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.     

Efferent projections of the deep mesencephalic nucleus (pars lateralis) in the rat

The projections of the lateral part of the deep mesencephalic nucleus (DMN) were traced by autoradiography and retrograde horseradish peroxidase (HRP) techniques. At the level of the DMN, projections from its lateral part crossed the midline and terminated in the medial and lateral part of the contralateral DMN. Furthermore, two labeled tracts passed rostrally from the lateral part of the DMN. One tract coursed dorsolaterally from the lateral DMN to terminate in the ipsilateral lateral thalamic nucleus. The second tract coursed ventrally and rostrally over the substantia nigra toward the ipsilateral zona incerta. At the caudal part of the zona incerta these fibers divided into two bundles. One bundle coursed superiorly to terminate bilaterally in the mediodorsal nucleus of the thalamus. The second bundle of fibers passed anteriorly to enter the ipsilateral zona incerta. Some of these fibers terminated upon neurons of the zona incerta and the ventromedial part of the subthalamic nucleus. The remaining fibers within the zona incerta coursed anteriorly to enter the internal capsule. These fibers terminated in the entopeduncular nucleus and medial part of the globus pallidus. These findings indicate that the lateral part of the DMN is likely to be involved in the ascending activating system of the reticular formation by connections with thalamic nuclei. Furthermore, the lateral part of the DMN may play a part in suprasegmental motor control via connections with rostral brain stem motor centers.     

Efferent tectal pathways of the opossum (Didelphis virginiana)

Efferent tectal pathways have been determined for the opossum, Didelphis virginiana, by employing the Nauta-Gygax technique ('54) on animals with tectal lesions of varying sizes. The superior colliculus projected tectothalamic fascicles to the suprageniculate nucleus, the central nucleus of the medial geniculate body, the lateral posterior thalamus, the pretectal nucleus, the ventral lateral geniculate nucleus, the fields of Forel and zona incerta, the parafascicular complex, the paracentral thalamic nucleus and in some cases to restricted areas of the anterior thalamus. Degenerating fibers from superior collicular lesions showed profuse distribution to the deeper layers of the superior colliculus on both sides and to the midbrain tegmentum, but only minimally to the red nucleus and substantia nigra. Fibers of tectal origin did not distribute to the motor nuclei of the oculomotor or trochlear nerves. At pontine levels, efferent fascicles from the superior colliculus were present as an ipsilateral tectopontine and tectobulbar tract and as a crossed predorsal bundle. The tectopontine tract ended mostly within the lateral and ventral basal pontine nuclei, whereas the ipsilateral tectobulbar tract distributed to certain specific areas of the reticular formation throughout the pons and medulla, minimally to the most medial portion of the motor nucleus of the facial nerve and to the nucleus of the inferior olive. The predorsal tract contributed fascicles to certain nuclei of the pontine raphe, extensively to the medial reticular formation of the pons, to the central and ventral motor tegmental nuclei of the reticular formation within the pons and medulla, to the paraabducens region, minimally to cells within restricted portions of the motor nucleus of the facial nerve, to certail specific regions of the caudal medulla and to the cervical cord as far caudally as the fourth segment. The tectospinal fascicles were few but some ended related to the spinal accessory nucleus and the ventral medial nucleus of the ventral horn. Lesions of the inferior colliculus resulted in degenerating fibers which distributed rostrally to the rostral nucleus of the lateral lemniscus and parabrachial region, to the suprageniculate nucleus, the parabigeminal nucleus and to the central nucleus of the medial geniculate body. The inferior colliculus also contributed fibers to the ipsilateral tectopontine and tectobulbar tracts. The latter bundle was traced as far caudally as the medulla and may arise from cells of the superior colliculus which are situated dorsal to the nucleus of the inferior colliculus.     

Spino-bulbar, spino-thalamic and medical lemniscal connections in the American opossum, Didelphis marsupialis virginiana

Projections from the spinal cord and dorsal column nuclei to more rostral levels of the neuraxis were investigated in seventeen adult opossums by the Nauta-Gygax and Fink-Heimer techniques. In all cases with spinal cord lesions a greater number of degenerating fibers distributed to the medulla and pons than to the midbrain and diencephalon. Numerous degenerating fibers ended within the medial reticular formation of the medulla and caudal pons, and within the lateral reticular formation of the rostral pons and midbrain. Degenerating fibers were numerous in the reticular formation following cervical and thoracic lesions, but sparse in specimens with damage restricted to either the lumbar or sacral spinal cord. The dorsal column nuclei received afferent connections from the well known dorsal funicular pathway and, although to a much lesser extent, from the main ventrolateral spinal bundle. Although most of the latter fibers ended in the subnucleus dorsalis and spinal vestibular nucleus, some penetrated into the gracile and cuneate nuclei. Conspicuous terminal degeneration was present within the inferior olivary nucleus following cervical and thoracic lesions, but was lacking in cases of either caudal lumbar or sacral cord lesions. The location of terminal degeneration within the lateral reticular nucleus is dependent upon the level of the lesion in the spinal cord. Degenerating fibers ended within the lateral vestibular nucleus in all cases of spinal cord hemisection, and within the medial portion of the facial nucleus in cases with a lesion rostral to C-4. After cervical and thoracic hemisections terminal fiber degeneration was present within the midbrain tegmentum, the periaqueductal gray, the intercollicular nucleus (Mehler,'69), the posterior thalamic nucleus, the ventrobasal nucleus, the parafascicular nuclei and the caudal nucleus ventralis lateralis. All thalamic nomenclature was taken from Oswaldo-Cruz and Rocha-Miranda, '68. In animals with more caudal lesions, no fiber degeneration was evident within the nucleus ventralis lateralis and so little within the ventrobasal nucleus that it was impossible to ascertain a somatotopic pattern of spinothalamic projections. Lesions of the dorsal column nuclei caused terminal degeneration within the inferior olivary nucleus, the pars lateralis of the nucleus of the inferior colliculus, the zona incerta, the posterior thalamic nucleus, the caudal part of the ventral lateral thalamic nucleus and the ventrobasal nucleus of the thalamus. Diffuse connections with the reticular formation, periaqueductal gray, midbrain tegmentum and the parafascicular complex were also observed. The results from small lesions indicate that the input to the ventrobasal nucleus in the opossum is organized in the typical mammalian fashion.     

An autoradiographic study of the efferent connections of the superior colliculus in the cat

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.     

Ascending tracts of the lateral columns of the rat spinal cord: a study using the silver impregnation and horseradish peroxidase techniques.

The location of projection areas and cells of origin of the ascending fiber tracts of the spinal cord lateral columns were examined in the rat. Projection areas were localized after unilateral microtransection of lateral column fibers at C2 or T10, using silver impregnation of preterminal and fiber degeneration. Cells of origin were localized by unilateral microtransection and subsequent application of horseradish peroxidase (HRP). Two groups of fibers projected to the dorsal medulla. One group projected to nucleus intercalatus, commissuralis, and the dorsal column nuclei. The second group projected via the inferior cerebellar peduncle to the vestibular complex, with additional fibers continuing dorsally to the cerebellum. The most extensive system of ascending fibers projected to the reticular formation. Most spinoreticular fibers coursed through the ventral hindbrain and projected to the lateral reticular nucleus, ventral reticular nucleus, nucleus gigantocellularis, and nucleus subceruleus. Spinotectal and spinocentral gray fibers coursed through the ventral portion of the medulla and then dorsally through the pons. Spinocentral gray fibers projected to the caudal portion of the central gray matter, ipsilaterally. Spinotectal fibers projected to the intercollicular nucleus and adjacent portions of the superior colliculus, bilaterally. Two projections to the thalamus were observed after anterolateral column transection. Preterminal degeneration was observed in the ventrobasal complex ipsilaterally, and bilaterally in the intralaminar nuclei. In conjunction with previous results the present HRP data suggest that the cells of origin of spinothalamic tract fibers were situated in laminae IV, V, and VI. The location of spinal cord cells of origin of additional ascending tracts is discussed.     

The origins of supraspinal projections to the cervical and lumbar spinal cord at different stages of development in the gray short-tailed Brazilian opossum, Monodelphis domestica.

We have used the retrograde transport of Fast blue (FB) to study the origins of supraspinal projections to the lumbar and cervical spinal cord at different stages of development in the Brazilian, short-tailed opossum, Monodelphis domestica. Monodelphis was chosen for study because its young are born in a very immature state, 14-15 days after copulation, making it possible to manipulate its nervous system in an embryonic state without intra-uterine surgery. When injections of FB were made into the lumbar cord at postnatal day (PD) 1, neurons were labeled within several areas of the reticular formation (the retroambiguus nucleus, the ventral and dorsal reticular nuclei of the medulla, the gigantocellular reticular nucleus, the lateral paragigantocellular reticular nucleus, and the pontine reticular nucleus), the presumptive coeruleus complex, and the lateral vestibular nucleus. In many cases, labeled neurons were also found within the caudal raphe and the presumptive interstitial nucleus of the medial longitudinal fasciculus. The results of immunocytochemical studies provided evidence for catecholaminergic and serotoninergic neurons in the brainstem at PD1 and for axons of both phenotypes in the spinal cord. By PD3, labeled neurons were found within the ventral gigantocellular and ventral pontine nuclei of the reticular formation, the spinal trigeminal nucleus, and the presumptive paraventricular nucleus of the hypothalamus. When injections were made at PD4, neurons were also labeled within the medial and inferior vestibular nuclei, the red nucleus, the mesencephalic nucleus of the trigeminal nerve, the presumptive nucleus of Edinger-Westphal and the lateral hypothalamus. By at least PD7, the pattern of supraspinal labeling was similar to that obtained at older ages and in the adult animal. When FB was injected into the cervical cord at PD1, neurons were labeled in all of the areas labeled by lumbar injections at the same age and in larger numbers. In addition, labeled neurons were found within the ventral gigantocellular and spinal trigeminal nuclei. When cervical injections were made at PD15, labeled neurons were found within the deep cerebellar nuclei and amygdala and by PD17 they were also present within the superior colliculus and cerebral cortex. In some cases, cortical labeling was present outside the areas labeled by comparable injections in adult animals.(ABSTRACT TRUNCATED AT 400 WORDS)     

The efferent projections of the periaqueductal gray in the rat: A Phaseolus vulgaris-leucoagglutinin study. II. Descending projections

The descending projections of the periaqueductal gray (PAG) have been studied in the rat using the anterograde tracer Phaseolus vulgaris-leucoagglutinin. The tracer was injected into the dorsolateral or ventrolateral subdivisions of the PAG at rostral or caudal sites. It was found that the patterns of the descending projections of the rostral and caudal parts of the dorsolateral PAG were the same and that the patterns of the descending projections of the rostral and caudal parts of the ventrolateral PAG were the same. However, the patterns of projections of the dorsolateral and ventrolateral PAG subregions were substantially different. These results suggest that the dorsolateral and ventrolateral parts of the PAG are organized into longitudinal columns that extend throughout the length of the PAG. The axons of PAG neurons descended through the pons and medulla via two routes. A small fiber bundle was present in the periaqueductal gray and in the periventricular area. This bundle distributed fibers and terminals locally within the periaqueductal gray and in the locus coeruleus and Barrington's nucleus. A larger bundle had a diffuse arrangement in the pontine reticular formation, however, and it had a more restricted distribution in the medulla, where it occupied a position dorsolateral to the pyramid. This bundle supplied structures in the pontine and medullary tegmentum. The dorsolateral column preferentially supplied the locus coeruleus, subcoeruleus, the gigantocellular nucleus pars alpha, the rostral part of the paragigantocellular nucleus, and the region of the A5 noradrenergic cell group. The ventrolateral column preferentially supplied the nucleus raphe magnus, the caudal part of the lateral paragigantocellular nucleus, and the rostroventrolateral reticular nucleus. © 1995 Willy-Liss, Inc.     

Dorsal mesencephalic projections to pons, medulla, and spinal cord in the cat: limbic and non-limbic components.

The vertebrate dorsal mesencephalon consists of the superior colliculus, the dorsal portion of the periaqueductal gray, and the mesencephalic trigeminal neurons in between. These structures, via their descending pathways, take part in various behavioral responses to environmental stimuli. This study was undertaken to compare the origins and trajectories of these pathways in the cat. Injections of horseradish peroxidase into the cervical spinal cord and upper medullary medial tegmentum retrogradely labeled cells mainly in the contralateral intermediate and deep superior colliculus, and in the ipsilateral dorsal and lateral periaqueductal gray and adjacent tegmentum. Only injections in the medullary lateral tegmental field labeled mesencephalic trigeminal neurons ipsilaterally. Autoradiographic tracing results, based on injections across the dorsal mesencephalon, revealed three efferent fiberstreams. A massive first fiberstream (limbic pathway), consisting of thin fibers, descended ipsilaterally from the dorsal and lateral periaqueductal gray and adjacent superior colliculus through the mesencephalic and pontine lateral tegmentum, terminating in these areas as well as in the ventral third of the caudal pontine and medullary medial tegmentum. A few fibers from the dorsal periaqueductal gray matter (PAG) were distributed bilaterally to the dorsal vagal, solitary, and retroambiguus nuclei. The second fiberstream (the predorsal bundle) descended contralaterally from the superior colliculus (SC) and consisted of both thick and thin labeled fibers. The thin fibers terminated bilaterally in the dorsomedial nucleus reticularis tegmenti pontis and the medial half of the caudal medial accessory inferior olive. The thick fibers targeted the contralateral dorsal two thirds of the caudal pontine and medullary medial tegmental fields, and the facial, abducens, lateral reticular, subtrigeminal, and prepositus hypoglossi nuclei. A few fibers recrossed the midline to terminate in the ipsilateral medial tegmentum. Caudal to the obex, fibers terminated laterally in the tegmentum and upper cervical intermediate zone. From the lateral SC, fibers terminated bilaterally in the lateral tegmental fields of the pons and medulla and lateral facial subnuclei. The third fiberstream (mesencephalic trigeminal or Probst tract) terminated in the supratrigeminal and motor trigeminal nuclei, and laterally in the tegmentum and upper cervical intermediate zone. In summary, neurons in the PAG and in the deep layers of the SC give rise to a massive ipsilateral descending pathway, in which a medial-to-lateral organization exists. A similar topographical pattern occurs in the crossed SC projections. The possibility that these completely different descending systems cooperate in producing specific defensive behaviors is discussed.     

Corticobulbar projections of the marsupial phalanger (Trichosurus vulpecula). I. Projections to the pons and medulla oblongata

A total of 27 adult phalangers was employed to investigate the pattern of neocortical projections to the pontine and medullary portions of the brain stem. Lesions restricted to neocortical areas rostral to the orbital sulcus resulted in fiber degeneration which distributed mainly to midline and medial areas of the pontine and medullary reticular formation. The greatest amount of fiber degeneration was located within the superior central nucleus, the nucleus of the pontine raphe, the nucleus pontis centralis oralis and the nucleus pontis centralis caudalis. However, a few degenerating fibers were present within the nucleus gigantocellularis and the magnocellular portion of the medullary raphe. In contrast, lesions which were located just caudal to the orbital sulcus resulted in fiber degeneration chiefly within the more lateral parvocellular reticular formation and within the subnucleus dorsalis of the nucleus medullae oblongatae centralis. In such cases, additional degenerating fibers were present within the dorsal column nuclei and within more medial areas of the reticular formation. In those brains with ventral parietal ablations, degenerating fibers were present within the chief sensory and spinal nuclei of the trigeminal complex and the closely adjacent reticular formation. All of the above neocortical lesions resulted in fiber degeneration within the basilar pontine gray. In those specimens subjected to caudal (striate and peristriate) or ventrocaudal (temporal) lesions, degenerating fibers were present within the basilar pontine gray, but not within other areas of the pons or the medulla oblongata.     

Neocortical projections to the pons and medulla of the nine-banded armadillo (Dasypus novemcinctus)

The pattern of neocortical projections to the pons and medulla was determined by employing the Nauta-Gygax technique ('54) on the brains of armadillos subjected to neocortical ablations. The results of this study indicate that the pretrigeminal basilar pontine gray receives input from a considerable portion of the neocortex. Degenerating fibers resulting from a lesion of the frontal tip of the neocortex terminated within the dorsal medial, the medial and the ventral medial areas of the rostral basilar pontine gray. Corticopontine fibers from the mid-presupraorbital neocortex ended throughout the rostral to caudal extent of the basilar pontine gray, and terminated within the dorsal medial, the medial and the ventral medial areas; whereas degenerating fibers resulting from a lesion of the neocortex immediately rostral to the supraorbital sulcus terminated within the medial, the ventral and the ventral lateral areas of the basilar pontine gray. The neocortex immediately caudal to the supraorbital sulcus distributed corticopontine fibers to the ventral, the ventral lateral, the dorsal lateral and to the dorsal areas of the basilar pontine gray, while degenerating fibers resulting from lesions of the caudal one-third and most caudal tip of the neocortex projected to the ventral and lateral portions of the basilar pontine gray. Neocortical projections to the pontine and medullary reticular formation originated mainly from cortical areas rostral and immediately caudal to the supraorbital sulcus. The neocortex rostral to the supraorbital sulcus distributed to the rostral and medial portions of the pontine reticular formation, whereas corticoreticular fibers from the neocortex immediately caudal to the suprarbital sulcus, also distributed degenerating fascicles to the spinal trigeminal nucleus, the nucleus of the solitary tract and to the nucleus cuneatus. No degenerating fibers were seen to terminate within motor nuclei of cranial nerves located within either the pons or medulla.     

Bulbar and pontine sources of catecholaminergic innervation of the spinal cord of the rat studied using monoamine fluorescence and retrograde labeling technics

Organization of the neuroanatomical substrate providing the supraspinal catecholaminergic innervation of upper thoracic spinal cord in rat was studied by the retrograde neuronal labelling by means of primuline and HRP combined with simultaneous catecholamine fluorescence. It was shown that the pontine catecholaminergic neurons located within the ventral part of nucleus locus coeruleus (group A6), reticular formation (subcoeruleus, group A7) as well as lateral to the superior olivary complex (group A5) project to the spinal cord. At the same time there are only few neurons located within the rostral part of the medullary catecholaminergic group A1 which give rise to the funicular projections. It is suggested that the pontine catecholaminergic neurons taking part in the spinal innervation are noradrenaline-containing neurons whereas those of medulla oblongata--adrenaline-containing ones.     

Supraspinal projections to the ventromedial lumbar spinal cord in adult male rats

In the present study, the fluorescent tract tracing compound Fluorogold was used to study the afferents of the SNB (spinal nucleus of the bulbocavernosus), which is found in the ventromedial spinal grey and innervates penile muscles of the male rat. Fluorogold was iontophoretically injected into the SNB, which was located by recording antidromic activation of the motoneurons after stimulating the bulbocavernosus muscle. Retrogradely labeled cells were found in laminae I, V-IX, and area X of the lumbar spinal cord, suggesting segmental input to the SNB. Supraspinally, the greatest number of labeled cells were in the medulla oblongata, particularly in the lateral vestibular nucleus, gigantocellular reticular nucleus, and ventral and alpha divisions of the gigantocellular reticular nucleus. Labeled cells were also observed in the medullary raphe nuclei, the ventral medullary nucleus, and the spinal vestibular nucleus. In the pons, labeled cells were observed in the nucleus locus coeruleus, nucleus subcoeruleus, and caudal pontine reticular nucleus. No labeled cells were present in the cerebellum, rostral pons, mesencephalon, and cerebral cortex. The most rostral occurrence of labeled cells was in the medial parvicellular division of the hypothalamic paraventricular nucleus. These potential afferents to the SNB identified in male rats imply that the inputs to motoneurons that innervate sex-specific muscles involved in male reproductive behavior may be similar to the inputs to lumbar motoneurons described in the female rat that innervate muscles involved in female sexual behavior.     

Autoradiographic demonstration of the projections from the mesencephalic locomotor region

An autoradiographic tracing technique was used to examine the projections of the classically defined mesencephalic locomotor region (MRL). Injections of [3H]proline and [3H]leucine were made into sites in the caudal mesencephalon which can be stimulated to produce locomotion. The injection sites were confined to the cuneiform nucleus (stereotaxic coordinates P2.0, L4.0, H-1.0). Descending projections were primarily ipsilateral to the gigantocellular and magnocellular reticular formation of the pons and medulla, the dorsal tegmental reticular nucleus, and the nucleus raphe magnus. Some sparse contralateral projections were also observed within the magnocellular and gigantocellular reticular formation. Direct axonal connections with the spinal cord were not consistently observed. Ascending projections were observed to the subthalamic nucleus, caudal hypothalamic nuclei, the centrum medianum nucleus of the thalamus, the ventral tegmental area of Tsai, the superior colliculus, and the periaqueductal gray region. The ascending projections were also ipsilateral, with sparse contralateral labeling confined to areas which received ipsilateral projections. Projections to the contralateral cuneiform nucleus were also consistently observed. The results, when compared to those of another study, suggest that the classical MLR is anatomically distinct from the more medial sites in the mesencephalon which can also induce locomotion.     

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

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

Autoradiographic study of descending pathways from the pontine reticular formation and the mesencephalic trigeminal nucleus in the rat

Descending projections were studied in autoradiographically prepared material after injections of tritiated leucine in the pontine tegmentum of rats. Injections involving the medial pontine reticular formation resulted not only in labeling commissural fibers, the medial reticulospinal tract, and the dorsal cap of the inferior olive, but also, in two cases, in labeling a cerebellar projection that originated from a region near the midline and clearly dorsal to the nucleus reticularis tegmenti pontis. The labeled fibers passed ventral in the midline to the pontine gray, then laterally through the gray and into the middle cerebellar peduncle to terminate as mossy fibers primarily in the flocculus, lobulus simplex, and Crus I of the ansiform lobule. Injections involving the mesencephalic nucleus of the trigeminal nerve (Vmes), resulted in labeling of Probst's tract, which descends in the dorsolateral reticular formation. Probst's tract gave off extensive terminal branches to the lateral medullary reticular formation and weaker projections to restricted portions of the descending trigeminal nucleus, the solitary nucleus, and the hypoglossal nucleus. In one case, fibers could be traced into the dorsal horn of the upper cervical cord.     

The vestibular nuclei and vestibuloreticular connections in the mallard (Anas platyrhynchos L.). An anterograde and retrograde tracing study

The vestibular apparatus provides information about the position and movements of the head. Craniocervical muscles position the head with respect to the upper part of the neck. Motoneurons innervating these muscles are located in the supraspinal nucleus and ventral horn of the rostral cervical cord. Premotor neurons of craniocervical muscles have been found in the medial two-thirds of the medullary reticular formation: the ventromedial part of the parvocellular reticular formation and the gigantocellular reticular formation. In the present study, projections from vestibular nuclei upon craniocervical premotor neurons were investigated using anterograde and retrograde tracers. Vestibulospinal fibers run bilaterally in the medial vestibulospinal tract and ipsilaterally in the lateral vestibulospinal tract. Vestibuloreticular projections are mainly ipsilateral, and originate from the n. vestibularis lateralis pars ventralis and pars dorsalis, and from the n. vestibularis descendens. Terminal labeling is found in the border zone between the parvocellular and gigantocellular reticular formation. These projections show that in addition to direct bilateral vestibulo-craniocervical projections an indirect vestibular pathway to craniocervical motor nuclei exists. The direct pathway probably is the neural substrate for the vestibulocollic reflex, whereas the vestibular projection upon the reticular formation might influence head orientation during various kinds of activities, such as pecking, preening and so on.     

Fastigial efferent projections in the monkey: an autoradiographic study.

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.     

Spinal projections from the lower brain stem in the cat as demonstrated by the horseradish peroxidase technique. II. projections from the dorsolateral pontine tegmentum and raphe nuclei

The descending projections to the spinal cord arising from the dorsolateral pontine tegmentum and brain stem raphe nuclei have been investigated by means of the horseradish peroxidase (HRP) technique. Particular attention was taken to clarify the cells of origin and the funicular trajectory of these spinal projections.After injections of HRP into the spinal cord, a significant number of HRP labeled neurons were observed in the following dorsolateral pontine tegmental structures: (1) an area ventral to the nucleous cuneiformis; (2) principal locus coeruleus; (3) locus coeruleus α; (4) locus subcoeruleus; (5) Kölliker-Fuse nucleus; and (6) nucleus parabrachialis lateralis. As a rule, the projections are ipsilateral and the descending fibers course in the ventral part of the lateral funiculus.As concerns the raphe-spinal projections, we have demonstrated that the nucleus raphe dorsalis also sends axons to the cervical segment of the spinal cord. Furthermore, in accord with previous reports, HRP labeled cells were also identified in the nucleus raphe magnus, pallidus and obscurus, but not in the nucleus raphe centralis superior and pontis.On the whole the present study further clarified the organization of spinal projections from the dorsolateral pons and raphe nuclei and provided some additional anatomical data for the physiology of the tegmentospinal and raphe-spinal projections.     

Developmental sequence in the origin of descending spinal pathways. Studies using retrograde transport techniques in the North American opossum (Didelphis virginiana)

The origin of descending pathways to thoracic and cervical levels of the spinal cord has been investigated with retrograde tracing techniques in a series of pouch young and adult opossums. The opossum was chosen because it is born in a very immature state, 12-13 days after conception, and has a protracted development in an external pouch. A few neurons in the pontine reticular formation and nucleus coeruleus were labeled by horseradish peroxidase (HRP) injections of the thoracic cord as early as postnatal day (PND) 3. By PND 5, similar injections labeled neurons in the same areas as well as in the medullary reticular formation, the raphe nuclei of the caudal pons and medulla, the spinal trigeminal nuclei, the vestibular complex, the accessory oculomotor nuclei and the interstitial nucleus of Cajal. When Nuclear Yellow (NY) was employed, neurons were also labeled in the red nucleus, the hypothalamus and possibly in the nucleus of the solitary tract. Regardless of the technique employed, neurons in the dorsal column nuclei were not labeled by thoracic injections until at least PND 14. Axons from the nucleus ambiguus, the fastigial and interposed nuclei of the cerebellum as well as the intermediate and deep layers of the superior colliculus reach cervical levels of the cord, where they are specifically targeted, by at least PND 17. They do not significantly overgrow those levels during development. Corticospinal axons are the last of the major descending pathways to innervate the spinal cord. Cortical neurons cannot be labeled by cervical injections of either HRP or NY until at least PND 30. Evidence for transient brainstem-spinal and corticospinal projections was obtained.