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PubMed2004

Fiber connections of the lateral valvular nucleus in a percomorph teleost, tilapia (Oreochromis niloticus).

Fiber connections of the lateral valvular nucleus were investigated in a percomorph teleost, the tilapia (Oreochromis niloticus), by tract-tracing methods. Following tracer injections into the lateral valvular nucleus, neurons were labeled in the ipsilateral dorsal part of dorsal telencephalic area, corpus glomerulosum pars anterior, dorsomedial thalamic nucleus, central nucleus of the inferior lobe, mammillary body, semicircular torus, valvular and cerebellar corpus, in the bilateral rostral regions of the central part of dorsal telencephalic area, dorsal region of the medial part of dorsal telencephalic area, habenula, anterior tuberal nucleus, posterior tuberal nucleus, and spinal cord, and in the contralateral lateral funicular nucleus. Labeled fibers and terminals were found in the ipsilateral cerebellar corpus and bilateral valvula of the cerebellum. Tracers were injected into portions of the telencephalon, pretectum, inferior lobe, and cerebellum to confirm reciprocally connections with the lateral valvular nucleus and to determine afferent terminal morphology in the lateral valvular nucleus. Telencephalic fibers terminated mainly in a dorsolateral portion of the lateral valvular nucleus. Terminals from the corpus glomerulosum pars anterior, central nucleus of the inferior lobe, and mammillary body showed more diffuse distributions and were not confined to particular portions of the lateral valvular nucleus. Labeled terminals in the lateral valvular nucleus were cup-shaped or of beaded morphology. These results indicate that the lateral valvular nucleus receives projections from various sources including the telencephalon, pretectum, and inferior lobe to relay information to the valvular and cerebellar corpus. In addition, the corpus glomerulosum pars anterior in tilapia is considered to be homologous to the magnocellular part of superficial pretectal nucleus in cyprinids.

Animals↗
PubMed2005

Octavolateral projections and organization in the medulla of a teleost fish, the sleeper goby (Dormitator latifrons).

This study is the first to employ simultaneous labeling with different colored fluorescent dyes and confocal microscopy to investigate the central projections of the octavolateral nerves in any fish. Three-dimensional reconstructions of the hindbrain octavolateral nuclei were made and overlap of octavolateral projections was assessed in a teleost, the sleeper goby (Dormitator latifrons). The octavolateral nerves, which innervate the otolithic organs, semicircular canals, and lateral lines, project to seven hindbrain nuclei in diverse, complex patterns. The medulla is generally organized with auditory regions dorsal to vestibular regions. The intermediate subdivision of the descending octaval nucleus (DON) receives interdigitating projections from the otolithic organs, and the dorsomedial DON likely integrates multiple auditory inputs. Afferents from the three otolithic organs (the utricle, saccule, and lagena) project to the intermediate DON in approximately equal proportion, supporting physiological evidence that suggests auditory roles for all three otolithic organs in the sleeper goby. The anterior octaval nucleus receives partially segregated inputs from the octavolateral organs. The dorsal division of the magnocellular octaval nucleus (MgON) receives highly overlapping otolithic organ and semicircular canal input, and we propose that this region is a major octaval integration center. Regions in the ventral medulla (the tangential octaval nucleus, ventral DON, and ventral MgON) receive mainly utricular and semicircular canal inputs, suggesting vestibular roles. Each semicircular canal nerve projects to distinct regions of the hindbrain, with little overlap in most octaval nuclei. Efferent neurons receive bilateral input and project unilaterally to the octavolateral organs.

Afferent Pathways↗
PubMed1975

The structure of the inferior lobe of the teleost hypothalamus.

Electron microscopic and Golgi studies on the inferior lobes of sunfish and goldfish are described. The inferior lobe consists primarily of a nucleus ventricularis of densely packed cells surrounding the lateral recess of the third ventricle, and a peripherally situated nucleus diffusus consisting mostly of scattered neurons. A cell-sparse zone of dense neuropil is located between the two cellular areas. Neurons of both nuclei have spiny dendrites and axons which originate from basal dendrites. In some cases axons are found to send a collateral into the cell-sparse zone. Neurons of the nucleus diffusus possess collaterals that extend a considerable distance within the nucleus itself. The ultrastructure of cells of both nuclei reveals cytoplasmic organelles typical of most neurons. Synapses containing dense-cored and clear vesicles are present on the spines and shafts of the dendrites of both neuronal types. In only rare cases synapses were observed on the soma of neurons of the nucleus ventricularis. Possible anatomical substrates involved in the control of feeding and aggression in teleosts are considered in light of the present findings. Morphological similarities of the inferior lobes and related areas in various fishes and amphibians are discussed and their possible significance for the understanding of the evolution of hypothalamic mechanisms is considered.

Aggression↗
PubMed1978

Comparison of Mauthner cell size in teleosts.

The Mauthner cells (M-cells) are a pair of neurons found in the medulla oblongata of most fish and amphibians. This neuron is not the same size in all teleosts. Based on the hypothesis that differences in M-cell size might be related to fish family and possibly fish habitat, M-cell and nuclear size were compared between fish families. In order to minimize effects of fish length on cell or nuclear size, statistical treatment of the data was made for four separate length classes. The results indicate at least three groupings by cell or nuclear size. The cell is large in fish from the Salmonidae, Catostomidae and Cyprinidae, small in the Stichaeidae, Cottidae and Pleuronectidae and absent in Batrachoididae, Lophiidae, Ogcocephalidae and Cylopteridae. In general a correlation exists between fish that lack or have small M-cells and a demersal habitat. Since these fish may rely on camouflage for protection against predation, the M-cells may have altered excitability or function as compared to more active fish in which the M-cell is known to function in initiating the startle response (larval zebrafish and goldfish). Differences in input to M-cells of different sizes in conjunction with known electrophysiological properties of the goldfish M-cell are discussed in relation to the function of this neuron.

Animals↗
PubMed1978

Cerebellar afferents in teleost catfish (Ictaluridae).

The cerebellar afferents in the bullhead catfish (Teleostei) were labeled by relying on the retrograde transport of horseradish peroxidase (HRP). Retrogradely labeled neurons were seen in: spinal cord, lateral cuneate nucleus, inferior olive, reticular nuclei, vestibular nuclei, nucleus subeminentialis, n. lateralis valvulae, locus coeruleus, n. mesencephalicus dorsalis, the basal optic nuclei, and a nucleus at the isthmic level which may be equivalent to the pontine nuclei of birds and mammals. Inputs to the molecular layer arise from the inferior olive, locus coeruleus and n. lateralis valvulae in addition to subjacent granule cells. No projections to cerebellum were seen to arise from either the optic tectum or from the inferior lobe. The so-called "lobo-cerebellar" tract in teleosts was reported by Goldstein, amongst many others, who mistook the superior secondary gustatory nucleus for a deep cerebellar nucleus.

Afferent Pathways↗
PubMed1982

Fiber connections of the corpus glomerulosum in a teleost, Navodon modestus.

Fiber connections of the corpus glomerulosum (CG) in a teleost, Navodon modestus, were studied by means of horseradish peroxidase (HRP) and the Fink-Heimer methods. The CG is divided into a pars anterior (GA) and a pars rotunda (GR). Both the GR and the GA have the same cell components and glomeruli. The GR is composed of four layers arranged concentrically around a central fiber net in the following order (Ito and Kishida, '75): a glomerular layer, a fibrous layer, a small-cell layer, and a peripheral fibrous capsule including large cells. The GA consists of a central glomerular layer and a peripheral small-cell layer which contains some large cells. Following HRP injections into the GR, HRP-positive cells were found bilaterally in the nucleus corticalis and ipsilaterally in the nucleus intermedius of Bricker ('29). Lesions of the nucleus corticalis produced degenerating terminals bilaterally in glomeruli in the CG. The course of the fiber connections was coincident with that of the commissura horizontalis. Lesions of the nucleus intermedius resulted in degenerating terminals in the fibrous layer of the GR and the small-cell layer of the GA. Following the destruction of the GR, degenerating terminals occurred in the ipsilateral lobus inferior. Both small and large cells in the ipsilateral CG were labeled after HRP injections into the lobus inferior.

Animals↗
PubMed1982

Cytoarchitecture, fiber connections, and ultrastructure of nucleus isthmi in a teleost (Navodon modestus) with a special reference to degenerating isthmic afferents from optic tectum and nucleus pretectalis.

Cytoarchitecture and fiber connections of the nucleus isthmi in a teleost (Navodon modestus) were studied by means of Nissl, Bodian, toluidine blue, Golgi, and Fink-Heimer methods. Synaptic terminals were classified by the ultrastructural characteristics, and their origins were determined by electron microscopic degeneration experiments. The nucleus isthmi is composed of an outer cellular area or shell and an inner noncellular area or core. The shell covers anterior, dorsal, and ventral aspects of the core. The cell bodies in the shell are oval (15 x 20 micrometers) with an anteroposterior long axis, and have many somatic spines. Spines are also seen on the initial segment of the axon. Primary dendrites extend posteromedially and branch out in the core. The core contains thin and thick myelinated fibers, which originate in the optic tectum and in the nucleus pretectalis, respectively. At least two types of axon terminal were distinguished in the nucleus isthmi: S type, containing spherical vesicles, and F type, containing flattened vesicles. S terminals are derived from thin myelinated fibers and are only seen in the core where they form asymmetric synapses with dendrites. Frequently a portion of the S terminal membrane near the usual synaptic cleft is in close apposition with the membrane of an adjacent small dendrite or spine. F terminals, which derived from thick myelinated fibers, make symmetric synaptic contacts with both cell bodies in the shell and dendrites in the core. S terminals degenerate after ipsilateral ablation of the optic tectum, whereas F terminals degenerate after destruction of the nucleus pretectalis.

Animals↗
PubMed1983

Extrinsic and intrinsic fiber connections of the telencephalon in a teleost, Sebastiscus marmoratus.

Extrinsic and intrinsic fiber connections of the telencephalic subdivisions of Nieuwenhuys ('62) in a teleost, Sebastiscus marmoratus, were studied by means of horseradish peroxidase (HRP) and Fink-Heimer methods. The olfactory bulb projects bilaterally to area dorsalis pars posterior, area ventralis pars ventralis, pars lateralis, pars posterior, pars intermedia, and the nucleus posterior tuberis of Peter et al. ('75) and receives fibers from ipsilateral area dorsalis pars centralis, pars posterior, area ventralis pars dorsalis, and pars supracommissuralis. Area dorsalis pars posterior sends numerous fibers to the ipsilateral ventral region of area dorsalis pars medialis, from which fibers of the medial forebrain bundle arise and terminate in the inferior lobe and nucleus posterior tuberis. Area dorsalis pars lateralis, pars dorsalis, and the dorsal region of pars medialis are the main targets of extratelencephalic ascending afferents. Area dorsalis pars lateralis receives fibers from the ipsilateral nucleus prethalamicus of Meader ('34), where tectal projections terminate massively. Area dorsalis pars dorsalis and the dorsal region of pars medialis receive afferents from the ipsilateral nucleus preglomerulosus of Schnitzlein ('62), nucleus posterior tuberis, area preoptica pars medialis of Crosby and Showers ('69), and nucleus entopeduncularis of Sheldon ('12). Raphe nuclei and locus ceruleus project bilaterally to area dorsalis pars centralis, pars dorsalis, pars lateralis, and the dorsal region of pars medialis. Area dorsalis pars centralis, pars dorsalis, and the dorsal region of pars medialis are important sources of extratelencephalic efferents. These subdivisions give rise to the lateral forebrain bundle and project to the ipsilateral nucleus prethalamicus, nucleus preglomerulosus, inferior lobe, nucleus paracommissuralis of Ito et al. ('82), optic tectum, torus semicircularis, and the bilateral mesencephalic tegmentum. Within the telencephalon, most of the ventral subdivisions project to ipsilateral area dorsalis pars centralis, pars dorsalis, pars lateralis, and the dorsal region of pars medialis. Area dorsalis pars centralis has reciprocal connections with ipsilateral area dorsalis pars lateralis, pars dorsalis, pars posterior, and the dorsal region of pars medialis. A dorsal part of the anterior commissure is composed of axons of the ventral region of area dorsalis pars medialis destined to the contralateral ventral region of area dorsalis pars medialis. A ventral part of the anterior commissure contains axons of area dorsalis pars centralis destined to contralateral area dorsalis pars lateralis.

Animals↗
PubMed1983

Cytoarchitecture and ultrastructure of nucleus prethalamicus, with special reference to degenerating afferents from optic tectum and telencephalon, in a teleost (Holocentrus ascensionis).

Histological structure and neuronal geometry of the nucleus prethalamicus of holocentrid teleosts, which is homologous to the nucleus rotundus of reptiles and birds and to the nucleus lateralis posterior-pulvinar complex of mammals, were studied by means of the Bodian, Nissl, toluidine blue, and Golgi methods. Synaptic terminals were classified electron microscopically, and terminal types originating from the telencephalon and the optic tectum were determined by electron microscopy in degeneration experiments. The nucleus prethalamicus is composed of four layers, in the following order from medial to lateral: a small-cell layer, a plexiform layer, a large-cell layer, and a marginal layer. Six types of terminals (U, L, Sp, Sd, F, and P) were distinguished in the nucleus, and the distribution pattern for each type of terminal was determined by counting its relative number in each layer. Sp terminals make synaptic contacts with small-cell dendrites or somata in the small-cell layer, and degenerate after telencephalic ablations. Sd terminals synapse exclusively with spines of large-cell dendrites in both marginal and large-cell layers, and degenerate after tectal ablations. Because only large neurons have been labeled after HRP injections into the telencephalon (Ito et al., '80, '82; Ebbesson, '80; Murakami et al., '83), it is considered that these neurons relay visual information from the optic tectum onto the telencephalon. It is hypothesized that the small neurons in the nucleus, which receive telencephalic input, might modulate the large neurons' relay function.

Animals↗
PubMed1984

Diameters and terminal patterns of retinofugal axons in their target areas: an HRP study in two teleosts (Sebastiscus and Navodon).

Studies in various vertebrate classes, particularly amphibians and mammals, have revealed that retinal ganglion cells with different functional properties project by means of axons of correspondingly different diameters onto specific target regions. Whether a similar pattern exists in teleosts is partly investigated in the present study. HRP was injected into the optic nerve of Sebastiscus and Navodon. The calibers of intraretinal HRP-labeled axons were classed as fine (ca. 0.8 micron), medium (ca. 1.3 micron), and coarse (ca. 2.5 microns). The calibers of HRP-labeled retinofugal axons were then determined in their target areas, and these can be summarized as follows: Optic hypothalamus: fine, medium. Lateral geniculate nucleus: fine. Dorsolateral thalamic nucleus: fine, medium. Area pretectalis: fine. Nucleus of the posterior commissure: fine, medium. Area ventralis lateralis, contralateral: fine, medium, coarse; ipsilateral: coarse. Optic tectum, stratum opticum: fine, medium; stratum fibrosum et griseum superficiale: fine, medium, coarse, segregated in sublayers; stratum album centrale: fine, medium, coarse. Therefore, fine fibers were found to reach all target areas except the ipsilateral area ventralis lateralis, and these were the only fibers found in the lateral geniculate nucleus, area pretectalis, and stratum griseum centrale of the optic tectum. Coarse fibers, on the other hand, were found only in the area ventralis lateralis and the optic tectum (stratum fibrosum et griseum superficiale and stratum album centrale). Terminal patterns of these fibers were also studied. Most fine fibers take tortuous courses giving off a few branches and terminate with many varicosities, and medium and coarse fibers give off several finer branches and terminate with bulbous swellings. The physiological significance of these findings is discussed. In addition, retrogradely labeled (retinopetal) cells were found in the olfactory bulb and the area ventralis pars ventralis of the telencephalon, as well as in the preoptic area and the dorsolateral thalamic nucleus.

Animals↗
PubMed1984

Connections of the auditory midbrain in a teleost fish, Cyprinus carpio.

Central auditory pathways were traced in Japanese carp, Cyprinus carpio, using electrophysiological mapping and HRP tract-tracing methods. Multiunit recordings made from the carp torus semicircularis, the major midbrain area for processing octavolateralis information, revealed a mediolateral segregation of auditory and lateral line sensory modalities. Iontophoretic injections of HRP were made into the medial torus to trace afferent and efferent projections of the carp auditory midbrain. Following unilateral HRP injections into the medial torus, retrogradely labeled neurons were observed within six nuclei of the carp medulla. Two octaval nuclei, the anterior octavus nucleus and descending octavus nucleus, contained HRP-filled neurons. Labeled neurons were also observed within the ipsilateral superior olive, scattered among fibers of both lateral lemnisci, and bilaterally within the medullary reticular formation. In addition, bilateral retrograde cell labeling was found within a group of Purkinje-like cells located adjacent to the IVth ventricle, just rostral to the level of the VIIIth nerve. Few labeled neurons were found within the nucleus medialis, a principal target for lateral line afferents within the medulla. At midbrain levels, retrogradely labeled neurons were observed within the contralateral torus semicircularis and the ipsilateral optic tectum. Three forebrain nuclei project to the carp auditory midbrain. Within the diencephalon, descending projections originate from the anterior tuberal nucleus, bilaterally, and from the ipsilateral central posterior thalamic nucleus. The ipsilateral caudal telencephalon also projects to the carp auditory midbrain via large multipolar neurons within area dorsalis pars centralis. Anterograde labeling of fibers and terminals revealed efferent projections of the carp auditory midbrain to the following targets: the ipsilateral superior olive, the ipsilateral medullary reticular formation, the deep layers of the optic tectum, the contralateral torus semicircularis, the anterior tuberal nucleus, and the central posterior thalamic nucleus. These results, together with recent studies of lateral line pathways in teleosts (Finger, '80, '82a), demonstrate that central auditory and lateral line pathways are anatomically distinct in the carp, at least from medullary to diencephalic levels. Furthermore, there are striking similarities in the organization of the central auditory pathways of the carp and those of amphibians and land vertebrates.

Afferent Pathways↗
PubMed1986

Fine structure of the optic fiber termination layer in the tectum of the teleost Rutilus: a stereological and morphometric study.

The stratum fibrosum et griseum superficiale (SFGS) of the Rutilus optic tectum, which receives a massive fiber projection from the contralateral retina, was studied by electron microscopy. The qualitative and quantitative analysis of the laterodorsal (LD) portion of the stratum involved both a stereological examination of the different elements and a morphometric study of the various profiles containing synaptic vesicles (PCSVs). The relative volume of each element in the LD SFGS was as follows: myelinated and unmyelinated axons, 6.6%; PCSVs, 38%; dendrites without vesicles, spines, and cell bodies, 41.7%; glia, 10.5%. With the fixation employed, 35% of PCSVs showed spheroidal synaptic vesicles. These profiles could be subdivided into three types: (1) S1 (23.5%) represented optic terminals, since they degenerated after retinal ablation or were labeled after intraocular injection of HRP or [3H] proline. Three subgroups of S1 were identified: S1m--profiles containing clear mitochondria;S1c--profiles that were contiguous with S1m and lacked mitochondria;S1i--isolated profiles without mitochondria. (2) S2 (9.3%) were characterized mainly by their dark mitochondria. (3) S3 (2.2%) corresponded to small nonvisual terminals that were isolated and lacked mitochondria. The PCSVs with pleiomorphic synaptic vesicles (65%) were subdivided into three groups: P1 (38%), P2 (19%), and P3 (8%). P1 and P2 were axonal in nature; P2 could be distinguished from P1 by a greater density of synaptic vesicles. P3 was of dendritic origin. Analysis of synaptic patterns revealed a small number of serial synapses. The presynaptic elements were optic boutons, whereas the intermediate profiles were dendrites with synaptic vesicles (P3). Results are compared with ultrastructural data obtained in the superficial tectal layers of other teleosts and other vertebrate groups.

Animals↗
PubMed1986

Telencephalic ascending acousticolateral system in a teleost (Sebastiscus marmoratus), with special reference to the fiber connections of the nucleus preglomerulosus.

Acousticolateral systems were examined by means of the horseradish peroxidase tracing method in a teleost (Sebastiscus marmoratus). The torus semicircularis projected bilaterally to the optic tectum, nucleus ventromedialis thalami of Schnitzlein ('62), and reticular formation; contralaterally to the torus semicircularis; and ipsilaterally to the nucleus preglomerulosus of Schnitzlein ('62) and the inferior olive. No topographic organization was detected between the torus semicircularis and the nucleus preglomerulosus. Ipsilateral inputs to the torus were from dorsal telencephalic areas (pars centralis, Dc; pars dorsalis, Dd; and the dorsal part of pars medialis, dDm) and the optic tectum. Contralateral inputs to the torus were from the torus semicircularis, a caudal part of the cerebellum, and a portion of the trigeminal complex. The torus also received bilateral input from the nucleus ventromedialis thalami, nucleus of lemniscus lateralis, nucleus medialis, anterior octaval nucleus, descending octaval nucleus, and the reticular formation. Retrogradely labeled cells in the octaval nuclei were seen predominantly subsequent to HRP injections in the medial torus, while cells in the nucleus medialis were retrogradely labeled following injections into the lateral torus. HRP injections into the nucleus preglomerulosus labeled cells in the superficial region of the torus, while injections into the nucleus ventromedialis thalami labeled cells in the deep region. The nucleus preglomerulosus received inputs bilaterally from the nucleus of the lemniscus lateralis and reticular formation and ipsilaterally from the dorsal telencephalic areas (Dc, Dd, and dDm) and the torus semicircularis. In turn the nucleus preglomerulosus projected to Dd and Dm. Fibers arising in the nucleus ventromedialis thalami ended in Dc, Dd, Dm, and area ventralis pars supracommissuralis (Vs). Homology between the nucleus preglomerulosus and the central thalamic nucleus in amphibians, the nucleus reuniens in reptiles, the nucleus ovoidalis in birds, and the medial geniculate body in mammals is discussed.

Afferent Pathways↗
PubMed1986

Thalamic fiber connections in a teleost (Sebastiscus marmoratus): visual somatosensory, octavolateral, and cerebellar relay region to the telencephalon.

Fiber connections of the nucleus ventromedialis thalami (VM) of Schnitzlein (J. Comp. Neurol. 118:225-267, '62) in a teleost (Sebastiscus marmoratus) were examined by means of the horseradish peroxidase (HRP) tracing method. This nucleus receives fibers from the ipsilateral telencephalon (area dorsalis pars centralis), contralateral retina, contralateral VM, ipsilateral optic tectum, ipsilateral torus semicircularis, contralateral corpus cerebelli, contralateral sensory nucleus of the trigeminal nerve, bilateral bulbospinal reticular formation, contralateral obex region, and contralateral dorsal portion of upper spinal segments. In turn, axons arising from VM terminate in the dorsal telencephalic areas (pars centralis, pars dorsalis, and pars medialis) ipsilaterally, ventral telencephalic area (pars supracommissuralis) bilaterally, nucleus prethalamicus of Meader (J. Comp. Neurol. 60:361-407, '34) bilaterally, nucleus dorsomedialis thalami bilaterally, VM contralaterally, optic tectum bilaterally, torus semicircularis bilaterally, and nucleus lateralis valvulae ipsilaterally. Based on the cytoarchitecture and fiber connections, VM is subdivided into rostral and caudal components. The caudal part of VM in Sebastiscus is considered to be a multimodal thalamic complex that contains some cells that constitute the dorsal thalamus in other vertebrate groups.

Afferent Pathways↗
PubMed1987

Distribution of choline acetyltransferase-immunoreactive neurons in the brain of a cyprinid teleost (Phoxinus phoxinus L.).

The distribution of putative cholinergic neurons in the brain of a cyprinid teleost was investigated by immunocytochemistry, with well-characterized polyclonal antibodies to porcine choline acetyltransferase (ChAT), correlated with acetylcholinesterase (AChE) histochemistry. AChE-positive neurons were more numerous than ChAT-immunoreactive (ChAT-IR) neurons. Regions with ChAT-IR neurons generally also contained AChE-positive ones, but regions with AChE-positive neurons often did not contain (or contained only small numbers of) ChAT-IR neurons. ChAT-IR neurons were located in the brainstem cranial nerve motor nuclei, in the brainstem reticular formation, in the nucleus lateralis valvulae and an adjacent subnucleus "a," in the nucleus isthmi, and in the stratum griseum periventriculare of the tectum opticum. All neurons in these areas were AChE positive. ChAT-IR neurons were also observed within the boundaries of the nucleus sensibilis nervi trigemini and the n. descendens nervi trigemini. The periventricular hypothalamus and the paraventricular organ, the pineal organ, and (possibly) the nucleus suprachiasmaticus also contained ChAT-IR neurons. In these areas, AChE activity was either low or located mainly in neurons other than the ChAT-IR ones. A small population of ChAT-IR neurons was observed in area ventralis telencephali pars lateralis. This was the only telencephalic ChAT-IR cell group. Furthermore, some previously unrecognized cell groups were observed. A small number of ChAT-IR neurons, located on the dorsal aspect of the fasciculus longitudinalis medialis (caudal to n. raphe dorsalis), emitted axons that passed caudally along the raphe midline and innervated some of the large reticular neurons. Another group of ChAT-IR neurons was observed caudal to the thalamic nucleus centralis posterior and was tentatively designed n. tractus rotundus, on the basis of the neuronal morphology. The almost Golgilike staining of some of the ChAT-IR cell groups permitted the identification of their efferent connections and the areas covered by their dendrites.

Animals↗
PubMed1987

Morphology and distribution of the projection neurons in the cerebellum in a teleost, Sebastiscus marmoratus.

Cerebellar efferent neurons in a teleost, Sebastiscus marmoratus, were studied by means of the horseradish peroxidase (HRP) tracing and Golgi impregnation methods. The cerebellar efferents or eurydendroid neurons are classified into two types (A and B) on the basis of the morphology of the dendrites, intracerebellar distribution, and other afferent connections. Type A neurons form a cell cluster in the lobus caudalis and have one thick primary dendrite from which several branches with sparse but long spines extend into the molecular layer of the lobus caudalis. Type B neurons, observed in both the valvula and corpus cerebelli, have two or three primary dendrites running along the ganglion cell layer, and the distal dendritic branches are distributed in molecular layer perpendicularly to the cerebellar surface. Small spines are densely studded on the dendrites of type B neurons. Somata of type A and B neurons are located in and just beneath the ganglion cell layer. The cerebellum projects to the ipsilateral nucleus lateralis valvulae and torus longitudinalis and bilaterally, but mostly contralaterally to the nucleus ventromedialis thalami of Schnitzlein ('62), nucleus ruber, the vicinity of the oculomotor complex, torus semicircularis, and brainstem reticular formation. Type A neurons send axons primarily to the vicinity of the oculomotor complex and partly to the nucleus ventromedialis thalami and the nucleus ruber, whereas type B cells project to all main cerebellar targets. In addition, type B cells are organized topographically in the cerebellum in relation to the efferent targets in the brainstem.

Animals↗
PubMed1987

Antibodies against retinal photoreceptor-specific proteins reveal axonal projections from the photosensory pineal organ in teleosts.

With the aid of specific antisera to the retinal proteins S-antigen and alpha-transducin and to the rhodopsin apoprotein opsin, we have labeled various cell populations in the pineal organ, parapineal organ, habenular nucleus, and subcommissural organ in two teleost species: the rainbow trout and the European minnow. Although these proteins are associated with photoreceptor functions, not only photoreceptor cells but also the majority of parenchymal cells in the pineal organ were immunoreactive. Immunoreactive cells with dendrite- and axonlike processes were observed also in the parapineal organ and the habenular nucleus. Furthermore, S-antigen-immunoreactive, long, axonal processes were observed in the pineal organ and could be traced from the pineal organ to the habenular nucleus and to the pretectal area. In the light of recent HRP electron microscopical and immunocytochemical studies we propose (1) that not only the classical pineal photoreceptor cells of poikilothermic vertebrates but also other types of CSF-contacting neurons may be the phylogenetic ancestors of mammalian pinealocytes, and (2) a close interrelationship between the pineal organ and the limbic system, effectuated by the direct projections from pineal photoreceptors/CSF-contacting neurons/pinealocytes to the habenular nucleus, and by displaced "pinealocytelike" elements scattered in the habenular nucleus.

Animals↗
PubMed1988

Cholinergic neurons in the brain of a teleost fish (Porichthys notatus) located with a monoclonal antibody to choline acetyltransferase.

A monoclonal antibody (Ab8) to choline acetyltransferase (ChAT) was used to locate structures showing ChAT-like immunoreactivity (ChAT-IR) in the brain of a teleost fish, the midshipman (Porichthys notatus). ChAT is the synthetic enzyme for acetylcholine found in neurons using that neurotransmitter; thus ChAT-IR may be interpreted as indicating putative cholinergic activity. Robust staining is seen in all cranial nerve motor nuclei. In addition, the brainstem of Porichthys is distinguished by two other expansive ChAT-IR zones: a sonic motor nucleus, which innervates swimbladder "drum" muscles, and an octavolateralis efferent nucleus, which innervates acoustic, vestibular, and lateral line end organs. Scattered labeled cells are found in several cranial sensory nuclei--the vagal lobe, and the main and descending trigeminal nuclei. ChAT-IR cells form restricted subpopulations in other noncranial nerve nuclei, including the granule cell layer of the cerebellum; superior, medial, and inferior divisions of the reticular formation; the stratum periventriculare of the midbrain's optic tectum; and the nucleus isthmi in the midbrain tegmentum. In the telencephalon, a dense population of ChAT-IR cells is found in the ventral nucleus of area ventralis; terminals and fine fibers are found in the dorsal, medial, and central nuclei of area dorsalis. Together, the data represent the first complete report of ChAT-IR cell bodies in the brain of any nonmammal with the monoclonal antibody Ab8, which has already been extensively used on a variety of vertebrate brains. The results are thus discussed from a comparative viewpoint, considering reports of ChAT-IR in different taxa.

Acetylcholine↗