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PubMed1977

Efferent projections of the main and the accessory olfactory bulb in the tree shrew (Tupaia glis).

The projections of the main and the accessory olfactory bulb in the tree shrew (Tupaia glis) have been analyzed with anterograde degeneration and autoradiographic methods for identifying axonal projections, and with the horseradish peroxidase method for identifying the distribution of neurons from which these projections originate. The cytoarchitectonic features of the paleocortical areas which receive projections from the main and the accessory olfactory bulb have also been described. The efferent projections of the accessory olfactory bulb are distributed to the bed nucleus of the accessory olfactory tract, the medial amygdaloid area, the posteromedial cortical amygdaloid area, and to the caudal portion of the bed nucleus of the stria terminalis. In contrast, the efferent projections of the main olfactory bulb are distributed to the anterior olfactory nucleus, the tenia tecta, the olfactory tubercle, the pyriform cortex, the anterior cortical amygdaloid area, the posterolateral cortical amygdaloid area, and to the lateral entorhinal cortex. These observations are consistent with the notion that the olfactory system can be divided into at least two major subsystems: one related to the vomeronasal organ and accessory olfactory bulb, and another related to the main olfactory organ and main olfactory bulb. The paleocortical areas receiving olfactory projections have three basic layers: a superficially positioned plexiform layer (layer I), a pyramidal cell layer (layer II), and a polymorphic cell layer (layer III). The projections of both the main and the accessory olfactory bulb terminate in the outer portion of the plexiform layer (sublamina Ia). Sublamina Ia contains the distal segments of dendrites which originate from a heterogeneous population of neurons located in layer II and, to a lesser extent, layer III. Although the efferent projections of the main and the accessory olfactory bulb are segregated, evidence for a more refined topographical organization within these projections was not obtained. However, the distribution of retrogradely labeled neurons in the main olfactory bulb, following injections of horseradish peroxidase into its various paleocortical targets, indicates that the olfactory projections to these areas may not all originate from the same population of cells.

Amygdala↗
PubMed1978

Organizational features of the cat and monkey cerebellar nucleocortical projection.

The organization of the cerebellar nucleocortical projection in the cat and the monkey has been studied using orthograde and retrograde neuroanatomical tracing techniques. Injections of tritiated leucine in the cat cerebellar nuclei orthogradely labeled nucleocortical fibers throughout their course to the cerebellar cortex. Their branch points in the corpus medullare, in the folial white matter, and in the granular layer were evident from the dense, continuous distribution of silver grains overlying these labeled axons. The results from the cat showed that the cerebellar nucleocortical projection is organized principally into three rostrocaudally oriented longitudinal cortical zones. Fastigial nucleocortical fibers were directed principally to the medial 1.5-2.5 mm of the ipsilateral vermis, with a lighter projection to the lateral vermis ipsilaterally and to the medial area of the vermis contralaterally. The interposed nuclei projected mainly to the paravermis-medial hemispheric zone of the cerebellar cortex. Nucleocortical fibers from the posterior interposed nucleus projected principally to the paramedian lobule, to the medial hemispheric area of Crus I and the lobus simplex, and to the flocculus and paraflocculus. Nucleocortical projections from the anterior interposed nucleus coursed to the anterior lobe paravermis and to the ventral folia of the paramedian lobule. A lighter projection from the interposed nuceli was found to the lateral edge of the vermis and into intermediate areas of the hemisphere. Dentatocortical fibers were directed into the lateral folia of Crus I and Crus II of the lateral hemispheric zone, with a ligher projection to intermediate areas of the hemisphere of the posterior lobe and along the lateral edge of the anterior lobe hemisphere. Along the periphery of each cortical zone, the nucleocortical projection from adjacent deep nuclei overlapped slightly. The retrograde transport of horseradish peroxidase (HRP) from injection sites in the lateral hemisphere, in the medial hemisphere--paravermis, and in the vermis labeled neurons localized mainly within the dentate, interposed, and fastigial nuclei, respectively. Retrograde labeling experiments carried out in monkeys indicated that the organization of the nucleocortical projection in this species is different than that of the cat. In the primate, the nucleocortical projection to the lateral hemisphere, to the medial hemisphere--paravermis, and to the vermis appeared to arise principally from the dentate nucleus. There was a secondary input to the paravermis and vermis arising from the interposed and fastigial nuclei, respectively. This evidence suggests that the cerebellar nucleocortical system undergoes a significant phylogenetic change in its organization between the cat and primate. These organization differences are discussed in light of possible functional implications.

Animals↗
PubMed1979

Anomalous ipsilateral retinotectal projections in Syrian hamsters with early lesions: topography and functional capacity.

Retinotectal topography, response properties of neurons in superior colliculus, and visual orienting behavior were studied in hamsters whose superior colliculi were innervated by one or the other of two types of anomalous ipsilateral projections. For the first type, an abnormally large uncrossed projection was created by monocular enucleation on the day of birth. This projection extended over the superficial part of the rostral half of the colliculus. The upper visual field was represented medially, and the lower visual field laterally, which corresponds to a normal projection. The rostrocaudal axis was disordered, but showed a slight tendency for nasal visual field to be represented rostrally and temporal field caudally; this tendency corresponds to an inversion of the normal ipsilateral projection, fitting instead the pattern of a contralateral projection. For the second type of anomalous ipsilateral projection, an abnormal intertectal decussation of optic tract fibers was created by neonatal ablation of the superficial layers of one superior colliculus and removal of the ipsilateral eye (Schneider, '73). Retinotectal topography observed in this recrossing projection was predominantly mirror-symmetric to the normal contralateral projection; however, some distortions in retinotopic order were observed, including misplaced fields and local inversions of the mirror-symmetric topography, and distortions of local magnification factor. Response properties of single units found medially in the left colliculus were similar to those found in normal colliculus. Units found more laterally were underresponsive, showing response decrements with repeated stimulation which is abnormal for units in the superficial gray, and many had abnormally large receptive fields. This physiological pattern was reflected in the pattern of errors made in visual orienting to small targets. It was concluded that polarity cues exist in the tectum sufficient to order the terminals of the retinotectal projection independent of the direction of fiber arrival or order in the optic tract as it enters the tectum. In addition, the functional competence of the abnormal recrossing retinotectal projection has been demonstrated by both electrophysiological and behavioral methods.

Animals↗
PubMed1979

Projections of lamprey spinal neurons determined by the retrograde axonal transport of horseradish peroxidase.

The spinal cords of larval sea lampreys (Petromyzon marinus) and adult river lampreys (Ichthyomyzon unicuspis) were injected with horseradish peroxidase through a transection 1 cm caudal to the last gill. Some animals also had a spinal hemisection 1 cm caudal to the injection. After recovery periods of 1 to 52 days, the spinal cords were treated with diaminobenzidene and hydrogen peroxide, and the projections of various cell types determined in wholemount slides. From these observations the following conclusions were drawn. Most dorsal cells (primary sensory cells) are bipolar with a long rostral projection and a short caudal projection of no more than 5-10 mm. Both processes travel in the ipsilateral dorsal column. Their peripheral processes enter the dorsal roots as branches of their central axons. Some dorsal cells send processes out three or more dorsal roots both rostral and caudal to the cell body. Myotomal motoneurons have characteristic locations in the medial gray column and send prominent transversely oriented dendrites into the lateral columns. A few motoneurons are unusually large. In addition to giant interneurons the majority of smaller rostrally projecting interneurons also have decussating axons. A recently described cell type, the oblique bipolar cell, appears to have an exclusively crossed rostral projection. Although most edge cells project rostrally, as many as 20% may have a caudal projection or both rostral and caudal projections. Edge cells project equally to the ipsilateral and contralateral spinal hemicord, but their processes do not extend more than about 18 mm in sea lamprey larvae and 37 mm in adult river lampreys. Lateral cells project exclusively to the ipsilateral caudal hemicord. A few cells which resemble lateral cells in location and in possessing large lateral dendrites, project rostrally. However, these have atypical morphologic features which probably distinguish them from true lateral cells. Thus far, regardless of cell type, all decussating axons seem to pass ventral to the central canal, while decussating medial dendrites pass dorsally.

Animals↗
PubMed1980

Topology of ascending brainstem projections to nucleus parabrachialis in the cat.

The afferent projections to nucleus parabrachialis (NPB) and nearby pontine areas from the lower brainstem were studied in cats using retrograde horseradish peoxidase (HRP) and anterograde autoradiographic tracing techniques. Two groups of medullary neurons send major projections to NPB and the Kölliker-Fuse nucleus (KF): 1) the solitary complex, especially the medial nucleus of the solitary tract (SM), nearby smaller cells of the dorsal motor nucleus of the vagus (DMV) and the commissural nucleus; and 2) the lateral tegmental field (FTL), or parvocellular reticular formation. Autoradiographic tracing from these areas demonstrated terminal fields in NPB/KF and emphasized a ventrolateral route to NPB from both sources, with axons ascending between the facial nerve and superior olive and passing rostral to the trigeminal nuclei. Minor projections to NBPB/KF originate in the ventrolateral nucleus of the solitary tract, area subpostrema, the alaminar spinal trigeminal nucleus, the gigantocellular and magnocellular tegmental fields, and an area dorsal to the ipsilateral inferior olive. Topographical features of the major projections were studied by correlating the locus of overlap of injection sites with the locations of HRP-positive cells. Medial areas of SM/DMV project mostly to medial parts of NPB, while lateral areas near the solitary tract project to lateral parts of NPB and KF. Crossing projections from SM/DMV favor dorsolateral NPB and KF. FTL neurons in dorsomedial areas project more to medial NPB, and ventrolateral areas project to lateral NPB/KF. Using a new coordinate system to locate and normalize the positions of FTL neurons, data from many brains were collated. FTL cells projecting to NPB/KF were found to be on discrete longitudinal sheets, running radially with respect to the fourth ventricle. This substructure and related evidence suggest a preferred pattern for neuroanatomical connections and information processing in the lateral reticular areas of the brainstem, and help in understanding the topography of the projections to NPB/KF.

Animals↗
PubMed1980

Tangential organization of thalamic projections to the neocortex in the mouse.

Using the anterograde degeneration technique, we examine the tangential organization of a thalamofugal axon population (class I of Frost and Caviness, '80) whose terminations are preferentially distributed to the middle tier (located in layers III and/or IV) of three radially separated tiers of thalamic projections to the neocortex. Less extensive data are also presented on the tangential organization of thalamofugal axon populations (class II of Frost and Caviness, '80) that do not terminate preferentially in the middle tier, but that are otherwise heterogeneous with respect to their radial pattern of intracortical termination. The projections of class I axons are distributed to all neocortical fields with the possible exception of fields 13,25, and 35. The class I projections to a given cortical field (with the possible exception of the cortex of the second somatosensory representation) originate in only one thalamic nucleus. The class I projections of an individual thalamic nucleus form a cortical representation of the nucleus that constitutes a "first order line-to-line" (topologic) transformation of the nuclear volume. The ensemble of class I projections forms a cortical representation of the corresponding thalamic regions that constitutes a "second order line-to-line" (non-topologic) transformation of the thalamic volume. Class II axons project to all neocortical fields. Classs II and class I projections contrast in that the class II projections of multiple thalamic nuclei overlap in the tangential plane of any given sector of the cortex. While the class II projections of the intralaminar nuclei and the widely projecting ventromedial nucleus are known to be topologically organized, the tangential organization of class II projections arising in other nuclei is incompletely understood.

Afferent Pathways↗
PubMed1981

Thalamic connections with limbic cortex. II. Corticothalamic projections.

The corticothalamic projections from the cat limbic cortex have been investigated with anterograde and retrograde axonal transport techniques. Five limbic cortical areas-the anterior limbic area, the cingular area, the granular and dysgranular retrosplenial areas, and the presubiculum-were identified on the basis of their cytoarchitecture. Emphasis was placed on determining the laminar distribution of the cells of origin of the efferent projections, the projection pathways, and the sites of termination within the thalamus. Projections to the thalamus originate in layers V and VI of limbic cortex. In the cingular region the cells of origin are predominantly in layer V and to a lesser extent in layer VI, while the majority of cells projecting from the more caudal retrosplenial areas and presubiculum are in layer VI. There are two fiber pathways from each cortical area to the thalamus. One system of fibers passes through the internal capsule and lateral thalamic peduncle, and a second system travels in the cingulate fasciculus before piercing the corpus callosum to join the postcommissural fornix. The lateral dorsal nucleus and the anterior nuclear group, including the anterior dorsal, anterior ventral, and anterior medial nuclei, are the major thalamic recipients of projections from limbic cortex. Corticothalamic projections also terminate sparsely in the midline and intralaminar nuclear complex, including the central lateral, central dorsal, paracentral, central medial, rhomboid, and reuniens nuclei. Projections from the anterior limbic area project predominantly to the anterior medial, central lateral, and paracentral nuclei. the anterior ventral nucleus, anterior medial nucleus, and lateral dorsal nucleus are the major thalamic recipients of projections from the cingular area, the granular and dysgranular retrosplenial areas, and the presubiculum. It appears that the anterior dorsal nucleus receives afferents only from the dysgranular retrosplenial area. Bilateral cortico-thalamic projections were found in the anterior medial, dorsal medial, central lateral, central medial, paracentral, and reuniens nuclei.

Animals↗
PubMed1981

Brain stem origins of spinal projections in the lizard Tupinambis nigropunctatus.

In order to study brainstem origins of spinal projections, ten Tegu lizards (Tupinambis nigropunctatus) received complete or partial hemisections of the spinal cord at the first or second cervical segment. Their brains were processed for conventional Nissl staining. The sections were surveyed for the presence or absence of retrograde chromatolysis. Based on analysis and comparison of results from lesions in the various spinal cord funiculi, the following conclusions were reached: The interstitial nucleus projects ipsilaterally to the spinal cord via the medial longitudinal fasciculus, as does the middle reticular field of the metencephalon. The red nucleus and dorsal vagal motor nucleus both project contralaterally to the spinal cord via the dorsal part of the lateral funiculus. The superior reticular field in the rostral metencephalon and the ventrolateral vestibular nucleus project ipsilaterally to the spinal cord via the ventral funiculus. The dorsolateral metencephalic nucleus and the ventral part of the inferior reticular nucleus of the myelencephalon both project ipsilaterally to the spinal cord via the dorsal part of the lateral funiculus. Several brainstem nuclei in Tupinambis project bilaterally to the spinal cord. The ventrolateral metencephalic nucleus, for example, projects ipsilaterally to the cord via the medial longitudinal fasciculus and contralaterally via the dorsal part of the lateral funiculus. The dorsal part of the inferior reticular nucleus projects bilaterally to the spinal cord via the dorsal part of the lateral funiculus. The nucleus solitarius complex projects contralaterally via the dorsal part of the lateral funiculus but ipsilaterally via the middle of the lateral funiculus. The inferior raphe nucleus projects bilaterally to the spinal cord via the middle part of the lateral funiculus. These data suggest that supraspinal projections in reptiles, especially reticulospinal systems, are more highly differentiated than previously thought. On the other hand, recent findings in cat, opossum, and monkey reveal that the organization of supraspinal pathways in the Tegu lizard bears a striking resemblance to that observed in mammals.

Animals↗
PubMed1981

Organization of thalamic afferents to anterior dorsal ventricular ridge in turtles. I. Projections of thalamic nuclei.

Dorsal ventricular ridge (DVR) is a thalamorecipient, subcortical telencephalic structure in reptiles and birds. Although there is a fair amount of information about sources of afferents to DVR, little is known about the relationship of projections from individual thalamic nuclei to the organization of the structure. This study examines the relationship between thalamic projections and both areal and zonal divisions of anterior DVR (ADVR; Balaban, '78a) of emydid turtles with orthograde degeneration, autoradiographic and horseradish peroxidase techniques. Individual thalamic nuclei contribute either a diffuse or a restricted projection to ADVR. Diffuse projections arise primarily from the dorsomedial anterior nucleus. These fine-caliber axons distribute bilaterally over a wide region of the telencephalon via both medial and lateral thalamotelencephalic pathways. The terminal regions include septum, striatum and the medial bank of cortex caudal to the lamina terminalis. In ADVR, the fibers are distributed sparsely in zones 2-4 of dorsal, medial and ventral areas. Restricted projections to ADVR originate in nucleus rotundus, nucleus reuniens and nucleus caudalis. They ascend ipsilaterally in the lateral thalamotelencephalic pathway (lateral forebrain bundle), and enter ADVR rostral to the anterior commissure. Nucleus rotundus projects to zone 4 of dorsal area, nucleus caudalis projects to zones 2-4 of dorsal division of medial area, and nucleus reuniens projects to zones 2-4 of both the ventral division of medial area and the ventral area. Comparison of these results with thalamotelencephalic projections in mammals suggests that diffuse and restricted thalamic projection systems are a common feature of both groups. Restricted thalamic projections in reptiles, birds and mammals terminating in anatomically distinct regions, also appear to be associated with different sensory modalities. The significance of diffuse systems is not clear.

Afferent Pathways↗
PubMed1981

Orderly anomalous retinal projections to the medial geniculate, ventrobasal, and lateral posterior nuclei of the hamster.

Experiments were performed to determine (1) under what conditions early brain surgery can cause sensory afferents to the thalamus to form connections at abnormal thalamic sites and (2) the extent to which such ectopic projections are receptotopically organized. In newborn Syrian hamsters, two of the retina's principal synaptic targets, the superior colliculus and dorsal lateral genicultae nucleus, were destroyed, respectively, by a direct lesion and by retrograde degeneration following a lesion of the occipital cortex. In th same brains, alternative terminal space for the retinofugal axons was made available in auditory (medical geniculate) or somatosensory (ventrobasal)thalamic nuclei by lesions of ascending auditory or somatosensory pathways, respectively; additional terminal space was made in the lateral posterior nucleus by degeneration of afferents from the superior colliculus. The projections of the contralateral retina were traced in neonatally operated adults by making one or two small peripheral retinal lesions and intraocular injections of 3H-proline 5 days and 1 day, respectively, prior to sacrifice. The neonatal surgery reliably produced anomalous crossed retinal projections to the partially deafferented structures. These projections terminate preferentially at the nuclear surfaces. Computer reconstructions from serial sections demonstrated several signs of spatial order suggestive of receptotopic organization in the anomalous retinothalamic projections. In order of increasing stringency, these signs (which are not mutually exclusive) are: (1) In each nucleus, a restricted retinal sector gives rise to a limited part of the abnormal projection. (2) In each nucleus, different parts of the retina give rise to different parts of the anomalous projection. (3) In each nucleus, there is more or less consistent polarity of the anomalous connection. Each small retinal sector appears to be represented along a "line of projection" in each of its abnormal thalamic targets, as it normally is in the dorsal and ventral lateral geniculate nuclei and in the superior colliculus. In some brains, some of the abnormal projections produce only a partial representation of the retina. However, in a single animal, a retinal sector not represented in the anomalous projections to one nucleus can contribute to the abnormal connections with another nucleus. In additional experiments, and attempt was made to direct developing auditory and somatosensory fibers normally terminating in the medial geniculate and ventrobasal nuclei, respectively, to anomalous thalamic targets. The axons were deprived of some of their normal thalamic sites of termination and alternative terminal space was made available in another thalamic sensory nucleus. These experiments failed to produce reliable evidence of ectopic auditory or somatosensory thalamic projections.

Animals↗
PubMed1981

The organization of centrifugal projections from the anterior olfactory nucleus, ventral hippocampal rudiment, and piriform cortex to the main olfactory bulb in the hamster: an autoradiographic study.

The centrifugal projections from the various subdivisions of the anterior olfactory nucleus (AON) can be categorized into four groups based on the organization of terminal fields in the main olfactory bulb (MOB). Pars lateralis and dorsalis have bilaterally asymmetric laminar projections to the MOB. The ipsilateral projections terminate primarily in the superficial half of the granule cell layer and in the deep third of the glomerular layer, whereas the contralateral projections terminate primarily in the superficial half of the granule cell layer and do not extend into the glomerular layer. Pars ventralis and posterior have bilaterally symmetric laminar projections with heavy terminations both in the superficial half of the granule cell layer and in the deep third of the glomerular layer. Pars medialis sends predominantly ipsilateral projections to the deep half of the granule cell layer. Pars externa has predominantly contralateral projections with a very narrow terminal field immediately deep to the internal plexiform layer. The projections to the MOB from the ventral hippocampal rudiment (HR) and the piriform cortex (PC) are exclusively ipsilateral. The projections from the ventral HR terminate primarily in the deep half of the granule cell layer. The projections from the PC also terminate predominantly in the granule cell layer, but there is a progressive shifting of terminal fields from the superficial half of this layer toward deeper regions for centrifugal axons arising from progressively more caudal levels of the PC. The laminar termination patterns of cortical afferents to the ipsilateral MOB thus are correlated with the mediolateral axis of the olfactory peduncle and the rostrocaudal axis of the piriform cortex. The centrifugal axons from these various sources enter directly into the granule cell layer of the caudal MOB or pass through the internal plexiform layer of the accessory olfactory bulb to reach the middle and anterior part of the MOB. We have termed these two routes the final common bulb pathway. The centrifugal axons from the laterally situated sources join the anterior and bulbar limbs of the anterior commissure before entering the final common bulbar pathway. In contrast, the centrifugal axons from pars medialis and the ventral HR travel diffusely in the cellular layer of the ipsilateral olfactory peduncle. A small component of the centrifugal projections from the PC travels in association with the lateral olfactory tract.

Animals↗
PubMed1982

Afferent projections to the deep mesencephalic nucleus in the rat.

Afferent projections to the deep mesencephalic nucleus (DMN) of the rat were demonstrated with axonal transport techniques. Potential sources for projections to the DMN were first identified by injecting the nucleus with HRP and examining the cervical spinal cord, brain stem, and cortex for retrogradely labeled neurons. Areas consistently labeled were then injected with a tritiated radioisotope, the tissue processed for autoradiography, and the DMN examined for anterograde labeling. Afferent projections to the medial and/or lateral parts of the DMN were found to originate from a number of spinal, bulbar, and cortical centers. Rostral brain centers projecting to both medial and lateral parts of the DMN include the ipsilateral motor and somatosensory cortex, the entopeduncular nucleus, and zona incerta. at the level of the midbrain, the ipsilateral substantia nigra and contralateral DMN likewise project to the DMN. Furthermore, the ipsilateral superior colliculus projects to the DMN, involving mainly the lateral part of the nucleus. Afferents from caudal centers include bilateral projections from the sensory nucleus of the trigeminal complex and the nucleus medulla oblongata centralis, as well as from the contralateral dentate nucleus. The projections from the trigeminal complex and nucleus medullae oblongatae centralis terminate in the intermediate and medial parts of the DMN, whereas projections from the contralateral dentate nucleus terminate mainly in its lateral part. In general, the afferent connections of the DMN arise from diverse areas of the brain. Although most of these projections distribute throughout the entire extent of the DMN, some of them project mainly to either medial or lateral parts of the nucleus, thus suggesting that the organization of the DMN is comparable, at least in part, to that of the reticular formation of the pons and medulla, a region in which hodological differences between medial and lateral subdivisions are known to exist.

Afferent Pathways↗
PubMed1982

Cortical and subcortical projections of the middle temporal area (MT) and adjacent cortex in galagos.

Projections of the middle temporal visual area, MT, and of visual cortex adjoining MT were investigated with autoradiographic methods in the prosimian primate, Galago senegalensis. Ipsilateral cortical targets of MT included area 17, area 18, cortex caudal to MT, cortex ventral to MT, and parietal-occipital cortex dorsal to MT. This pattern of projections suggests that extrastriate cortex contains a number of visual subdivisions in addition to MT. Contralateral projections were to MT and parietal-occipital cortex. Projections from MT to areas 17 and 18 connected regions representing similar parts of the visual hemifield while the location of callosal projections in MT matched the location of the injection site in the other hemisphere. Label in area 17 was concentrated in layers I, III, and VI whereas other cortical areas were most densely labeled in the granular and supragranular layers. Subcortical projections of MT included the reticular nucleus of the thalamus, the lateral posterior nucleus, the superior pulvinar, the inferior pulvinar, the superior colliculus, and the pontine nuclei. The projection pattern to the superior and inferior pulvinar nuclei suggests that MT projects in a topographic manner to two subdivisions within each of these structures. Injections in cortex just outside of MT labeled area 18, inferotemporal cortex, parietal-occipital cortex, and, to a lesser extent, MT. The projections to inferotemporal cortex clearly distinguish the bordering cortex from MT. Contralateral cortical terminations were in locations corresponding to the injection site. Subcortical targets were generally similar to those seen after MT injections, although additional projections were observed depending on the location of the injection. Comparison of these results from the prosimian galago with studies in New and Old World monkeys indicates there are substantial similarities in projections. Thus, some of the cortical and thalamic subdivisions described for monkeys appear to exist in prosimians.

Animals↗
PubMed1983

Ascending auditory projections to the inferior colliculus in the adult gerbil, Meriones unguiculatus.

Ascending auditory projections to the inferior colliculus (IC) of the adult gerbil were studied using the retrograde transport of horseradish peroxidase. Our results indicate that in gerbils, the IC receives afferent projections from most brainstem auditory nuclei. A strong contralateral projection originates in the cochlear nuclear complex (CN). A smaller but consistent projection from all three divisions of ipsilateral CN is also present. The medial superior olive (MSO), superior parolivary nucleus, and ventral nucleus of the lateral lemniscus all maintain ipsilateral projections to the IC. Bilateral projections arise from the lateral superior olive, lateral nucleus of the trapezoid body, and dorsal nucleus of the lateral lemniscus. Previous investigations in other mammalian species provide conflicting data concerning the magnitude of a direct ipsilateral projection from CN to the IC. Our quantitative data indicate that the ipsilateral projection from CN in the gerbil is nearly one third as large as the projection from ipsilateral MSO. The projection from contralateral CN is six times larger than the MSO projection. The distribution of labeled cells across the rostrocaudal extent of MSO and the three divisions of the cochlear nuclear complex are presented.

Animals↗
PubMed1984

Projections from the superior olivary complex to the cochlear nucleus in the tree shrew.

The origins and targets of projections from the superior olivary complex to the cochlear nuclei were studied in the tree shrew by placing small injections of horseradish peroxidase (HRP) in the cochlear nucleus and small injections of 3H-leucine in the superior olivary complex. The results show that the descending pathways originate in periolivary cell groups surrounding the medial and lateral superior olives and that periolivary nuclei differ from one another in their patterns of projections to the cochlear nucleus. For example, cell groups may project either ipsilaterally or bilaterally. Cells in the lateral nucleus of the trapezoid body project only to the ipsilateral cochlear nucleus. Other periolivary cell groups project bilaterally, although some of these may project more heavily to one side than the other. Some pathways have widespread targets in the cochlear nucleus whereas others have relatively specific targets. Diffuse projections to all divisions of the cochlear nucleus arise from the lateral nucleus of the trapezoid body ipsilaterally and from the medial perioliviary nucleus bilaterally. The targets of other descending pathways are more restricted. The anterolateral, dorsal, and dorsolateral periolivary nuclei project mainly to the anteroventral cochlear nucleus; the ventral nucleus of the trapezoid body and the posterior periolivary nucleus project mainly to the dorsal and posteroventral cochlear nuclei. All of these specific projections are bilateral. These results suggest that projections from the periolivary cell groups to the cochlear nucleus consist of multiple components with different degrees of specificity.

Animals↗
PubMed1984

Pretectal and brain stem projections of the medial terminal nucleus of the accessory optic system of the rabbit and rat as studied by anterograde and retrograde neuronal tracing methods.

The projections of the medial terminal nucleus (MTN) of the accessory optic system have been studied in the rabbit and rat following injection of 3H-leucine or 3H-leucine/3H-proline into the MTN and the charting of the course and terminal distribution of the MTN efferents. The projections of the MTN, as demonstrated autoradiographically, have been confirmed in retrograde transport studies in which horseradish peroxidase (HRP) has been injected into nuclei shown in the autoradiographic series to contain fields of terminal axons. The following projections of the MTN have been identified in the rabbit and rat. The largest projection is to the ipsilateral nucleus of the optic tract and dorsal terminal nucleus (DTN) of the accessory optic system. Labeled axons course through the midbrain reticular formation and the superior fasiculus, posterior fibers of the accessory optic system, to reach the nucleus of the optic tract and the DTN in both rabbit and rat. Axons also run forward to traverse the lateral thalamus and to distribute to rostral portions of the nucleus of the optic tract in rat only. A second, large projection is to the contralateral dorsolateral portion of the nucleus parabrachialis pigmentosus of the ventral tegmental area together with an adjacent segment of the midbrain reticular formation. The patchy terminal field observed has been named the visual tegmental relay zone (VTRZ). This fiber projection courses within the posterior commissure and along its path to the VTRZ, provides terminals to the interstitial nucleus of Cajal and the nucleus of Darkschewitsch, both bilaterally. A third, large MTN projection distributes ipsilaterally to the deep mesencephalic nucleus, pars medialis, and the oral pontine reticular formation. Further, this projection also supplies input to the medial nucleus of the periaqueductal gray matter, bilaterally in the rabbit and rat, and in the rabbit also to the ipsilateral superior and lateral vestibular nuclei. A fourth projection crosses the midline and courses caudally to reach, contralaterally, the dorsolateral division of the basilar pontine complex and the above nuclei of the vestibular complex. A fifth projection of the MTN utilizes the medial longitudinal fasciiculus to reach the rostral medulla, in which its axons distribute ispilaterally to the dorsal cap, its ventrolateral outgrowth, and the beta nucleus of the inferior olivary complex. There is also a contralateral contingent of this projection that leaves the medial longitudinal fasciculus to innervate a small rostral segment of the contralateral dorsal cap.(ABSTRACT TRUNCATED AT 400 WORDS)

Animals↗
PubMed1984

The postnatal development of corticotrigeminal projections in the cat.

The postnatal development of corticotrigeminal projections was studied in kittens following 3H-amino acid injections into the face area of the primary somatosensory cortex. Corticofugal axons grow into the brainstem and form the pyramidal tract prenatally. Corticotrigeminal projections begin to develop at the end of the first postnatal week. The earliest corticotrigeminal axons grow out of the pyramidal tract caudally and project into laminae III-V of the spinal trigeminal (Vs) nucleus caudalis. During the second postnatal week, corticotrigeminal axons grow out of the pyramidal tract in a caudal to rostral sequence and project up to the ventromedial borders of Vs-interpolaris, Vs-oralis, and to the principal trigeminal nucleus. Corticotrigeminal axons pause at the periphery of these nuclei for 1-2 days before penetrating the trigeminal neuropil and forming terminal arborizations in a centripetal direction. Coincident with the development of cortical projections to the principal trigeminal nucleus, some of the labeled axons which were in lamina III of Vs-caudalis project into lamina I and terminate. This sequence of development of corticotrigeminal projections closely parallels, albeit at a later time, the sequence of formation of the trigeminal nuclei, suggesting that the temporal sequence of cytogenesis of trigeminal neurons may be a factor which regulates their order of innervation by afferents. Corticotrigeminal projections develop bilaterally and, during the second postnatal week, are relatively equal in density in the ipsilateral and contralateral nuclei. Many of the ipsilateral corticotrigeminal projections are lost, however, after the second postnatal week, so that by the fourth postnatal week, corticotrigeminal projections are mainly contralateral and adultlike in their distribution. It remains to be determined whether the transience of ipsilateral corticotrigeminal projections is due to selective elimination of axon collaterals or to neuronal death.

Animals↗
PubMed1984

Cerebellar efferents in the lizard Varanus exanthematicus. II. Projections of the cerebellar nuclei.

The projections of the cerebellar nuclei have been studied in the lizard Varanus exanthematicus with various experimental anatomical techniques. In anterograde degeneration experiments (lesions of the cerebellar peduncle) both ascending and decending contralateral projections were found. Ascending fibers which could be traced from the cerebellar commissure ventralward decussated at the level of the trochlear and oculomotor nuclei. These fibers coursed rostralward to the mesodiencephalic junction. With anterograde tracing techniques (3H-leucine and HRP) this tract was found to terminate in the nucleus ruber and the interstitial nucleus of the fasciculus longitudinalis medialis. Moreover, retrograde tracer studies (HRP, "Fast Blue") showed that this tract appeared to arise mainly in the lateral cerebellar nucleus. With both anterograde degeneration and tracing techniques (3H-leucine and HRP) a bundle of fibers could be followed, which decussates in the basal part of the cerebellum and passes dorsally around the contralateral medial cerebellar nucleus to the lateral side of the brainstem. This contralaterally descending projection system was found, lateral to the vestibular nuclear complex, and as far caudally as the descending vestibular nucleus, to terminate on various vestibular nuclei. Horseradish peroxidase studies showed that this contralaterally descending projection system originates mainly in the medial cerebellar nucleus, but ipsilaterally descending projections were also found. With the fluorescent double labeling technique ("Fast Blue" and "Nuclear Yellow") the projections of the cerebellar nuclei described above were confirmed. Furthermore, double labeling revealed neurons in both cerebellar nuclei (especially the medial nucleus) that project to both the mesencephalon and the cervical spinal cord. The present results indicate that the efferent connections of the cerebellar nuclei in the lizard Varanus exanthematicus are organized as two main projections, an ascending projection comparable to the mammalian brachium conjunctivum arising in the lateral cerebellar nucleus, and a descending projection comparable to the mammalian hook bundle (fasciculus uncinatus), originating mainly in the medial cerebellar nucleus. Such projections are common for terrestrial vertebrates.

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