Fiber connections of the nucleus isthmi in the carp (Cyprinus carpio) and tilapia (Oreochromis niloticus)

The nucleus pretectalis (NP) is a prominent nucleus in the percomorph pretectum and has been shown to project to the nucleus isthmi in the filefish by an HRP tract-tracing method [Ito et al., 1981], but a homologous nucleus to the NP is apparently lacking in ostariophysans. The present study examined fiber connections of the nucleus isthmi in an ostariophysan teleost, the carp (Cyprinidae, Cyprinus carpio), to identify a nucleus homologous to the percomorph nucleus pretectalis. Identical studies in a percomorph tilapia (Cichlidae, Oreochromis niloticus) were also performed. Injections of biotinylated dextran amine (BDA) or biocytin to the carp nucleus isthmi labeled cells in the ipsilateral optic tectum and nucleus ruber of Goldstein [1905]. Labeled tectal neurons were located in the stratum periventriculare (SPV) and the stratum fibrosum et griseum superficiale (SFGS). The somata in the SPV were pyriform and those in the SFGS were fusiform. No labeled cells were found in the pretectum. Labeled terminals were seen in the ipsilateral nucleus pretectalis superficialis pars parvocellularis (PSp), optic tectum, and bilateral nucleus ruber. Terminals in the nucleus ruber appear to come from tectal neurons in the SFGS labeled by isthmic injections. Thus the nucleus isthmi has reciprocal fiber connections with the ipsilateral optic tectum, receives projections from the ipsilateral nucleus ruber, and projects to the ipsilateral PSp. The nucleus pretectalis homologue is apparently absent in the carp. Studies in tilapia showed that the nucleus isthmi receives bilateral projections from the NP and optic tectum. In addition, the present study revealed a previously unknown afferent from the nucleus ruber to the percomorph nucleus isthmi. The tilapia nucleus isthmi projects to the same targets as in the carp. Isthmic projection neurons in the tilapia optic tectum were located in the SPV and pyriform with a similar shape to the carp SPV neurons that project to the nucleus isthmi. No labeled cells were found in the SFGS of tilapia optic tectum. The fusiform neurons in the SFGS of the carp optic tectum possess various hodological similarities with the NP and may correspond to the NP neurons of percomorphs.     

Periventricular efferent neurons in the optic tectum of rainbow trout

The efferent connections and axonal and dendritic morphologies of periventricular neurons were examined in the optic tectum of rainbow trout to classify periventricular efferent neurons in salmonids. Among the target nuclei of tectal efferents, tracer injections to the following four structures labeled periventricular neurons: the area pretectalis pars dorsalis (APd), nucleus pretectalis superficialis pars magnocellularis (PSm), nucleus ventrolateralis of torus semicircularis (TS), and nucleus isthmi (NI). Two types of periventricular neurons were labeled by injections to the APd. One of them had an apical dendrite ramifying at the stratum fibrosum et griseum superficiale (SFGS), with an axon that bifurcated into two branches at the stratum griseum centrale (SGC), and the other had an apical dendrite ramifying at the SGC. Two types of periventricular neurons were labeled after injections to the TS. One of them had an apical dendrite ramifying at the boundary between the stratum opticum (SO) and the SFGS, and the other had dendritic branches restricted to the stratum album centrale or stratum periventriculare. Injections to the PSm and NI labeled periventricular neurons of the same type with an apical dendrite ramifying at the SO and a characteristic axon that split into superficial and deep branches projecting to the PSm and NI, respectively. This cell type also possessed axonal branches that terminated within the tectum. These results indicate that periventricular efferent neurons can be classified into at least five types that possess type-specific axonal and dendritic morphologies. We also describe other tectal neurons labeled by the present injections.     

Fiber connections of the torus longitudinalis and optic tectum in holocentrid teleosts

Fiber connections of the torus longitudinalis (TL) and target(s) of toral recipient tectal neurons (pyramidal cells) in the optic tectum were examined by tract-tracing methods in holocentrids. Injections into the stratum marginale (SM) labeled neurons in the stratum opticum and stratum fibrosum et griseum superficiale (SFGS). They had superficial spiny dendrites, with a fan-shaped branching pattern in SM and a thick basal dendrite that gave rise to bushy horizontal branches at the boundary between the SFGS and the stratum griseum centrale (SGC), where an axon and a thin dendrite arose. The axon terminated in a middle cellular layer of the SGC, and the thin dendrite ramified slightly deeper to this cellular layer. The SM injections also labeled cells in the ipsilateral TL. Injections into either the lateral or the medial part of TL labeled terminals in the ipsilateral SM and neurons in the bilateral nucleus paracommissuralis (NPC) and nucleus subvalvularis and ipsilateral nucleus subeminentialis. Only medial TL injections labeled cells in the ipsilateral SGC. These neurons had a basal dendrite that branched in the middle cellular layer of SGC, suggesting that they receive inputs from the pyramidal cells and project back to the TL to form a closed circuit. Only lateral TL injections labeled terminals in the corpus cerebelli. A visual telencephalic portion projects to the NPC and sublayers of SGC, where dendrites of the pyramidal cells and SGC neurons ramify. The present results therefore suggest that the TL and SM are components of an intricate circuitry that exerts telencephalic descending visual influence on the optic tectum and corpus cerebelli.     

Synaptic interrelationships between the optic tectum and the ipsilateral nucleus isthmi in Rana pipiens

The nucleus isthmi is reciprocally connected to the ipsilateral optic tectum. Ablation of the nucleus isthmi compromises visually guided behavior that is mediated by the tectum. In this paper, horseradish peroxidase (HRP) histochemistry and electron microscopy were used to explore the synaptic interrelationships between the optic tectum and the ipsilateral nucleus isthmi. After localized injections of HRP into the optic tectum, there are retrogradely labeled isthmotectal neurons and orthogradely labeled fibers and terminals in the ipsilateral nucleus isthmi. These terminals contain round. Clear vesicles of medium diameter (40–52 nm). These terminals make synaptic contact with dendrites of nucleus isthmi cells. Almost half of these postsynaptic dendrites are retrogradely labeled, indicating that there are monosynaptic tectoisthmotectal connections. Localized HRP injection into the nucleus isthmi labels terminals primarily in tectal layers B, E, F, and 8. The terminals contain medium-sized clear vesicles and they form synaptic contacts with tectal dendrites. There are no instances of labeled isthmotectal terminals contacting labeled dendrites. Retrogradely labeled tectoisthmal neurons are contacted by unlabeled terminals containing medium-sized and small clear vesicles. Fifty-four percent of the labeled fibers connecting the nucleus isthmi and ipsilateral tectum are myelinated fibers (average diameter approximately 0.6 μm). The remainder are unmyelinated fibers (average diameter approximately 0.4 μm). © 1994 Wiley-Liss, Inc.     

Tectal projection neurons to the retinopetal nucleus in the filefish

Following horseradish peroxidase (HRP) injections into the preoptic retinopetal nucleus (PRN), neurons in the ipsilateral optic tectum were labeled retrogradely. Labeled neurons exhibited a 'Golgi-like' appearance, somata of these neurons were pyriform or round, and most of them were located in the stratum album centrale (SAC) or the stratum periventriculare (SPV). These neurons had a long apical dendrite, which ramified in the upper-half of SGC into horizontally arborized dendritic fields. The main trunk of the apical dendrites also gave off several branches in the stratum fibrosum et griseum superficiale (SFGS) and reached the stratum opticum (SO). These neurons resemble the 'large pyriform neurons' of Vanegas et al. (Vanegas, H., Laufer, M. and Amat, J., The optic tectum of a perciform teleost. I. General configuration and cytoarchitecture, J. Comp. Neurol., 154 (1974) 43-60) except that in the tecto-PRN neurons the axons originates from the apical dendritic shaft at or near the level of the SAC. Judging from their dendritic patterns, the tectal neurons projecting indirectly to the retina may receive non-retinal inputs besides the retinal input.     

Organization of nucleus rotundus, a tectofugal thalamic nucleus in turtles. III. The tectorotundal projection

Nucleus rotundus is the primary thalamic recipient of projections from the optic tectum in pond turtles. Although the projection of the retina to the optic tectum is known to be topographically organized, earlier studies suggest that the tectorotundal projection is not topographically organized. Three types of analyses are used in this paper to characterize the organization of the projection of the optic tectum to nucleus rotundus. First, large iontophoretic injections of horseradish peroxidase into the optic tectum anterogradely fill axons with reaction product after the use of a cobalt-enhanced diaminobenzidine procedure. These preparations show that shafts of axons in the tectothalamic tract give rise to thinner, primary collaterals that enter nucleus rotundus from its caudolateral aspect and form sparsely branching arbors within the nucleus. Very thin secondary collaterals branch from these collateral bear terminal collaterals with frequent varicosities. Although the total size of such arbors is unknown, the evidence suggests that each arbor is large in relation to the size of nucleus rotundus. Thus, injection sites restricted to central tectum label axons throughout nucleus rotundus. Second, subtotal lesions of the tectum produce degeneration throughout nucleus rotundus in silver degeneration preparations. Finally, analysis of electron microscopic degeneration material indicates that tectal boutons are distributed along the full lengths of the dendrites of rotundal neurons, but not on their somata. These boutons form asymmetric synaptic junctions and contain round synaptic vesicles. In view of the relatively large size of the dendritic fields of rotundal neurons, these data suggest that the tectorotundal projection is both strongly convergent on individual neurons and strongly divergent from single tectorotundal axons. This type of organization is consistent with physiological evidence that rotundal neurons have receptive fields that cover at least one-half of the contralateral visual field and often include the entire hemifield. It seems unlikely that nucleus rotundus can be involved in neuronal transactions that preserve detailed spatial information, but it may be involved in processing information on other visual parameters such as stimulus velocity or color.     

青蛙前视盖与视顶盖间神经传导的细胞内电生理研究(英文)

目的已有许多研究报告了青蛙的前视盖对视顶盖起抑制作用,但关于此神经活动的特性尚不清楚。本研究探讨了这种复杂的神经活动的机理。方法用细胞内记录方法,通过电刺激前视盖的神经细胞核来记录视顶盖细胞的神经活动。结果前视盖的电刺激在同侧视顶盖主要唤起了两种神经反应:一种是兴奋性(excitatory postsynaptic potential,EPSP)和抑制性突触后电位(an inhibitory postsynaptic potential,IPSP)同时出现,另一种是单纯的IPSP,后者在本记录中占主导地位。另外我们也记录到了某些投射到前视盖的视盖投射细胞的神经电位。它揭示了视顶盖和前视盖之间存在着交叉性的相互作用。短潜时的EPSP可能是通过单突触进行传导的,而大多数的IPSP是通过多突触方式进行神经信息传递的。几乎98%被记录的视盖细胞对前视盖的刺激显示出了抑制性反应。结论前视盖的神经细胞对视顶盖的神经活动发挥了强烈的抑制性作用。     

Isthmic afferent neurons identified by the retrograde HRP method in a teleost, Navodon modestus

Isthmic afferent neurons were investigated by the retrograde horseradish peroxidase (HRP) method in a teleost, Navodon modestus. Following HRP injections into the nucleus isthmi, large pyriform neurons are labeled in the ipsilateral optic tectum. Very large and multipolar neurons are also labeled in the ipsilateral nucleus pretectalis. No labeled neurons were found in other areas.     

Topographic projections between the nucleus isthmi and the optic tectum in a teleost,Navodon Modestus

Following horseradish peroxidase injections into the optic tectum of a teleost,Navodon modestus, reciprocal and topographic projections between the nucleus isthmi and the ipsilateral optic tectum were determined. The isthmo-tectal fibers diverge to the optic tectum while maintaining the spatial arrangements of the isthmic cells from which the fibers originate. The tecto-isthmic projections also keep the spatial arrangements in the optic tectum. The tectal fibers converge near the nucleus isthmi and terminate in the non-cellular portion of the nucleus. The reciprocal topography is apparent in the combined results of 9 experiments with one tectal injection in each region. No labeled cells and fibers were found in the contralateral nucleus isthmi.     

Thalamo-tectal projections in the frog

The optic tectum of the leopard frog was examined for evidence of terminal degeneration following lesions in forebrain structures. No evidence was found of a telencephalic tectal projection. Degeneration following lesions in forebrain sites which give rise to tectal afferents are located in the dorsal thalamus, specifically the corpus geniculatum laterale in the rostral thalamus and the nucleus posterolateralis in the caudal thalamus. Corpus geniculatum projects to the ipsilateral tectum where it distributes in both the superficial and deep laminae over the rostromedial one-third of that structure. The rostral portion of the nucleus posterolateralis projects rather sparsely to the ipsilateral tectum. In contrast, the posterior portion of the posterolateral nucleus projects to both the superficial and deep laminae of the rostral two-thirds of the ipsi- and contralateral tectum. The significance of these and reciprocal tectothalamic projections for behavioral expression is considered.     

Retinofugal and retinopetal projections in the green sunfish, Lepomis cyanellus

The retinofugal and retinopetal connections in the green sunfish were studied by autoradiographic and horseradish peroxidase methods. All retinofugal fibers decussate in the optic chiasm. Some fibers project to contralateral preoptic and hypothalamic nuclei while others recross to project to the comparable ipsilateral nuclei. Contralaterally, the medial optic tract projects to the periventricular thalamic and pretectal nuclei and, sparsely, to the rostral optic tectum. The dorsal optic tract projects to the parvocellular portion of the superficial pretectal nucleus, the central pretectal nucleus, nucleus corticalis, and the rostral portion of the optic tectum. The ventral optic tract primarily projects to the caudal portion of the optic tectum, giving off fibers in route to innervate various nuclei, including the parvocellular superficial pretectal nucleus and the dorsal and ventral accessory optic nuclei. The axial optic tract projects to the dorsal accessory optic nucleus, the central pretectal nucleus, and the caudal optic tectum. Retinal fibers reach the ipsilateral thalamus, pretectum and other sites via a redecussation through the posterior commissure. From outgroup analysis it is concluded that such redecussating fibers are an independently derived character within actinopterygians and are homoplasous to nondecussating ipsilateral retinal projections in other vertebrates. Neurons retrogradely labeled with horseradish peroxidase were found to form a rostrocaudal column from the olfactory bulb and nerve through the ventral telencephalon to caudal diencephalic levels along the medial aspect of the optic tract. It is possible that all these neurons consist of one population of migrated ganglion cells of the nervus terminalis.     

Somatomotor connectivity in the midbrain of Rana pipiens

The mesencephalic oculomotor nuclei of Rana pipiens and their surrounding cell groups were investigated using the anterograde and retrograde transport of horseradish peroxidase and Golgi techniques. The cell groups surrounding the oculomotor and trochlear nuclei were divided into the nucleus interstitialis (nInt) groups A, B, and C, the basal optic nucleus, and the nucleus reticularis tegmenti. Afferents to the ventral mesencephalon originate from the retina and from vestibular, cerebellar, visual, and accessory oculomotor nuclei. These afferents produce a sequence of terminal arborizations in which visual afferents are found in the outer neuropil, and accessory oculomotor, vestibular, and cerebellar afferents are found along the inner neuropil and central gray. The oculomotor neurons in anurans have extensive dendritic fields, extending to the outer margins of the neuropils, as do many large cells along the margin of nInt. Other neurons in nInt have dendritic fields restricted to the proximal portions of the neuropil. Efferents from nInt area A project to the cerebellum and bilaterally to the spinal cord. Area B nInt projects to the ipsilateral spinal cord, contralateral nInt, pretectal nucleus lentiformis mesencephali, and ipsilateral trochlear nucleus. Efferents from area C nInt reach the deep tectal layers and ipsilateral spinal cord. The outer portions of the neuropil contain the nucleus of the basal optic root which comprises ganglionic elongate and stellate neurons and projects to the pretectum. In the center of the neuropil peri-nBOR neurons have dendrites directed towards the visual terminal fields and axons towards the central gray and oculomotor neurons. The nucleus reticularis tegmenti receives afferents from the tectum and lateral forebrain bundle and projects to the deep tectal layers. In anurans, the oculomotor neurons receive a variety of visual, somatic, and vestibular afferents and appear relatively undifferentiated, whereas the nInt appears more developed.     

青蛙前视盖与视顶盖间神经传导的细胞内电生理研究

目的已有许多研究报告了青蛙的前视盖对视顶盖起抑制作用,但关于此神经活动的特性尚不清楚。本研究探讨了这种复杂的神经活动的机理。方法用细胞内记录方法,通过电刺激前视盖的神经细胞核来记录视顶盖细胞的神经活动。结果前视盖的电刺激在同侧视顶盖主要唤起了两种神经反应：一种是兴奋性（excitator ypostsynaptic potential,EPSP）和抑制性突触后电位（an inhibitory postsynaptic potential,IPSP）同时出现,另一种是单纯的IPSP,后者在本记录中占主导地位。另外我们也记录到了某些投射到前视盖的视盖投射细胞的神经电位。它揭示了视顶盖和前视盖之间存在着交叉性的相互作用。短潜时的EPSP可能是通过单突触进行传导的,而大多数的IPSP是通过多突触方式进行神经信息传递的。几乎98％被记录的视盖细胞对前视盖的刺激显示出了抑制性反应。结论前视盖的神经细胞对视顶盖的神经活动发挥了强烈的抑制性作用。     

Distribution, laminar location, and morphology of tectal neurons projecting to the isthmo-optic nucleus and the nucleus isthmi, pars parvocellularis in the pigeon (Columba livia) and chick (Gallus domesticus): a retrograde labelling study.

Retrograde transport of Phaseolus vulgaris leucoagglutinin (PHA-L), fluorogold, fast blue, rhodamine labelled microspheres, and horseradish peroxidase (HRP) was employed to study the distribution, laminar location within the optic tectum, and morphology of tectal cells projecting upon the isthmo-optic nucleus (ION) and the nucleus isthmi, pars parvocellularis (Ipc), in the pigeon and chick. Following injections into the ION, all retrograde markers labelled tecto-ION neurons and their dendrites in the ipsilateral tectum. The cells were located within a relatively narrow band at the border between layers 9 and 10 of the stratum griseum et fibrosum superficiale (SGFS). Retrogradely labelled neuronal somata were different in both dendritic branching and shape; however, tecto-ION neurons generally possessed non-spiny radially oriented and multi-branched dendrites. The apical processes extended into the retino-recipient layers (2-7) of the SGFS and basal dendrites extended into layers 12-14 of the SGFS. Positive neuronal somata were observed throughout the rostro-caudal extent of the optic tectum. The average distance between adjacent tecto-ION neurons varied from one region to another. Specifically, retrogradely labelled cells were more numerous in the caudal, lateral, and ventral tectum, and less numerous at rostro-dorsal levels. Approximately 12,000 tecto-ION neurons were labelled within the ipsilateral optic tectum following either PHA-L or fluorescent dye injections. While the regional distribution of tecto-Ipc neurons was not examined, the morphology indicated that the cells had a single radially oriented dendritic process. Therefore, the apical dendrites are more restricted than those of tecto-ION cells. Moreover, the dendrites were spiny and arborized within layers 3, 5, and 9 of the ipsilateral optic tectum. The axon of tecto-Ipc cells arise from the apical process as a shepherd's crook and descend into the deep layers of the optic tectum. These results indicate that 1) tecto-ION and tecto-Ipc neurons are possibly monosynaptically activated by retinal input, 2) tecto-ION neurons are heterogeneous in morphology, and 3) there is a differential distribution of the tecto-ION neurons throughout the rostro-caudal extent of the optic tectum, suggesting a greater representation of the caudo-ventral portion of the optic tectum within the ION. The discussion primarily concerns the organization of the retino-tecto-ION-retinal circuit in light of the distribution and morphology of tecto-ION neurons within the optic tectum.     

The nucleus isthmi as an intertectal relay for the ipsilateral oculotectal projection in the frog, Rana pipiens

Reconstruction of serial sections through the nucleus isthmi in the frog Rana pipiens shows that the cortex of the nucleus consists of a sheet of cells which is folded back on itself to form two more or less parallel faces. Cyto-architectural features allow three regions to be distinguished: a 7“rim region,” which previous work had suggested may be involved in the physiological pathway from one eye to the ipsilateral tectal lobe, and two additional regions which are here termed the anterior and posterior “nonrim cortex,” re-spectively. The cytoarchitectural features which distinguish the rim region from the other two regions are largely absent in the tadpole. Analysis of retrograde transport of horseradish peroxidase (HRP) following widespread injections into one tectal lobe indicates that the anterior nonrim cortex projects ipsilaterally while the rim cortex and posterior nonrim cortex both project contralaterally. The differing projections of the three regions are paralleled by the pattern of retrograde degeneration observed after unilateral tectal lesions. We have studied the topographic organization of the connections between the nucleus isthmi and the two tectal lobes by making small injections of HRP at tectal loci with known visual field input. Patterns of retrograde cellular labelling show that the anterior nonrim cortex projects topographically to the entirety of the tectal lobe on the same side of the brain. The rim region projects topographically to the binocularly activated part of the opposite tectal lobe; the posterior nonrim cortex projects to the monocularly activated part. There is a discontinuity in the mapping from the nucleus to the opposite tectal lobe which corresponds to the border between binocular and monocular tectum. Patterns of anterograde labelling indicate that the afferent projection from the ipsilateral tectal lobe is topographic and organized so that afferents from a given tectal locus contact cells in the rostral part of the nucleus which project back to that locus. Afferents from tectal re-gions representing binocular visual field in addition continue across the nucleus to terminate within the rim region. The organization of the afferent and efferent projections of this region is such as to link tectal loci which relate to the same direction in visual space. Our findings provide new evidence that the nucleus isthmi is involved in the pathway from one eye to the ipsilateral tectal lobe. They also show how the nucleus is organized to distribute information from a given locus in one tectal lobe to cells which project to the visually corresponding but in general anatomically different pairs of loci in the two tectal lobes. Finally, our findings confirm the existence of a projection from the nucleus isthmi to the opposite monocular tectum and suggest that this may be part of an intertectal circuit linking anatomically corresponding rather than visually corresponding pairs of tectal loci.     

Differential sensitivities of the two visual pathways of the chick to labelling by fluorescent retrograde tracers.

This study investigates the neurone structure-specific differences of sensitivities of fluorescent tracers. The tracers were used for retrograde labelling of contralateral projections in the two visual pathways of the chick. Rhodamine B Isothiocyanate (RITC), Fluorogold (FG) and True blue (TB) were injected into either the visual Wulst (thalamofugal pathway) or the nucleus rotundus (Rt; tectofugal pathway) and the retrogradely labelled neurones in the nucleus geniculatus lateralis pars dorsalis (GLd) or the optic tectum, respectively, were counted. Differential retrograde labelling in the two pathways was observed. In the thalamofugal pathway, both the contralateral and ipsilateral GLd cells were labelled by all three tracers (RITC, FG and TB). However, in the tectofugal pathway, whereas RITC labelled both the ipsilateral and contralateral tectal neurones, FG or TB labelled effectively only the ipsilateral tectal neurones. It was clear that FG and TB were taken up by the nerve endings and transported part-way along the axon but failed to be transported to the cell bodies of the contralateral tectal neurones. In addition, red beads and green beads were also injected into Rt and the differential labelling was also observed. Red beads labelled both ipsilateral and contralateral tectal neurones but green beads labelled only the ipsilateral tectal neurones. Since the contralateral tectal projections consist of divergent axon collaterals, the present study suggests that various retrograde tracers are not transported in these axon collaterals to label cell bodies. The contralaterally projecting neurones in the thalamofugal pathway are not axon collaterals and they were labelled by all of the tracers used.     

Tectal efferents in the banded water snake,Natrix sipedon

Visual information reaches the dorsal thalamus by two distinct routes in most reptiles. Retinal efferents terminate directly in the dorsal lateral geniculate nucleus (DLGN). Retinal information is also channeled indirectly through the tectum to nucleus rotundus. Retinal projections to DLGN and tectum are also well esablished in snakes, but the status of the tecto-rotundal link of the indirect visual pathway is uncertain. Thus, tectal efferents were studied with Fink-Heimer methods in banded water snakes (Natrix sipedon). The tectum gives rise to crossed and uncrossed projections to the brainstem reticular formation. Commissural connections are effected with the contralateral tectum via the tectal and osterior commissures. tectum projects densely to the ipsilateral basal optic nucleus. Bilateral ascending projections reach the pretectal area, nucleus lentiformis mesencephali, lateral habenular nuclei, and posterodorsal nuclei. Ascending projections reach the ventral lateral geniculate and suprapeduncular nuclei. there is a diffuse projection to the central part of the caudal thalamus and a dense, bilaternal projection to the DLGN. These results indicate that the relation of the tectum to the dorsal thalamus is different in snakes than in other reptiles. Nucleus rotundus is either absent or poorly differentiated and there is a strong convergence of the direct and indirect visual pathways at DLGN.     

Visual, lateral line, and auditory ascending pathways to the dorsal telencephalic area through the rostrolateral region of the lateral preglomerular nucleus in cyprinids

Fiber connections of the rostrolateral region of the lateral preglomerular nucleus (PGlr) were studied by tract-tracing methods in carp and goldfish. The PGlr receives fibers from the optic tectum, ventrolateral nucleus of semicircular torus, ventromedial thalamic nucleus, medial pretoral nucleus, anterior tuberal nucleus, subglomerular nucleus, and (unexpectedly) also from the retina. Dendritic morphology of tecto-preglomerular neurons suggests that they receive retinal inputs. The PGlr can be further subdivided into dorsal (PGlr-d) and ventral (PGlr-v) zones, both of which are composed of somata and neuropil layers. Retinal and tectal fibers terminate mostly in the neuropil layer of the PGlr-d with the retinal terminals concentrated medially and tectal terminals laterally. Lateral line toral fibers terminate mainly in a lateral portion and ventromedial thalamic fibers in a medial portion of the somata layer of the PGlr-d. Auditory fibers from the medial pretoral nucleus and anterior tuberal nucleus terminate in the PGlr-v. The central nucleus of the semicircular torus also projects sparse fibers to the PGlr-v. The PGlr projects to the lateral, central, and medial parts of the dorsal telencephalic area, and the latter telencephalic part sends descending fibers to the PGlr. Differential distribution patterns of PGlr-d and PGlr-v fibers are noted within the dorsal telencephalic parts, suggesting that different sensory modalities may be represented in distinct regions at least to a certain degree.     

Caudal topographic nucleus isthmi and the rostral nontopographic nucleus isthmi in the turtle, Pseudemys scripta

Isthmotectal projections in turtles were examined by making serial section reconstructions of axonal and dendritic arborizations that were anterogradely or retrogradely filled with HRP. Two prominent tectal-recipient isthmic nuclei--the caudal magnocellular nucleus isthmi (Imc) and the rostral magnocellular nucleus isthmi (Imr)--exhibited strikingly different patterns of organization. Imc cells have flattened, bipolar dendritic fields that cover a few percent of the area of the cell plate constituting the nucleus and they project topographically to the ipsilateral tectum without local axon branches. The topography was examined explicitly at the single-cell level by using cases with two injections at widely separated tectal loci. Each Imc axon terminates as a compact swarm of several thousand boutons placed mainly in the upper central gray and superficial gray layers. One Imc terminal spans less that 1% of the tectal surface. Imr cells, by contrast, have large, sparsely branched dendritic fields overlapped by local axon collaterals while distally, their axons nontopographically innervate not only the deeper layers of the ipsilateral tectum but also ipsilateral Imc. Imr receives a nontopographic tectal input that contrasts with the topographic tectal input to Imc. Previous work on nucleus isthmi emphasized the role of the contralateral isthmotectal projection (which originates from a third isthmic nucleus in turtles) in mediating binocular interactions in the tectum. The present results on the two different but overlapping ipsilateral tecto-isthmo-tectal circuits set up by Imc and Imr are discussed in the light of physiological evidence for selective attention effects and local-global interactions in the tectum.     

Axon terminals from the nucleus isthmi pars parvocellularis control the ascending retinotectofugal output through direct synaptic contact with tectal ganglion cell dendrites

The optic tectum in birds and its homologue the superior colliculus in mammals both send major bilateral, nontopographic projections to the nucleus rotundus and caudal pulvinar, respectively. These projections originate from widefield tectal ganglion cells (TGCs) located in layer 13 in the avian tectum and in the lower superficial layers in the mammalian colliculus. The TGCs characteristically have monostratified arrays of brush‐like dendritic terminations and respond mostly to bidimensional motion or looming features. In birds, this TGC‐mediated tectofugal output is controlled by feedback signals from the nucleus isthmi pars parvocellularis (Ipc). The Ipc neurons display topographically organized axons that densely ramify in restricted columnar terminal fields overlapping various neural elements that could mediate this tectofugal control, including the retinal terminals and the TGC dendrites themselves. Whether the Ipc axons make synaptic contact with these or other tectal neural elements remains undetermined. We double labeled Ipc axons and their presumptive postsynaptic targets in the tectum of chickens (Gallus gallus) with neural tracers and performed an ultrastructural analysis. We found that the Ipc terminal boutons form glomerulus‐like structures in the superficial and intermediate tectal layers, establishing asymmetric synapses with several dendritic profiles. In these glomeruli, at least two of the postsynaptic dendrites originated from TGCs. We also found synaptic contacts between retinal terminals and TGC dendrites. These findings suggest that, in birds, Ipc axons control the ascending tectal outflow of retinal signals through direct synaptic contacts with the TGCs. J. Comp. Neurol. 524:362–379, 2016. © 2015 Wiley Periodicals, Inc.