Cortical neurons projecting to the pontine nuclei in the cat. An experimental study with the horseradish peroxidase technique

Summary Horseradish peroxidase (HRP) injections in various portions of the cat pontine nuclei resulted in retrograde labeling of neurons in layer V of the ipsilateral cerebral cortex.Corticopontine neurons, pyramidal in type, have been found to be labeled in the entire cortex, confirming the previous findings of anterograde degeneration studies. Most (91%) of the labeled cells were 14–26 m in diameter (mean 19.4±4.5 m SD). Small (10–20 m) and medium (20–40 m) cells represent 51.5% and 47.7%, respectively, of the total number of the labeled neurons. The populations of the neurons of various sizes were almost identical in different cortical areas, and were different from the populations of corticoreticular and corticospinal cells.Corticopontine cells were well labeled in experimental cases of 3-days' survival time, confirming the topographical organization established previously by degeneration studies for this projection system. However, in cases of shorter survival time (20–27 h), the number of labeled neurons was very small.The relative paucity of labeled Corticopontine neurons in the sigmoid and lateral gyri is discussed with reference to other cortical descending neurons (e.g., the corticotectal, corticoreticular and corticospinal) which have hitherto been identified morphologically as well as physiologically.Abbreviations AL gyrus lateralis anterior - ASigm gyrus sigmoideus anterior - ASup gyrus suprasylvius anterior - Br.p. brachium pontis - Cor gyrus coronalis - L left - L.m. lemniscus medialis - MEct gyrus ectosylvius medius - MSup gyrus suprasylvius medius - N.dl. nucleus dorsolateralis - N.l. nucleus lateralis - N.m. nucleus medianus - N.p. nucleus peduncularis - N.pm. nucleus paramedianus - N.r.t. nucleus reticularis tegmenti pontis - N.v. nucleus ventralis - Ped corticospinal and corticopontine fibers in cerebral peduncle - PSigm gyrus sigmoideus posterior - R right     

Cerebellotectal projections studied in cats with horseradish peroxidase or tritiated amino acids axonal transport

Summary After injections of horseradish peroxidase (HRP) into various parts of the superior colliculus (SC) in 14 cats, retrogradely labeled neurons were found in parts of all deep cerebellar nuclei. The present study demonstrated that there are three main origins of the cerebellotectal projections in regard to the locations of the cell bodies: (1) the caudal half approximately of the fastigial nucleus (NM) including the subnucleus medialis parvocellularis (SMP), (2) the ventral and lateral parts of the posterior interpositus nucleus (NIP), and (3) the ventral part of the dentate nucleus (NL) including the subnucleus lateralis parvocellularis (SLP).The pathways and terminations of these projections have also been shown autoradiographically. Thus, fibers from NM crossed within the cerebellum and terminated in the intermediate and deep gray layers of the bilateral SC. Fibers from NIP and NL passed within the superior cerebellar peduncle, which crossed in the tegmentum (decussation of the peduncle) and ended in the two layers of the contralateral SC. In addition, some cerebellofugal fibers were found to terminate in the nuclei interstitialis of Cajal and Darkschewitsch, as well as in parts of pretectum and thalamus.The tecto-ponto- (and olivo-) cerebellotectal loop (cf. Kawamura 1980) has been established morphologically and it is briefly commented on in correlation with the propagation of the teleceptive (optic and acoustic) impulses.Abbreviations AI Stratum album intermedium - AP Stratum album profundum - Cc Crus cerebri - CM Corpus mamillare - EW Nucleus of Edinger-Westphal - f.apm. Ansoparamedian fissure - Flm Fasciculus longitudinalis medialis - f.p.l. Posterolateral fissure - f.ppd. Prepyramidal fissure - f.pr. Fissura prima - f.p.s. Posterior superior fissure - f.sec. Fissura secunda - GI Stratum griseum intermedium - GP Stratum griseum profundum - GS Stratum griseum superficiale - L. Left - MG Medial geniculate body - ND Nucleus of Darkschewitsch - NIA Nucleus interpositus anterior - Nint Nucleus interstitialis of Cajal - NIP Nucleus interpositus posterior - NL Nucleus lateralis (dentatus) - NL-NIA Transition area of nucleus lateralis (dentatus) and nucleus interpositus anterior - NM Nucleus fastigii - Npa Nucleus pretectalis anterior - Npc Nucleus of posterior commissure - Npm Nucleus pretectalis medialis - Npp Nucleus pretectalis posterior - NR Nucleus ruber - Nto Nucleus of optic tract - N.III Oculomotor nerve - O Stratum opticum - PC Posterior commissure - pm. Paramedian lobule - Pg Periaqueductal gray substance - R. Right - Rf Fasciculus retroflexus - SC Superior colliculus - SCC Commissure of SC - Z Stratum zonale - III Nucleus of oculomotor nerve - V, VI, VIIA, VIIB, VIIIA, VIIIB, IX Cerebellar lobules of Larsell Working in the Anatomical Department of Iwate Medical University for six months (several periods during the year 1981)     

The cerebellotectal pathway in the grey squirrel

Summary In the well laminated superior colliculus of the grey squirrel the cells of origin of the crossed descending pathway to the brainstem gaze centers are contained within the inner sublamina of the intermediate grey layer. The technique of anterograde transport of horseradish peroxidase was used to determine whether the pathway from the cerebellum to the superior colliculus terminates in this region. The technique of retrograde transport of horseradish peroxidase was used to localize the source of this pathway within the cerebellum and to determine the morphology of the cerebellotectal neurons. The grey squirrel cerebellotectal pathway provides two terminal fields to the superior colliculus: a diffuse projection into the deep grey layer and a more concentrated, interrupted projection into the inner sublamina of the intermediate grey layer. The more concentrated projection overlies precisely the tectal sublamina that contains the cells of origin of the predorsal bundle. In contrast to animals with frontal eyes, the cerebellotectal pathway in the grey squirrel was found to project almost entirely contralaterally and the vast majority of the cells of origin for the pathway were distributed ventrally, in the caudal pole of the posterior interpositus nucleus and the adjacent region of the dentate. The labelled cells in both cerebellar nuclei were large and displayed similar morphologies.Abbreviations BC Brachium conjunctivum - BP Brachium pontis - CN Cochlear nuclei - D Dentate nucleus of the cerebellum - DLG Dorsal lateral geniculate nucleus - DLPG Dorsal lateral pontine grey - I Interpositus nucleus of the cerebellum - IC Inferior colliculus - III Oculomotor nucleus - IO Inferior olive - ITB Ipsilateral tectobulbar pathway - F Fastigial nucleus of the cerebellum - MG Medial geniculate nucleus - NRTP Nucleus reticularis tegmenti pontis - OPT Stratum opticum - PAG Periaqueductal grey - PDB Predorsal bundle - PB Parabigeminal nucleus - PH Prepositus hypoglossi - PUL Pulvinar nucleus - PT Pretectum - RN Red nucleus - SAI Stratum album intermediale (intermediate white layer) - SAP Stratum album profundum (deep white layer) - SGI Stratum griseum intermediale (intermediate grey layer) - SGP Stratum griseum profundum (deep grey layer) - SGS Stratum griseum superficiale (superficial grey layer) - SN Substantia nigra - sV Sensory division of the trigeminal complex - Ve Vestibular nuclei - VII Facial nucleus - VLG Ventral lateral geniculate nucleus     

大白鼠上丘传入性联系的HRP法研究

将HRP溶液(33％)注射到21只成体大白鼠的一侧上丘,存活1～2天后,脑切片作DAB或TMB反应,在另一侧上丘及其它脑区观察标记的神经元,结果如下: 1.当注射的深度达到上丘中间灰层或其以下各层时,无论注射点位于上丘的吻、尾端或其之间,标记神经元在另一侧上丘的区域分布与注射的HRP位置大体对应;当注射的深度较浅,即在视觉层及其以上各层时,在对侧上丘未观察到标记的神经元。 2.在上丘的带状层和表面灰层未发现标记的细胞。标记细胞在中间灰层(SGI)最多(53.6％),视觉层为16.5％,深部各层(SGI及其以下各层)标记细胞占标记细胞总数的83.5％。 3.根据标记神经元的形态分为:垂直的梭形神经元,水平的梭形神经元和多极神经元。它们的分布无明显规律。 4.除在同侧的视皮层观察到大量的标记神经元外,在两侧的下丘、外侧丘系背核和丘系旁核、黑质及外侧被盖核、同侧的外膝体腹核、对侧的前顶盖区及网状结构中都发现了标记的神经元。     

Origins of the projections of the superior colliculus to the dorsal lateral geniculate nucleus and the pulvinar in the rabbit

The origins of the projections of the superior colliculus to the dorsal lateral geniculate nucleus and to the pulvinar in Dutch-belted rabbits were investigated using horseradish peroxidase (HRP) methods. Following injections of HRP in the dorsal lateral geniculate nucleus, retrogradely labeled neurons were found in the upper two-thirds of the stratum griseum superficiale of the ipsilateral superior colliculus. Most of the labeled somata were spindle-shaped, and their major axes tended to be perpendicular to the surface of the superior colliculus. In contrast, following injections of the pulvinar, labeled neurons were found in the lower third of the ipsilateral stratum griseum superficiale. In these cases, the labeled somata were larger than those labeled following dorsal lateral geniculate injections and were multipolar in shape.     

GABAergic neurons comprise a major cell type in rodent visual relay nuclei: an immunocytochemical study of pretectal and accessory optic nuclei

Summary The enzyme glutamic acid decarboxylase (GAD) has been localized in sections of rodent brains (gerbil, rat) using conventional immunocytochemical techniques. Our findings demonstrate that large numbers of GAD-positive neurons and axon terminals (puncta) are present in the visual relay nuclei of the pretectum and the accessory optic system. The areas of highest density of these neurons are in the nucleus of the optic tract (NOT) of the pretectum, the dorsal and lateral terminal accessory optic nuclei (DTN, LTN), the ventral and dorsal subdivisions of the medial terminal accessory optic nucleus (MTNv, MTNd), and the interstitial nucleus of the posterior fibers of the superior fasciculus (inSFp). The findings indicate that 27% of the NOT neurons are GAD-positive and that these neurons are distributed over all of the NOT except the most superficial portion of the NOT caudally. The GAD-positive neurons of the NOT are statistically smaller (65.9 m²) than the total population of neurons of the NOT (84.3 [j,m2) but are otherwise indistinguishable in shape from the total neuron population. The other visual relay nuclei that have been analyzed (DTN, LTN, MTNv, MTNd, inSFp) are similar in that from 21% to 31% of their neurons are GAD-positive; these neurons are smaller in diameter and are more spherical than the total populations of neurons. The data further show that a large proportion of the neurons in these visual relay nuclei are contacted by GAD-positive axon terminals. It is estimated that approximately one-half of the neurons of the NOT and the terminal accessory optic nuclei receive a strong GABAergic input and have been called GAD-recipient neurons. Further, the morphology of the GAD-positive neurons combined with their similar distribution to the GAD-recipient neurons suggest that many of these neurons are acting as GABAergic, local circuit neurons. On the other hand, the large number of GAD-positive neurons in the NOT and MTN (20–30%) in relation to estimates of projection neurons (75%) presents the possibility that some may in fact be projection neurons. The overall findings provide morphological evidence which supports the general conclusion that GABAergic neurons play a significant role in modulating the output of the visually related NOT and terminal accessory optic nuclei.Abbreviations to Figures A Cerebral aqueduct - CP Posterior commissure - DK Nucleus of Darkschewitsch - DMN Deep mesencephalic nucleus - DTN Dorsal terminal nucleus, accessory optic system - HITr Habenulointerpeduncular tract - IGL Intergeniculate leaflet - INC Interstitial nucleus of Cajal - inSFp Interstitial nucleus, superior fasciculus, posterior fibers - LGNd Dorsal lateral geniculate nucleus - LGNv Ventral posterior nucleus - LP Lateral posterior nucleus - LTN Lateral terminal nucleus, accessory optic system - MB Mammillary body - MGN Medial geniculate nucleus - ML Medial lemniscus - MTNd Medial terminal nucleus, dorsal subdivision, accessory optic system - MTNv Medial terminal nucleus, ventral subdivision, accessory optic system - NOT Nucleus of the optic tract - NPC Nucleus of posterior commissure - OT Optic tract - PA Anterior pretectal nucleus - PAG Periaqueductal gray - pbp Nucleus parabrachialis pigmentosus - pC Cerebral peduncle - PM Medial pretectal nucleus - pn Nucleus paranigralis - PO Pretectal olivary nucleus - pp Posterior pretectal nucleus - PPN Peripeduncular nucleus - RNm Magnocellular division, red nucleus - RNp Parvocellular division, red nucleus - SC Superior colliculus - SGP Stratum griseum profundus, superior colliculus - SGS Stratum griseum superficiale, superior colliculus - SGM Stratum griseum medium, superior colliculus - SNc Substantia nigra, pars compacta - SNr Substantia nigra, pars reticulata - SO Stratum opticum, superior colliculus - VB Ventrobasal complex - ZI Zona incerta - 3N Oculomotor nerve, root fibers - 3V Third ventricle Supported by USPHS grants EY03642, NS15669, NS20228, EY03018, and NS15321. C.E.R. is the recipient of a Klingenstein Fellowship in the Neurosciences; R.H.I.B. is a Research Career Development Fellow of the National Eye Institute; and J.H.F. is a Research Career Development Fellow of the National Institutes of Health     

Time of origin of neurons of the rat superior colliculus in relation to other components of the visual and visuomotor pathways

Summary Groups of pregnant rats were injected with two successive daily doses of ³H-thymidine from gestational day 12 and 13 (E12+E13) until the day before parturition (E21+22) in order to label all the multiplying precursors of neurons. At 60 days of age the proportion of neurons generated (or no longer labelled) on specific days was determined in the separate layers of the superior colliculus. Neurogenesis begins with the production of a few large multipolar neurons in layers V and IV on day E12; the bulk (87%) of these cells are generated on day E13. This early-produced band of large neurons, the intermediate magnocellular zone, divides the superior colliculus into two cytogenetically distinct regions. In both the deep and the superficial superior colliculus neuron production is relatively protracted. In the deep superior colliculus neuron production peaks on day E15 in layer VII, on day E15 and E16 in layer VI, and on day E16 (the large neurons excluded) in layer V, indicating an inside-out sequence. In the superficial superior colliculus peak production time of layer III cells is on day E15 and of layer IV cells on day E16; peak production time of both layer I and II is on day E16 but in the latter region neuron production is more prolonged and ends on day El8. One interpretation of these results is that the two pairs of superficial layers are produced in an outside-in sequence. These three cytogenetic subdivisions of the superior colliculus may be correlated with its structural-functional parcellation into an efferent spinotectal, a deep somatomotor and a superficial visual component.A comparison of neurogenesis in different components of the visuomotor and visual pathways of the rat indicates that the motor neurons of the extraocular muscles, the abducens, trochlear and oculomotor nuclei, and neurons of the nucleus of Darkschewitsch are produced first. Next in line are source neurons of efferents to the bulb and the spinal cord: those of the Edinger-Westphal nucleus and the intermediate magnocellular zone of the superior colliculus. These are followed by the relay neurons of the dorsal nucleus of the lateral geniculate body. The neurons of the superficial superior colliculus and of the visual cortex implicated in visual sensori-motor integrations are produced last.Abbreviations A aqueduct - ap stratum album profundum (layer VII) - bi brachium of the inferior colliculus - c caudal - CGd central gray, pars dorsalis - CGl central gray, pars lateralis - CGv central gray, pars ventralis - dm deep magnocellular zone - EW Edinger-Westphal nucleus - gi stratum griseum intermediale (layer IV) - gp stratum griseum profundum (layer VI) - gs stratum griseum superficiale (layer II) - IC inferior colliculus - im intermediate magnocellular zone - LGd lateral geniculate nucleus, pars dorsalis - ll lateral lemniscus - lm stratum lemnisci (layer V) - MG medial geniculate nucleus - ND nucleus of Darkschewitsch - NO nucleus of the optic tract - op stratum opticum (layer III) - ot optic tract - r rostral - SC superior colliculus - vIII third ventricle - ZO stratum zonale (layer I) - III oculomotor nucleus - IV trochlear nucleus - Vm mesencephalic nucleus of the trigeminal - VI abducens nucleus     

Identification of geniculo-tectal relay neurons in the rat's ventral lateral geniculate nucleus

Summary In the rat's ventral lateral geniculate nucleus (vLGN), geniculo-tectal relay neurons (GTR-neurons) could be identified by the retrograde transport of horseradish peroxidase (HRP) after injection in the superior colliculus (SC). GTR-neurons correspond to class III cells described by Brauer and Schober (1973) in Golgi preparations of the rat's vLGN. The distribution of GTR-neurons is restricted to the lateral subnucleus of vLGN. According to Swanson et al. (1974), the axons of these cells terminate in lower Stratum griseum superficiale and in Stratum opticum, Stratum griseum intermedium and Stratum album intermedium of SC.The GTR-neurons are characterized by very thick and long proximal dendritic segments which have a smooth surface. Dendrites branch preponderantly in their distal regions and only in this part form many multiform protrusions. There is some evidence that retinal axons terminate on these dendritic surface structures. The supposed differences in the afferent patterns between GTR-neurons in the vLGN and geniculo-cortical relay neurons in the dorsal lateral geniculate nucleus are discussed.Sponsored by a grant of the Ministry of Science and Technology of the GDR     

Nigral and cerebellar synaptic terminals in the intermediate and deep layers of the cat superior colliculus revealed by lesioning studies

The presence of degenerating nigral and cerebellar synaptic terminals in the intermediate and deep layers of the cat superior colliculus was demonstrated by electron microscopy following lesions of the substantia nigra or brachium conjunctivum. The superior colliculus was taken for analysis 4–5 days after operation. Nigral terminals underwent a dark type of degeneration following kainic acid lesion of the pars reticulata of the substantia nigra. The majority of nigral degenerating terminals and axons were found in the stratum griseum intermediate with a few in the stratum griseum profundum. Two kinds of cerebellar terminals were distinguished by general appearances such as size, type of synaptic contact and type of synaptic vesicle and by the pattern of degenerative changes following electrical lesion of the brachium conjunctivum. Large elongated synaptic terminals 4–7 μm in diameter, were found mainly in the stratum griseum profundum. They often had double termination with conventional dendrites and with vesicles containing dendrites. This kind of terminal had a filamentous type of degeneration. A second type of degenerating cerebellar terminal, characterized by an electron-lucent type of degeneration, was predominantly located in the stratum griseum intermediale. These terminals were circular, about 4 μm in diameter, and did not have synaptic contact with vesicle-containing profiles. The finding of the two types of degenerating terminal after lesion of the brachium conjunctivum can be considered as evidence of the coexistence of at least two kinds of cerebellar terminals in the superior colliculus. The presence of nigral and cerebellar terminals in the intermediate and deep layers of the superior colliculus implicates the involvement of the substantia nigra and cerebellum in control of collicular visuomotor function.     

The nigrotectal projection and tectospinal neurons in the rat. A light and electron microscopic study demonstrating a monosynaptic nigral input to identified tectospinal neurons

In order to investigate the nigro-tecto-spinal pathway in the rat, the pattern of termination of nigrotectal fibres and the distribution of tectospinal neurons have been investigated in a light and electron microscopic study of the superior colliculus. In addition, the pattern of termination of nigrotectal fibres was compared to the pattern of acetylcholinesterase staining. The light microscopic studies showed that the nigrotectal fibres, which had been identified by anterograde transport of horseradish peroxidase from the substantia nigra, terminated in a distinctive clustered pattern throughout the rostrocaudal extent of the stratum griseum intermedium, stratum album intermedium and adjacent dorsal portion of the stratum griseum profundum of the ipsilateral superior colliculus. The clusters of nigrotectal terminals formed a series of branching, interconnected longitudinal columns which largely corresponded with the pattern of acetylcholinesterase staining. The tectospinal neurons, which had been identified by retrograde transport of horseradish peroxidase from the spinal cord, had mainly large-sized somata, were stellate in shape with multiple long dendrites, and formed variable-sized clusters of 4-15 neurons within lateral regions of the ventral stratum album intermedium and dorsal stratum griseum profundum. In experiments where both the nigrotectal terminals and the tectospinal neurons were labelled by the transport of horseradish peroxidase, the clusters of tectospinal neurons largely corresponded with the regions of densest nigrotectal fibre termination in the lateral regions of the superior colliculus. In addition, a small contralateral nigrotectal projection was localized in the rostrolateral region of the superior colliculus where the crossed fibres terminated in a clustered pattern in alignment with clusters of tectospinal neurons in this region. Electron microscopic examination of the superior colliculus following ibotenic acid lesions in the substantia nigra and horseradish peroxidase injections in the spinal cord showed multiple degenerating nigrotectal boutons in synaptic contact with the soma and the mainstem and secondary dendrites of labelled tectospinal neurons in the lateral regions of the stratum album intermedium and stratum griseum profundum of the superior colliculus. The majority of the degenerating nigrotectal boutons showed electron-lucent degenerative changes and were in axodendritic contact. All of the identified nigrotectal synapses were of the symmetrical type.(ABSTRACT TRUNCATED AT 400 WORDS)     

Distribution of calbindin, parvalbumin and calretinin in the lateral geniculate nucleus and superior colliculus in Cebus apella monkeys

We studied the distribution of the calcium-binding proteins calbindin, parvalbumin and calretinin, in the superior colliculus and in the lateral geniculate nucleus of Cebus apella, a diurnal New World monkey. In the superior colliculus, these calcium-binding proteins show different distribution patterns throughout the layers. After reaction for calretinin one observes a heavy staining of the neuropil with few labeled cells in superficial layers, a greater number of large and medium-sized cells in the stratum griseum intermediale, and small neurons in deep layers. The reaction for calbindin revealed a strong staining of neuropil with a large number of small and well stained cells, mainly in the upper half of the stratum griseum superficiale. Intermediate layers were more weakly stained and depicted few neurons. There were few immunopositive cells and little neuropil staining in deep layers. The reaction for parvalbumin showed small and medium-sized neurons in the superficial layers, a predominance of large stellate cells in the stratum griseum intermediale, and medium-sized cells in the deep layers. In the lateral geniculate nucleus of Cebus, parvalbumin is found in the cells of both the P and M pathways, whereas calbindin is mainly found in the interlaminar and S layers, which are part of the third visual pathway. Calretinin was only found in cells located in layer S. This pattern is similar to that observed in Macaca, showing that these calcium-binding proteins reveal different components of the parallel visual pathways both in New and Old World monkeys.     

Laminar origin of ipsilateral tectopontine pathways

The purpose of these experiments was to identify the cells of origin of the ipsilateral tectopontine pathways in the grey squirrel (Sciurus carolinensis). Following injections of tritiated amino acids into individual collicular laminae, labelled fibers could be traced to the dorsolateral pontine nuclei and overlying lateral pontine tegmentum. Fibers originating in stratum griseum superficiale terminated most heavily within the pontine nuclei whereas those arising from stratum griseum profundum terminated most heavily within the tegmentum. After horseradish peroxidase was injected into the dorsolateral pontine nuclei, cells labelled with reaction product were found in all 3 grey laminae of the superior colliculus, but the majority were located in stratum griseum superficiale. In contrast, when horseradish peroxidase was injected into the tectorecipient pontine tegmentum, most of the labelled cells were located in stratum griseum profundum.These results indicate that each of the 3 grey laminae of the superior colliculus projects to both the dorsolateral pontine nuclei and the lateral pontine tegmentum. However, the pathway to the pontine nuclei arises chiefly in stratum griseum superficiale while the tectotegmental pathway arises chiefly in stratum griseum profundum.     

Connections of the anterior ectosylvian visual area (AEV)

Summary We have previously described a visual area situated in the cortex surrounding the deep infolding of the anterior ectosylvian sulcus of the cat (Mucke et al. 1982). Using orthograde and retrograde transport methods we now report anatomical evidence that this anterior ectosylvian visual area (AEV) is connected with a substantial number of both cortical and subcortical regions. The connections between AEV and other cortical areas are reciprocal and, at least in part, topographically organized: the rostral AEV is connected with the bottom region of the presylvian sulcus, the lower bank of the cruciate sulcus, the rostral part of the ventral bank of the splenial sulcus, the rostral portion of the lateral suprasylvian visual area (LS) and the lateral bank of the posterior rhinal sulcus; the caudal AEV is connected with the bottom region of the presylvian sulcus, the caudal part of LS, the ventral part of area 20 and the lateral bank of the posterior rhinal sulcus. Subcortically, AEV has reciprocal connections with the ventral medial thalamic nucleus (VM), with the medial part of the lateralis posterior nucleus (LPm), as well as with the lateralis medialis-suprageniculate nuclear (LM-Sg) complex. These connections are also topographically organized with more rostral parts of AEV being related to more ventral portions of the LPm and LM-Sg complex. AEV also projects to the caudate nucleus, the putamen, the lateral amygdaloid nucleus, the superior colliculus, and the pontine nuclei. It is concluded that AEV is a visual association area which functionally relates the visual with both the motor and the limbic system and that it might play a role in the animal's orienting and alerting behavior.Abbreviations Ac aqueductus cerebri - AEs anterior ectosylvian sulcus - ALLS anterolateral lateral suprasylvian area - AMLS anteromedial lateral suprasylvian area - ASs anterior suprasylvian sulcus - Cd caudate nucleus - CL central lateral nucleus - Cl claustrum - Cos coronal sulcus - Crs cruciate sulcus - DLS dorsal lateral suprasylvian area - GI stratum griseum intermediale - GP stratum griseum profundum - IC inferior colliculus - LAm lateral amygdaloid nucleus - LGNd dorsal nucleus of lateral geniculate body - LGNv ventral nucleus of lateral geniculate body - Llc nucleus lateralis intermedius, pars caudalis - LM nucleus lateralis medialis - LPl nucleus lateralis posterior, pars lateralis - LPm nucleus lateralis posterior, pars medialis - Ls lateral sulcus - MD nucleus mediodorsalis - MG medial geniculate body - MSs middle suprasylvian sulcus - Ndl nucleus dorsolateralis pontis - Nl nucleus lateralis pontis - Np nucleus peduncularis pontis - Npm nucleus paramedianus pontis - Nrt nucleus reticularis tegmenti pontis - Nv nucleus ventralis pontis - Ped cerebral peduncle - PEs posterior ectosylvian sulcus - Pg periaqueductal gray - PLLS posterolateral lateral suprasylvian area - PMLS posteromedial lateral suprasylvian area - PSs presylvian sulcus - Pul pulvinar - Put putamen - R red nucleus - Sg suprageniculate nucleus - SN substantia nigra - Sps splenial sulcus - Syls sylvian sulcus - T trapezoid body - VA ventral anterior nucleus - VL ventral lateral nucleus - VLS ventral lateral suprasylvian area - VM ventral medial nucleus - VPL ventral posterolateral nucleus - VPM ventral posteromedial nucleus Sponsored by Max-Planck-Society during part of the studySponsored by Thyssen FoundationSponsored by Alexander von Humboldt-Foundation     

Specialized subregions in the cat motor cortex: Anatomical demonstration of differential projections to rostral and caudal sectors

Summary (1) Ipsilateral cortico-cortical and thalamo-cortical projections to the cat motor cortex were determined from the locations of retrogradely labeled neurons following single small intracortical injections of HRP in area 4. These projections were also examined by studying the distribution of anterogradely transported axonal label following multiple injections of HRP or of tritiated amino acids in areas 1–2 of SI and in area 2pri (SII). (2) The number of retrogradely labeled cells in areas 1–2 and in area 2pri differed markedly between HRP injection sites located in the precruciate (anterior sigmoid gyrus) and postcruciate (posterior sigmoid gyrus) subregions of area 4. These associational projections from primary and secondary somatosensory cortices were dense to postcruciate subrogions but weak to the precruciate subregions. (3) The associational projections from areas 1–2 and from area 2pri to the postcruciate subregion of area 4 were topographically organized, but no clear topographic organization could be demonstrated for the precruciate projection. (4) Anterograde terminal labeling following injection of either HRP or tritiated amino acids into areas 1–2 and area 2pri confirmed the preferential projection of somatosensory cortex to the postcruciate subregion of motor cortex. The projection from somatosensory areas 1–2 was uniform over its terminal field, but that from area 2pri was more patchy and complex. (5) HRP injections in area 4 gave rise to lamellae of labeled neurons in the ventrolateral nucleus of thalamus (VL). A topographic relationship was found between the site of injection and the location of the lamella of labeled neurons. (6) The percentage of retrogradely labeled neurons in the shell zone surrounding the border of the ventrolateral nucleus and the ventrobasal complex (VB) was greater following postcruciate than precruciate injections, whereas fewer retrogradely labeled neurons were found in central lateral nucleus (CL) after postcruciate injections than after precruciate injections. (7) These observations support the hypothesis that differential cortical and thalamic projections to different subregions of area 4 may give rise to the different physiological properties of neurons observed in these subregions (Vicario et al. 1983; Martin et al. 1981).     

Brain stem projections to the pulvinar-lateralis posterior complex of the cat

Summary The present experiments were undertaken to define the areas of projection of pretectum and superior colliculus to the pulvinar and n. lateralis posterior, respectively, and to define other brain stem structures projecting to these thalamic nuclei in cats. For this purpose the technique of retrograde transport of horseradish peroxidase (HRP) has been used.After injection of the enzyme in the pulvinar, neurons were labeled in all subdivisions of the pretectal area. The majority of the labeled cells were located in the n. pretectalis posterior and n. tractus opticus although cells filled with HRP were present also in the n. pretectalis anterior pars compacta and area pretectalis medialis. Neurons projecting to the pulvinar were also found in the periaqueductal gray, reticular formation and locus coeruleus.When HRP was injected in the n. lateralis posterior, labeled neurons were present in the II and III subdivisions of the second layer of the superior colliculus. The location of these cells shifted from medial to lateral as the injections were shifted from posterior to anterior within the lateralis posterior. Neurons projecting to this nucleus were also present in the intermediate layers of the superior colliculus, lateral hypothalamus and parabigeminal nucleus.The possible role of the pretectal area and superior colliculus in mediating somesthetic input to the pulvinar and lateralis posterior, respectively, and the role of these structures in the control of ocular movements, are discussed.Abbreviations APM area pretectalis medialis - Cu nucleus cuneiformis - CS nucleus centralis superior - fr fasciculus retroflexus - Gp pontine gray - Hb nucleus habenulae - IC inferior colliculus - LC locus coeruleus - LGB lateral geniculate body - LP lateralis posterior - MGB medial geniculate body - nPA_c nucleus pretectalis anterior pars compacta - nPA_r nucleus pretectalis anterior pars reticularis - nPC nucleus posterior commissurae - nPP nucleus pretectalis posterior - nTO nucleus tractus opticus - PAG periaqueductal gray - PB nucleus parabigeminalis - Pi pulvinar inferior - PO nucleus posterior of the thalamus - Pul pulvinar - Pt pretectum - RF reticular formation - Rtp tegmental reticular nucleus - SC superior colliculus Supported by H. de Jur Foundation and USPHS Grant TWO 2718Present address: Max-Planck-Institut für biophysikalische Chemie, Postfach 968, D-3400 Göttingen, Federal Republic of Germany     

Integration of visual and auditory information in bimodal neurones in the guinea-pig superior colliculus

Summary We have investigated the responses of neurones in the guinea-pig superior colliculus to combinations of visual and auditory stimuli. When these stimuli were presented separately, some of these neurones responded only to one modality, others to both and a few neurones reliably to neither. To bimodal stimulation, many of these neurones exhibited some form of cross-modality interaction, the degree and nature of which depended on the relative timing and location of the two stimuli. Facilitatory and inhibitory interactions were observed and, occasionally, both effects were found in the same neurone at different inter-stimulus intervals. Neurones whose responses to visual stimuli were enhanced by an auditory stimulus were found in the superficial layers. Although visual-enhanced and visual-depressed auditory neurones were found throughout the deep layers, the majority of them were recorded in the stratum griseum profundum. Neurones that responded to both visual and auditory stimuli presented separately and gave enhanced or depressed responses to bimodal stimulation were found throughout the deep layers, but were concentrated in the stratum griseum intermediale and extended into the stratum opticum.     

Retinofugal projections in hedgehog-tenrecs (Echinops telfairi and Setifer setosus)

Summary Using the autoradiographic tracing technique the retinal projections were studied in the tenrecs, Echinops telfairi and Setifer setosus (insectivora, tenrecidae). Bilateral projections were found to the n. suprachiasmaticus, the anterior hypothalamic area, the dorsal and ventral lateral geniculate bodies, the pretectal olivary nucleus and the superior colliculus. The contralateral projections were usually more intense than the ipsilateral ones except the retinohypothalamic connections. A partial segregation of the projection fields from both eyes was present in the dorsal and ventral lateral geniculate bodies. In the superior colliculus retinal fibers predominantly involved the stratum zonale and the upper portion of the stratum griseum superficiale on both sides. The projections to the deeper portion of the colliculi were rather faint, particularly on the ipsilateral side. Target areas receiving contralateral projections exclusively were the periamygdaloid area (labeled only in Setifer), the terminal accessory nuclei including the n. tractus optici and the inferior colliculus. The data are compared with other species. The most striking finding may concern the projection to the medial terminal nucleus being quite prominent in marsupials and most eutherian mammals (including the erinaceomorphous hedgehogs), but greatly reduced in tenrecs and primates.Abbreviations ae commissura anterior - AmP periamygdaloid area - Col colliculus inferior - CoS colliculus superior - cp cerebral peduncule - Ec Echinops telfairi/lesser hedghog-tenrec - GLD corpus geniculatum laterale, pars dorsalis - GLV corpus geniculatum laterale, pars ventralis - GLVa-d subdivisions of GLV - GM corpus geniculatum mediale - HbM n. habenulae medialis - HyA anterior hypothalamic area - oc chiasma opticum - on nervus opticus - ot tractus opticus - PT pretectum - PTO n. olivarius praetectalis - Ru n. ruber - SCh n. suprachiasmaticus - Se Setifer setosus/greater liedgehog-tenrec - SGI stratum griseum intermedium - SPG stratum griseum profundum - SGS stratum griseum superficiale - SO stratum zonale - To n. motorius nervi trochlearis - TmD n. terminalis dorsalis - TmL n. terminalis lateralis - TmM n. terminalis medialis - TrO n. tractus optici     

Comparison of the ultrastructure of cortical and retinal terminals in the rat superior colliculus

We compared the ultrastructure and synaptic targets of terminals of cortical or retinal origin in the stratum griseum superficiale and stratum opticum of the rat superior colliculus. Following injections of biotinylated dextran amine into cortical area 17, corticotectal axons were labeled by anterograde transport. Corticotectal axons were of relatively small caliber with infrequent small varicosities. At the ultrastructural level, corticotectal terminals were observed to be small profiles (0.44 +/- 0.27 microm(2)) that contained densely packed round vesicles. In tissue stained for gamma amino butyric acid (GABA) using postembedding immunocytochemical techniques, corticotectal terminals were found to contact small (0.51 +/- 0.69 microm(2)) non-GABAergic dendrites and spines (93%) and a few small GABAergic dendrites (7%). In the same tissue, retinotectal terminals, identified by their distinctive pale mitochondria, were observed to be larger than corticotectal terminals (3.34 +/- 1.79 microm(2)). In comparison to corticotectal terminals, retinotectal terminals contacted larger (1.59 +/- 1.70 microm(2)) non-GABAergic dendrites and spines (73%) and a larger proportion of GABAergic profiles (27%) of relatively large size (2.17 +/- 1.49 microm(2)), most of which were vesicle-filled (71%). Our results suggest that cortical and retinal terminals target different dendritic compartments within the neuropil of the superficial layers of the superior colliculus.     

Velocity response profiles of collicular neurons: parallel and convergent visual information channels.

We have recorded from single neurons in the retinorecipient layers of the superior colliculus of the cat. We distinguished several functionally distinct groups of collicular neurons on the basis of their velocity response profiles to photic stimuli. The first group was constituted by cells responding only to photic stimuli moving at slow-to-moderate velocities across their receptive fields (presumably receiving strong excitatory W-type input but not, or only subthreshold, Y-type input). These cells were recorded throughout the stratum griseum superficiale and stratum opticum and constituted 50% of our sample. The second group of cells exhibited excitatory responses only at moderate and fast velocities (presumably receiving excitatory Y-type but not W-type input). These cells constituted only about 7% of the sample and were located principally in the lower stratum griseum superficiale. The third group of cells was constituted by cells excited over the entire range of velocities tested (1-2000 /s) and presumably received substantial excitatory input from both W- and Y-channels. These cells constituted almost 26% of our sample and were located in the lower stratum griseum superficiale, stratum opticum and the upper part of the stratum griseum intermediale. Overall, cells receiving excitatory Y-type input, i.e. the sum of group two and group three cells, constituted about a third of the sample and their excitatory discharge fields were significantly larger than those of cells receiving only W-type input. A fourth distinct group of collicular neurons was also constituted by cells responding over a wide range of stimulus velocities. These cells were excited by slowly moving stimuli, while fast-moving photic stimuli evoked purely suppressive responses. The excitatory discharge fields of these cells (presumably, indicating the spatial extent of the W-input) were located within much larger inhibitory fields, the extent of which presumably indicates the spatial extent of the Y-input. These low-velocity-excitatory/high-velocity-suppressive cells were recorded from the stratum griseum superficiale, stratum opticum and stratum griseum intermediale and constituted about 17% of the sample. The existence of low-velocity-excitatory/high-velocity-suppressive cells in the mammalian colliculus has not been previously reported. Low-velocity-excitatory/high-velocity-suppressive cells might play an important role in activating "fixation/orientation" and "saccade" premotor neurons recorded by others in the intermediate and deep collicular layers. Overall, in the majority (57%) of collicular neurons in our sample there was no indication of a convergence of W- and Y-information channels. However, in a substantial minority of collicular cells (about 43% of the sample) there was clear evidence of such convergence and about 40% of these (low-velocity-excitatory/high-velocity-suppressive cells) appear to receive excitatory input from the W-channel and inhibitory input from the Y-channel.     

Possible induction of [Met]enkephalin-Arg6-Gly7-Leu8 immunoreactivity in neurons of the rat superior colliculus following eye enucleation

The distribution of [Met]enkephalin-Arg6-Gly7-Leu8 (MEAGL)-immunoreactive (-IR) neurons and its modification after enucleation have been investigated in the rat superior colliculus. In normal rats and on the ipsilateral side of monocular-enucleated rats, small sized vertically elongated fusiform-shaped weakly immunostained neurons were dispersed throughout the sublamina of the stratum griseum superficiale (SGS). In bilaterally enucleated rats and on the contralateral side of monocular-enucleated rats, many small strongly immunoreactive MEAGL-containing neurons, projecting processes horizontally or obliquely toward the surface, appeared in the deepest part of the SGS and the superficial part of the stratum opticum (SO), in contrast to the disappearance of the fusiform-shaped weakly stained neurons in the SGS. MEAGL-IR fibers increased in density throughout the sublamina of the SGS, being densest in the deep SGS, accompanying their increase in the neighboring SO. Sporadically found MEAGL-IR neurons in the deep SO and the stratum griseum intermediale did not show the detectable change of immunoreactivity. These results indicate that enkephalin biosynthesis is undergone by different type of neurons in the normal and the ocular-derived superior colliculus, and suggest that some neurons in the adult superior colliculus have a potentiality to express the peptidergic phenotype.