescent dyes into various cortical areas demonstrate that hypothalamic neurons in general have rather restricted cortical terminal fields. Only occasional neurons are found, primarily in LHAt, which are double labeled by injections into different cytoarchitectonic areas.(ABSTRACT TRUNCATED AT 400 WORDS)

Afferent Pathways↗
PubMed1985

The projection of three extrathalamic cell groups to the cerebral cortex of the turtle Pseudemys.

Three extrathalamic subcortical inputs to the part of the cerebral cortex that is known to receive thalamic fibers in the turtle were examined in the present study. Direct projections from the locus coeruleus, the superior medial raphe nucleus, and a wide area of the basal telencephalon that lies ventromedial to the globus pallidus were demonstrated with the horseradish peroxidase method. Fluorescence histochemistry confirmed the presence of catecholamine-containing fibers in the rostral half of dorsal cortex and also demonstrated a dense network of serotoninergic fibers. Biochemical analysis showed the concentration of both monoamines to be relatively high; the norepinephrine concentration was 709 ng/g and the serotonin concentration was 1,750 ng/g. No evidence was found to suggest the existence of either a dopamine fiber projection to cortex comparable to that of mammalian neocortex or the presence of an epinephrine pathway to turtle cortex equivalent to the epinephrine-containing fibers in the pallium of amphibians. The coexistence of the projections from the thalamus with noradrenergic projections from the locus coeruleus, serotoninergic projections from the superior medial raphe nucleus, and presumably cholinergic projections from the basal telencephalon provide at least four distinct subcortical inputs to the reptilian dorsal cortex. Neither thalamic nor similar extrathalamic inputs have been demonstrated in the dorsal pallium of amphibia. Mammalian neocortex, in contrast, has even more elaborately differentiated inputs of both types. These results support the idea that thalamic and extrathalamic inputs to cortex appear at the same time in vertebrate evolution, and that both types of inputs are required for the normal development and function of neocortex.

Animals↗
PubMed1985

Projections from the nucleus tractus solitarii to the rostral ventrolateral medulla.

Projections from the nucleus tractus solitarii (NTS) to autonomic control regions of the ventrolateral medulla, particularly the nucleus reticularis rostroventrolateralis (RVL), which serves as a tonic vasomotor center, were analyzed in rat by anterograde, retrograde, and combined axonal transport techniques. Autonomic portions of the NTS, including its commissural, dorsal, intermediate, interstitial, ventral, and ventrolateral subnuclei directly project to RVL as well as to other regions of the ventrolateral medulla. The projections are organized topographically. Rostrally, a small cluster of neurons in the intermediate third of NTS, the subnucleus centralis, and neurons in proximity to the solitary tract selectively innervate neurons in the retrofacial nucleus and nucleus ambiguus. Neurons generally located in more caudal and lateral sites in the NTS innervate the caudal ventrolateral medulla (CVL). The RVL, CVL, and nucleus retroambiguus are interconnected. A combined retrograde and anterograde transport technique was developed so as to prove that projections from the NTS to the ventrolateral medulla specifically innervate the region of RVL containing neurons projecting to the thoracic spinal cord or the region of the nucleus containing vagal preganglionic neurons. When the retrograde tracer, fast blue, was injected into the thoracic spinal cord, and wheat germ agglutinin-conjugate horseradish peroxidase (HRP) was injected into the NTS, anterogradely labeled terminals from the NTS surrounded the retrogradely labeled neurons in the RVL and in the nucleus retroambiguus in the caudal medulla. Among the bulbospinal neurons in the RVL innervated by the NTS were adrenaline-synthesizing neurons of the C1 group. When fast blue was applied to the cervical vagus, and HRP was injected into the NTS, anterogradely labeled terminals from the NTS surrounded retrogradely labeled neurons in the rostral dorsal motor nucleus of the vagus, the region of the nucleus ambiguus, the retrofacial nucleus, and the dorsal portion of the RVL, a region previously shown to contain cardiac vagal preganglionic neurons. This combined anterograde and retrograde transport technique provides a useful method for tracing disynaptic connections in the brain. These data suggest that the RVL is part of a complex of visceral output regions in the ventrolateral medulla, all of which receive afferent projections from autonomic portions of the NTS. Bulbospinal neurons in the RVL, in particular the C1 adrenaline neurons, may provide a portion of the anatomic substrate of the baroreceptor and other visceral reflexes.

Afferent Pathways↗
PubMed1985

Laminar organization of geniculocortical projections in Galago senegalensis and Aotus trivirgatus.

The projections of the lateral geniculate nucleus to striate cortex were traced by anterograde and retrograde transport of WGA-HRP in two primates, Galago and Aotus. The goal was to determine the laminar organization of the terminals of individual layers of the lateral geniculate nucleus. The results show that in both species the magnocellular layers project to cortical layer IV alpha, the parvicellular layers project to IV beta, and the intercalated geniculate layers (which term includes layers 4 and 5 in Galago) project to layers III and I. The distribution of terminals in layer III is periodic, which is to say, there are regularly spaced regions of terminals separated by regions devoid of terminals. When the two species are compared to Saimiri, it is clear that the basic organization of the three pathways relaying in the lateral geniculate nucleus is common to all three primates. At the same time, there are some significant species differences. The total pattern of projections in Galago is compressed in comparison to that in the monkey, and this compression seems to be related to the poorer differentiation of cortical layers in the prosimian. For example, layer IIIC is distinct only in the two monkeys and at the same time it is spared from geniculate terminations. Both Galago and Aotus differ from Saimiri in that they lack a projection from the parvicellular geniculate layers to the layer IIIB. These species comparisons are relevant to the questions of the functional significance of the three pathways and the evolution of the primate striate cortex.

Animals↗
PubMed1986

Cortical projections originating from the cat's insular area and remarks on claustrocortical connections.

The cortical projections originating in the cat's insular cortex and claustrum were investigated with the aid of the horseradish peroxidase retrograde tracing technique. Twenty small injections of horseradish peroxidase were distributed along lateral and medial regions of the hemisphere. Labeling in the insular cortex occurred following all injections except those six situated along the lateral gyrus--that is, within the visual cortex. In the claustrum labeled neurons were found following all injections, except following the injection situated in the posterior temporal area. Claustral labeling was frequently more intense than insular labeling. The injections into the occipital cortex that revealed no insular innervation nevertheless received a considerable number of claustral projections. As the insular cortex itself receives at most a minor projection from the claustrum the differing cortical projection patterns of insula and claustrum have to be considered unrelated. Our findings confirm the view that the claustrum projects to most regions of the cerebral cortex; these projections are at least in part topographically organized. A topographical pattern can also be constructed for the insular cortex, though it is less stringent than for the claustrocortical connections. Both the afferent and efferent connections of the insula show similarities to those of the prefrontal cortex. Nevertheless, the insula differs in that it receives strong input from the sensory associative nuclei of the thalamus. Consequently, and in line with behavioral observations following its ablation, we consider the insula as involved in the temporal structuring of perceived patterns.

Animals↗
PubMed1986

Projections from the anteroventral cochlear nucleus to the lateral and medial superior olivary nuclei.

The projections from the cochlear nucleus to the lateral and medial superior olivary nuclei were studied in the cat by use of retrograde transport of horseradish peroxidase to demonstrate the connections. The medial superior olivary nucleus receives input only from the anterior and posterodorsal subdivisions of the anterior division of the anteroventral cochlear nucleus (AA and APD, respectively; Brawer, Morest, and Kane: J. Comp. Neurol. 155: 251-300, 1974). These two subdivisions are populated almost exclusively by spherical bushy cells. Like the medial superior olivary nucleus, the lateral superior olivary nucleus receives inputs from AA and APD. In addition, the lateral superior olivary nucleus receives projections from the posterior subdivision (AP) of the anterior division and also from the posterior division of the anteroventral cochlear nucleus. The projections to the medial superior olivary nucleus are bilateral, whereas the projections to the lateral superior olivary nucleus are almost entirely ipsilateral. One implication of the results is that the medial superior olivary nucleus receives inputs from only one cell type--the spherical bushy cell--but that, at the least, two cell types project to the lateral superior olivary nucleus. Both the olivary nuclei receive input from most, if not all, of the dorsoventral extent of the anteroventral cochlear nucleus, implying that both receive input from neurons arrayed across the entire frequency representation of the anteroventral cochlear nucleus. All of the projections appear to be organized topographically such that frequency representation is preserved.

Animals↗
PubMed1986

Afferent projections to the interpeduncular nucleus in the rat, as studied by retrograde and anterograde transport of wheat germ agglutinin conjugated to horseradish peroxidase.

We examined the afferent projections to the subnuclei of the interpeduncular nucleus (IPN) in the rat by means of retrograde and anterograde transport of wheat germ agglutinin conjugated to horseradish peroxidase (WGA-HRP). We observed locations of retrogradely labeled cells following injections of WGA-HRP into the IPN, and distributions of anterogradely labeled fibers and terminals within the IPN following injections into the areas that contain cells of origin of afferents. Results of the retrograde and anterograde experiments have clarified the detailed organization of the IPN afferents. A part of the nucleus incertus, located dorsomedial to the dorsal tegmental nucleus, projects to the contralateral half of the rostral subnucleus of the IPN; the pars caudalis of the dorsal tegmental nucleus projects sparsely to the rostral lateral, dorsal lateral, lateral, caudal, and apical subnuclei predominantly contralaterally; the laterodorsal tegmental nucleus, to most of the subnuclei predominantly contralaterally; the ventromedial central gray rostral to the dorsal tegmental nucleus and lateral to the dorsal raphe nucleus projects to the rostral lateral and dorsal lateral subnuclei predominantly contralaterally; the median raphe nucleus, substantially to all subnuclei; the medial habenular nucleus, in a topographic manner, to the rostral, central, and intermediate subnuclei, to the rostral lateral and lateral subnuclei predominantly ipsilaterally, and to the dorsal lateral subnucleus predominantly contralaterally; the supramammillary nucleus and areas around the origin of the mammillothalamic tract and near the third ventricle project sparsely to the ventral part of the rostral subnucleus and to the central, lateral, caudal and apical subnuclei; the nucleus of the diagonal band, sparsely to the rostral, central, dorsal lateral, caudal, and apical subnuclei. These differential projections of the afferents to the subnuclei of the IPN may reflect its complex functions within the limbic midbrain circuit.

Afferent Pathways↗
PubMed1986

The topography of expanded uncrossed retinal projections following neonatal enucleation of one eye: differing effects in dorsal lateral geniculate nucleus and superior colliculus.

The topographic organization of the uncrossed retinal projections to the dorsal lateral geniculate nucleus (dLGN) and superior colliculus (SC) was studied in normal adult hooded rats and in rats subjected to unilateral ocular enucleation on the day of birth. Sections were stained for anterograde degeneration products following discrete retinal lesions at various locations. The projection from the temporal crescent to the dLGN in neonatally enucleated rats had an expanded but topographically normal organization, with the nasotemporal and dorsoventral retinal axes displaying polarities identical to those in normal adults. Neonatal enucleation permits the remaining uncrossed retinogeniculate projection to extend primarily along the "lines of projection" into neuropil normally recipient of binocularly conjugate crossed projections. In the SC, the dorsoventral axis of the temporal crescent showed a normal polarity, but the nasotemporal axis failed to display any topographic organization. Retinal loci in the temporal crescent projected throughout the rostrocaudal extent of the ipsilateral SC. Retinal lesions placed outside the temporal crescent failed to produce any substantial degeneration in ipsilateral dLGN or SC. These topographically distinct effects in dLGN and SC following unilateral eye removal on the day of birth are discussed in the context of differing constraints upon axonal ingrowth and connectivity during early development, which may normally bring about the characteristically distinct features of retinogeniculate and retinocollicular organization.

Animals↗
PubMed1986

Cerebellar nucleocortical projection with a survey of factors affecting the transport of radioactive tracers.

The nucleocortical projection has been studied with the method of anterograde transport of tritiated amino acids and autoradiography. It was observed that this projection is made up of a small number of fibers. Counts of silver grain aggregates in projection sites of the granular layer were compared with counts from material on the cuneocerebellar projection. As it had been concluded in previous studies that the projection is quantitatively important, several modifications of the experimental conditions were tested. Radioactive leucine of high or low specific activity as well as a mixture of amino acids were used. It was observed that labeling is always more intense with a high specific activity tracer. Variations of the aspect and density of the projection were observed with survival periods lasting from a few hours to several days. With survival times between 9 and 15 hours, round aggregates of silver grains measuring from 10 to 20 microns were observed in the granular layer of labeled regions. At longer survival periods, the terminal structures in the granular layer appeared as coarse linear aggregates. It is suggested that the latter represent preterminal labeled fragments while the round accumulations correspond to terminal rosettes. Maximum density of the labeling in the granular layer occurred between 9 and 15 hours. At 2 days, the density was lowest, and at 5 or 6 days it was somewhat higher. Even under optimal conditions, the density of the nucleocortical terminals was low.

Afferent Pathways↗
PubMed1987

Topography of the corticofugal projection to the lateral reticular nucleus in the monkey.

The cortical projection to the lateral reticular nucleus (LRN) was explored in monkeys prepared for autoradiography and horseradish peroxidase (HRP) histochemistry. An unambiguous projection was revealed only in cases with injections of the precentral forelimb and hindlimb areas. The forelimb area projection occupied centromedial segments, the hindlimb area projection occupied ventrolateral segments of the LRN with very little overlap. Some sparse labeling was also seen with injections of the supplementary motor area (SMA), but only when the lectin-bound tracer HRP was injected and not when autoradiography was used. Retrogradely labeled cortical cells occupied a larger cortical area in one case with injection of free HRP into the LRN. Since the additional expanse of cortex, however, was not examined in anterograde cases, and since the injected marker substance had diffused to neighboring structures, the significance of the labeled cells outside the precentral motor cortex is questionable. There was no evidence for a projection from the precentral face area with either anterograde tracing method. The corticoreticular projection was bilateral and only slightly more marked contralateral to the injection. The labeling was largely confined to the magnocellular division with minor amounts in the parvicellular division (especially in the hindlimb cases). The subtrigeminal portion was spared in all cases. It is concluded that the LRN constitutes another somatotopically organized precerebellar nucleus relaying signals from the motor cortex to the cerebellum. Compared with the corticopontocerebellar pathway in monkeys, however, the LRN is only a minor component of the corticocerebellar transmission system.

Animals↗
PubMed1987

Neostriatal projections from cytoarchitectonically defined gyri in the prefrontal cortex of the dog.

The cytoarchitecture and neostriatal projections of the canine prefrontal cortex (PFC) were examined by using Nissl, silver degeneration, autoradiographic, and horseradish peroxidase techniques. Cytoarchitectonically, the PFC can be divided into six major gyral areas with each area corresponding to one of the major gyri--proreal, polar, pregenual, subproreal, paraorbital, and orbital--defined myeloarchitectonically by Kreiner (J. Comp. Neurol. 116:117-133, '61). Of the six major areas, only the proreal gyrus displays a distinctly granular layer IV. In all other gyri, layer IV is more difficult to distinguish. In both the orbital and polar gyri, layer IV is poorly defined and consists of scattered clusters of small cells between layers III and V. In the pregenual, subproreal, and paraorbital gyri, layer IV is not detectable. In all gyri, layer V consists of a thin lamina of small and medium-size pyramidal cells. The transition from layer III to layer V is marked by changes in cell density and size as well as staining intensity. Borders between layers V and VI are generally less distinct than those between layers III and V, with the exception of the pregenual gyrus, in which layer V is separated from layer VI by a distinct cell-poor lamina. In the subproreal and paraorbital gyri, the border between the underlying white matter and layer VI is particularly distinct, with large numbers of neurons oriented tangentially to the white matter. In contrast, the border between layer VI of the orbital gyrus and the white matter is less distinct and consists of palisades of neurons extending well into the white matter. The silver degeneration and autoradiographic methods revealed that prefrontostriatal projections terminate as dorsoventrally oriented longitudinal bands within the medial half of the head and body of the caudate nucleus. Projections from the polar and dorsal proreal gyri terminate most medially in the nucleus while projections from the lateral part of the proreal, subproreal, orbital, and paraorbital gyri terminate progressively more laterally within the medial half of the nucleus. There is apparent overlap between adjacent projection fields. A sparse projection was also noted to a small part of the putamen adjacent to the internal capsule. Injections of horseradish peroxidase into the medial and ventromedial parts of the head of the caudate nucleus resulted in widespread retrograde labeling in parts of the proreal, pregenual, paraorbital, subproreal, and central precruciate gyri. Labeled neurons were located primarily in the superficial part of layer V with smaller numbers of labeled cells in layers III, IV, and VI.(ABSTRACT TRUNCATED AT 400 WORDS)

Amino Acids↗