Nucleus tegmenti pedunculopontinus: Efferent connections with special reference to the basal ganglia,studied in the rat by anterograde and retrograde transport of horseradish peroxidase

The efferent connections of the brain stem nucleus tegmenti pedunculopontinus were studied in the rat using the techniques of anterograde and retrograde transport of the enzyme horseradish peroxidase, laying particular emphasis on that part of pedunculopontinus which receives direct descending projections from the basal ganglia and related nuclei. In a preliminary series of experiments horseradish peroxidase was injected into either the entopeduncular nucleus or the subthalamic nucleus and, following anterograde transport of enzyme, terminal labelling was identified in nucleus tegmenti pedunculopontinus, surrounding the brachium conjunctivum in the caudal mesencephalon.In a subsequent series of experiments, horseradish peroxidase was injected into that region of nucleus tegmenti pedunculopontinus which receives entopeduncular and subthalamic efferents and its efferent projections were studied by anterograde transport of the enzyme. The results indicate that nucleus tegmenti pedunculopontinus gives rise to widely distributed efferent projections which terminate rostrally in mesencephalic, diencephalic and telencephalic structures and caudally in the pontine tegmentum. In the mesencephalon, terminal labelling was found in the pars compacta of the ipsilateral substantia nigra and sometimes in the adjoining ventral tegmental area. Labelling was also found in the ipsilateral half of the periaqueductal grey. In the diencephalon terminal labelling occurred bilaterally in the subthalamic nucleus and ipsilaterally in the intralaminar nuclei of the thalamus. Further rostrally, terminal labelling was particularly evident in the ipsilateral pallidal complex, especially in the caudal two-thirds of the entopeduncular nucleus and the ventral half of the caudal third of the globus pallidus. Caudal to pedunculopontine injection sites dense labelling was observed in the reticular formation of the pontine tegmentum.In a final series of experiments, confirmation of apparent pedunculopontine efferent projections was sought using the retrograde transport of horseradish peroxidase. Enzyme was injected into sites possibly receiving pedunculopontine efferents and the peribrachial area of the brain stem was examined for retrograde cell labelling. In this way, pedunculopontine projections were confirmed to the globus pallidus, entopeduncular nucleus, subthalamic nucleus, substantia nigra, parafascicular nucleus and pontine reticular formation. Injections into the globus pallidus or subthalamic nucleus gave rise to retrograde cell labelling bilaterally in pedunculopontinus. In addition, retrograde transport studies alone demonstrated projections from pedunculopontinus to the cerebral cortex and to the spinal cord.It is concluded that the nucleus tegmenti pedunculopontinus has reciprocal relationships with parts of the basal ganglia and some functionally related nuclei (in particular, the pallidal complex, subthalamic nucleus and substantia nigra). These connections support the view that nucleus tegmenti pedunculopontinus is likely to be involved in the subcortical regulation and mediation of basal ganglia influences upon the lower motor system. This suggests a potential role for pedunculopontine afferent and efferent pathways in the pathophysiology of basal ganglia related disorders of movement.     

Brain stem afferents to the anterior dorsal ventricular ridge in a lizard (Varanus exanthematicus)

Summary The anterior dorsal ventricular ridge (ADVR), a large intraventricular protrusion in the reptilian forebrain, receives information from many different sensory modalities and in turn, projects massively onto the striatum. The ADVR possesses functional similarities to the mammalian isocortex and may perform complex sensory integrations. The ADVR in lizards is composed of three longitudinal zones which receive visual, somatosensory and acustic information, respectively. These projections are relayed via thalamic nuclei. Previous retrograde tracer studies also suggested brain stem projections to the ADVR arising in the midbrain reticular formation and in certain monoaminergic brain stem nuclei (substantia nigra, locus coeruleus and nucleus raphes superior). In the present study the powerful retrograde fluorescent tracer. Fast Blue was applied as a slow-release gel to the ADVR of the savanna monitor lizard, Varanus exanthematicus. Thalamic projections were confirmed and various direct brain stem projections to the ADVR were demonstrated. Brain stem afferents to the ADVR were found from the laminar nucleus of the torus semicircularis (possibly comparable to the mammalian periaqueductal gray), from the midbrain reticular formation, from the substantia nigra (pars compacta and reticulata) and the adjacent ventral tegmental area, from the nucleus raphes superior, from the locus coeruleus, from the parabrachial region, from the nucleus of the lateral lemniscus and even from the most caudal part of the brain stem (a few neurons in the nucleus of the solitary tract and lateral reticular formation, possibly comparable to the mammalian A₂ and A₁ groups, respectively). These data strongly suggest direct ADVR projections from the parabrachial region (related to visceral and taste information) as well as distinct catecholaminergic (presumably dopaminergic: substantia nigra, ventral tegmental area and, noradrenergic: locus coeruleus, respectively) and serotonergic projections (nucleus raphes superior).     

Subthalamic nucleus efferent projection to the cerebral cortex

A direct projection from the subthalamic nucleus to the dorsal cerebral cortex has been demonstrated in the rat using a retrograde axonal transport technique. Injections of horseradish peroxidase into the cerebral cortex gave rise to retrogradely-labelled neuronal cell bodies in the ipsilateral subthalamic nucleus. Labelled cells were restricted to the lateral half of the nucleus. In addition, retrograde-labelling was observed in the rostral and caudal portions of the entopeduncular nucleus. Injections of horseradish peroxidase into the striatum underlying the cortical region receiving subthalamic efferents failed to label any subthalamic nucleus or entopeduncular nucleus neurones.These findings add the cerebral cortex to the other known projection areas (globus pallidus, substantia nigra, nucleus tegmenti pedunculopontinus) of the subthalamic nucleus and might have implications for the way in which the subthalamic nucleus influences motor activity.     

Striatal axons to the globus pallidus, entopeduncular nucleus and substantia nigra come mainly from separate cell populations in cat

The extent to which individual striatal neurons send collaterals to the globus pallidus, entopeduncular nucleus and substantia nigra in the cat brain was determined by double-retrograde tracing with rhodamine fluorescent latex microspheres in combination with either horseradish peroxidase or the fluorescent nuclear dye Diamidino Yellow. In each case, two of the three target nuclei were injected, each with a different tracer, until all three possible combinations of two had been obtained several times. In all cases in which the tracer encroaches upon a striatal target, there are cells labeled in the striatum of a size and shape that is consistent with the observation that they mainly belong to the category of medium striatal cells. Since the striatal projections to the globus pallidus, entopeduncular nucleus and substantia nigra are each topographically organized, the zones of cell-labeling within the striatum vary depending upon the portion of the target nucleus involved by the deposit. Thus, in many cases the fields of striatal cells containing one label overlap only slightly with those in which cells containing the other label occur. In other cases, however, there is extensive overlap of the striatal zones containing cells marked with either tracer. In all cases, very few double-labeled cells can be found, even where hundreds of cells labeled with either tracer are freshly intermingled. Doubly labeled cells occur somewhat more frequently in those cases where the tracers are placed in the entopeduncular nucleus and substantia nigra than in those with the other two combinations, suggesting that striatal axons branch more often to the entopeduncular nucleus and substantia nigra than to the globus pallidus and nigra or globus pallidus and entopeduncular nucleus. These findings confirm, that, in the cat as in the primate, the striatal axons to the substantia nigra arise from cells that are largely separate from the striatopallidal population, and further show that the axons to the globus pallidus and entopeduncular nucleus also emanate mainly from different cells.     

Substantia nigra projections to the reticular formation,superior colliculus and central gray in the rat,cat and monkey

After horseradish peroxidase injections in different parts of the lower brain stem retrogradely labeled neurons were observed in the substantia nigra, mainly ipsilateral pars reticulata. These findings demonstrate that the substantia nigra projects not only to the striatum and thalamus but also to brain stem areas which give rise to descending spinal projections. These nigral projections to brain stem structures may play an important role in a variety of behaviors and may be involved in clinical syndromes associated with nigral lesions.     

The fasciculus longitudinalis medialis in the lizard Varanus exanthematicus. 1. Interstitiospinal, reticulospinal and vestibulospinal components

Summary With the horseradish peroxidase (HRP) technique the various descending components of the medial longitudinal fasciculus (flm) have been studied in the lizard Varanus exanthematicus. After wheat germ agglutinin conjugated HRP injections at the spinomedullary border, retrogradely labeled fibers passing via the flm could be traced to various parts of the magnocellular rhombencephalic reticular formation, the descending and ventromedial vestibular nuclei and the interstitial nucleus of the flm. By implanting HRP slow-release gels into the flm the trajectory and site of termination of various components of the flm have been analysed. The interstitiospinal tract passes via the dorsal part of the flm. Reticulospinal fibers arising in the nucleus reticularis superior and nucleus reticularis medius take a position ventral to the interstitiospinal fibers. Vestibulospinal projections via the flm are found in its ventral part and arise mainly in the contralateral ventromedial and descending vestibular nuclei. A strong vestibulocollic projection to cervical motoneurons should be noted.The positional relations of the various fiber components within the flm found in a lower vertebrate such as the lizard Varanus exanthematicus are comparable to those in mammals.     

Ascending projections of presumed dopamine-containing neurons in the ventral tegmentum of the rat as demonstrated by horseradish peroxidase

The projections of presumed dopamine-containing neurons in the zona compacta of the substantia nigra and the ventral tegmental area were examined by stereotaxic injections of horseradish peroxidase into diverse cortical and subcortical regions which are known to include dopamine-containing terminals. Neurons in the lateral half of the substantia nigra pars compacta were labelled after injections into the caudolateral aspect of the caudate-putamen, while neurons in the medial part of the substantia nigra pars compacta and lateral aspect of the ventral tegmental area projected to the anteromedial portion of the caudate putamen. Injections of horseradish peroxidase into the amygdala resulted in the appearance of reactive neurons in the anterior portion of the ventral tegmental area, but the more caudally located entorhinal cortex received projections from the posterior half of the ventral tegmental area. Injections of horseradish peroxidase into the frontal cortex, anterior to the genu, produced scattered labelled cells in the rostral half of the ventral tegmental area, whereas more posterior injections into the cingulate cortex resulted in the appearance of reactive cells which were confined to the medial one-quarter of the substantia nigra pars compacta. The near-midline structure, the lateral septum, was innervated by neurons with cell bodies primarily in the medial half of the ventral tegmental area. Injections of horseradish peroxidase into the nucleus accumbens, which contains very high levels of dopamine, resulted in the appearance of many labelled neurons throughout the ventral tegmental area and some reactive neurons in the medial part of the substantia nigra pars compacta. A few labelled cells were also occasionally observed in the contralateral ventral tegmental area after accumbens injections.These results suggest that although there is considerable overlap, and that the same subdivisions within the substantia nigra pars compacta and the ventral tegmental area appear to innervate diverse regions of the forebrain, there also exists a general topographical organization with respect to the projections of these neurons.Injections of horseradish peroxidase into some of the forebrain regions also resulted in the appearance of reactive cells in mesencephalic nuclei not known to contain dopaminergic perikarya. For example, labelled cells were observed in the supramamillary nucleus after injections into the frontal cortex, entorhinal cortex, accumbens and lateral septum. Injections into the amygdala produced reactive cells in the suprageniculate nucleus, the peripeduncular nucleus, and the magnocellular nucleus of the medial geniculate. These latter results are discussed with reference to the possibility that such pathways may mediate the responsiveness of cells in the amygdala to a wide range of sensory stimuli.     

Basal ganglia and other afferent projections to the peribrachial region in the rat: A study using retrograde and anterograde transport of horseradish peroxidase

The afferent projections to the peribrachial region in the rat were studied using retrograde and anterograde transport of horseradish peroxidase. Particular attention was paid to descending projections from the basal ganglia and related nuclei to the region of nucleus tegmenti pedunculopontinus. Following injection of peroxidase into nucleus tegmenti pedunculopontinus, few retrogradely-labelled neurons were found in the entopeduncular nucleus proper, but larger numbers were found with a wide distribution within the boundaries of the internal capsule and cerebral peduncle. Labelled cells were also consistently observed in the amygdala, the caudal globus pallidus, the subthalamus including zona incerta and subthalamic nucleus, the hypothalamus, the substantia nigra and the ventral tegmental area. Following iontophoretic injections of horseradish peroxidase into the entopeduncular nucleus, lateral hypothalamus, subthalamic nucleus or ventral tegmental area, terminal labelling was observed in and around the branchium conjunctivum in an area apparently corresponding to nucleus tegmenti pedunculopontinus in the rat.     

Projections of the basal ganglia to the zona incerta of the dog diencephalon

Retrograde axonal transport of horseradish peroxidase was used to show that the projections of the globus pallidus, entopeduncular nucleus, substantia nigra, and pedunculopontine tegmental nucleus in dogs are directed to all segments of the zone incerta. The experiments reported here identified no topical features in the organization of these projections in dogs, as application of marker to different areas of the zona incerta yielded similar distributions of labeled neurons in the basal ganglia. No striatal projections to the zone incerta were found.     

Topographic projections from the basal ganglia to the nucleus tegmenti pedunculopontinus pars compacta of the cat with special reference to pallidal projections

Summary Projections from the basal ganglia to the nucleus tegmenti pedunculopontinus pars compacta (TPC) were studied by using anterograde and retrograde tracing techniques with horseradish peroxidase conjugated with wheat germ agglutinin (WGA-HRP) in the cat. Following WGA-HRP injections into the medial TPC area, a substantial number of retrogradely labeled cells were seen in the entopeduncular nucleus (EP) and medial half of the substantia nigra pars reticulata (SNr), whereas following WGA-HRP injections into the lateral TPC area, labeled cells were marked in the caudal half of the globus pallidus (GP) and lateral half of the SNr. To confirm the retrograde tracing study, WGA-HRP was injected into the EP or the caudal GP, and anterograde labeling was observed in the TPC areas. Terminal labeling was located in the medail TPC area in the EP injection case, while terminal labeling was observed in the lateral TPC area in the caudal GP injection case. Projections from the striatum to the pallidal complex (the EP and the caudal GP) were also studied autoradiographically by injecting amino acids into various parts of the caudate nucleus and the putamen. Terminal labeling was distributed over the whole extent of the EP and the rostral GP following injections into the rostral striatum (the head of the caudate nucleus or the rostral part of the putamen), while terminal labeling was distributed over the caudal GP following injections into the caudal striatum (the body of the caudate nucleus or the caudal part of the putamen). From these findings, we conclude that there exists a medio-lateral topography in the projection from the basal ganglia to the TPC: The EP receives afferent projections from the rostral striatum and projects to the medial TPC area, whereas the caudal GP receives projections from the caudal striatum and sends fibers to the lateral TPC area.Abbreviations BC brachium conjunctivum - CD caudate nucleus - CP cerebral peduncle - DBC decussation of the brachium conjunctivum - EP entopeduncular nucleus - GP globus pallidus - IC internal capsule - ICo inferior colliculus - LH lateral habenular nucleus - ML medial lemniscus - PN pontine nuclei - PUT putamen - SCo superior colliculus - SI substantia innominata - SN substantia nigra - SNc substantia nigra pars compacta - SNr substantia nigra pars reticulata - STN subthalamic nucleus - TH thalamus - TPC nucleus tegmenti pedunculopontinus pars compacta     

Quantitative evaluation of crossed and uncrossed projections from basal ganglia and cerebellum to the cat thalamus

Quantitative and qualitative analysis of crossed vs uncrossed projections from the substantia nigra, entopeduncular nucleus and individual cerebellar nuclei to the thalamus was undertaken in nine adult cats using retrograde labeling with horseradish peroxidase and fluorescent dyes. The results indicate that about 90% of entopeduncular nucleus neurons and 50% of substantia nigra neurons give rise to ipsilateral projections to the thalamus whereas the contralateral component of these projections originates from about 10 and 7% neurons of entopeduncular nucleus and substantia nigra, respectively. Some of the fibers constituting the contralateral component are represented by branching axon collaterals of the neurons projecting ipsilaterally. In the basal ganglia thalamic projection, its minor component (contralateral) targets the ventral anterior and ventral medial nuclei the same as its major component (ipsilateral). However, some preferential distribution of the contralateral projections to the ventral medial nucleus appears to exist. In regard to the cerebellothalamic projections it was found that about 90% of neurons located in the dentate and interpositus nuclei and 50% of neurons in the fastigial nucleus project to the contralateral thalamus while 16% of dentate nucleus neurons and 40% of fastigial nucleus neurons give rise to the ipsilateral cerebellothalamic projections. A considerable number of ipsilateral cerebellothalamic fibers are represented by divergent axon collaterals of the same neurons projecting to the contralateral thalamus. The cerebellothalamic projections from all cerebellar nuclei including the fastigial nucleus are targeted primarily to the ventral lateral nucleus both contra- and ipsilaterally. The ventral medial nucleus receives bilateral input from the fastigial nucleus which originates from about one quarter of the thalamus projecting neurons in this nucleus. Of all other cerebellar nuclei only the dentate nucleus projects to the ventral medial nucleus and this projection is exclusively contralateral.     

Retinal projection to the formatio reticularis tegmenti mesencephali in the Old World monkeys

Summary We studied the retinal projections of Old World monkeys using the anterograde transport of tritiated amino acid and wheat germ agglutinin conjugated to horseradish peroxidase. In addition to well-known retinal connections, these methods revealed that a small number of labeled retinofugal fibers might terminate in a small area of the contralateral formatio reticularis tegmenti mesencephali between the red nucleus and the substantia nigra. In the autoradiographic cases, a few labeled retinal terminals were also found in the same area on the ipsilateral side. In order to reach their terminal field, these labeled fibers appeared to leave the accessory optic tract in the vicinity of the dorsal border of the lateral terminal nucleus and run medially through the substantia nigra.     

大鼠下边缘皮质的皮质下端脑,间脑,脑干的传入投射

实验用ＨＲＰ导入大鼠下边缘皮质研究了皮质下端脑、间脑和脑干至下边缘皮质的传入投射。结果：皮质下端脑至下边缘皮质的传入主要来自同侧屏状核,背侧梨状内核,杏仁基底外侧核和杏仁基底内侧核,其次来自杏仁外侧核,杏仁皮质核等。     

Interactions between the basal ganglia, the pontine parabrachial region, and the trigeminal system in cat

Anatomical studies utilizing wheat germ lectin-bound horseradish peroxidase demonstrated direct connections between the pontine parabrachial region and the substantia nigra pars reticulata and to a lesser extent, the entopeduncular nucleus as well as a number of other forebrain regions including the amygdala, hypothalamus, thalamus, bed nucleus stria terminalis and substantia innominata. The pontine parabrachial region was also shown to receive direct inputs from the spinal trigeminal system and to send axons to areas surrounding trigeminal and hypoglossal motor areas. Once the anatomical connections were determined, electrophysiological studies were undertaken to investigate some of the functional aspects of these connections between the pontine parabrachial, basal ganglia and trigeminal systems. Extracellular single unit recordings were obtained from 228 cells in the dorsal pontine parabrachial region of the cat. These cells were tested for responsiveness to trigeminal sensory stimulation and activation of basal ganglia outputs (i.e. substantia nigra and entopeduncular nucleus). Twenty-two percent of pontine parabrachial cells responded to only trigeminal stimulation; 4% responded to entopeduncular nucleus only; 37% responded to substantia nigra only, and 28% responded to both substantia nigra and trigeminal stimulation. Furthermore, 43% of pontine parabrachial cells with both substantia nigra and sensory response had the sensory response altered by a preceding stimulus to the substantia nigra. Thus, the substantia nigra is shown to exert influences on both the spontaneous activities and afferent responses of pontine parabrachial neurons. The significance of these findings are discussed in relation to the importance of descending basal ganglia influences and ascending influences from the pontine parabrachial region on various sensorimotor activities.     

An anatomical and electrophysiological investigation of the serotonergic projection from the dorsal raphe nucleus to the substantia nigra in the rat

Evidence for a projection from the dorsal raphe nucleus to the substantia nigra was obtained by the demonstration of reactive perikarya in the dorsal raphe nucleus after injections of horseradish peroxidase into the substantia nigra of the rat. No labelled cells were observed in the median raphe nucleus. Stereotaxic injections of [³H]leucine into the dorsal raphe nucleus resulted in the appearance of autoradiographic grains over both the zona compacta and zona reticulate of the substantia nigra, although the concentration of grains was higher over the zona compacta. Electrolytic lesions of the dorsal raphe nucleus reduced nigral and striatal 5-hydroxytryptamine content by 61.5 and 70% respectively. Stimulation of the dorsal raphe nucleus was found to inhibit the unit activity of cells in both the zona compacta and zona reticulate of the substantia nigra and this inhibition could be blocked by 60–72 h pretreatment with p-chlorophenylalanine. Stimulation of the median raphe nucleus produced no consistent effects upon nigral unit activity. para-Chlorophenylalanine pretreatment did not significantly affect the rate of striatal dopamine depletion produced by injections of α-methyl-para-tyrosine, suggesting that the serotonergic raphe-nigral projection exerts a phasic rather than a tonic inhibitory influence over the dopaminergic neurons of the nigro-striatal projection.The results are discussed with reference to the possibility that the projections of the dorsal raphe nucleus to the substantia nigra and the striatum may mediate some of the interactions between central serotonergic and dopaminergic mechanisms.     

Dissociation of crossed and uncrossed nigrostriatal projections with respect to site of origin in the rat

In the present study we have investigated the relative rostrocaudal position of the neurons in the substantia nigra, which project to the ipsilateral or contralateral neostriatum. The retrograde tract tracer horseradish peroxidase was implanted into the striatum on one side. The substantia nigra, ventral tegmental area and retrorubral area ipsilateral and contralateral to the site of implantation were examined for labeled cells. The distributions of the cells which give rise to the crossed and uncrossed nigrostriatal projections were found to be inverse. More labeled cells were found in the rostral than the caudal part of the substantia nigra ipsilateral to the site of horseradish peroxidase implantation. In contrast, there was a greater likelihood of finding labeled cells in the middle and caudal parts of the contralateral substantia nigra than in the rostral part. Sparse projections from the ipsilateral and contralateral retrorubral area and ventral tegmental area were also found.     

Organization of Projections of the Zona Incerta of the Diencephalon to Pallidal Structures in the Dog Brain

Detailed studies of the organization of individual sectors in the zona incerta of the diencephalon to functionally diverse pallidal structures in the dog brain were performed by antero- and retrograde axon transport of horseradish peroxidase. The results showed that neurons in the caudal sector of the zona incerta innervate the globus pallidus and entopeduncular nucleus, which receive more extensive innervation from motor structures. The same pallidal structures receive projections from occasional neurons in the dorsal and causal sectors of the zona incerta. No connections of the zona incerta with the limbic ventral pallidum were found.     

Somatosensory systems and the milk-ejection reflex in the rat. I. Lesions of the mesencephalic lateral tegmentum disrupt the reflex and damage mesencephalic somatosensory connections

Bilateral electrolytic lesions and unilateral tracer injections were performed in lactating rats in order to study the participation of the mesencephalic lateral tegmentum in the milk-ejection reflex. The release of oxytocin was detected as a rise in intramammary pressure during each milk ejection. In animals with lesions, the lateral part of the deep grey layers of the superior colliculus, the intercollicular area and the rostromedial portion of the external nucleus of the inferior colliculus were destroyed. The mesencephalic lateral tegmentum of animals in which the milk-ejection reflex was blocked sustained a larger damage than in rats where the frequency of the milk-ejection response was only slowed down. Solutions of True Blue, horseradish peroxidase or horseradish peroxidase coupled to wheat germ agglutinin were injected in the mesencephalic lateral tegmentum of rats with and without lesions. Retrogradely labelled cells were found in several nuclei of the somatosensory pathways: the principal sensory and spinal parts of the trigeminal complex, the cuneate and gracile nuclei, the lateral cervical nucleus and the nucleus proprius of the spinal cord. Labelled cells were also found in the ventral nucleus of the lateral lemniscus, the ventral parabrachial nucleus, the gigantocellular reticular nucleus, the lateral nucleus of the substantia nigra, the prerubral nucleus of the thalamus, the hypothalamic ventromedial nucleus, the zona incerta and in the anterior and lateral hypothalamic areas. Labelled fibres and "terminal-like" labelling were found in the anterior pretectal area, in the thalamic parafascicular nucleus, in the posterior nucleus and the ventroposterior complex, in the zona incerta and in the fields of Forel, but none were observed in the supraoptic or paraventricular nuclei. Injections made in the area of the lateral cervical nucleus and in the cuneate and gracile nuclei labelled fibres and "terminal-like" fields in the external nucleus of the inferior colliculus, the intercollicular area, the deep grey layers of the superior colliculus and in the mesencephalic lateral tegmentum. After injections in the posterior nucleus and ventroposterior complex of the thalamus, retrogradely labelled cells were found in the lateral tegmentum, the intercollicular area and the external nucleus of the inferior colliculus. These results indicate that bilateral lesioning of the mesencephalic lateral tegmentum, which disrupts the milk-ejection response, could damage somatosensory projections originating from the dorsal horn of the spinal cord, the lateral cervical nucleus, the dorsal column nuclei and the sensory and spinal trigeminal nuclei.(ABSTRACT TRUNCATED AT 400 WORDS)     

Branched output neurons of the rat subthalamic nucleus: electrophysiological study of the synaptic effects on identified cells in the two main target nuclei, the entopeduncular nucleus and the substantia nigra

The synaptic responses of entopeduncular and nigral cells to subthalamic stimulation were studied with extracellular recording techniques in rats with and without chronic lesions. Entopeduncular output cells were identified by antidromic activation from the lateral habenula, ventral anterior thalamic nucleus and tegmenti pedunculopontine nucleus. Nigral cells projecting to superior colliculus were identified by antidromic discharge. Stimulation of the subthalamic nucleus produced a short latency suppression of spontaneous activity (10-60 ms duration) of 89% of the entopeduncular cells tested in chronically lesioned rats. Of these cells, 50% were identified as projecting to lateral habenula. On the other hand, subthalamic nucleus stimulation produced a short latency excitation of 73% of the nigral cells tested (4.16 +/- 0.07 ms). Forty-eight percent of these cells projected to superior colliculus. The subthalamic fibres which terminate in entopeduncular nucleus and substantia nigra, come from the same neuronal population since the majority, if not all, rat subthalamic neurones send branched projections to both these nuclei. Therefore, the two different types of responses recorded in these nuclei are elicited by the activation of a single neuronal population. This dual effect could be easily explained if one of the responses is mediated by local interneurones. If not, the same transmitter induces the two responses. The entopeduncular nucleus and substantia nigra which are the main target nuclei of the subthalamic nucleus, are also the only known outputs of the striatum. The subthalamic efferent cells could thus modulate the activity of the entire striatal descending output. It is noteworthy that this subthalamic control is different in entopeduncular nucleus than in substantia nigra.     

Amygdaloid projections to the mesencephalon,pons and medulla oblongata in the cat

Summary Amygdalotegmental projections were studied in 26 cats after injections of horseradish peroxidase (HRP) in the diencephalon, midbrain and lower brain stem and in 6 cats after injection of ³H-leucine in the amygdala. Following HRP injections in the posterior hypothalamus, periaqueductal gray (PAG) and tegmentum many retrogradely labeled neurons were present in the central nucleus (CE) of the amygdala, primarily ipsilaterally. Injections of HRP in the posterior hypothalamus and mesencephalon also resulted in the labeling of neurons in the basal nucleus, pars magnocellularis.Following ³H-leucine injections in CE and adjacent structures autoradiographically labeled fibers were present in the stria terminalis and ventral amygdalofugal pathways. In the mesencephalon heavily labeled fiber bundles were located lateral to the red nucleus. Labeled fibers and terminals were distributed to the mesencephalic reticular formation, substantia nigra, ventral tegmental area and PAG. In the pontine and medullary tegmentum the bulk of passing fibers was located laterally in the reticular formation. Many labeled fibers and terminals were distributed to the parabrachial nuclei, locus coeruleus, nucleus subcoeruleus and lateral tegmental fields. Many terminals were also present in the solitary nucleus and dorsal motor nucleus of the vagus nerve.The location of the cells of origin and the distribution of the terminals of the amygdalotegmental projection suggest that this pathway plays an important role in the integration of somatic and autonomic responses associated with affective defense.Abbreviations A nucleus ambiguus - AL lateral amygdaloid nucleus - AQ cerebral aqueduct - BC brachium conjunctivum - BL basal amygdaloid nucleus, pars magnocellularis - BM basal amygdaloid nucleus, pars parvocellularis - BP brachium pontis - CE central amygdaloid nucleus - CI internal capsule - CN cochlear nucleus - CO cortical amygdaloid nucleus - CP cerebral peduncle - DCN dorsal column nuclei - DMV dorsal motor nucleus of the vagus nerve - E entopeduncular nucleus - F fornix - FLA longitudinal association bundle - GP globus pallidus - H hippocampal formation - 1C inferior colliculus - INJ injection site - LC locus coeruleus - IO inferior olive - LG lateral geniculate nucleus - LRN lateral reticular nucleus - LT lateral tegmental field - M medial amygdaloid nucleus - MB mammilary body - MG medial geniculate nucleus - ML medial lemniscus - MT medial tegmental field - MV motor nucleus of the trigeminus - OC optic chiasm - OT optic tract - P putamen - PAG periaqueductal gray - PB parabrachial nuclei - PC posterior commissure - PH posterior hypothalamus - PT pyramidal tract - PV principal sensory nucleus of the trigeminus - PYR pyriform cortex - R red nucleus - RF reticular formation - S solitary nucleus - SC nucleus subcoeruleus - SN substantia nigra - SO superior olive - SOL solitary nucleus - SPV spinal trigeminal complex - ST stria terminalis - VC vestibular complex - VTA ventral tegmental area - VII facial nucleus - XII hypoglossal nucleus