Anterograde tracer study on the nucleus geniculatus dorsalis and its internal synaptic structure in chick brain

In the present study the terminals of retinal fibres and those of internal layer cells in ventral geniculate nucleus of chicks were labelled with the anterograde tracer biotinylated dextran amine. The tracer showed the connections from the internal cell layers of ventral geniculate nucleus to the medial part of the dorsal lateral geniculate nucleus. The labelled retinal terminals were located exactly in the lateral part of nucleus. The labelled terminals in the two parts of the nucleus were analysed with the electron microscope and showed a different synaptic organisation in the two parts of the dorsal lateral geniculate nucleus. In the lateral part, two kinds of synaptic glomeruli were found mostly in the vicinity of large dendrites, which are proximal dendrites of projection neurons. One type is a simple glomerulus containing a large dendrite, a large optic terminal and a large and/or series of asymmetrical synapses surrounded by glial processes. The other type is a complex synaptic unit with several pre- and postsynaptic components, among them synapses of GABA-positive axon terminals and/or dendraxons. No glomeruli were found in the medial part of the nucleus. In the medial part of the lateral geniculate nucleus, the terminals of internal layer cell axons established asymmetrical synapses with dendrites. Often, a large terminals and large dendritic profiles established serial asymmetrical synapses. GABA-positive myelinated fibres entered and ramified in both parts of the dorsal lateral geniculate nucleus, and GABA-positive terminals were seen to form synapses on the same dendrite near to the asymmetrical contacts. To our knowledge, this is the first report of the connection from ventral geniculate internal layer cells to the dorsal lateral geniculate nucleus in the chick.     

Fewer driver synapses in higher order than in first order thalamic relays

We used electron microscopy to determine the relative numbers of the three synaptic terminal types, RL (round vesicle, large terminal), RS (round vesicles, small terminal), and F (flattened vesicles), found in several representative thalamic nuclei in cats chosen as representative examples of first and higher order thalamic nuclei, where the first order nuclei relay subcortical information mainly to primary sensory cortex, and the higher order nuclei largely relay information from one cortical area to another. The nuclei sampled were the first order ventral posterior nucleus (somatosensory) and the ventral portion of the medial geniculate nucleus (auditory), and the higher order posterior nucleus (somatosensory) and the medial portion of the medial geniculate nucleus (auditory). We found that the relative percentage of synapses from RL terminals varied significantly among these nuclei, these values being higher for first order nuclei (12.6% for the ventral posterior nucleus and 8.2% for the ventral portion of the medial geniculate nucleus) than for the higher order nuclei (5.4% for the posterior nucleus, and 3.5% for the medial portion of the medial geniculate nucleus). This is consistent with a similar analysis of first and higher order nuclei for the visual system (the lateral geniculate nucleus and pulvinar, respectively). Since synapses from RL terminals represent the main information to be relayed, whereas synapses from F and RS terminals are modulatory in function, we conclude that there is relatively more modulation of the thalamic relay in the cortico-thalamo-cortical higher order pathway than in first order relays.     

gamma-Aminobutyric acid immunoreactivity in brainstem auditory nuclei of the chicken

Using an antiserum directed against gamma-aminobutyric acid (GABA), the presence of presumed GABAergic neurons is demonstrated in the chicken auditory brainstem nuclei: nucleus laminaris, nucleus angularis, superior olive, and the ventral nuclei of the lateral lemniscus. Nucleus magnocellularis contains no immunopositive neurons but numerous GABA-positive terminals surrounding the cells. Terminal labeling is also present in the other auditory nuclei, though scarcer and not always associated with cell bodies. These data suggest an involvement of GABAergic inhibition in auditory processing in the lower auditory pathway of birds.     

大白鼠脚间核的传入性联系

本实验应用微量注射和离子透入法经三种不同入路,将HRP输入大鼠脚间核内,追踪脚间核的传入性联系。三种不同进针方向,共同出现标记神经元的核团除了缰内侧核、缰外侧核、中缝背核、中央上核、被盖背核、被盖背外侧核、导水管周围灰质外侧与腹外侧区和蓝斑以外,尚有Broca氏斜角带核和伏隔核。组内侧核和脚间核的联系存在着明显的局部定位关系,即双侧缰内侧核内侧投射至脚间核中部的腹侧和腹外侧;双侧缰内侧核外侧投射至脚间核中部的背侧;同侧缰内侧核投射至脚间核中部的外侧;双侧缰内侧核纤维并不投射至脚间核的吻端和尾端。本研究还发现其它核团对脚间核的投射也存在一定的局部定位关系,如缰外侧核、被盖背核腹内侧和被盖背外侧核均投射到脚间核的尾侧;伏隔核尾端也有投射纤维至脚间核。     

Calretinin distribution in the thalamus of the rat: immunohistochemical and in situ hybridization histochemical analyses.

The distribution of calretinin-containing cells was examined by in situ hybridization histochemistry and compared with the immunohistochemical mapping of calretinin in the thalamus of the rat. Results revealed a close correspondence between the immunohistochemical localization of cell bodies and the messenger RNA label produced by the calretinin oligonucleotide probe. Calretinin cells were most prominent in the midline (paraventricular, reuniens, rhomboid) and intralaminar (central medial, paracentral) nuclei and in a group of cells along the rostral central gray which appeared continuous with the caudal extent of the midline nuclei. A subpopulation of calretinin cell bodies was also identified in the reticular nucleus. The mediorostral lateral posterior nucleus, subparafascicular, lateral geniculate and habenular nuclei also contained calretinin messenger RNA probe label. In contrast, no positive cells were found in the anterior, ventral or posterior thalamic nuclei. The distribution of calretinin cells did not correspond directly with that of other histochemical markers. Thus, the in situ hybridization histochemical and immunohistochemical results revealed calretinin as a unique identifying marker for distinct sets of thalamic neurons.     

Dorsal thalamic connections of the ventral lateral geniculate nucleus of rats

In order to understand better the organisation of the ventral lateral geniculate nucleus of the ventral thalamus, this paper has examined the patterns of connections that this nucleus has with various nuclei of the dorsal thalamus in rats. Injections of biotinylated dextran or cholera toxin subunit B were made into the parafascicular, central lateral, posterior thalamic, medial dorsal, lateral dorsal, lateral posterior, dorsal lateral geniculate, anterior, ventral lateral, ventrobasal and medial geniculate nuclei of Sprague-Dawley rats and their brains were processed using standard tracer detection methods. Three general patterns of ventral lateral geniculate connectivity were seen. First, the parafascicular, central lateral, medial dorsal, posterior thalamic and lateral dorsal nuclei had heavy connections with the parvocellular (internal) lamina of the ventral lateral geniculate nucleus. This geniculate lamina has been shown previously to receive heavy inputs from many functionally diverse brainstem nuclei. Second, the visually related dorsal lateral geniculate and lateral posterior nuclei had heavy connections with the magnocellular (external) lamina of the ventral lateral geniculate nucleus. This geniculate lamina has been shown by previous studies to receive heavy inputs from the visual cortex and the retina. Finally, the anterior, ventral lateral, ventrobasal and medial geniculate nuclei had very sparse, if any, connections with the ventral lateral geniculate nucleus. Overall, our results strengthen the notion that one can package the ventral lateral geniculate nucleus into distinct visual (magnocellular) and non-visual (parvocellular) components.     

Distribution of met-enkephalin immunoreactivity in the diencephalon and the brainstem of the dog

The endogenous opioid system, in particular the enkephalins, has been implicated in a vast array of neurological functions. The dog could be a suitable model for the study of complex interactions between behavioral state and regulatory physiology in which the opioid system appeared to be implicated. Moreover, opiate derivatives are currently used in veterinary clinic and sometimes pharmacologically tested in the dog. However, there are no anatomical data regarding the organization of the opioid system in this species. The present work represents the first attempt to map the distribution of Met⁵-enkephalin-like-immunoreactive (Met-enk-li) cell bodies and fibers in the diencephalon and the brainstem of the dog. In the diencephalon, labeled cells were present in all the mid-line and intralaminar thalamic nuclei; the lateral posterior, pulvinar and suprageniculate nuclei; the ventral nucleus of the lateral geniculate body and the medial geniculate body. Additionally, Met-enk-li cells were seen in every hypothalamic nucleus except in the supraoptic. Variable densities of labeled fibers were also seen in all these nuclei except in the medial geniculate body and in most areas of the lateral posterior and pulvinar nuclei. In the mesencephalon, positive cells were found in the periaqueductal gray, the Edinger–Westphal and interpeduncular nuclei, delimited areas of the superior and inferior colliculi and the ventral tegmental area. In the rhombencephalon, labeled cells were seen in the majority of the nuclei in the latero-dorsal pontine tegmentum, the nuclei of the lateral lemniscus, the trapezoid, vestibular medial, vestibular inferior and cochlear nuclei, the prepositus hypoglossal, the nucleus of the solitary tract and the dorsal motor nucleus of the vagus, the infratrigeminal nucleus and the caudal part of the spinal trigeminal nucleus and in the rhombencephalic reticular formation. The distribution of fibers included additionally the substantia nigra, all the trigeminal nerve nuclei, the facial nucleus and a restricted portion of the inferior olive. These results are discussed with regard to previous reports on the distribution of Met-enk in other species.     

An immunohistochemical study of somatostatin and neurotensin positive neurons in the septal nuclei of the rat brain

Summary Antibodies to the neuropeptides somatostatin (SOM) and neurotensin were used to study the distribution of the two peptides within the septum of the rat brain. In colchicine treated rats, numerous somatostatin-positive cell bodies were found in the dorsal and ventral subdivisions of the alteral septum, along the border of the nucleus accumbens, in the ventral tip of the horizontal limb of the diagonal band of Broca as well as in the anterior hippocampal rudiment, infralimbic area and several other structures of the basal forebrain (e.g., nucleus accumbens, olfactory tubercle and substantia innominata). Cell bodies containing immunoreactivity for neurotensin were situated in the intermediate and ventral subdivisions of the lateral septum, the medial septal nucleus, the diagonal band of Broca, the rostro-medial continuation of the substantia innominata and the olfactory tubercle.In untreated rats, somatostatin positive processes formed terminal plexuses in the medial septal nucleus and along an area close to the ventricular wall of the lateral ceptal nucleus. Other septal nuclei, such as the diagonal band of Broca contained a sparse innervation by somatostatin positive fibers. In contrast, the nucleus accumbens olfactory tubercle, and the substantia innominata contained a rich innervation by somatostatin positive axons and terminals. Within these structures the density of SOM positive processes show great variations with patches of densely packed terminals separated by areas of sparser or no innervation. The neurotensin positive terminals were situated predominantly within the intermediate part of the lateral septum and the medial septal nucleus. Both of these regions contained numerous pericellular baskets of neurotensin positive terminals around septal neurons. In addition to the septal innervation, several of the basal forebrain structures were rich in neurotensin positive processes with the densest innervation found in the nucleus accumbens and substantia innominata. Like the SOM-immunoreactivity distinct islands of dense neurotensin innervation separated by less or no innervation occur throughout the basal forebrain. Taken together, these findings suggest that somatostatin and neurotensin occur in separate neuronal populations and that each may influence important physiological functions within the individual septal nuclei.     

Distribution of somatostatinlike immunoreactivity in the brain of the little brown bat (Myotis lucifugus)

The distribution of somatostatinlike immunoreactive (SLI) perikarya, axons, and terminals was mapped in subcortical areas of the brain of the little brown bat, Myotis lucifugus, using light microscopic immunocytochemistry. A preponderance of immunoreactivity was localized in reticular, limbic, and hypothalamic areas including: (1) in the forebrain: the bed nucleus of the stria terminalis; lateral preoptic, dorsal, anterior, lateral and posterior hypothalamic areas; amygdaloid, periventricular, arcuate, supraoptic, suprachiasmatic, ventromedial, dorsomedial, paraventricular, lateral and medial mammillary, and lateral septal nuclei; the nucleus of the diagonal band of Broca and nucleus accilmbens septi; (2) in the midbrain: the periaqueductal gray, interpeduncular, dorsal and ventral tegmental, pretectal, and Edinger-Westphal nuclei; and (3) in the hindbrain: the superior central and parabrachial nuclei, nucleus incertus, locus coeruJeus, and nucleus reticularis gigantocellularis. Other areas containing SLI included the striatum (caudate nucleus and putamen), zona incerta, infundibulum, supramammiilary and premammillary nuclei, medial and dorsal lateral geniculate nuclei, entopeduncular nucleus, lateral habenular nucleus, central medial thalamic nucleus, central tegmental field, linear and dorsal raphe nuclei, nucleus of Darkschewitsch, superior and inferior colliculi, nucleus ruber, substantia nigra, mesencephalic nucleus of V, inferior olivary nucleus, inferior central nucleus, nucleus prepositus, and deep cerebellar nuclei. While these results were similar in some respects to those previously reported in rodents, they also provided interesting contrasts.     

Efferent fiber projections of the habenula and the interpeduncular nucleus. An experimental study in the opossum and cat

Summary A study of efferent fiber connections of the habenula and the inter-peduncular nucleus was conducted using anterograde degeneration techniques. Lesions were placed in the habenula of the opossum and the habenula and interpeduncular nucleus of the cat. Degeneration was studied by means of the Nauta and Fink-Heimer techniques.Fibers from the habenular nucleus of the opossum extended caudally and were traced bilaterally to the interpeduncular nucleus, dorsal tegmental nucleus of Gudden, deep (ventral) tegmental nucleus of Gudden, nucleus centralis superior and nucleus reticularis tegmenti pontis. Rostrally fibers were traced to the preoptic and septal region and the anterior and lateral hypothalamus.The medial and lateral habenular nuclei of the cat projected differentially to portions of the interpeduncular nucleus and the tegmental nuclei of Gudden. The medial habenular nucleus sent fibers to the paramedian subnucleus of the interpeduncular nucleus and to the deep tegmental nucleus; whereas the lateral habenular nucleus distributed to the apical and central subnuclei of the interpeduncular nucleus and the dorsal tegmental nucleus.Fibers from both the medial and lateral habenular nuclei were found to project bilaterally to the nucleus paraventricularis anterior, nucleus ventralis anterior, anterior medialis and anterior dorsalis of the thalamus, and the septal area.Fibers from the interpeduncular nucleus of the cat were represented bilaterally. Those passing rostral went to the lateral habenular nucleus, nucleus centromedianus and parafascicularis of the thalamus, and to the septal area. Those directed caudally projected to the nucleus centralis superior, and the dorsal and deep tegmental nucleus of Gudden.Abbreviations AC anterior commissure - AD nucleus anterior dorsalis - AM nucleus anterior medialis - AV nucleus anterior ventralis - BC brachium conjunctivum - CC corpus callosum - CD caudate nucleus - CI internal capsule - CL nucleus centralis lateralis - CM nucleus centromedianus - CP cerebral peduncle - DT dorsal tegmental nucleus (of Gudden) - EN entopeduncular nucleus - Fx fornix - GC central gray - GL lateral geniculate nucleus - GM medial geniculate nucleus - GP globus pallidus - HbPt habenulopeduncular tract - HVM ventromedial hypothalamic nucleus - IC inferior colliculus - IP interpeduncular nucleus - LHb lateral habenular nucleus - LL lateral lemniscus - LMN lateral mammillary nucleus - LP nucleus lateralis posterior - MD nucleus medialis dorsalis - MHb medial habenular nucleus - ML medial lemniscus - MMN medial mammillary nucleus - MP mammillary peduncle - NCM nucleus centralis medialis - OC optic chiasm - OT optic tract - Pf nucleus parafascicularis - Pul pulvinar - PUT putamen - RE nucleus reuniens - RN red nucleus - RPO preoptic area - RTP nucleus reticularis tegmenti pontisv (von Bechterew) - S stria medullaris - SC superior colliculus - SN substantia nigra - SPT septal area - VA nucleus ventralis anterior - VL nucleus ventralis lateralis - VM nucleus ventralis medialis - VPL nucleus ventralis posterolateralis - VPM nucleus ventralis posteromedialis - VT deep tegmental nucleus (of Gudden) - II optic nerve     

Calretinin immunoreactivity in the thalamus of the squirrel monkey

The distribution of the calcium-binding protein, calretinin, in the thalamus of the squirrel monkey (Saimiri sciureus) was studied with immunohistochemical methods. Calretinin was found to be heterogeneously distributed in the primate thalamus and to occur only in specific neuronal populations of certain thalamic nuclei. Neuronal cells and fibers in midline nuclei and their dorsolateral extension, which includes the parataenial and central superior lateral nuclei, displayed the most intense calretinin immunoreactivity. The immunoreactivity for cells and fibers in the intralaminar nuclei was moderate rostrally but very weak caudally. The centre médian nucleus, together with the medial habenular nucleus, were virtually devoid of calretinin immunostaining. The mediodorsal nucleus displayed a markedly heterogeneous staining, with numerous clusters of labeled cells and fibers in its central parvicellular part. Cell and fiber immunoreactivity ranged from moderate to high in the nuclei of the anterior and lateral groups, but was very weak in the nuclei of the ventral and posterior groups. There was a small to moderate number of heterogeneously distributed calretinin-immunoreactive cells and fibers in the lateral and medial geniculate bodies, as well as in the reticular nucleus. The present study provides the first evidence for the existence of calretinin in primate thalamus, where this protein is distributed according to a highly heterogeneous pattern. This specific pattern of distribution suggests that calretinin may play a role that is complementary to those of the other calcium-binding proteins parvalbumin and calbindin D-28k in the thalamus of primates.     

The superior colliculus neurons which project to the dorsal and ventral lateral geniculate nuclei in the cat

Summary Cells in the cat superior colliculus which project to the ventral and dorsal lateral geniculate nuclei (VLG and DLG) have been labeled by retro-grade transport of horseradish peroxidase (HRP). We studied the depth, area, and morphology of each labeled neuron quantitatively. Our measurements show that the projection neurons to both VLG and DLG vary in laminar position, size, and morphology. Labeled cells projecting to both nuclei were concentrated within the superficial gray layer, but were also scattered through the optic layer and, after DLG injections, in the intermediate gray layer as well. Labeled cells in both groups varied greatly in size, ranging from 49–344 m² cross-sectional area (mean 143 m²) for the VLG group and from 31–398 m² (mean 165 m²) for the DLG group. The labeled cells also varied in morphology after both VLG and DLG injections. The majority had a granule or vertical fusiform morphology. There were fewer with a stellate morphology and almost none with a horizontal morphology. At least three types of superior colliculus cells thus appear to project to the ventral and dorsal lateral geniculate nuclei. These cell types likely give rise to distinct functional channels to these nuclei.Abbreviations A lamina A of the dorsal lateral geniculate nucleus - A1 lamina A1 of the dorsal lateral geniculate nucleus - C lamina C of the dorsal lateral geniculate nucleus - CM central medial nucleus - CMM medial mammillary nucleus - CP cerebral peduncle - D nucleus of Darkschewitsch - FCT central tegmental tract - H habenular nuclei - HPM medial habenulo-peduncular tract - LP lateral posterior nucleus - MG medial geniculate nucleus - MIN medial intralaminar nucleus - NCP nucleus of the posterior commissure - NR reticular nucleus - OT optic tract - P pulvinar nucleus - PC posterior commissure - R red nucleus - SG suprageniculate nucleus - SN substantia nigra - VLA ventral anterolateral nucleus - VLG ventral lateral geniculate nucleus - VPL ventral posterolateral nucleus - VPM ventral postero-medial nucleus This study was supported by USPHS Research Grant EY02973 from the National Eye Institute, a New Faculty Research Grant from the State of Tennessee, and USPHS Postdoctoral Training Grant GM-00202     

Distribution of nerve growth factor receptor-like immunoreactivity in the adult rat central nervous system. Effect of colchicine and correlation with the cholinergic system--I. Forebrain

Nerve growth factor receptor, as recognized by the monoclonal antibody 192-IgG, was localized to multiple regions of the adult rat forebrain. Immunoreactive cell bodies and fibers were seen in both sensory and motor regions which are known to contain cholinergic and non-cholinergic neurons. Specifically, nerve growth factor receptor immunoreactivity was present in cells lining the olfactory ventricle, rostral portion of the lateral ventricle, in basal forebrain nuclei, caudate putamen, globus pallidus, zona incerta and hypothalamus. Immunoreactive cells which were situated subpially along the olfactory ventricle and anterior portions of the lateral ventricle, and in the arcuate nucleus resembled neuroglia but could not definitively identified at the light microscopic level. Animals pretreated with intracerebroventricular colchicine displayed significantly increased nerve growth factor receptor immunoreactivity in all previously positive neurons and particularly in the medial preoptic area and ventral premammillary nucleus of the hypothalamus. In such animals, receptor immunoreactivity also appeared in previously non-immunoreactive cells of the hippocampal CA3 region and polymorph layer of the dentate gyrus as well as in the mitral cell layer of the olfactory bulb. Nerve growth factor receptor-immunoreactive fibers and varicosities were seen in the olfactory bulb, piriform cortex, neocortex, amygdala, hippocampus, thalamus, olivary pretectal nucleus and hypothalamus. In most regions, such fiber-like immunoreactive structures likely represented axon terminals, although in some areas, neuroglial or extracellular localizations could not be excluded. In this context, diffuse, non-fibrillar receptor immunoreactivity occurred in the lateral habenular nucleus and medial terminal nucleus of the accessory optic tract. Furthermore, intense nerve growth factor receptor immunoreactivity occurred along certain regions of the pial surface on the ventral surface of the brain. The distribution of nerve growth factor receptor-immunoreactive cell bodies and fibers in multiple sensory and motor nuclei suggests wide-spread influences of nerve growth factor throughout the adult rat forebrain. There is a high degree of overlap with regions containing choline acetyltransferase immunoreactivity. However, significant disparities exist suggesting that certain nerve growth factor receptor-containing non-cholinergic neurons of the rat forebrain may also be affected by nerve growth factor.     

Segregation of lemniscal inputs and motor cortex outputs in cat ventral thalamic nuclei: application of a novel technique

Summary A double labeling method that permits accurate delineation of the terminals of medial lemniscal fibers was used to determine whether thalamic neurons projecting to motor cortex in the cat are in a position to be contacted by such terminals. Thalamic neurons in the VL nucleus were retrogradely labeled by injections of fluorogold placed in the cytoarchitectonically defined area 4, while lemniscal axons and their terminal boutons were anterogradely labeled, in a Golgi-like manner, from injections of Fast Blue placed under physiological control in different parts of the contralateral dorsal column nuclei. In additional experiments, spinothalamic fibers were similarly labeled by injections of Fast Blue in the spinal cord. The results reveal that there is no significant overlap in the distributions of lemniscal terminals and motor cortex-projecting neurons and that no somata or proximal dendrites of motor cortex-projecting neurons are in a position to receive lemniscal terminals. Spinothalamic terminals, on the other hand, end in clusters around motor cortex-projecting neurons in the VL nucleus as well as in other nuclei and are a more likely route for short latency somatosensory inputs to the motor cortex.Abbreviations AD anterodorsal nucleus - AM anteromedial nucleus - AP area postrema - AV anteroventral nucleus - C cuneate nucleus - CeM central medial nucleus - CL central lateral nucleus - CM centre médian nucleus - EC external cuneate nucleus - G gracile nucleus - L limitans nucleus - LD lateral dorsal nucleus - LP lateral posterior nucleus - MGM magnocellular medial geniculate nucleus - MD mediodorsal nucleus - MTT mamillothalamic tract - MV medioventral nucleus - Pc paracentral nucleus - Pf parafascicular nucleus - Po posterior nuclei - R reticular nucleus - RF fasciculus retroflexus - S solitary nucleus - SG suprageniculate nucleus - T spinal trigeminal nucleus - VA ventral anterior nucleus - VIN vestibular nuclei - VL ventral lateral nucleus - VMb basal ventral medial nucleus - VMp principal ventral medial nucleus - VPL ventral posterior lateral nucleus - VPM ventral posterior medial nucleus - ZI zona incerta - 1,2,3a,3b,4 fields of cerebral cortex - C4, C5, C6 spinal cord segments - 5SP,5ST spinal trigeminal nucleus and tract - 10, 12 vagal and hypoglossal nuclei     

Riboflavin-like inmunoreactive fibers in the monkey brain

Using an antiserum directed against the vitamin riboflavin, we studied the distribution of riboflavin-like immunoreactive structures in the monkey brain. In the mesencephalon, at the level of the mesencephalic-diencephalic junction, single riboflavin-like immunoreactive fibers were observed in its dorsal part, whereas a low density of immunoreactive fibers was found below the surface of the section and close to substantia nigra, and a high density was observed above the substantia nigra and close to the medial geniculate nucleus. In the thalamus, single riboflavin-like immunoreactive fibers were found in the ventral regions of the lateral posterior and the medial geniculate nuclei; a low density in the region located above the medial and lateral geniculate nuclei and a high density in the ventral part of the pulvinar nucleus and in the region extending from this latter to the caudate nucleus. Immunoreactive fibers were not observed in the medulla oblongata, pons, cerebellum, hypothalamus, basal ganglia and cerebral cortex. Moreover, no riboflavin-like immunoreactive cell bodies were observed in the monkey brain. The distribution of riboflavin-like immunoreactive fibers in the monkey suggests that this vitamin could be involved in several physiological mechanisms.     

A degeneration study of efferent connections of the habenular complex in the opossum

Parts of the medial and lateral habenular nuclei were removed unilaterally in each of thirteen opossums and the brains were studied for fiber degeneration by a modified Nauta method. Degeneration was seen in the ipsilateral, but not the contralateral, habenulopeduncular tract, which at the level of the interpeduncular nucleus underwent a partial decussation over it, whereas there were almost no degenerating fibers in the nucleus itself. Caudal to the nucleus extensive degeneration was present bilaterally among nuclei of the raphé and this extended into the predorsal fasciculus. Many terminals were observed in the nuclei of the raphé and within the deep tegmental nucleus. Although degenerating fibers were seen in the region of the dorsal tegmental nucleus, no terminals could be identified with certainty. Degeneration was also present in the superior colliculus. Bilateral degeneration occurred in the stria medullaris and extended to the preoptic area and the olfactory tubercle. In the dorsal preoptic area a small, but quite definite fiber bundle, separated from the posterior surface of the stria medullaris, traversed the lateral hypothalamus and passed dorsal to the mammillary bodies into the midbrain tegmentum, where it became intermingled with fibers of the habenulopeduncular tract just ventral to the red nucleus. Findings appear to indicate that in the opossum relatively few, if any, fibers of habenular origin terminate in the interpeduncular nucleus. In addition, fairly substantial evidence has been obtained to show that there are a number of efferent fibers within the stria medullaris.     

Retinofugal projections of an echolocating megachiropteran

The projection leading from the eye and the nuclear targets of the projection to the brainstem were identified in an echolocating megachiropteran (Rousettus aegyptiacus) following unilateral intraocular injections of radioactive amino acids. In the hypothalamus, the projection ended bilaterally in suprachiasmatic nuclei. In the ventral thalamus, it ended bilaterally in external and internal divisions of the ventral lateral geniculate nuclei. In the dorsal thalamus, the projection terminated bilaterally in the dorsal lateral geniculate nuclei and contralaterally in the lateral posterior nucleus. Input from the two eyes was segregated to laminae in the lateral division of the dorsal lateral geniculate nucleus. The contralateral projection ended in the dorsolateral and ventral portions of lamina 1, in lamina 2, the ventral portions of lamina 3, and an interlaminar fiber plexus. The ipsilateral projection ended in the dorsomedial portion of lamina 1, the dorsal portion of lamina 3, and the most superficial portion of lamina 1. Contralateral and ipsilateral input to the medial division of the dorsal lateral geniculate nucleus was for the most part segregated. The projection to the pretectum terminated in nuclei of the optic tract, pretectal olivary nuclei, and posterior pretectal nuclei. Although the input to the pretectal nuclei was bilateral, the contralateral projection was greater. The contralateral projection to the superior colliculus terminated throughout the rostral-caudal extent of the superficial gray layer. The ipsilateral projection to the superior colliculus ended in the superficial gray layer in the middle one-third of the superior colliculus only. On the contralateral side the projection to the outer portion of the superficial gray layer was especially heavy. The superior fascicle of the accessory optic tract was identified. It was traced to dorsal, lateral, and medial accessory optic nuclei. These results indicate that the visual system of Rousettus is more extensive than that of the echolocating microchiroptera and that it is similar to that described for nonecholocating Pteropus.     

Cyto- and chemoarchitecture of the dorsal thalamus of the monotreme Tachyglossus aculeatus,the short beaked echidna

We have examined the cyto- and chemoarchitecture of the dorsal thalamus of the short beaked echidna (Tachyglossus aculeatus), using Nissl and myelin staining, immunoreactivity for parvalbumin, calbindin, calretinin and non-phosphorylated neurofilament protein (SMI-32 antibody), and histochemistry for acetylcholinesterase and NADPH diaphorase. Immunohistochemical methods revealed many nuclear boundaries, which were difficult to discern with Nissl staining. Parvalbumin immunoreactive somata were concentrated in the ventral posterior, reticular, posterior, lateral and medial geniculate nuclei, while parvalbumin immunoreactivity of the neuropil was present throughout all but the midline nuclei. Large numbers of calbindin immunoreactive somata were also found within the midline thalamic nuclei, and thalamic sensory relay nuclei. Immunoreactivity for calretinin was found in many small somata within the lateral geniculate “a” nucleus, with other labelled somata found in the lateral geniculate “b” nucleus, ventral posterior medial and ventral posterior lateral nuclei. Immunoreactivity with the SMI-32 antibody was largely confined to somata and neuropil within the thalamocortical relay nuclei (ventral posterior medial and lateral nuclei, lateral and medial geniculate nuclei and the posterior thalamic nucleus). In broad terms there were many similarities between the thalamus of this monotreme and that of eutheria (e.g. disposition of somatosensory thalamus, complementarity of parvalbumin and calbindin immunoreactive structures), but there were some unique features of the thalamus of the echidna. These include the relatively small size of the thalamic reticular nucleus and the preponderance of calbindin immunoreactive neurons over parvalbumin immunoreactive neurons in the ventral posterior nucleus.     

Cyto- and chemoarchitecture of the dorsal thalamus of the monotreme Tachyglossus aculeatus, the short beaked echidna

We have examined the cyto- and chemoarchitecture of the dorsal thalamus of the short beaked echidna (Tachyglossus aculeatus), using Nissl and myelin staining, immunoreactivity for parvalbumin, calbindin, calretinin and non-phosphorylated neurofilament protein (SMI-32 antibody), and histochemistry for acetylcholinesterase and NADPH diaphorase. Immunohistochemical methods revealed many nuclear boundaries, which were difficult to discern with Nissl staining. Parvalbumin immunoreactive somata were concentrated in the ventral posterior, reticular, posterior, lateral and medial geniculate nuclei, while parvalbumin immunoreactivity of the neuropil was present throughout all but the midline nuclei. Large numbers of calbindin immunoreactive somata were also found within the midline thalamic nuclei, and thalamic sensory relay nuclei. Immunoreactivity for calretinin was found in many small somata within the lateral geniculate “a” nucleus, with other labelled somata found in the lateral geniculate “b” nucleus, ventral posterior medial and ventral posterior lateral nuclei. Immunoreactivity with the SMI-32 antibody was largely confined to somata and neuropil within the thalamocortical relay nuclei (ventral posterior medial and lateral nuclei, lateral and medial geniculate nuclei and the posterior thalamic nucleus). In broad terms there were many similarities between the thalamus of this monotreme and that of eutheria (e.g. disposition of somatosensory thalamus, complementarity of parvalbumin and calbindin immunoreactive structures), but there were some unique features of the thalamus of the echidna. These include the relatively small size of the thalamic reticular nucleus and the preponderance of calbindin immunoreactive neurons over parvalbumin immunoreactive neurons in the ventral posterior nucleus.     

Localization of chick retinal 24,000 dalton protein (visinin)-like immunoreactivity in the rat lower brain stem

The distribution of visinin, a 24,000 dalton peptide, in the lower brain stem of the rat was examined by means of an indirect immunofluorescent method. Visinin-immunoreactive structures were found to be unevenly distributed only in the neuronal elements. The following neuronal systems were strongly labeled by the antiserum; the Purkinje cell system, mammillotegmental system, habenulointerpeduncular system, the second layer of the superior colliculus, ventral tegmental area, substantia nigra pars lateralis, area medial to the medial geniculate body, parabrachial area, dorsal and ventral nuclei of the lateral lemniscus, pontine reticular formation just medial to the trigeminal principal nucleus, superior olivary nucleus, solitarii nucleus, external layer of the inferior colliculus and spinal trigeminal nucleus. The densities of the labeled fibers in these areas paralleled those of the labeled cells. In addition, highly dense visinin-immunoreactive fiber plexuses were seen in the zona compacta of the substantia nigra, lateral portion of the interpeduncular nucleus, ventral tegmental nucleus of Gudden and vestibular nucleus.