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PubMed1988

Retinal ganglion cell topography in teleosts: a comparison between Nissl-stained material and retrograde labelling from the optic nerve.

The retinal topography of cells within the ganglion cell layer of three teleost species is examined in Nissl-stained material in which all neuronal elements containing Nissl substance in the cytoplasm are counted. A topographic comparison is made with retrogradely labelled ganglion cells to differentiate the proportion of nonganglion cells not possessing an axon joining the optic nerve. In the three species studied 92%, 80%, and 66% were found to be the maximum proportion of true ganglion cells in the area centralis, horizontal streak, and periphery, respectively. The proportion of nonganglion cells in the total population of cells counted was 24%. The major contribution to this discrepancy is from peripheral nonspecialized regions of the retina. There is little difference in both topography and peak densities of retinal ganglion cells between the two techniques. The soma areas of both populations are analysed, with the homogeneous nonganglion cell population possessing cells between 5 and 15 micron2 and the heterogeneous ganglion cell soma between 5 and 68 micron2, increasing in size with eccentricity.

Animals↗
PubMed1988

Binding pattern of alpha-bungarotoxin on horizontal cells of a marine teleost retina.

A conjugate of alpha-bungarotoxin and a fluorescent marker (fluorescein isothiocyanate) has been used to localize "nicotinic" acetylcholine receptors on neurons in the outer plexiform layer of marine teleost retina. Toxin binding was confined to bipolar cell dendrites and to intermediate horizontal cells. The arrangement of labeled horizontal cells appears irregular in the whole retina, with a peak density in the ventral and dorsal quandrants. Alpha-bungarotoxin receptors on horizontal cells differ from those on bipolar cells and from those on dendrites in the inner plexiform layer in their sensitivity to agonists and antagonists such as d-tubocurarine and nicotine. They constitute a different type of "nicotinic" receptor that probably has a different function.

Animals↗
PubMed1989

Sound-generating (sonic) motor system in a teleost fish (Porichthys notatus): sexual polymorphism in the ultrastructure of myofibrils.

One mechanism used by teleost fishes to produce acoustic communication signals involves the contraction of sonic "drum" muscles that appose the lateral walls of the swimbladder. In one marine species, the midshipman (Porichthys notatus), there is a sex difference in the overall size of the swimbladder as well as in the ultrastructural properties of its myofibrils. Additionally, there are two classes of sexually mature males referred to as Type I and Type II. The peripheral sonic motor system of Type I males differs from that of Type II males and females (which resemble each other) in a number of ways: (1) the mass of their swimbladder and associated sonic muscles is 50% greater, (2) their muscle fibers are several times larger and have a characteristically large volume of sarcoplasm that surrounds the myofibrils and is densely filled with mitochondria, (3) the length of z-lines of their myofibrils is about 20-fold greater, and (4) their sarcoplasmic reticulum is more highly branched. The ultrastructure of the myofibrils of Type II males and females resembles that found in the sonic muscle of males and females in other related species. The larger mass and specializations of the sonic muscle in Type I males are considered to be adaptations related to their known role in sound production and the unique long duration "humming" sounds that they generate during the breeding season. The similarity in the sonic motor system between females and Type II males is considered to be related to the utilization of an "alternative mating strategy" by Type II males. To our knowledge, this is the first documentation of a sex difference or, for that matter, a sexual polymorphism in the ultrastructural features of a vertebrate myofibril.

Animals↗
PubMed1990

Catecholaminergic systems in the brain of a gymnotiform teleost fish: an immunohistochemical study.

The localization of catecholamines (CA) in the brain of Apteronotus leptorhynchus was studied with immunohistochemical techniques using antibodies to the enzymes tyrosine hydroxylase (TH), dopamine B-hydroxylase (DBH), phenylethanolamine-N-methyltransferase (PNMT), and the neurotransmitter dopamine (DA). Telencephalic TH and DA immunoreactive (ir) neurons were located in the following structures: olfactory bulb, area ventralis telencephali partes ventralis, centralis, dorsalis, and intermediate. Diencephalic TH ir neurons were distributed in: nucleus preopticus periventricularis pars anterior, floor of preoptic recess, n. suprachiasmaticus, n. preopticus periventricularis pars posterior, n. anterior periventricularis, area ventralis lateralis, rostral region of posterior periventricular nucleus (paraventricular organ of other authors), periventricular nucleus of posterior tuberculum, n. recessus lateralis, n. tuberis lateralis pars anterior, and n. tuberis posterior. Although most diencephalic TH ir structures were also DAir, the posterior periventricular nucleus, n. recessus lateralis pars medialis, n. recessus posterioris, and ventral region of nucleus lateralis tuberis pars anterior showed differences in the distribution of TH and DA immunoreactivity. The rhombencephalic structures contained cell groups with different combinations of catecholamines as follows: TH and DBH ir neurons in the isthmic tegmentum (locus coeruleus); TH and DBH ir cells in the rostral medullary tegmentum ventral to VIIth nerve; TH and PNMT ir cells in the sensory nucleus of the vagus nerve; TH, DBH, and PNMT ir cells in the dorsal medullary tegmentum, TH and DBH ir cells in the dorsomedian postobecular region, ventral to the descending trigeminal tract and lateral to the central canal at medullospinal levels. This study shows that: (1) with few exceptions TH and DA ir coincides, (2) gymnotiforms possess similar DBH ir rhombencephalic groups, but additional telencephalic and rhombencephalic TH ir groups, and PNMT ir cells that were not reported previously in teleosts, and (3) the presence of CAergic fibers in the electrosensory system supports findings of their modulatory function in communication and aggression.

Animals↗
PubMed1990

Immunohistochemical subpopulations of retinopetal neurons in the nucleus olfactoretinalis in a teleost, the whitespotted greenling (Hexagrammos stelleri).

Two subpopulations of retinopetal neurons in the nucleus olfactoretinalis (NOR) were revealed by means of general histological, tract tracing, and immunohistochemical methods in a marine teleost, the whitespotted greenling (Hexagrammos stelleri). Two types of cells in the NOR (M cell, L cell) were morphologically distinguishable from one another. The cell bodies of M cells were medium-size and fusiform, while those of L cells were large and ellipsoidal or irregular. M cells were located at the ventralmost region of the junction between the olfactory bulb and telencephalon, while L cells were scattered more rostrally along the ventromedial surface of the olfactory bulb. Following applications of HRP or Fluoro-Gold to the optic nerve, almost all M cells and about half of the L cells were labeled in the contralateral NOR. L cells showed strong immunoreactivities to gonadotropin releasing hormone (GnRH) and Phe-Met-Arg-Phe-NH2 (FMRFamide), whereas M cells showed only weak GnRH-immunoreactivity and no FMRFamide-immunoreactivity. Axons of L cells were detected in the optic nerve by means of GnRH- and FMRFamide-immunohistochemistry. The axons were concentrated in the myelinated edge (the oldest area) of the "ribbon" optic nerve. GnRH- and FMRFamide-immunoreactive fibers constituted a plexus at the junction between the inner nuclear layer and inner plexiform layer. The existence of two structurally separate classes of NOR cells suggests two functionally separate channels from the NOR to the retina.

Animals↗
PubMed1990

Interspecific variation in the projection of primary afferents onto the electrosensory lateral line lobe of weakly electric teleosts: different solutions to the same mapping problem.

We demonstrate that preterminal axons composing the primary afferent projection onto the four somatotopically organized electrosensory lateral line lobe (ELL) segments in weakly electric gymnotiform teleosts course in fundamentally different directions in the most commonly studied species. Afferents enter the deep fiber layer (dfl) of the ELL and course in variable, but species-specific, directions within a horizontal plane before turning dorsally to terminate within the deep neuropil layer of the ELL (dnl). Among the species considered here, apteronotids exhibit the tightest projection pattern. Afferents enter the rostral ELL from the anterior lateral line nerve ganglion (ALLNG) in a nonsomatotopic fashion. As they course horizontally, these fibers undergo a rostrocaudal somatotopic sorting along the ventrolateral border of the dfl, then turn within a horizontal plane to course medially across the ELL segments. These medially coursing horizontal fibers are sorted: they form sublaminae according to the nerve branch containing their peripheral axon. Horizontal axons then turn dorsally, form fascicles, and terminate within the dnl. Within the dorsal fascicles, axons run directly into the dnl with little deviation, and their terminal fields exhibit no appreciable spread. In sternopygids, dfl horizontal fibers course in directions orthogonal to those in apteronotids. Fibers enter the rostral ELL and course medially across segments before turning caudally within segments. Unlike apteronotids, sternopygid horizontal fibers do not sort tightly by nerve branch. As horizontal axons turn dorsally they also form tight fascicles. But rather than terminating directly and without spreading, as in apteronotids, sternopygid fibers disperse from these fascicles and become sorted horizontally a second time prior to terminating in the dnl.(ABSTRACT TRUNCATED AT 250 WORDS)

Animals↗
PubMed1990

Spatial and morphological differentiation of trigger zones in afferent fibers to the teleost utricle.

A morphological correlate of the trigger site (the locus of action potential initiation) was identified in afferent axons of the utricle in the ear of two species of teleost fish. These sites were identified by the ferric-ferrocyanide (Prussian blue) cytochemical procedure and they were correlated with the geometries of afferent intraepithelial arbors as visualized by means of a silver stain. The intraepithelial arbors of afferent fibers show regional distributions that correlate with axon diameter and Prussian blue staining. Afferent axons with diameters greater than 4-5 microns only innervate the striola regions of the epithelium and terminate as one of two distinct types of intraepithelial arbors. Afferent axons with diameters smaller than 4 microns are ubiquitously distributed throughout the epithelium. Arbors that stained by Prussian blue within the utricular epithelium are restricted to the striolar regions. These arbors possess nodal-like membrane in different branches as postsynaptic membrane. Afferents that innervate hair cells in the extrastriolar epithelial regions stained with Prussian blue only at the extraepithelial terminal heminode. The postsynaptic membrane of these afferents is passive or dendritic-like.

Afferent Pathways↗
PubMed1991

Sexually dimorphic distribution of a galanin-like peptide in the central nervous system of the teleost fish Poecilia latipinna.

Immunohistochemical techniques were used to visualize areas of the brain and spinal cord containing a galanin-like peptide in the teleost fish, the sailfin molly. Galanin-like immunoreactivity (GAL-LI) in both males and females was identified in neurons in the nucleus preopticus periventricularis, nucleus lateralis tuberis, and nucleus commissuralis. GAL-LI fibers had a comparable distribution in the forebrain, preoptic, hypothalamic, and visceral sensory areas of both sexes. In striking contrast to these areas, the optic tectum, torus semicircularis, brainstem tegmentum, and spinal cord of the male contained much higher levels of GAL-LI than the female. GAL-LI in these dimorphic areas in the female was limited to single fiber bundles in the ventromedial tegmentum and in the trigeminal system. Additionally, a population of neurons in the preoptic nucleus was found to contain GAL-LI in the male only. Sexual dimorphism was especially prominent in the spinal cord, where extensive GAL-LI fibers were found in the male only. These fibers were oriented in the longitudinal plane and confined largely to the gray matter. Comparative studies were performed on the goldfish spinal cord, in which GAL-LI was localized solely in the dorsal horn and exhibited no sexual dimorphism. Further, examination of spinal cord material from neonatal mollies revealed a lack of spinal GAL-LI at this developmental stage. As the extent of GAL-LI in the male molly spinal cord differs from both the goldfish and from that reported for the mammalian spinal cord, and a prominent sexual dimorphism in GAL-LI extends from the diencephalon to the caudal spinal cord, it is suggested that a galanin-like peptide may play a unique, sex-specific role in this species.

Animals↗
PubMed1991

Source of sexually dimorphic galanin-like immunoreactive projections in the teleost fish Poecilia latipinna.

A galanin-like peptide has a sexually dimorphic distribution in the teleost fish, the sailfin molly. An extensive system of galanin-like immunoreactive (GAL-LI) fibers has been described in the brainstem and spinal cord of the male molly, which is absent in the female (Cornbrooks and Parsons, companion paper). As GAL-LI in the mammalian spinal cord has been localized to neurons of origin in the dorsal root ganglia and dorsal and ventral horns, the present study was undertaken to determine whether the sexually dimorphic GAL-LI in the male molly may originate in part from corresponding sources in this species. Colchicine treatments of the spinal cord and dorsal root ganglia did not result in GAL-LI staining in neuronal somata in these regions. Following complete transection of the spinal cord and at any level of the spinal cord, there was a complete absence of GAL-LI caudal to the lesion site. In fish that received unilateral spinal transection, there was a loss of GAL-LI ipsilateral and caudal to the lesion. Finally, in fish that received lesions in the rostral hypothalamus, there was a complete loss of GAL-LI in the sexually dimorphic fiber system in the brainstem and spinal cord, but not in non-dimorphic GAL-LI regions of the brainstem. Thus the sexually dimorphic fiber system in the male molly may originate in neurons of the preoptic nucleus that are sexually dimorphic for a GAL-LI peptide. This preoptico-spinal pathway may mediate sex-specific behaviors in this species.

Animals↗
PubMed1991

Organization of the histaminergic system in the brain of the teleost, Trachurus trachurus.

To accumulate phylogenetic information on the central histaminergic system, we investigated the histaminergic system in the brain of a teleost, the jack mackerel (Trachurus trachurus), using the indirect immunofluorescent method with antiserum against histamine. A small number of histamine-immunoreactive cell bodies were observed in the posterior hypothalamus around the posterior recess. Histamine-immunoreactive fibers innervated the telencephalon, diencephalon, tegmentum, and rostral part of the medulla oblongata. The immunoreactive fibers were very sparse or absent in the olfactory bulb, optic tectum, cerebellum, caudal part of the medulla oblongata, spinal cord, and hypophysis. Ascending fiber bundles were seen in the basal hypothalamus, supplying fiber collaterals to the telencephalon and diencephalon, whereas descending fibers were observed in the midline of the lower brainstem. These findings suggest that the central histaminergic system of the jack mackerel is homologous to those of mammals, reptiles, and amphibians, although poorly developed compared with them. The histamine-immunoreactive neuronal cell bodies found in the border area between the mesencephalon and rhombencephalon of the river lamprey were not detected in the brain of the jack mackerel.

Animals↗
PubMed1991

Zebrin II immunoreactivity in the rat and in the weakly electric teleost Eigenmannia (gymnotiformes) reveals three modes of Purkinje cell development.

Monoclonal antibody (mab) anti-zebrin II recognizes a single 36-kD polypeptide in Purkinje cells in the rat and fish cerebellum. In the adult rat, zebrin II+ Purkinje cells form, in each hemicerebellum, seven parasagittal bands interposed by zebrin II- bands. We show that, in rats, immunoreactivity first appears caudally at postnatal day 5 and spreads; all Purkinje cells are labelled by postnatal day 12. Subsequently, immunoreactivity is selectively lost so that by day 18 the adult pattern of zebrin II+/-immunoreactive bands is created. This pattern indicates two types of Purkinje cells according to developmental trajectory, zebrin II-/+/-. In the adult gymnotiform teleost Eigenmannia, Purkinje cells in the corpus cerebelli (CCb), lateral valvula cerebelli (VCbl), and eminentia granularis anterior (EGa) are zebrin II+. Purkinje cells in the eminentia granularis posterior (EGp) and medialis (EGm) and the medial valvula cerebelli (VCbm) are zebrin II-. Zebrin II antigenicity is first present at 6 days postspawning (P6) in the EGa and at P8 in the CCb. In the valvula, labelling does not appear until P29. Immunoreactivity in the CCb, VCBl, and the EGa persists in the adult, whereas in the VCbm Purkinje cells become zebrin II- before reaching adulthood. These developmental histories (zebrin II-/+ and zebrin II-/+/-) correspond to the patterns of Purkinje cell development in mammals. Additionally, Eigenmannia has a third class of Purkinje cells, in the EGp and EGm, that never express zebrin II immunoreactivity, indicating that zebrin II expression is not an obligatory feature of Purkinje cell development in all vertebrates.

Animals↗
PubMed1992

Retinal growth and cell addition during embryogenesis in the teleost, Haplochromis burtoni.

Neurogenesis of the developing embryonic retina is described for the African cichlid fish, Haplochromis burtoni, from 4 days post fertilization until all cell phenotypes are generated (day 7). Cell addition and differentiation both begin at the same absolute location which later becomes the central retina. As observed in most other vertebrates, cones and ganglion cells differentiate first, followed by amacrine and bipolar cells. Rod photoreceptors, which are added late, differentiate last. Changes in retinal thickness, retinal stretching, cell size, and cell density were measured during development. From day 4 through 7, there is an increase in retinal thickness largely due to the expansion of the inner plexiform layer (IPL) and outer nuclear layer (ONL). The inner nuclear layer (INL) decreases in thickness and there is a transient decrease in the density of cells in the scleral portion of the INL. Cells increase in size in the ganglion cell layer (GCL) and the vitread INL, decrease in size in the sclerad INL, and remain the same in the ONL. Changes in the density of the cell layers were observed: the density of ONL cells increased, the density of GCL cells decreased, and INL cells increased then decreased. From day 4 to day 6, eye growth is entirely due to cell addition because no retinal stretching was observed in the ONL or the horizontal layer. During this same developmental period, the pattern and rate of neurogenesis were measured in the differentiated portion of the retina by means of 3H-thymidine labeling. A small number of cell divisions within the differentiated INL precede the onset of cell divisions in the ONL. The number of 3H-thymidine labeled cells within the INL increases at a low rate consistent with an asymmetric pattern of cell division characteristic of stem cells. In contrast, cell divisions in the ONL increase exponentially, consistent with a symmetric pattern of cell division characteristic of progenitor cells. Double-label experiments (3H-thymidine and a rod specific opsin antibody) show that some of the symmetrically dividing cells in the ONL express the rod specific opsin within 2 days, suggesting that these dividing cells are rod progenitors. Although we do not hae conclusive evidence, these developmental processes support the hypothesis that stem cells within the INL could be the source of rod precursors in the embryonic teleost retina.

Animals↗
PubMed1992

Galanin receptors in the brain of a teleost: autoradiographic distribution of binding sites in the Atlantic salmon.

The distribution of galanin (GAL) binding sites in the brain of the Atlantic salmon (Salmo salar) was investigated by means of radioligand binding in conjunction with autoradiography by using high-performance liquid chromatography (HPLC) characterized radio-iodinated porcine galanin ([125I]GAL). On slide-mounted sections of frozen salmon brain homogenate, [125I]GAL (4 nM) bound rapidly and reversibly to a single population of sites with a Kd of 1.0 +/- 0.08 nM (n = 3) and Bmax of 2.38 +/- 0.19 fmol/mg wet tissue. Specific [125I]GAL binding was found in cellular regions, in fiber tracts, and in neuropil areas throughout the brain, except for in the olfactory bulb, pineal organ, and cerebellum. Autoradiographic microdensitometric measurements revealed high total [125I]GAL binding in the ventral hypothalamus (inferior lobes; around 7-12 fmol/mg tissue), the dorsal spinal cord (between 6 and 12 fmol/mg tissue), sublayers of the optic tectum (around 8 fmol/mg), torus semicircularis (around 7 fmol/mg), and glomerular complex (around 6 fmol/mg). Intermediate densities of [125I]GAL binding (3-5 fmol/mg tissue) were found in the pituitary, telencephalon, dorsolateral thalamic nucleus, and raphe nuclei and in association with the forebrain bundles. Except for in the optic tectum, there is a good concordance of [125I]GAL binding sites and GAL-immunoreactive fiber projections in most brain areas of the salmon. The wide distribution of GAL binding sites provides further evidence that a GAL-like substance might be involved in a diversity of brain functions of teleosts. The topographic distribution of target sites in the hypothalamo-hypophyseal axis indicates that GAL-like substances may have both direct and indirect effect on pituitary functions while in extrahypothalamic areas, functional implications by GAL may include involvement in somatosensory, central gustatory, olfactory, and visual functions. This study provides evidence for the presence of a specific GAL receptor in the brain of the Atlantic salmon. Together the distribution of GAL binding and GAL-like molecules provide a covering delineation of the GAL neuronal system in the brain of the Atlantic salmon. Comparisons with mammals suggest that the GAL receptor molecule has been well preserved during evolution and that GAL-like substances may be present, and even possess similar functional properties, throughout the vertebrate phylogeny.

Animals↗
PubMed1993

Development of the dorsal root ganglion in a teleost, Oreochromis mossambicus (Peters).

The precursor crest cells of the spinal dorsal root ganglia (DRG) in the tilapia, Oreochromis mossambicus, were analysed by HNK-1 antibody staining, scanning electron microscopy, and DiI labeling techniques. The ontogeny of the DRG was followed in the embryos and young fry of the fish. Neural crest cells which contribute to the formation of the DRG were observed to commence their migration in the trunk region after 40 hours postfertilization. They do not penetrate the somites but travel through the space between the neural tube and the somite. Crest cells destined to become the DRG accumulate at the midsomitic region where the ventral root exits. At 50 to 80 hours postfertilization, they differentiate and become bipolar sensory cells. The DRG continues to grow and develop right through hatching at 115 hours. During the early larval stages, crest cells accumulate around the ventral root and the DRG eventually fuses with the motor root, giving rise to a situation in which the DRG contains not only the sensory cells but also motor fibres. The mixed nature of the DRG was confirmed by HRP retrograde labeling. We believe that this is the first report in describing the formation of the DRG in a teleost.

Animals↗
PubMed1993

Collateral sprouting in the electrosensory lateral line lobe of weakly electric teleosts (gymnotiformes) following ricin ablation.

Sprouted collateral axons were observed in the electrosensory lateral line lobe (ELL) of gymnotiform teleosts (Apteronotus leptorhynchus) following the ablation of the supraorbital branch of the anterior lateral line nerve. Ablation was accomplished by using microinjections of the toxic lectin ricin. Sprouted axons were followed for up to 26 weeks postablation. Ricin exposure severely reduced axonal numbers and the peripheral electroreceptors in the region innervated by these fibers. To visualize sprouted fibers, intact lateral line afferent nerve branches were anterogradely labelled with the neuronal tract tracers horseradish peroxidase or cobalt chloride, or the monoclonal antibody Q26A3. Within the four somatotopically organized ELL segments, sprouted collaterals were first observed two weeks after ricin injection in the medial and centromedial segments, and four weeks postinjection in the centrolateral and lateral segments. Sprouting involved intrasegmental, horizontally directed axons from adjacent nerve branch terminal fields, and mixed intra- and extrasegmental, dorsally directed axons from the ELL deep fiber layer. The sprouting response was robust but variable in its timing, peaking between 6 and 12 weeks. Subsequently, the intrasegmental, horizontally directed fibers were retained but the mixed dorsally directed fibers, including all extrasegmental axons, were retracted. Therefore, this sprouting response appears to consist of a collateral overproduction followed by a selective axonal retraction. In our view, the most likely explanation for this axonal retraction is that the descending inputs from the isthmus and the cerebellum, as well as commissural fibers from the contralateral ELL, maintain established somatotopic relationships by eliminating somatotopically mismatched sprouted collaterals.

Animals↗
PubMed1994

Comparative distribution of neurotensin-like immunoreactivity in the brain of a teleost (Carassius auratus), an amphibian (Hyla meridionalis), and a reptile (Gallotia galloti).

The distribution of neurotensin (NT) was studied in the brain of three species belonging to the three major classes of cold-blooded vertebrates: teleost fishes (Carassius auratus), anuran amphibians (Hyla meridionalis), and reptiles (Gallotia galloti; Lacertidae). By using antibodies directed against synthetic bovine NT in the three species, immunoreactive cell bodies were discovered mostly in the telencephalon and diencephalon, in particular at the level of the preoptic region the mediobasal hypothalamus, and the thalamus. In the frog and the lizard, additional immunoreactive (ir) structures were observed in the optic tectum and the tegmentum of the mesencephalon. In the goldfish pituitary, an extensive innervation was consistently observed at the level of the rostral pars distalis, whereas in both frog and lizard, positive fibers were only detected in the external layer of the median eminence. In the three species there is a striking overlap between the distribution of the NT-ir cell bodies and that of the target cells for sexual steroids. The results are discussed in relation with those reported in birds and mammals, and with the possible interactions among NT, sexual steroids, and the neuroendocrine control of pituitary hormone release, in particular prolactin and gonadotrophin.

Amino Acid Sequence↗
PubMed1995

Fine structure of the medullary lateral line area of Chelon labrosus (order perciformes), a nonelectroreceptive teleost.

The ultrastructure and synaptic organization of the nucleus medialis and cerebellar crest of the teleost Chelon labrosus have been investigated. The nucleus medialis receives projections from the anterior and posterior lateral line nerves. This nucleus consists of oval neurons and large crest cells ("Purkinje-like" cells) whose apical dendrites branch in the overlying molecular layer, the cerebellar crest. In the dorsal region of the nucleus medialis, the perikarya and smooth primary dendrites of the crest cells are interspersed among myelinated fibers and nerve boutons. The ventral layer of the nucleus medialis contains crest cell perikarya and dendrites as well as oval neurons. The cerebellar crest lacks neuronal bodies, but the apical dendrites of crest cells receive synapses from unmyelinated and myelinated fibers. In the cerebellar crest, two types of terminals are presynaptic to the crest cell dendrites: boutons with spherical vesicles that form asymmetric synapses with dendritic spines and boutons containing pleomorphic vesicles that form symmetric synapses directly on the dendritic shaft. Most axon terminals found on the somata and primary dendrites of crest cells in the nucleus medialis have pleomorphic vesicles and form symmetric contacts, though asymmetric synapses with spherical vesicles and mixed synapses can be observed; these mixed synapses exhibit gap junctions and contain spherical vesicles. Unlike crest cells, the oval neuron perikarya receive three types of contacts (symmetric, asymmetric, and mixed). The origins and functions of these different bouton types in the nucleus medialis are discussed.

Animals↗
PubMed1995

Localization of nicotinamide adenine dinucleotide phosphate-diaphorase activity in electrosensory and electromotor systems of a gymnotiform teleost, Apteronotus leptorhynchus.

The distribution of nicotinamide adenine dinucleotide phosphate-diaphorase (NADPH-d) activity was determined in electrosensory and electromotor systems of the weakly electric gymnotiform teleost Apteronotus leptorhynchus as an indicator of putative nitric oxide synthase-containing cells. NADPH-d activity was detected in electroreceptors and in afferent nerves of both ampullary and type I and type II tuberous organs. All cell bodies within the anterior lateral line nerve ganglion were positive for NADPH-d activity, as were the primary afferent axons and termination fields in the medullary electrosensory lateral line lobe. In the corpus cerebelli and valvula cerebelli, NADPH-d label was present in Purkinje cell somata, mossy fiber synaptic glomeruli, granule cells, and parallel fibers. In the midbrain, NADPH-d activity was apparent in layer VIIIB of the torus semicircularis dorsalis and in electrosensory laminae of the optic tectum. NADPH-d was particularly associated with diencephalic electrosensory and electromotor nuclei, including the prepacemaker nucleus, the nucleus subelectrosensorius, and the central posterior nucleus of the thalamus. Intense NADPH-d activity was present in pacemaker and relay cells of the medullary pacemaker nucleus but was absent from a novel class of smaller cells in this structure. Relay cell axons and spinal electromotor neurons and their axons within the electric organ were positive for NADPH-d activity. These results indicate that putative nitric oxide synthase-containing neurons in Apteronotus are localized preferentially to electrosensory and electromotor structures, suggesting a role for nitric oxide in determining the activity of cells involved in detecting or generating weakly electric fields.

Animals↗