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Showing papers in "The Journal of Comparative Neurology in 1977"


Journal ArticleDOI
TL;DR: The efferent connections of the hippocampal formation of the rat have been re‐examined autoradiographically following the injection of small quantities of 3H‐amino acids into different parts of Ammon's horn and the adjoining structures to indicate quite clearly that each component of the hippocampusal formation has a distinctive pattern ofefferent connections.
Abstract: The efferent connections of the hippocampal formation of the rat have been re-examined autoradiographically following the injection of small quantities of 3H-amino acids (usually 3H-proline) into different parts of Ammon's horn and the adjoining structures. The findings indicate quite clearly that each component of the hippocampal formation has a distinctive pattern of efferent connections and that each component of the fornix system arises from a specific subdivision of the hippocampus or the adjoining cortical fields. Thus, the precommissural fornix has been found to originate solely in fields CA1-3 of the hippocampus proper and from the subiculum; the projection to the anterior nuclear complex of the thalamus arises more posteriorly in the pre- and/or parasubiculum and the postsubicular area; the projection to the mammillary complex which comprises a major part of the descending columns of the fornix has its origin in the dorsal subiculum and the pre- and/or parasubiculum; and finally, the medial cortico-hypothalamic tract arises from the ventral subiculum. The lateral septal nuclei (and the adjoining parts of the posterior septal complex) constitute the only subcortical projection field of the pyramidal cells in fields CA1-3 of Ammon's horn. There is a rostral extension of the pre-commissural fornix to the bed nucleus of the stria terminalis, the nucleus accumbens, the medial and posterior parts of the anterior olfactory nucleus, the taenia tecta, and the infralimbic area, which appears to arise from the temporal part of field CA, or the adjacent part of the ventral subiculum. The projection of Ammon's horn upon the lateral septal complex shows a high degree of topographic organization (such that different parts of fields CA1 and CA3 project in an ordered manner to different zones within the lateral septal nucleus). The septal projection of “CA2” and field CA3 is bilateral, while that of field CA1 is strictly unilateral. In addition to its subcortical projections, the hippocampus has been found to give rise to a surprisingly extensive series of intracortical association connections. For example, all parts of fields CA1, CA2 and CA3 project to the subiculum, and at least some parts of these fields send fibers to the pre- and parasubiculum, and to the entorhinal, perirhinal, retrosplenial and cingulate areas. From the region of the preand parasubiculum there is a projection to the entorhinal cortex and the parasubiculum of both sides. That part of the postsubiculum (= dorsal part of the presubiculum) which we have examined has been found to project to the cingulate and retrosplenial areas ipsilaterally, and to the entorhinal cortex and parasubiculum bilaterally.

1,561 citations


Journal ArticleDOI
TL;DR: The mediodorsal nucleus of the rat thalamus has been divided into medial, central and lateral segments, and these segments have been shown by experiments using the autoradiographic method of demonstrating axonal connections to project to seven distinct cortical areas covering most of the frontal pole of the hemisphere.
Abstract: The mediodorsal nucleus of the rat thalamus has been divided into medial, central and lateral segments on the basis of its structure and axonal connections, and these segments have been shown by experiments using the autoradiographic method of demonstrating axonal connections to project to seven distinct cortical areas covering most of the frontal pole of the hemisphere. The position and cytoarchitectonic characteristics of these areas are described. The medial segment of the nucleus projects to the prelimbic area (32) on the medial surface of the hemisphere, and to the dorsal agranular insular area, dorsal to the rhinal sulcus on the lateral surface. The lateral segment projects to the anterior cingulate area (area 24) and the medial precentral area on the dorsomedial shoulder of the hemisphere, while the central segment projects to the ventral agranular insular area in the dorsal bank of the rhinal sulcus, and to a lateral part of the orbital cortex further rostrally. (The term "orbital" is used to refer to the cortex on the ventral surface of the frontal pole of the hemisphere.) A ventral part of this orbital cortex also receives fibers from the mediodorsal nucleus, possibly its lateral segment, but the medial part of the orbital cortex, and the ventrolateral orbital area in the fundus of the rhinal sulcus receive projections from the paratenial nucleus and the submedial nucleus, respectively. All of these thalamocortical projections end in layer III, and in the outer part of layer I. The basal nucleus of the ventromedial complex (the thalamic taste relay) has been shown to have a similar laminar projection (layer I and layers III/IV) to the granular insular area immediately dorsal to, but not overlapping, the mediodorsal projection field. However, the principal nucleus of the ventromedial complex appears to project to layer I, and possibly layer VI, of the entire frontal pole of the hemisphere. The anteromedial nucleus does not appear to project to layer III of the projection field of the mediodorsal nucleus, although it may project to layers I and VI, especially in the anterior cingulate and medial precentral areas. A thalamoamygdaloid projection from the medial segment of the mediodorsal nucleus to the basolateral nucleus of the amygdala has also been demonstrated, which reciprocates an amygdalothalamic projection from the basolateral nucleus to the medial segment. The habenular nuclei also appear to project to the central nucleus of the amygdala. These results are discussed in relation to the delineation and subdivision of the prefrontal cortex in the rat, and to amygdalothalamic and amygdalocortical projections which are described in a subsequent paper (Krettek and Price, '77).

1,259 citations


Journal ArticleDOI
TL;DR: Projections are described from the basolateral, lateral and anterior cortical nuclei of the amygdaloid complex, and from the prepiriform cortex, to several discrete areas of the cerebral cortex in the rat and cat and to the mediodorsasl thalamic nucleus in the rats.
Abstract: Projections are described from the basolateral, lateral and anterior cortical nuclei of the amygdaloid complex, and from the prepiriform cortex, to several discrete areas of the cerebral cortex in the rat and cat and to the mediodorsal thalamic nucleus in the rat. These projections are very well-defined in their origin, and in their area of laminar pattern of termination. The basolateral amygdaloid nucleus can be divided into anterior and posterior divisions, based on cytoarchitectonic and connectional distinctions. In both the rat and cat the posterior division projects to the prelimbic area (area 32) and the infralimbic area (area 25) on the medical surface of the hemisphere. The anterior division projects more lightly to these areas, but also sends fibers to the dorsal and posterior agranular insular areas and the perirhinal area on the lateral surface. Furthermore, in the cat the perirhinal area is divided into two areas (areas 35 and 36) and the anterior division projects to both of these and also to a ventral part of the granular insular area; this last area is adjacent to, but separate from the auditory insular area and the second cortical taste area. In most of these areas, the fibers from the basolateral nucleus terminate predominantly in two bands: one in the deep part of layer I and layer II, and a heavier band in layer V (in the rat) or layers V and VI (in the cat). The lateral amygdaloid nucleus projects heavily to the perirhinal area, and also to the posterior agranular insular area. These fibers terminate predominantly in the middle layers of the cortex, although the cellular lamination in these two areas is relatively indistinct. The anterior cortical amygdaloid nucleus and the prepiriform cortex both project to the infralimbic area and the ventral agranular insular area, and the anterior cortical nucleus also projects to the posterior agranular area and the perirhinal area. In all of these areas, the fibers from these olfactory-related structures terminate in the middle of layer I. In the rat, the two divisions of the basolateral nucleus also project to the medial segment of the mediodorsal thalamic nucleus, with the anterior division projecting mainly to the posterior part of this segment and the posterior division to the anterior part. The endopiriform nucleus, deep to the prepiriform cortex, projects to the central segment of the mediodorsal nucleus; this may constitute the major olfactory input into the mediodorsal nucleus, since little or no projection could be demonstrated from the prepiriform cortex itself. Projections to the mediodorsal nucleus have not been found in the cat.

781 citations


Journal ArticleDOI
TL;DR: The afferent connections of the habenular complex in the rat were examined by injecting horseradish peroxidase into discrete portions of theHabenular nuclei by microelectrophoresis.
Abstract: The afferent connections of the habenular complex in the rat were examined by injecting horseradish peroxidase (HRP) into discrete portions of the habenular nuclei by microelectrophoresis.

778 citations


Journal ArticleDOI
TL;DR: After lesions of inferior olive, survival times of 5 to 12 days and Nauta staining, degeneration is present in white matter and central cerebellar nuclei and Deiters' nucleus andOccasional labeling of mossy fiber terminals is explained by involvement of reticular nuclei.
Abstract: After lesions of inferior olive, survival times of 5 to 12 days and Nauta staining, degeneration is present in white matter and central cerebellar nuclei and Deiters' nucleus. Shorter survival times from 40 to 60 hours and Fink-Heimer impregnation reveal degenerating climbing fiber terminals in the molecular layer. With 3H-leucine autoradiography and survival times of three to seven days the entire trajectory of the climbing fibers can be traced. Olivocerebellar fibers cross in the brain stem and terminate contralaterally in cortex and central nuclei. Occasional labeling of mossy fiber terminals is explained by involvement of reticular nuclei. Small parts of the inferior olive connect with narrow longitudinal zones in the cortex through compartments in the white matter. The corresponding distribution of olivocerebellar fibers and Purkinje cell axons over these compartments suggests that the organization of the olivocerebellar and corticonuclear projection is essentially similar. Collaterals always terminate in the central cerebellar necleus which receives a corticonuclear projection from the zone in which the parent fibers terminate. Caudal medial accessory olive projects to medial vermal zone A and to fastigial nucleus, subnucleus beta projecting to lobule VII and caudal fastigial nucleus. Cadual dorsal accessory olive projects to lateral vermal zone B in lobules I-VI, Deiters' nucleus and dorsomedial subnucleus of interposed nucleus. The caudal principal olive (dorsal cap, ventrolateral outgrowth receiving visual and vestibular input) projects to flocculo-nodular lobe.

582 citations


Journal ArticleDOI
TL;DR: The differential projections of the three main cellular strata of the superior colliculus have been examined in the cat by the autoradiographic method and several of these projections are topographically organized.
Abstract: The differential projections of the three main cellular strata of the superior colliculus have been examined in the cat by the autoradiographic method. The stratum griseum superficiale projects caudally to the parabigeminal nucleus and rostrally to several known visual centers: the nucleus of the optic tract and the olivary pretectal nucleus in the pretectum; the deepest C laminae of the dorsal lateral geniculate nucleus; the large-celled part of the ventral lateral geniculate nucleus; the posteromedial, large-celled part of the lateral posterior nucleus of the thalamus. Several of these projections are topographically organized. The stratum griseum profundum gives rise to most of the descending projections of the superior colliculus. Ipsilateral projections pass to both the dorsolateral and lateral divisions of the pontine nuclei, the cuneiform nucleus, and the raphe nuclei, and to extensive parts of the brainstem reticular formation: the tegmental reticular nucleus, and the paralemniscal, lateral, magnocellular, and gigantocellular tegmental fields. Contralateral projections descending in the predorsal bundle pass to the medial parts of the tegmental reticular nucleus and of some of the tegmental fields, the dorsal part of the medial accessory nucleus of the inferior olivary complex, and to the ventral horn of the cervical spinal cord. Ascending projections of the stratum griseum profundum terminate in several nuclei of the pretectum, the magnocellular nucleus of the medial geniculate complex and several intralaminar nuclei of the thalamus, and in the fields of Forel and zona incerta in the subthalamus. The strata grisea profundum and intermediale each have projections to homotopic areas of the contralateral superior colliculus, to the pretectum, and to the central lateral and suprageniculate nuclei of the thalamus. However, the stratum griseum intermediale has few or no descending projections.

533 citations


Journal ArticleDOI
TL;DR: The retrograde, horseradish peroxidase technique has been used to demonstrate the cells of origin of corticofugal fiber systems arising in the rat somatic sensory cortex and projecting to the striatum, diencephalon, brainstem, and spinal cord.
Abstract: The retrograde, horseradish peroxidase technique has been used to demonstrate the cells of origin of corticofugal fiber systems arising in the rat somatic sensory cortex and projecting to the striatum, diencephalon, brainstem, and spinal cord. Correlative experiments conducted with the anterograde, autoradiographic method have been used to confirm the terminal distribution of many of these fiber systems. Corticofugal pathways directed to subcortical structures arise in the first and second somatic sensory areas exclusively from pyramidal cells of the infragranular layers, V and VI. Fibers which descend to the midbrain, pons, medulla and spinal cord arise exclusively from the largest pyramidal cells, the somata of which are found in the deep part of layer V (layer VB). There is some evidence for a sublaminar organization of the different classes of efferent cells within this layer. Fibers projecting to the diencephalon arise from somata situated throughout layer VI and to a lesser extent in layer V. Corticostriatal fibers arise only from cells with somata in layer V, but the somata are more superficially situated than those of the other classes of corticofugal neurons. The laminar distribution of the somata of corticofugal neurons differs considerably from that of commissural and ipsilateral corticocortical neurons.

515 citations


Journal ArticleDOI
TL;DR: Axonal projections are described from the lateral and hasolateral nuclei of the amygdaloid complex, and from the overlying periamygdaloids and pre‐piriform cortices and the endopiriform nucleus, to the lateral entorhinal area, the ventral part of the subiculum, and the parasubiculum in the cat and rat.
Abstract: Axonal projections are described from the lateral and basolateral nuclei of the amygdaloid complex, and from the overlying periamygdaloid and prepiriform cortices and the endopiriform nucleus, to the lateral entohinal area, the ventral part of the subiculum, and the parasubiculum in the cat and rat. All of these projections have well-defined laminar patterns of termination, which are complementary to those of other projections to the same structure. Based on these results, and on cytoarchitectonic distinctions, the lateral entohinal area has been divided into dorsal, ventral, and ventromedial subdivisions. The olfactory bulb and prepiriform cortex project to layers IA and IB, respectively, of all three subdivisions, but the lateral amygdaloid nucleus has a restricted projection to layer III of the ventral subdivision only. The periamygdaloid cortex projects to layer II of the ventromedial and adjoining parts of the ventral subdivisions. The ventral part of the subiculum receives fibers from the posterior division of the basolateral nucleus, which terminate in the cellular layer and the deep half to one-third of the plexiform layer. The periamygdaloid cortex and the endopiriform nucleus also project to the same part of the subiculum, but these fibers terminate in the outer part of the plexiform layer. None of these projections extend into the dorsal part of the subiculum. The posterior division of the basolateral nucleus also projects to the posterodorsal part of the parasubiculum ("parasubiculum a" of Blackstad, '56). These fibers end in the deeper part of the plexiform layer and the superficial part of the cellular layer.

515 citations


Journal ArticleDOI
TL;DR: The cells of origin of cortico‐cortical and sub cortical projections from the subfields of the somatic sensory area and from the motor cortex have been identified in cynomolgus and squirrel monkeys by the retrograde axonal transport method.
Abstract: The cells of origin of cortico-cortical and subcortical projections from the subfields of the somatic sensory area and from the motor cortex have been identified in cynomolgus and squirrel monkeys by the retrograde axonal transport method. The somata of the cells of origin of a particular fiber system have a specific laminar or sublaminar distribution. The somata of the majority of cortico-cortical cells lie in the supragranular layers. Those projecting to the opposite cortex are confined to the deeper half of layer III (layer IIIB). Ipsilateral cortico-cortical neurons lie mainly superficial to them in layers IIIA and II, but in the second somatic sensory area (SII) and in area 2 of the first (SI), small numbers are also found in layer V. Corticospinal cells lie in the deeper part of layer V and corticostriatal cells in the superficial part. Corticopontine, corticobulbar and corticorubral cells lie in between. The majority of corticothalamic cells lies in layer VI but a second, smaller population is found in the deep part of layer V. The cells giving rise to a particular set of efferent connections can be distinguished in terms of size and, with the exception of the corticospinal cells, their size does not vary greatly from area to area. In many cases, the size and laminar specificity indicates that cells sending axons to one site cannot have collateral branches projecting to another. In most of the fiber systems studied, labeled cells form single or multiple strips, 0.5–1 mm wide and oriented mediolaterally across the cortex. The strips appear in all of the subfields of the somatic sensory and motor areas and may form the basis of the clustering of like groups of efferent neurons demonstrable in physiological studies.

509 citations


Journal ArticleDOI
TL;DR: The efferent projections from the cortical area 8 (frontal eye field) have been re‐examined in four adult monkeys by injecting small amounts of H3 ‐proline into the rostral bank of sulcus arcuatus and using the autoradiographic tracing technique.
Abstract: The efferent projections from the cortical area 8 (frontal eye field) have been re-examined in four adult monkeys (Macaca fascicularis) by injecting small amounts of H3-proline into the rostral bank of sulcus arcuatus and using the autoradiographic tracing technique Ipsilateral cortical projections could be traced into specific areas of the depths of sulcus principalis, sulcus temporalis superior and sulcus intraparietalis Label was found contralaterally in area 8 Subcortical connections were observed ipsilaterally to n caudatus, putamen, claustrum, n ventralis anterior pars magnocellularis, n medialis dorsalis pars multiformis and pars densocellularis, n centralis lateralis and paracentralis, n parafascicularis, n pulvinar oralis, zone incerta, n subthalamicus, pretectal area, colliculus superior and griseum pontis as well as the ipsi- and contralateral n reticularis tegmenti pontis Negative results were obtained with respect to the oculomotor nuclei, n interstitials and Darkschewitsch as well as to the paramedian pontine reticular formation

496 citations


Journal ArticleDOI
TL;DR: The results indicate that, contrary to previous reports which had suggested a projection to only the head of the caudate nucleus, area 9 of Brodmann projects to the entire length of the nucleus.
Abstract: The distribution of prefronto-caudate fibers in the caudate nucleus was studied autoradiographically in monkeys of various ages in which tritiated amino acids had been injected into the middle one-third of the length of the dorsal bank of the principal sulcus. The results indicate that, contrary to previous reports which had suggested a projection to only the head of the caudate nucleus, area 9 of Brodmann projects to the entire length of the nucleus. In the head of the caudate nucleus the cortico-caudate fibers are distributed in a pattern which is remarkable in two respects. First, the grains are not uniformly distributed but rather are segregated into clusters separated from one another by territories in which grain density does not exceed background. Second, individual clusters of grains, circular or elliptical in shape, surround grain free cores. These patterns of fiber distribution within the head of the nucleus are more sharply defined in newborn than in older monkeys. Our findings suggest that the caudate nucleus is organized more as an anatomic and functional mosaic than as the homogeneously organized structure that it is commonly considered to be.

Journal ArticleDOI
TL;DR: The manner in which new cells are added to the growing adult goldfish retina was examined using 3H‐thymidine radioutography, suggesting that the rods must be changing their synaptic connections as the retina grows.
Abstract: The manner in which new cells are added to the growing adult goldfish retina was examined using 3H-thymidine radioautography. Cell proliferation leading to the formation of neurons is restricted to the retinal margin at the ora terminalis. New retina is added in concentric rings, with slightly more growth dorsonasally. The rate of cell addition is variable, averaging 12,000 cells/day. These new cells account for about 20% of the total increase in retinal area; the remaining 80% is due to hypertrophy, or expansion, of the retina. In contrast to all of the other retinal cells, the rods do not appear to participate in the retinal expansion. This hypothesized immobility of the rods would create a shearing strain between the retinal layers resulting in a shift in their position relative to the other cells. Were they to maintain synaptic contacts with the same horizontal and bipolar cells, the rod axons would have to be elongated peripherally or the post-synaptic cell dendrites displaced centrally. Since neurons with this morphology have not been found in the goldfish retina, these observations suggest that the rods must be changing their synaptic connections as the retina grows.

Journal ArticleDOI
TL;DR: An analysis of cell densities in various regions throughout the retina showed that the cells are distributed nearly homogeneously, which implies the formation of even more new synapses, and suggests the adult goldfish retina as a model for both neuro‐ and synaptogenesis.
Abstract: The retinas of adult goldfish, one to four years of age, 4-23 cm in length, were examined with standard paraffin histology to determine if new cells were being added with growth. Retinal cell nuclei were counted and the area of the retina was measured. An analysis of cell densities in various regions throughout the retina showed that the cells are distributed nearly homogeneously. The density (No./mm2 of retinal surface) of ganglion cells, inner nuclear layer cells and cones decreases with growth, but the density of rods remains constant. Thus the rods account for a larger proportion of the cells in larger retinas; The total number of cells per retina increases: the ganglion cells from 60,000 to 350,000; the inner nuclear layer cells from 1,500,000 to 4,000,000; the cones from 250,000 to 1,400,000; the rods from 1,500,000 to 15,000,000. This increase in the number of retinal neurons implies the formation of even more new synapses, and suggests the adult goldfish retina as a model for both neuro- and synaptogenesis.

Journal ArticleDOI
TL;DR: The autoradiographic tracing method has been used to identify the various descending tectofugal pathways and their targets in the rhesus monkey (Macaca mulatta).
Abstract: The autoradiographic tracing method has been used to identify the various descending tectofugal pathways and their targets in the rhesus monkey (Macaca mulatta). The present data reveal that the majority of descending tectofugal axons arise from collicular laminae which lie ventral to the stratum opticum (layer 3). Such descending axons can be grouped into two major bundles or tracts, i.e., the ipsilateral tectopontine-tectobulbar tract and the crossed tectospinal tract (or the predorsal bundle). There is, in addition to these two major pathways, a smaller, commissural projection. The ipsilateral pathway courses laterally and ventrocaudally to terminate within the parabigeminal nucleus, the mesencephalic reticular formation, the dorsal lateral pontine gray (in several discrete patches), the dorsal lateral wing of the nucleus reticularis tegmenti pontis, and within the nucleus reticularis pontis oralis. Other ipsilateral targets of the deep tectal layers are the cuneiform nucleus and the external nucleus of the inferior colliculus. In several experiments transported protein is also apparent within the substantia nigra. Axons which comprise the tectospinal tract, or the predorsal bundle, cross within the dorsal tegmental decussation and descend within the brainstem in a position slightly lateral to the midline. The most rostral and quite extensive target of the predorsal bundle is the nucleus reticularis tegmenti pontis. As the predorsal bundle courses caudally within the pontine tegmentum, labeled axons enter the dorsal and medial regions of both the oral and the caudal divisions of the nucleus reticularis pontis. At caudal medullary levels, the mojority of the labeled axons comprising the predorsal bundle pass ventrally to end quite profusely with the subnucleus b of the medial accessory nucleus of the inferior olivary complex. Caudal to this only a few scattered, labeled axons can be followed into the cervical spinal cord. Labeled axons also pass to the opposite, or contralateral colliculus via the tectal commissure. Such axons appear to arise and end primarily within the deeper tectal layers. In one experiment, the injection invaded the mesencephalic nucleus of the trigeminal nerve. Labeled axons were apparent within the motor nucleus, the chief sensory nucleus (quite profusely) and within the spinal or descending nucleus of the trigeminal nerve.

Journal ArticleDOI
TL;DR: The cells of origin of the corticostriatal projection have been identified in squirrel monkeys by the use of the retrograde horseradish peroxidase method and are unlikely to be collaterals of axons projecting to other sites.
Abstract: The cells of origin of the corticostriatal projection have been identified in squirrel monkeys by the use of the retrograde horseradish peroxidase method. In the subfields of the somatic sensory, motor, parietal and frontal areas of the cortex, cells projecting to the ipsilateral striatum are relatively sparsely distributed and form a group of small- to medium-sized pyramidal cells with an average somal diameter from area to area of 14-16 mum. Such cells are found only in layer V of the cortex (mainly in the more superficial parts of the layer). Since they are consistently smaller than the pyramidal cells of layer V that project to the brainstem and spinal cord and since they lie outside layer VI which gives rise to corticothalamic axons, the corticostriatal axons are unlikely to be collaterals of axons projecting to other sites. The cells of origin of the crossed corticostriatal projection are also found in layer V and are pyramidal cells with somal diameters in the same range as above. They are found only in areas 4, 8, and 6. Studies with the anterograde, autoradiographic method in rhesus, cynomologous and squirrel monkeys, indicate that the somatic sensory areas project to most of the antero-posterior extent of the ipsilateral putamen. Subareas 3a, 3b, 1 and 2 of the somatic sensory cortex project to the same region and the projection overlaps similarly extensive projections from the motor and certain other areas of the cortex. However, in each case the pattern of terminal labeling is in the form of interrupted clusters, strips and bands. A single small injection of the cortex is associated with only one or two such clusters of terminal labeling. This seems to imply that individual corticostriatal fibers end in a very restricted manner and that the terminal ramifications of fibers from one cortical area may alternate in the putamen with those arising in other areas.

Journal ArticleDOI
TL;DR: The connections of the pretectal complex in the cat have been examined by anatomical methods which utilize the anterograde axonal transport of tritiated proteins or the retrograde axonal Transport of the enzyme horseradish peroxidase.
Abstract: The connections of the pretectal complex in the cat have been examined by anatomical methods which utilize the anterograde axonal transport of tritiated proteins or the retrograde axonal transport of the enzyme horseradish peroxidase. Following injections of tritiated amino acids into the eye, label can be seen in the contralateral and ipsilateral nucleus of the optic tract and olivary nucleus where it appears as two or three finger-like strips. Following large injections of tritiated amino acids into the pretectal complex transported label accumulates ipsilaterally in a region dorsolateral to the red nucleus, the central and pericentral divisions of the tegmental reticular nucleus, the intermediate layers of the superior colliculus, the nucleus of Darkschewitch, the thalamic reticular nucleus, zona incerta and fields of Forel, the central lateral nucleus, the pulvinar nucleus and the ventral lateral geniculate nucleus. Contralaterally label accumulates in the nucleus of the posterior commissure, the interstitial nucleus of Cajal, the anterior, posterior and medial pretectal nuclei, and the ventral lateral geniculate nucleus From smaller injections, more or less well confined to single nuclei, the following patterns of connections are demonstrated. The nucleus of the optic tract projects to the ipsilateral ventral lateral geniculate nucleus and pulvinar nucleus and to the contralateral nucleus of the posterior commissure. The anterior pretectal nucleus projects to the ipsilateral central lateral nucleus, the reticular nucleus, zona incerta, fields of Forel, the region dorsolateral to the red nucleus and to the contralateral anterior pretectal nucleus. The posterior pretectal nucleus seems to project only to the ipsilateral reticular nucleus and zona incerta. The central tegmental fields deep to the pretectum project to the tegmental reticular nucleus of the brainstem. When the injection involves the nucleus of the posterior commissure label is seen in the ipsilateral nucleus of Darkschewitch, and in the contralateral nucleus of the posterior commissure and interstitial nucleus of Cajal but no nucleus of the pretectum could be positively identified as projecting to any of the motor nuclei of cranial nerves III, IV, and VI. Following large injections of horseradish peroxidase into the pretectal complex, labeled cells are seen in the superficial layers of the ipsilateral superior colliculus, in the ipsilateral ventral lateral geniculate nucleus, reticular nucleus and zona incerta and in the contralateral anterior, medial and posterior pretectal nuclei, nucleus of the optic tract and ventral lateral geniculate nucleus.

Journal ArticleDOI
TL;DR: The efferent connections of the paramedian pontine reticular formation have been studied in the cat in autoradiographic experiments designed to analyze direct and indirect preoculomotor pathways.
Abstract: The efferent connections of the paramedian pontine reticular formation have been studied in the cat in autoradiographic experiments designed to analyze direct and indirect preoculomotor pathways. Injections of tritium-labelled amino acids were placed (1) near the border between the oral and caudal subdivisions of the nucleus pontis centralis, (2) in more rostral and dorsal parts of the pontine tegmentum, (3) at the pontomesencephalic border, and (4) at the pontomedullary border. Tegmental injections of the first group were unique in labelling a direct ipsilateral pathway to the abducens nucleus and nucleus prepositus hypoglossi. More rostral injections failed to produce discrete labelling of the nuclei of the extraocular muscles but labelled nearby tegmentum and central gray substance. Caudal deposits, involving the pontomedullary reticular formation at its junction with the abducens, perihypoglossal and vestibular nuclei, labelled a decussating fiber system reaching the contralateral abducens nucleus, nucleus prepositus hypoglossi and parts of the vestibular complex. In a single additional case, an injection placed in the oculomotor complex produced heavy labelling of the abducens nuclei. All tegmental injections labelled discrete reticulo-reticular and other variably complex longitudinal pathways. Most injections of (a) the pontomedullary and (b) the pontomesencephalic zones elicited labelling of the pretectum including the nucleus of the optic tract. An incidental finding in the latter group was dense labelling of the pars compacta of the substantia nigra, subthalamic nucleus, and (1 case) entopeduncular nucleus; in one case of each of these groups, labelled fibers were traced to the external pallidum. These observations suggest that, with respect to its efferent oculomotor affiliations, the paramedian pontine tegmentum may be divided into compartments whose supranuclear connections are distinct but for the most part heavily weighted toward influencing the abducens nucleus and periabducens region. Considered within the framework of behavioral and physiological studies of the so-called pontine gaze center, and studies of pontine afferents, the findings are interpreted as suggesting a functional differentiation of these tegmental zones with respect to their influence on eye-head coordination.

Journal ArticleDOI
TL;DR: Most cells of the dorsal lateral geniculate nucleus of rats are generated of fetal days 12 to 14 and their axons invade the telencephalon on fetal day 16 and run in the intermediate zone just below the cortical plate, reaching the visual area on Fetal day 18.
Abstract: Most cell of the dorsal laterial geniculate nucleus of rats are generated on fetal days 12 to 14. Their axons invade the telencephalon on fetal day 16 and run in the intermediate zone just below the cortical plate, reaching the visual area of fetal day 18. The axons do not invade the cortical plate significantly until close to birth (day 22 of gestation) and reach their zone of terminal distribution between postnatal days 1 and 4. In subsequent days the projection becomes progressively more heavily distrubuted in layers IV and I, and synapses of thalamic origin can be identified in these layers. While cells destined for layers IV cross the intermediate zone at the time that thalamic axons first arrive, this coincidence of growth does not seem to be a factor which determines the specificity of patterns of thalamocortical connections since the cells reach layer IV several days before the axons. It is unclear why the axons should wait several days in the region immediately below the cortical plate before invading; although there is a parallel in previous studies on the development of the chick retinotectal pathway (Crossland et al., '75).

Journal ArticleDOI
TL;DR: The rod and cone fields of horizontal cell bodies were found to be nearly coextensive in space, arguing against the notion that substantial rod input came from distant, rod‐dominated terminal arborizations.
Abstract: The responses of horizontal cell bodies and cones in the retina of the cat have been studied by means of intracellular recording and Procion dye injection in an isolated, arterially perfused eyecup preparation. Comparison of the hyperpolarizing responses of these units to red and blue stimuli of different intensities indicated that all morphological varieties of horizontal cells and, additionally, cones themselves, had mixed rod and cone input. The rod input into horizontal cell bodies is thus explained on the basis of cone physiology. The half-saturating intensity of 441 nm stimuli for the rod input into cones and horizontal cells was about 400 quanta/mum2/sec and about 160,000 quanta/mum2/sec for the cone input. Little of this difference can be related to the different quantum catching abilities of rods and cones. The spatial properties of horizontal cell bodies and cones have been characterized using stimuli consisting of long slits in conjunction with a continuous cable model. Space constants for horizontal cells ranged from 210 mum to 410 mum, whereas those for cones ranged from 50 mum, or possibly less, to 180 mum. It is argued that horizontal cell bodies of the cat retina form electrical networks, and that the sizes of the receptive fields generated in these networks may be limited by the diameters of the primary and secondary dendrites of horizontal cells. The rod and cone fields of horizontal cell bodies were found to be nearly coextensive in space, arguing against the notion that substantial rod input came from distant, rod-dominated terminal arborizations.

Journal ArticleDOI
TL;DR: The distribution of cortical projections from areas 17, 18, and 19 to the lateral thalamus, pretectum, and superior colliculus was investigated with the autoradiographic tracing method and clear retinotopic organization was not demonstrable.
Abstract: The distribution of cortical projections from areas 17, 18, and 19 to the lateral thalamus, pretectum, and superior colliculus was investigated with the autoradiographic tracing method. Cortical areas 17, 18 and 19 were demonstrated to project retinotopically and in register upon the dorsal lateral geniculate nucleus, medial interlaminar nucleus, lateral zone of the lateral posterior complex, nucleus of the optic tract and superior colliculus. Area 19 was shown to project retinotopically upon the pulvinar nucleus. Clear retinotopic organization was not demonstrable in the projections of areas 17, 18 and 19 to the reticular complex of the thalamus and ventral lateral geniculate nucleus, or in the projection of area 19 to the anterior pretectal nucleus. The cortical projections were employed to define the retinotopic organization of the nucleus of the optic tract, pulvinar nucleus, and lateral zone of the lateral posterior complex. The cortical projections show the vertical meridian to be represented caudally, with the lower visual field represented laterally, and the upper visual field medially, within the nucleus of the optic tract. The projections of area 19 to the pulvinar nucleus demonstrate the lower visual field to be represented rostrally and the upper visual field caudally in this nucleus; the vertical meridian to be represented at the lateral border and the visual field periphery to be represented at the medial border of the pulvinar nucleus. Cortical projections to the lateral zone of the lateral posterior complex demonstrate the lower visual field to be represented rostrally and the upper visual field caudally; the vertical meridian to be represented at the medial limit and the visual field periphery at the lateral border of the termination zones. On the basis of the experimental findings, a new terminology is introduced for the feline lateral posterior complex. Divisions are proposed which correspond to zones with demonstrably distinct afferent input. The pulvinar nucleus is defined by the distribution of projections from area 19. Three flanking divisions are defined within the lateral posterior complex; a lateral division recipient of projections from area 17, 18 and 19, an interjacent division recipient of projections of the superficial layers of the superior colliculus, and a medial division flanking the tectorecipient zone medially.

Journal ArticleDOI
TL;DR: Attempts were made to determine fastigial projections in the monkey using autoradiographic tracing technics, and cells in rostral, caudal and all parts of the FN were labeled with [3H] amino acids.
Abstract: Because fastigial efferent fibers partially decussate within the cerebellum and cerebellar corticovestibular projections pass near, or through, the fastigial nucleus (FN), degeneration studies based on lesions in the nucleus leave unresolved questions concerning fastigial projections. Attempts were made to determine fastigial projections in the monkey using autoradiographic tracing technics. Cells in rostral, caudal and all parts of the FN were labeled with [3H] amino acids. Selective labeling of neurons in either rostral or caudal parts of the FN results in transport of isotope primarily via fibers of the contralateral uncinate fasciculus (UF) and the ipsilateral juxtarestiform body (JRB). Fastigial projections to the vestibular nuclei are mainly to ventral portions of the lateral (LVN) and inferior (IVN) vestibular nuclei, are nearly symmetrical and are quantitatively similar on each side. Fastigiovestibular projections to cell groups f and x arise from all parts of the FN and are mainly crossed; modest projections to the medial vestibular nucleus are uncrossed. No fastigial efferent fibers end in the superior vestibular nucleus on either side, or in dorsal regions of the LVN. Crossed fibers descending in IVN terminate in the nucleus parasolitarius. Fastigioreticular fibers arise predominately from rostral regions of the FN, are entirely crossed and project mainly to: (1) medial regions of the nucleus reticularis gigantocellularis, (2) the dorsal paramedian reticular nucleus and (3) the magnocellular part of the lateral reticular nucleus. Fastigiopontine fibers, emerge with the UF, bypass the vestibular nuclei and terminate upon the contralateral dorsolateral pontine nuclei. Crossed fastigiospinal fibers separate from fastigiopontine fibers and descend in the ventrolateral tegmentum beneath the spinal trigeminal tract; in the medulla and upper cervical spinal cord these fibers are intermingled with those of the vestibulospinal tract. Fastigiospinal fibers terminate in the anterior gray horn at C-1 and probably descend further. Ascending fastigial projections arise from caudal parts of the FN, are entirely crossed and ascend in dorsal parts of the midbrain tegmentum. Label is transported bilaterally to the superior colliculi and the nuclei of the posterior commissure. Contralateral fastigiothalamic projections terminate in the ventral posterolateral (VPLc and VPLo) and in parts of the ventral lateral (VLo) thalamic nuclei. The major region of termination of fastigiothalamic fibers is in VPLo. Fastigiothalamic projections, probably conveying impulses concerned with equilibrium and somatic proprioception, appear to impinge upon thalamic neurons receiving inputs from less specialized receptors that signal information concerning position sense and body movement. More modest fastigial projections to VLo could directly influence activity of neurons in the primary motor cortex.

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TL;DR: Stimulation of the dorsomedial or ventrolateral perforant pathways resulted in quantitatively different extracellularly recorded EPSPs in the fascia dentata of the rat in agreement with Hjorth‐Simonsen's ('72) evidence for the separateness of the two pathways.
Abstract: Stimulation of the dorsomedial or ventrolateral perforant pathways resulted in quantitatively different extracellularly recorded EPSPs in the fascia dentata of the rat. The two potential differed in latency to peak and in width at half amplitude in a manner consistent with the different locus of termination of the two pathways on the granule cell dendrites. Both potentials were able to follow brief stimulus trains of 100 Hz, which suggests that they are monosynaptic. Medially elicited responses had their peak negativity approximately 100 to 180 μm deeper in the molecular layer than laterally elicited responses. Stimulation at short intervals along a dorsomedial to ventrolateral track in the angular bundle yielded a step function rather than a continuum of EPSP peak latency and half-width, in agreement with Hjorth-Simonsen's ('72) evidence for the separateness of the two pathways. Both pathways were able to induce granule cell discharge. Laterally elicited spikes, however, were delayed. Stimulation at intermediate locations frequently elicited double spikes from granule cell population. Population spikes elicited by either pathway were inhibited for as long as 100 msec after a single discharge. Both pathways showed facilitation with double stimuli at short intervals, and both showed post-tetanic potentiation lasting at least 30 minutes. Under conditins where it could be shown that the two pathways at least partially converged onto the same granule cells, the response of one pathway did not increase when long lasting potentiation was induced on the other.

Journal ArticleDOI
TL;DR: The growth of corticospinal axons into the spinal cord has been demonstrated using the autoradiographic and the Fink‐Heimer silver degeneration methods and several types of placing reactions has been studied.
Abstract: The growth of corticospinal axons into the spinal cord has been demonstrated using the autoradiographic and the Fink-Heimer silver degeneration methods. In addition, the development of several types of placing reactions have been studied. After unilateral injections of radioactive proline or unilateral ablations of the somatosensory-motor cortex, corticospinal axons were found to extend into the contralateral dorsal funiculus of the lower cervical cord at one day postnatally, into mid-thoracic segments at three days, into upper lumbar cord by five days and into coccygeal segments by nine days. Corticospinal axons are first present in the contralateral spinal gray of lower cervical cord at day 5 and in the contralateral spinal gray of lower lumbar and sacral cord by day 9. Little change in the topographical distribution or in the density of the projection is found at all levels of the spinal gray after the fourteenth postnatal day. Comparable results were found with both experimental techniques. Forelimb placing is first seen between 4 to 7 days and hind limb placing between 9 to 13 days. The last placing response to appear in both the forelimbs and the hindlimbs is placing in response to tactile and light proprioceptive stimuli. After the initial onset of the placing reactions, there is a gradual increase in the frequency and speed of the responses until 14 to 17 days postnatally, at which time the reactions appear to be mature. While a causative relationship between the growth of corticospinal axons into the spinal cord and the development of placing has not been established, a close temporal relationship has been found between first: the appearance of fore-or hindlimb placing responses and the appearance of corticospinal axons within the spinal gray at the appropriate levels of the cord and second: between the completion of the primary growth of corticospinal axons at the light microscopic level and the maturation of the placing reactions.

Journal ArticleDOI
TL;DR: By using the barrels to identify prospective layer IV in immature cortex, it is determined that layers V and VI attain their adult height during the sixth postnatal day — an age when prospective layers I‐IV are only half their adultheight.
Abstract: Barrels of the PMBSF of the mouse somatosensory cortex become apparent in Nissl-stained tangential sections simultaneously, on the fourth postnatal day. At this time they are miniatures of those in the adult and are situated in the deepest sublamina of the trilaminar cortical plate. An early barrel appears as a patch of decreased cell density: the prospective hollow of the barrel. Septa become noticeable during the sixth postnatal day. From that period to adulthood, the relative contribution of the PMBSF to the total cortical surface area increases -- an increase that goes against one's expectation: the barrel related periphery matures very early and so does the central, lateral region of the cortex. Barrel growth parallel to the pial surface is greater along the major axes than along the minor axes. By using the barrels to identify prospective layer IV in immature cortex, we could determine that layers V and VI attain their adult height during the sixth postnatal day -- an age when prospective layers I-IV are only half their adult height. The onset of barrel formation coincides with the moment after which injury to the pertinent somatosensory periphery (the vibrissal papillae) no longer causes profound alterations in barrel morphology.

Journal ArticleDOI
TL;DR: Three variants of the Golgi method were employed to examine the cell types, their dendritic fields and organization and azonal trajectories within the substantia nigra of albino and hooded rats.
Abstract: Three variants of the Golgi method were employed to examine the cell types, their dendritic fields and organization and axonal trajectories within the substantia nigra of albino and hooded rats. In both sagittal and coronal sections, large, medium and small neurons were classified on the basis of soma size, extent of dendritic fileds and dendritic caliber. In general nigral cells have three to five primary dendrites that branch relatively infrequently. Some dendrites of all cell types have thinly scattered spines or varicosities. Small cells, found in all areas of the nucleus, have thin dendrites and small, nondirectional dendritic fields. These are considered to be interneurons. The medium cells found in pars compacta, presumed to be the dopaminergic cells of the nigroneostriatal pathway, send long dendrites into pars reticulata perpendicular to the course of pars compacta. In addition, these cells have a number of dendrites which remain in pars compacta. These cells have axons that run medio-dorsally. No axon collaterals were detected. Both large and medium cells are found in pars reticulata. Cells in the dorso-medial aspect of pars reticulata orient rostro-caudally and roughly perpendicular to the course of pars compacta, while cells in the peripeduncular area show a strict orientation which is parallel to the crus cerebri. Some pars reticulata cells emit axon collaterals while others remain unbranced for their observable lenght. Both large and medium cells are also seen in pars lateralis. These cells send long dendrites ventrally into pars reticulata where they run parallel to the crus cerebri, while some shorter dendrites remain in pars lateralis. In total, the substantia nigra appears to have a layered organization: the superior layer is the cellular pars compacta, the second is the dorso-medial area of pars reticulata where both pars compacta and pars reticulata dendrites run rostro-caudally and dorso-ventrally and the third layer is the peripeduncular region where dendrites from all areas run parallel to the crus cerebri.

Journal ArticleDOI
TL;DR: A quantitative study of the rat olfactory bulb during aging was carried out by directly measuring or calculating the following parameters at 3, 12, 24, 27, and 30 months: the volume of the glomerular, external plexiform, and internal granular layers, a relative measure of the size of theOlfactory nerve layer, the mean volume of mitral cell nuclei and perikarya, and number of Mitral cells.
Abstract: A quantitative study of the rat olfactory bulb during aging was carried out by directly measuring or calculating the following parameters at 3, 12, 24, 27, and 30 months: The volume of the glomerular, external plexiform, and internal granular layers, a relative measure of the size of the olfactory nerve layer, the mean volume of mitral cell nuclei and perikarya, a relative measure of the mean volume of the mitral cell dendritic tree as well as the total length and mean cross-sectional area of its constituent dendrites, and number of mitral cells. In addition, measurements of the size and number of mitral cells in the accessory olfactory bulb were performed. Data were analyzed with analysis of variance, multiple range tests for differences means at the various ages, and simple, partial, and multiple product-moment correlations. From 3 to 24 months a linear increase of approximately 50% occurs in all layers of the olfactory bulb. During this time the mean perikaryal volume and dendritic volume of mitral cells increases, also in a linear fashion, approximately 100%. No significant change occurs in the number of mitral cells. From 24 to 30 months a significant decrease occurs in the volume of the layers. Although the total volume of mitral cell dendritic trees decreases slightly from 24 to 27 months, the volume of individual mitral cell dendritic treess, as well as perikaryal and nuclear size, increases sharply during this period, apparently in compensation for a sharp decrease in the number of mitral cells which occurs at this time. From 27 to 30 months no further decrease in mitral cell number occurs, but the size of mitral cell perikarya, and especially dendritic trees, decreases sharply. The coordinated increase in olfactory bulb size from 3 to 24 months appears to be a comtinuation into adult life of earlier postnatal increases. The atrophy from 24 to 30 months appears not to be associated with peripheral rhinitis, since the glomerular and olfactory nerve layers do not show greater atrophy than the other layers, and atrophy also occurs in the accessory olfactory bulb, which is supplied by nerves from the vomeronasal organ, a structure not normally subject to rhinitis.

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TL;DR: In this article, it was shown that the X-and Y-cells described physiologically in the A laminae of the cat's dorsal lateral geniculate nucleus (LGN) are two morphologically distinct cell types recognizable in Golgi preparations.
Abstract: This study presents evidence that the X- and Y-cells described physiologically in the A laminae of the cat's dorsal lateral geniculate nucleus (LGN) are two morphologically distinct cell types recognizable in Golgi preparations. It is shown firstly that the three cell types seen in Golgi preparations of the A laminae (large and medium-sized principal cells and small interneurons-types 1,2 and 3 in the classification of Guillery, '66) may be identified in 1-mum Epon sections of osmicated material. While cell-diameter histograms prepared from serial 1-mum sections show a unimodal distribution of cell sizes, three populations can be distinguished if attention is paid to the presence or absence of large cytoplasmic inclusions (laminar bodies). These three populations consist of large cells lacking laminar bodies (Class I), medium-sized cells possessing laminar bodies (Class II) and small cells lacking them (Class III). That these three classes correspond to the three morphological types has been shown by (i) size comparisons, and (ii) direct demonstration of laminar bodies in the Golgi-impregnated cell bodies of Guillery's type 2 cells. Histograms prepared in this way for samples taken at various positions in the LGN show that the numbers of class II cells decline from the representation of the area centralis to the monocular segment. This decline is compensated by a corresponding rise in the numbers of class I cells. This pattern of distribution is similar to the physiologically observed distribution of X- and Y-cells, indicating that X-cells are likely to be class II cells and Y-cells class I cells. The cortical projections of the various cell types have been examined by the horseradish peroxidase method. Class II cells project to area 17 only. Most class I cells also project to area 17 only, but a few very large class I cells project to area 18. From our results, it appears that very few if any cells in the A laminae have branching axons supplying both 17 and 18. The class III cells do not project to the visual cortex, a finding consistent with their identification as interneurons. Class I and II cells are also found in lamina C and in the MIN. In both these regions there is a predominance of very large class I cells, which project to area 18. Laminae Cl-C3 contain small cells lacking laminar bodies. These cells may project to both areas 17 and 18 with branching axons. They are likely to correspond to Guillery's type 4 cells (small relay cells confined to the C laminae) and to the physiologically described W-cells. Long-term monocular deprivation causes cell shrinkage which is much more severe for class I than for class II cells. There is in addition a decrease in the relative numbers of class I cells. This decrease is found in binocular deprivation also. These observations provide an anatomical basis for the reported loss of Y-cells from deprived laminae of the LGN. It is suggested that the effects of deprivation on Y-cells may be accounted for in terms of competition for synaptic space.

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TL;DR: The results revealed that Nucleus lateralis posterior (NLP) projects to a large peristriate cortical field that includes areas 18A, 7, and the anterior portion of area 18, and to a circumscribed temporal area corresponding to Krieg's ('46a,b) area 20.
Abstract: The organization of thalamic afferents to the rat's visual cortex was investigated autoradiographically and through the retrograde transport of horseradish peroxidase (HRP) following injections into striate and peristriate cortex. The results revealed that Nucleus lateralis posterior (NLP) projects to a large peristriate cortical field that includes areas 18A, 7, and the anterior portion of area 18, and to a circumscribed temporal area corresponding to Krieg's ('46a,b) area 20. The dorsal lateral geniculate nucleus (LGNd) was shown to project to two spatially discontinuous cortical areas. The largest geniculate receiving area is partially coextensive with Krieg's area 17, but an extension of this projection posterior and medial to the striate cortex was found. In addition, a geniculate projection to a restricted field located in the lateral peristriate cortex was identified. Concurrent investigations were designed to assess the pattern discrimination abilities of rats prepared with striate cortical ablations, lesions in NLP and combined striate-cortical and thalamic ablations. Comparison of these animals with normal control subjects revealed that the striate cortex in the rat (as in the cat [Doty, '71; Sprague et al., '77] and the tree shrew [Killackey and Diamond, '71; Ware et al., '74]) is not necessary for successful pattern discrimination, and that the geniculo-striate and NLP-extra-striate projection systems are both involved in mediating the visual discriminative abilities of the rat. The results add species generality to the concept that the central connections to the visual cortex are characterized by parallel-conducting thalamic channels and contribute to the growing number of demonstrations that the extra-striate cortex and associated thalamic cell groups contribute significantly to the process of visual-pattern recognition.

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TL;DR: Experiments using anterograde and retrograde tracing techniques have been used to identify projections to and from the region of mouse SmI cortex which contains the posteromedial barrel subfield, finding that diffusion of the injection was limited to cortex above and below the PMBSF in layer IV.
Abstract: Experiments using anterograde and retrograde tracing techniques have been used to identify projections to and from the region of mouse SmI cortex which contains the posteromedial barrel subfield (PMBSF, Woolsey and Van der Loos, '70). Microinjections containing horseradish peroxidase (HRP) and tritiated amino acids were placed unilaterally into the topographic center of the PMBSF. Brains were perfuse-fixed and frozen sectioned. All sections were reacted for HRP and alternate sections were autoradiographed. Examination of sections cut tangential to the pial surface in the region of the injection site showed that diffusion of the injection was limited to cortex above and below the PMBSF in layer IV (i.e., PMBSF cortex). A “column” of HRP reaction product and developed silver grains was present in ipsilateral cortical area 40, in the face area of SmII. HRP positive cell bodies were mainly in layer III and VI of this “column.” A similar “column” was present in ipsilateral cortical area 6, in a region which in the rat corresponds to the vibrissal area of MsI (Hall and Lindholm, '74), but here HRF positive cells bodies were situated mainly in layer V. HRP labeled cells bodies were also present in layer V of ipsilateral cortical area 29c. The ipsilateral nucleus ventralis thalami pars lateralis and the nucleus posterior thalami contained many HRP positive cell bodies and were associated with dense aggregations of developed silver grains. Numerous silver grains were also present over portions of the ipsilateral caudate, reticular nucleus of the thalamus and ventral pontine nuclei, but no HRP positive cell bodies occurred in these regions. HRP-filled axons left the injection site and traveled via the corpus callosum to contralateral PMBSF cortex where HRF labeled cell bodies were present mainly in layers III and V. Usually only one or two labeled somata were located superficial or deep to a contralateral PMBSF barrel. A few HRF positive cell bodies were also present in layers II and III of contralateral pyriform cortex. These results indicate that PMBSF cortex is reciprocally connected with ipsilateral cortical areas 6 and 40 and with the ipsilateral ventral and posterior nuclei of the thalamus. A small, homotopic callosal connection with contralateral PMBSF cortex has been demonstrated, and it is presumed that this projection is also reciprocal. PMBSF cortex projects to, but receives no projections from the ipsilateral caudate, reticular nucleus of the thalamus and the ventral pontine nuclei. Thus, many of the same projections of primary somatosensory cortex in higher animals, such as the monkey have been shown to occur in the mouse.

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TL;DR: The morphological maturation of several varieties of neurons of cortical area 17 have been followed in Golgi Rapid preparations from Macaque monkeys ranging in age from fetal day 127 to maturity and a developmental sequence common to all varieties of neuron is described.
Abstract: The morphological maturation of several varieties of neurons of cortical area 17 have been followed in Golgi Rapid preparations from Macaque monkeys ranging in age from fetal day 127 to maturity. A developmental sequence common to all varieties of neuron is described. Maturation occurs at the same rate at all cortical depths and appears to relate to the size of the neuron rather than to factors such as generation time, arrival at a final laminar position or cell type. The characteristic laminar patterns of cell type distribution and the specific axonal and dendritic arborisations seen in the adult are generated in the earliest stages of growth and do not occur as the result of elimination from a wider, less precise, distribution. During the period from birth to postnatal week 8 a marked increase in the numbers of dendritic spines is seen in all varieties of neuron including those which will be spine-free in the adult. Following this period an equally marked reduction in spine numbers occurs, initially rapid but continuing at a slower rate even nine months postnatally. Possible relationships between these postnatal dendritic spine changes and the extreme sensitivity of the system to visual input during the early postnatal weeks are discussed.