Funicular location of ascending axons of lamina I cells in the cat spinal cord

The laminar distribution of spinal cord neurons projecting suprasegmentally through different funiculi was determined in the cat using horseradish peroxidase (HRP) injections combined with selective spinal cord lesions. The lesions were designed to limit the caudal transport of HRP to either the ventral funiculi or the dorsolateral funiculus. HRP injections in the ventromedial or ventrolateral funiculi resulted in labeling primarily within laminae IV–VIII and a virtual lack of labeling within lamina I. When the dorsolateral funiculus was injected, 20–25% of all labeled cells were located in lamina I, bilaterally. These results demonstrate that the ascending lamina I projections are through the dorsolateral funiculus.     

Funicular course of catecholamine fibers innervating the lumbar spinal cord of the cat

The purpose of this study was to determine the funicular location of descending catecholamine (CA) fibers innervating the lumbar spinal cord from the dorsolateral pons (DLP). The locations of catecholamine-containing cell bodies which project to the lumbar spinal cord were determined by combining the use of the retrogradely transported fluorescent dye, Evans Blue (EB), with the glyoxylic acid histofluorescence technique. Lumbar injections of Evans Blue were combined with thoracic lesions of the dorsolateral funiculi (DLF) or ventrolateral funiculi (VLF) in order to retrogradely label those CA-containing or non-CA-containing cell bodies whose axons descend within the spared hemispinal cord. By this technique it was determined that descending CA fibers innervating the lumbar spinal cord of the cat project through both the DLF and the VLF. The nucleus subcoeruleus, the Kolliker-Fuse nucleus and the CA cell bodies in the area of A5 each contain a significant number of CA-containing cells whose fibers descend both within the DLF and the VLF, while the nucleus locus coeruleus projects to the lumbar cord primarily through the VLF. Catecholamine cells of the DLP innervate the lumbar spinal cord bilaterally, although there is an ipsilateral predominance. The CA-containing cells of the DLP which innervate the contralateral spinal cord were shown by ipsilateral or contralateral thoracic hemisection to decussate both above and below the thoracic lesion. Non-CA-containing cells from the DLP also crossed at all levels of the spinal cord; however, cells from the caudal pons had a larger number of cells which crossed above the thoracic lesion while cells of the more rostral pons had a larger number of cells which crossed below the lesion.     

Graded unilateral cervical spinal cord injury in the rat: evaluation of forelimb recovery and histological effects

The purpose of this study was to develop a model of unilateral cervical (C4-C5) spinal cord contusion injury in the rat and to characterize the functional and histological consequences following three injury levels using a new weight-drop spinal cord injury device. We evaluated forepaw/forelimb and hindlimb functions by: (1) a horizontal ladder beam measuring paw misplacements and slips; and (2) the forelimb preference test which measures the forelimb used for pushing off to rear, for support, and to land on after rearing. Rats with a mild spinal cord injury displayed primarily a forepaw deficit (forepaw misplacements) for 8 weeks after injury. Paw preference also improved after injury, but failed to reach control levels even after 12 weeks. These rats had damage primarily to the rubrospinal, spinocervicothalamic, and the uncrossed lateral corticospinal tracts in the dorsolateral funiculus a well as some loss of the lateral spinothalamic tracts in the lateral funiculus. Rats with a moderate injury had a prominent forepaw deficit still evident at 12 weeks after injury as well as a mild but not significant hindlimb deficit. Paw preference improved slightly 12 weeks. There was a larger lesion in the dorsolateral and lateral funiculi than in mildly injured rats which extended into the ventrolateral funiculi. There was a significant loss of gray matter compared to rats with a mild injury. Rats with a severe injury displayed significant forelimb and hindlimb deficits throughout the 12 week testing period compared to rats with a mild or moderate injury, and also had a more severe paw preference bias (90%). The lesion encompassed the entire dorsolateral, lateral and ventrolateral funiculi with some disruption of the ventral funiculus. There was more significant gray matter necrosis compared to rats with either a mild or moderate injury. Thus, the spinal cord injury device we used may be useful for studying graded cervical spinal cord injury in rats and potential treatments or interventions, because both the behavioral and histological effects are reproducible and consistent.     

Distribution of spinal cord projections from the medullary subnucleus reticularis dorsalis and the adjacent cuneate nucleus: A phaseolus vulgaris- leucoagglutinin study in the rat

The distribution and organization of descending spinal projections from the dorsal part of the caudal medulla were studied in the rat following injections of Phaseolus vulgaris leucoagglutinin into small areas of the subnucleus reticularis dorsalis (SRD) and the adjacent cuneate nucleus (Cu). The caudal aspect of the Cu projected only to the dorsal horn of the ipsilateral cervical cord via the dorsal funiculus. These projections were mainly to laminae I, IV, and V. More ventrally located reticular structures projected to the full length of the cord. Fibers originating from the SRD travelled through the ipsilateral dorsolateral funiculus and terminated within the deep dorsal horn and upper layers of the ventral horn, mainly in laminae V–VII. Fibers originating from subnucleus reticularis ventralis (SRV) travelled ipsilaterally through the lateral and ventrolateral funiculi and bilaterally through the ventromedial funiculus. These fibers terminated within the ventral horn. The density of labeling within the gray matter varied at different levels of the cord was as follows: cervical > sacral > thoracic > lumbar. The reciprocal connections between the caudal medulla and the spinal cord suggest that the former is an important link in feedback loops that regulate spinal outflow. © 1995 Wiley-Liss, Inc.     

Spinal projections from the mesencephalic and pontine reticular formation in the North American Opossum: a study using axonal transport techniques.

The results from several experimental approaches lead to the following conclusions. The nucleus cuneiformis projects to at least lumbar levels of the spinal cord. Its axons course through the ipsilateral sulcomarginal and ventral funiculi to distribute within lamina VIII and adjacent portions of lamina VII. Neurons within the nucleus reticularis pontis (RP), particularly within more medial parts of the nucleus, project through comparable routes to the same laminae. In addition, however, neurons within the lateral and dorsolateral RP relay through the lateral and dorsolateral funiculi, ipsilaterally, and the dorsolateral funiculus, contralaterally. Axons could be traced from the dorsolateral tracts to laminae IV through VII, lamina X and, in some instances, to laminae I and II. Injections of the dorsolateral pons also label the intermediolateral cell column and an area presumed to be the sacral parasympathetic nucleus. Many of the neurons which contribute to the contralateral bundle are located adjacent to the ventral nucleus of the lateral lemniscus. The nucleus reticularis gigantocellularis projects mainly via the sulcomarginal, ventral and lateral funiculi to laminae VIII and adjacent portions of lamina VII. The nucleus reticularis gigantocellularis pars ventralis innervates the same laminae; but, in addition, projects heavily to laminae I and II, to lateral portions of laminae IV through VII; to laminae IX and X and to the intermediolateral cell column. Axons destined for laminae I and II, as well as IV through VII and X, traverse the dorsolateral funiculi as described for the cat by Basbaum et al. ('78). Neurons within the nucleus reticularis parvocellularis project to cervical levels, mainly through the ventral funiculi. In general our results show that reticulospinal projections are more complex than suggested by degeneration methods and that laminae I, II. lateral parts of laminae IV-VII, laminae IX and X, as well as the intermediolateral cell column and sacral parasympathetic nucleus are targets of axons from specific areas.     

Anatomical correlates of locomotor recovery following dorsal and ventral lesions of the rat spinal cord

The present study was designed to relate functional locomotor outcome to the anatomical extent and localization of lesions in the rat spinal cord. We performed dorsal and ventral lesions of different severity in 36 adult rats. Lesion depth, spared total white matter, and spared ventrolateral funiculus were compared to the locomotor outcome, assessed by the BBB open-field locomotor score and the grid walk test. The results showed that the preservation of a small number of fibers in the ventral or lateral funiculus was related to stepping abilities and overground locomotion, whereas comparable tissue preservation in the dorsal funiculus resulted in complete paraplegia. The strongest relation to locomotor function was between the BBB score and the lesion depth as well as the BBB score and the spared white matter tissue in the region of the reticulospinal tract. Locomotion on the grid walk required sparing in the ventrolateral funiculus and additional sparing of the dorsolateral and dorsal funiculus, where the cortico- and rubrospinal tracts are located.     

An autoradiographic and HRP study of vestibulocollic pathways in the pigeon

This study examines the connections underlying the vestibulocollic system in the adult pigeon by using retrogradely transported horseradish peroxidase (HRP) to identify neck muscle motoneurons in one set of animals, and transneural anterograde transport of tritiated proline-fucose to delineate the descending medial (MVST) and lateral (LVST) vestibulospinal tracts in a second set of animals. Correlations of location and distribution of HRP-labeled motoneurons and autoradiographically labeled fiber tracts and terminal fields were performed between the two sets of experiments. The right biventer cervicis and complexus neck muscles were subdivided into rostral and caudal halves in ten animals and HRP injected into only half of one of the two muscles in each experiment. Following a 16–48-hour survival, the brain was fixed by intracarotid catheterization and perfusion and the HRP in the brain sections reacted with the tetramethylbenzidine (TMB) blue reaction process. Three groups of HRP-labeled motoneurons were identified in the ipilateral ventral horn of the upper cervical spinal cord: a ventromedial and ventrolateral group within lamina VIII innervating the biventer cervicis and the more rostral part of the complexus muscle, and a dorsolateral group of motoneurons within lamina VII innervating the caudal part of the complexus muscle. The dorsolateral motoneurons with their HRP-labeled axons leaving the cord through the dorsal root are homologous to the spinal accessory nucleus of mammals. Labeled motoneurons were also noted in the ipsilateral medulla adjacent to the medial longitudinal fasiculus (ELM) in a location previously identified as the hy-poglossal nucleus. Additional experiments were performed in which HRP was injected directly into the base of the tongue. The resultant HRP-labeled hypoglossal motoneurons were separate and dorsolateral to the collic motoneurons. Descending vestibulospinal projections from one vestibular labyrinth were identified autoradiographicalry (ARG) by transneural anterograde transport of ³H-proline-fucose injected into the left labyrinthine endolytine endolymph in five animals. Heavily labeled MVST fibers were observed crossing the midline of the brain to enter and descend in the contralateral ELM. Labeled MVST fibers were noted to leave the contralateral FLM and surround the previously identified collie motoneurons in the medulla with intense terminal fields suggestive of synaptic contact. Labeled MVST fibers in the contralateral ventral funiculus of the cord were also noted to innervate the HRP-identified ventromedial and ventrolateral cervical motoneurons, but not the dorsolateral motoneurons in lamina VII. Ipsilateral (left) descending MVST and LVST fibers were less heavily labeled at all levels in the medulla and upper cervical cord. Labeled ipsilateral (left) vestibulospinal fibers were also observed to leave the lateralmost aspect of the left ventrolateral funiculus in the upper cervical cord to terminate among left ventrolateral motoneurons. Our findings are compared and contrasted with previous studies of vestibulocollic pathways.     

Dendritic organization of phrenic motoneurons in the adult rat

The dendritic organization of the phrenic nucleus as a whole was studied after injections of the B-subunit of cholera toxin conjugated to horseradish peroxidase were made into the diaphragm of adult rats. Transverse, sagittal, and horizontal sections through the phrenic nucleus (C3-C5) were incubated according to a modified tetramethylbenzidine HRP technique. The conjugated form of HRP used in this study has a special affinity for the GM1 ganglioside receptors on neuronal cell surfaces. As a result, extensive labeling of the terminal dendritic fields of a large number of phrenic motoneurons occurred simultaneously. The results showed that the majority of the dendrites of phrenic motoneurons were tightly organized rostrocaudally and confined to the boundaries of the column made up of the phrenic cell bodies. In addition, analysis of transverse and horizontal sections revealed dendritic bundles radiating at right angles to the long axis of the cell column in the following directions: dorsolateral into the dorsal half of the lateral funiculus, lateral into the lateral funiculus, ventromedial into the lateral half of the anterior funiculus, ventrolateral into the ventral half of the lateral funiculus, and dorsal into the intermediate gray matter. Some dendritic bundles were measured as far as 900 microns from phrenic cell bodies into the white matter. The horizontal sections also showed that there was a periodicity in the arrangement of the dendritic fascicles in that they were separated by distances ranging from 180 to 250 microns. From the analysis of phrenic dendritic distribution the present results suggest that the majority of synaptic input to phrenic motoneurons occurs within the column of the phrenic cell bodies. In addition, there is evidence to suggest that a synaptic input may also occur directly on distal phrenic dendrites in the lateral and ventral funiculi of the spinal cord white matter.     

Spinal projections from the lower brain stem in the cat as demonstrated by the horseradish peroxidase technique. I. Origins of the reticulospinal tracts and their funicular trajectories

Using a retrograde tracer technique with horseradish peroxidase (HRP) attempts were made to determine the origins of reticulospinal tracts and their funicular trajectories. Reticulospinal tracts originating from the mesencephalic reticular formation (RF) were composed of: (1) descending projections arising from the cluster of cells located just lateral to the periaqueductal gray that course in the anterior funiculus (AF) and ventral part of the lateral funiculus (LF) with ipsilateral predominance; and (2) projections from the cluster of cells located dorsal to the brachium conjunctivum that course in the ipsilateral LF. Origins of the pontine reticulospinal tracts arising from the n. reticularis pontis oralis (Poo) have been divided qnto three parts: (1) medial one-third; (2) middle; and (3) ventrolateral. The axons from the medial part descend ipsilaterally via the medial part of the AF, while the axons from the ventrolateral part of the Poo give rise to diffuse descending projections in the AF and LF. The middle part of the Poo has been further subdivided into: (1) dorsal part that gives rise to spinal projections ipsilaterally in the ventrolateral funiculus (VLF); and (2) ventral, particularly its upper part, whose axons descend bilaterally via the DLF. Origins of reticulospinal tracts from the n. reticularis pontis caudalis (Poc) could be divided into three parts: (1) medial; (2) dorsolateral; and (3) ventrolateral. The medial part of the Poc is a source of axons via the medial part of the ipsilateral AF, while the ventrolateral part of the nucleus is a source of axons via the contralateral LF. The spinal projections from the dorsolateral part of the Poc appears to course diffusely in the AF and LF, but with DLF predominance. The n. reticularis gigantocellularis (Gc) was found to be a main medullary source of the spinal projections in the ipsilateral AF, while n. reticularis magnocellularis (Mc) is the major source of the fibers coursing ipsilaterally in the VLF. The most medial part of the Mc descends ipsilaterally via the medial part of the AF, while the ventrolateral part of the nucleus together with the n. reticularis lateralis of Meesen and Olszewski descends ipsilaterally via the DLF. It has also been found that the axons from the n. reticularis paramedianus pass via both the AF and LF with ipsilateral predominance, while the n. reticularis dorsalis and ventralis course via the LF with ipsilateral predominance.     

Descending modulation of monosynaptic reflexes after traumatic injury of the cat spinal cord

Studies of the descending modulation of monosynaptic reflex responses have revealed that electrical stimulation of dorsolateral, ventrolateral and ventral funiculi in C2 facilitated and suppressed test responses of intact animals, but evoked only suppression of spinal reflexes after injury of the spinal cord. The obtained data have shown that descending pathways which transmit facilitatory influences are more vulnerable to injury of the spinal cord.     

Funicular organization of avian brainstem-spinal projections.

The purpose of this study was to determine which reticulospinal projections need to be preserved to allow voluntary walking and to differentiate between those pathways descending within the ventrolateral funiculus versus the ventromedial funiculus. Retrogradely transported tracers (True Blue, Fast Blue, Diamidino Yellow dihydrochloride, fluorescein-conjugated dextran-amines) were used alone as discrete funicular injections (4-5 microliters) into the lumbar cord (L1), or in conjunction with a more rostral subtotal lesion of the low thoracic cord, to determine the trajectories of brainstem-spinal projections in adult ducks and geese. No difference was found between the species. The major components of the ventromedial funiculus include projections from the medullary reticular formation, pontine reticular formation, raphe obscurus and pallidus, lateral vestibular nucleus, and interstitial nucleus, and to a minor extent from the locus coeruleus, lateral hypothalamus, and nucleus periventricularis hypothalami. The components of the ventrolateral funiculus (VLF) include projections from the nucleus of the solitary tract, nucleus alatus, pontomedullary reticular formation, raphe pallidus, raphe magnus, locus coeruleus, subcoeruleus, lateral vestibular, and descending vestibular nuclei. The principal descending projections within the dorsolateral funiculus (DLF) arose from the red nucleus, the paraventricular nucleus, locus coeruleus, subcoeruleus, dorsal division of the caudal medullary reticular formation, and raphe magnus. The functional implications of the distribution of these descending pathways are discussed with regard to locomotion. Since birds were able to walk despite bilateral lesion of the DLF or VMF but were unable to walk following a bilateral lesion of the VLF, this suggests that medullary reticulospinal pathways coursing within the VLF are essential for the provision of locomotor drive.     

Inhibition of nociceptive neurons in the shell region of nucleus ventralis posterolateralis following conditioning stimulation of the periaqueductal grey of the cat. Evidence for an ascending inhibitory pathway.

Recordings were made from neurons in the ventroposterior lateral nucleus (VPL) of urethane chloralose-anaesthetised cats, following both noxious mechanical stimulation of the integument, and electrical stimulation of the inferior cardiac nerve. The effects of stimulating the periaqueductal grey (PAG), or the nucleus raphe dorsalis (NRD) on the responses obtained from these units were also investigated. Units responding to noxious mechanical stimulation of the integument, with inferior cardiac nerve input, were found only around the periphery of the posterior half of VPL. Responses elicited from these units by electrical stimulation of the inferior cardiac nerve were inhibited following electrical stimulation of either the ventral PAG or the NRD. Inhibition following PAG or NRD stimulation could still be demonstrated after bilateral section of the dorsolateral funiculi at the junction between C3 and C4, although the degree of inhibition decreased. Responses elicited from these units by electrical stimulation of the anterolateral funiculus were also inhibited following PAG or NRD stimulation. These data suggest that PAG or NRD stimulation-produced inhibition of these units may be partially mediated by an ascending pathway, in addition to the well-known descending spinal pathways in the dorsolateral funiculi of the spinal cord.     

Spinal input pathways affecting the medullary gigantocellular reticular nucleus

Single neurons were recorded in nucleus reticularis gigantocellularis of anesthetized or decerebrate cats. Most of the neurons were isolated using contralateral dorsal funicular stimulation to initially identify the neuron, and all were tested for responsiveness to, or modulation by, input from the contralateral dorsal funiculus and the ipsilateral ventrolateral tracts in the presence of either complete spinal transection sparing the dorsal funiculi or transection of the dorsal half of the spinal cord. Two-thirds of the neurons were excited by way of both spinal pathways when the stimulus was applied rostal to the spinal lesion. The remaining one-third of the neurons were excited by one pathway (90% via dorsal funiculus and 10% via ventrolateral tracts) and inhibited by the other pathway. Most neurons responded within 2 to 8 ms after stimulation of either pathway, and 4.5% were driven antidromically from the ventrolateral tracts. In cats with only the dorsal funiculi intact, all neurons tested for cutaneous responsiveness had small excitatory receptive fields; 90% responded to touch and 10% to hair bending. The thresholds to peripheral nerve stimulation suggested that these neurons were excited by way of the large Aα fibers. Nearly three-fourths of the neurons tested responded to stimulation of the medial lemniscus just caudal to the thalamus; most responded within 5 ms. In cats with only the ventral half of the spinal cord intact, nearly all neurons tested responded to electrical stimulation of each of the four paws, but only 19% responded to cutaneous stimulation (tap or noxious pinch). Clear interactions were found between the two input pathways in nearly all neurons, the pattern of effects (inhibitory and facilitatory) varying with the nature of the effects from each pathway alone. In 4% of the neurons, spontaneous discharge was found to be increased (only ventral half of spinal cord intact) or decreased (only dorsal funiculi intact) during noxious pinching of the skin. Clearly, input by way of both spinal pathways can affect most, if not all, neurons in the gigantocellular nucleus of the medullary reticular formation.     

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.     

Funicular trajectories of brainstem neurons projecting to the lumbar spinal cord in the monkey (Macaca fascicularis): a retrograde labeling study

Brainstem nuclei projecting to the lumbar spinal cord in the monkey were identified by using horseradish peroxidase and the fluorescent dye granular blue. These retrogradely transported tracers were used in fluid and/or gel forms to determine the funicular trajectories of the brainstem-spinal projections. The major descending components of the dorsal funiculus arose from the n. gracilis, n. cuneatus, and the n. of the solitary tract. Major components of the dorsolateral funiculus (DLF) came from the raphe complex, medullary and pontine reticular formation, locus coeruleus, Edinger-Westphal n., and red n. Other nuclei giving rise to minor contributions to the DLF included n. gracilis, n. cuneatus, n. of the solitary tract, medial and spinal vestibular n., subcoeruleus, periaqueductal gray, interstitial n. of Cajal, n. of Darkschewitsch, and the anteromedian n. The major components of ventral cord paths (ventrolateral and ventral funiculi) arose from the raphe complex, the medullary and pontine reticular formation, lateral and spinal vestibular n., and the coerulean complex. Minor contributions to the ventral paths descended from the dorsal motor n. of X, n. of the solitary tract, medial vestibular n., paralemniscal reticular formation, dorsal parabrachial n., n. cuneiformis, periaqueductal gray, K?lliker-Fuse n., and red n. The possible functional implications of the funicular distribution of these descending pathways are discussed from the perspective of descending inhibition and pain modulation.     

Evidence for an Anuran Homologue of the Mammalian Spinocervicothalamic System: An In Vitro Tract-tracing Study in Xenopus laevis

Evidence is presented for an anuran homologue of the mammalian spinocervicothalamic system. In vitro tract-tracing experiments with biotinylated dextran amine in Xenopus laevis show that ascending spinal fibres from all levels of the spinal cord, passing via the dorsolateral funiculus, terminate in a cell area ventrolateral to the dorsal column nucleus. This cell area can be considered a possible homologue of the mammalian lateral cervical nucleus. After tracer applications to the ventral thalamus or to the torus semicircularis (both targets for somatosensory projections), the anuran lateral cervical nucleus was retrogradely labelled contralateral to the application sites. Tracer applications to the dorsolateral funiculus at the obex level and rostral spinal cord resulted in labelling of the cells of origin of the spinocervical tract. These were found, mainly ipsilaterally, in the ventral part of the dorsal horn, and were rather evenly distributed throughout the spinal cord. These data suggest the presence of an anuran homologue of the mammalian spinocervicothalamic system. A brief survey of the literature shows that such a system is much more common in vertebrates than previously thought.     

Spinal ascending pathways in amphibians: Cells of origin and main targets

As part of a research program on the evolution of somatosensory systems in vertebrates, the various components of ascending spinal projections were studied with in vivo and in vitro tract-tracing techniques in representative species of amphibians (the large green frog, Rana perezi, the clawed toad, Xenopus laevis and the ribbed newt, Pleurodeles waltl). Three main ascending sensory channels, each with largely separate targets, were demonstrated: 1. Ascending projections via the dorsal funiculus include primary and nonprimary projections that ascend to terminate mainly in the dorsal column nucleus at obex levels. A small component ascends farther rostralwards to terminate in the reticular formation, the octavolateral area, the trigeminal nuclear complex, and in the granular layer of the cerebellum. 2. Projections ascending via the dorsolateral funiculus reach other spinal and supraspinal targets than the dorsal funicular fibers, mainly ipsilaterally. At upper cervical cord and obex levels, many fibers innervate a region considered the amphibian homologue of the lateral cervical nucleus of mammals. In the medulla, these fibers ascend ventral to the descending trigeminal tract to terminate in the dorsal column and the solitary tract nuclei, and more rostrally, in the reticular formation, the descending trigeminal nucleus and the medial aspect of the ventral octaval nucleus. Major projections reach the area between the facial motor nucleus and the ventral octaval nucleus, and a mediolateral subcerebellar band. These projections arise in neurons located mainly in the ipsilateral deep dorsal and lateral fields throughout the spinal cord. 3. Ascending spinal projections via the ventral quadrant of the spinal cord (the ventral and ventrolateral funiculi) ascend throughout the brainstem up to the diencephalon. Along its course, this component innervates various parts of the reticular formation, the octavolateral area, the granular layer of the cerebellum, the region ventromedial and ventrolateral to the isthmic nucleus, and the subcerebellar region. In the mesencephalon, the torus semicircularis, the midbrain tegmentum and, sparsely, the tectum mesencephali are innervated. Beyond the midbrain, various dorsal and particularly ventral thalamic nuclei and the posterior tubercle are innervated by this ascending sensory channel. The cells of origin of some of these projections were observed in the dorsal, and to a lesser extent, in the lateral and ventral spinal fields of the spinal cord. Evidence for the presence of these three main ascending sensory channels throughout vertebrates will be discussed. The presence of such channels appears to be a shared character in the brain of both amniotes and anamniotes. J. Comp. Neurol. 378:205–228, 1997. © 1997 Wiley-Liss, Inc.     

Localization of enkephalin immunoreactivity in the spinal cord of the long-tailed ray Himantura fai

Enkephalin-like immunoreactivity (ENK-LI) was found throughout the spinal cord of the long-tailed ray Himantura fai. The densest ENK-LI was in the superficial portion of lamina A of the dorsal horn. Lamina B and the deeper parts of lamina A contained radially oriented, labelled fibres. Laminae C, D, and E contained many longitudinally orientated fascicles which were surrounded by a reticulum of transversely orientated, labelled fibres, some of which projected into the ventral and lateral funiculi. Labelled fibres were found in the dorsal commissure and around the central canal, but the later did not cross the midline. One-third of all enkephalinergic cells were found throughout laminae A and B, while two-thirds were located in the medial half of C, D, and E. Occasionally a labelled cell was located in the lateral funiculus. The ventral horn (laminae F and G) contained many enkephalinergic fibres but no labelled nuclei. A few dorsal column axons contained ENK-LI. In the lateral funiculus there were two groups of labelled axons, a superficial, dorsolateral group, and a deeper group, occupying a crescent-shaped region. The ventral funiculus also contained many labelled axons. The central projection of the dorsal root passed through the substantia gelatinosa and divided into rostrally and caudally projecting fascicles within lamina C. The root, and these fascicles, both lacked ENK-LI. In contrast, the fascicles in laminae D and E did contain enkephalinergic fibres. The origin of the various fibre systems and the role of enkephalin in the regulation of sensory processing and motor output are discussed. © 1996 Wiley-Liss, Inc.     

Spinal cord substrate of the turning behavior induced by unilateral lesion of the entopeduncular nucleus

The neural pathways in the spinal cord mediating circling behavior in animals with unilateral kainic acid lesion of the entopeduncular nucleus were studied in rats. The circling activity toward the lesioned side was indiced by i.p. administration of apomorphine (3 mg/kg). Section of the lateral funiculus ipsilateral to the lesioned entopeduncular nucleus, reduced significantly the rate of drug induced rotations. The above was a common lesion of ventrolateral and dorsolateral transections of the cervical spinal cord. However, the latter transection was more effective than the former to block the circling. On the other hand, lesion of the contralateral spinal cord fails to modify turning behavior. These findings suggest that crossed fibers descending in the dorsolateral quadrant directly from the basal ganglia or mediating synaptic relay in the lower brainstem may be the anatomical substrate of the circling produced by striatal stimulation.     

Effectivess of synaptic influences of the ascending tracts of different spinal cord funiculi on reticulospinal neurons in cats]

Extracellular recording of the responses of the reticulospinal neurons evoked by stimulation of the dorsal, dorsolateral, ventral and ventrolateral spinal funiculi were performed in cats under chloralose anesthesia. It is found that dorsal funiculi of the spinal cord are an effective source of ascending influences on the reticulospinal neurons. Correlation of synaptic responses of the reticulospinal neurons with antidromatic responses in the peripheral nerves set up by stimulation of the dorsal funiculi shows that the former can be evoked by low threshold muscle (groups I and II) and cutaneous (group II) afferent fibres. The role of the ascending tracts in the transmission of the spino-bulbo-spinal activity is discussed.