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R Kishida

Publications and source records attributed to R Kishida.

At least 55 records · Page 3Linked to original sources
PubMed1987

Primary neurons of the lateral line nerves and their central projections in hagfishes.

The hagfish lateral line system was studied by horseradish peroxidase transganglionic transport. The anterior lateral line nerve innervates the group of lateral line canals situated anteriorly to the eye, and the posterior lateral line nerve innervates the group of canals situated posteriorly to the eye. Although both nerves pass through the muscle fascia at the same point, each runs a different course to the brain. The anterior lateral line nerve runs near the trigeminal nerve and its ganglion is closely attached to the trigeminal ganglion, but both systems are completely independent. The posterior lateral line nerve runs independently of any other cranial nerve and makes a peculiar U-turn at the point of entry to the brain capsule. The anterior lateral line ganglion contains both cutaneous sensory cells (small to large cells) and lateral line sensory cells (small cells); from this ganglion projections run to both the trigeminal sensory nucleus (fine and thick fibers) and medial nucleus of the area acousticolateralis (fine fibers). The posterior lateral line ganglion contains only small lateral line cells that project fine fibers to the medial nucleus of the area acousticolateralis. There are no efferent components in this lateral line system, and its only afferent terminal field is the medial nucleus of the area acousticolateralis.

Afferent Pathways↗
PubMed1987

Chemoarchitectonics of the brainstem in infrared sensitive and nonsensitive snakes.

The crotaline snake Agkistrodon possesses infrared receptors, whereas the colubrid Elaphe quadrivirgata does not. We compared the histochemical activity of succinate dehydrogenase (SDH), monoamine oxidase (MAO), and acetylcholinesterase (AChE) in the brainstem of these 2 species, by the method of Nachlas et al. (1957), Glenner et al. (1957), and Koelle and Friedenwald (1949), respectively, and made the following observations. Visual system: The tectum opticum (TO) exhibited strong or moderate AChE and SDH activity in areas receiving retinal projections, i.e. the str. zonale (sz), str. fibrosum et griseum superficiale (sfgs), and narrow areas between small tight fasciculi of the tr. opticus. The sfgs was divided into 2 sublayers, a superficial and a deep, by the intensity of AChE activity. The deep sublayer of the sfgs and sfc of Agkistrodon were stained more strongly than other layers. Numerous fibers within the TO showed MAO activity. The entire sfgs of Agkistrodon was thinner than in Elaphe. The nucl. posterodorsalis showed moderate AChE, and weak SDH and MAO activity in Agkistrodon, but lack of AChE, weak SDH, and moderate MAO activity in Elaphe. Infrared system: This system was present only in Agkistrodon. The nucl. of the lateral descending trigeminal tract (dlV) and the nucl. reticularis caloris (rc) showed to moderate SDH activity in the main neuropil and/or perikarya. These nuclei were not conspicuous in AChE preparations. The marginal neuropil of the dlV had weak SDH, and moderate AChE and MAO activity. Common sensory trigeminal system: Moderate activity of the 3 enzymes was seen in the nucl. tr. descendens n. trigemini (dl). In the dorsomedial part of the nucl. interpolaris, the round limited portion was stained strongly for SDH and AChE. Cells of the nucl. tr. mesencephalicus n. trigemini showed strong SDH and AChE activity. Other regions: In Elaphe, there was strong to moderate AChE and SDH activity in the nucl. of the fasciculus longitudinalis medialis, nucl. centralis superior, raphe nuclei, and reticular nuclei, but only weak activity in Agkistrodon. We also found the following similarities in the 2 species. Strong to moderate AChE and SDH activity was observed in the motor nuclei of the cranial nerves, pretectal nuclei excepting the nucl. posterodorsalis, nucl. opticus basalis, and nucl. posterolateralis tegmentalis. Strong to moderate activity of the 3 enzymes together was detected in the nucl. interpeduncularis as found in other animals previously studied, and in the nucl. commissurae cornae dorsalis, nucl. cochlearis angularis, and the molecular and granular layer of the cerebellum.(ABSTRACT TRUNCATED AT 400 WORDS)

Acetylcholinesterase↗
PubMed1986

Organization of the trigeminal and facial motor nuclei in the hagfish, Eptatretus burgeri: a retrograde HRP study.

We studied the trigeminal and facial motor nuclei of the hagfish by the retrograde HRP method. We distinguished 4 components in a single column of the motor nuclei of the trigeminal nerve and the facial nerve, viz., the pars magnocellularis of the trigeminal motor nucleus (mVm), the anterior part of the pars parvocellularis of the trigeminal motor nucleus (mVp1), the posterior part of the pars parvocellularis of the trigeminal motor nucleus (mVp2) and the facial motor nucleus (mVII). Although in Nissl preparations only the mVm could be distinguished from the rest of the nucleus, the boundaries of the other 3 components were clearly demarcated in HRP preparations. Intramuscular injections into two representative antagonistic jaw muscles revealed that there was no apparent topological organization of the neurons pertaining to the opening and closing muscles in the mVm and mVp1, but both antagonistic muscles were innervated bilaterally. Although the hagfish does possess a cartilaginous jaw, the organization pattern of the motor nuclei of the jaw muscles seems to be the most primitive of all living vertebrates.

Animals↗
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↗
PubMed1985

Primary sensory ganglion cells projecting to the principal trigeminal nucleus in the mallard, Anas platyrhynchos.

The trigeminal and glossopharyngeal ganglia of the adult mallard were studied following HRP injections into the principal trigeminal nucleus (PrV). The PrV consists of the principal trigeminal nucleus proper (prV) and the principal glossopharyngeal nucleus (prIX). After an injection into the prV, the labeled cells were found in the ipsilateral trigeminal ganglion. After an injection into the prIX, labeled cells were found in the ipsilateral distal glossopharyngeal ganglion, but not in the proximal ganglion of the IX and X cranial nerve (pGIX + X). In Nissl preparations, two types of ganglion cells in the trigeminal ganglion, pGIX + X, and distal ganglion of N IX could be distinguished: larger light cells and smaller dark cells. We could not determine whether the HRP-labeled cells belonged to both types or to one of them; but because all the labeled cells were over 20 microns, we concluded that the smallest cells (10-19 microns) in the trigeminal ganglion and distal ganglion of N IX did not project to the PrV. The labeling of the cells in the distal ganglion of N IX (average 34.5 microns) was uniformly moderate. In the trigeminal ganglion there were two types of labeled cells: heavily labeled cells (average 29.1 microns) and moderately labeled cells (average 35.1 l microns). These two types of labeling (moderate and heavy) may reflect two types of primary sensory neurons: cells with ascending, nonbifurcating axons, and cells with bifurcating axons. We speculate that the former are proprioceptive neurons and the latter tactile neurons. Labeled bifurcating axons in the sensory trigeminal complex gave off collaterals to all parts of the descending trigeminal nucleus except to the caudalmost laminated spinal part.

Animals↗
PubMed1985

Primary vestibular projections in the hagfish, Eptatretus burgeri.

The VIIIth cranial nerve projections in the hagfish, which has only one circular canal in the ear, were studied by transganglionic HRP transport. This nerve has two branches, the nervus utricularis (N. utr.) and the nervus saccularis (N. sac.), each with its own ganglion, the ganglion utriculare (G. utr.) and the ganglion sacculare (G. sac.), respectively. Although the G. sac. has uniformly small cells, the G. utr. consists of two separate cell masses, a ventral mass of large cells and a dorsal mass of small cells. The small cells were labeled in both ganglia after horseradish peroxidase (HRP) injection into the endolymphatic space. The greater part of the terminal areas of these two branches overlapped in the ventral nucleus of the area acoustico-lateralis, but the terminals of the N. sac. extended slightly further in a caudal direction. No projections to the primordial cerebellum and no retrogradely labeled cells in the brain were found. The large cells in the ventral part of the G. utr. seem to be general cutaneous neurons, and the dorsal part of the area acousticolateralis seems to receive lateral line input.

Animals↗
PubMed1984

Vagal afferent C fibers projecting to the lateral descending trigeminal complex of crotaline snakes.

The primary vagal axons and terminals in the lateral descending trigeminal complex (dlv-DLV complex) in crotaline snakes were studied following HRP injections into the vagal nerve. Labeled fibers and terminals were found in the marginal neuropil, which was made up entirely of unmyelinated fibers, i.e., C fibers. The general features of vagal input to the dlv-DLV complex in snakes with infrared sensitivity (Boidae and Crotalinae) are discussed.

Afferent Pathways↗
PubMed1983

Primary vagal nerve projections to the lateral descending trigeminal nucleus in boidae (Python molurus and Boa constrictor).

The primary vagal axons and terminals within the lateral descending trigeminal tract (dlv) and nucleus (DLV) of two species of Boidae are studied following HRP injections of the vagal nerve. Labeled fibers and terminals are found in the tail portion of the dlv and DLV, partly forming a neuropil at its margin. The labeled thin fibers and neuropil seem to correspond to the C-fibers and marginal neuropil of Crotalinae.

Afferent Pathways↗
PubMed1982

Infrared sensory neurons in the trigeminal ganglia of crotaline snakes: transganglionic HRP transport.

Trigeminal neurons were labeled by inserting HRP into holes cut in the pit receptor membranes of a crotaline snake, Agkistrodon blomhoffi brevicaudus. Neurons were labeled in the ophthalmic ganglion and the maxillary division of the maxillo-mandibular ganglion, and the HRP was further transported across the ganglia and through the lateral descending trigeminal tract (dlv) to label axon terminals exclusively in the dlv nucleus (DLV). In 6 successful preparations, 7.1-19.3% of totals of 5568-5986 cells in the maxillary division of the ganglion were labeled, but none at all were labeled in the mandibular division. Only a few or none at all were labeled in the ophthalmic ganglion. Cells in the two ganglia ranged in size from 10 to 55 micrometers, but large cells (greater than or equal to 40 micrometers) were scarce (4.9% of the total population). All HRP-labeled neurons fell in the median range of 20-39 micrometers. We concluded that these ganglion cells were infrared neurons, and were therefore the origin of the A delta fibers in the pit membrane. There were no HRP-labeled neurons above or below this range, in spite of the fact that smaller cells (less than or equal to 19 micrometers) made up 35.8% of the total population. In normal Nissl preparations we found both light- and dark-staining cells, but the size range of neither corresponded to the size range of infrared neurons.

Animals↗
PubMed1981

Chemoarchitectonics of the forebrain of the hagfish, Eptatretus burgeri.

The brain of the hagfish, Eptatretus burgeri, was investigated by enzyme histochemical methods to locate roughly the areas which have somatic, visceral, and correlative functions. From the results of previous investigations, it seems that, as a rule, AChE is found in the correlation areas and in a part of the visceral and somatic areas, whereas SDH and MAO are detected in the somatic and visceral areas, respectively. Therefore, the activities of these three enzymes can be used to indicate the functional areas. In addition, G6PD is used to detect areas related to the pentose cycle. Areas with remarkable AChE activity are layer 4 (neuropil), layer 3 (perikarya), layer 5 (perikarya and neuropil), the primordium hippocampi of Jansen (neuropil and a small number of perikarya), the median sagittal lamina of the habenula (neuropil and perikarya), some cells in the pars dorsalis thalami of Jansen (neuropil), the nucleus tuberculi posterior of Jansen (neuropil), and the hypophysis. Activity of SDH, MAO, and G6PD appears in the neuropil. Regions showing activity of both SDH and MAO are the olfactory nerves and glomeruli, the septal area, layer 1 and 4 including the neostriatum of Crosby and Schnitzlein, the primordium hippocampi of Jansen, the preotic area, the habenula, and the caudal part of the medial hypothalamus, this last being the circumference of the hypothalamic ventricle. Furthermore, the anterior part of the amygdala of Crosby and Schnitzlein shows SDH activity. Activity of G6PD is distributed in the same regions showing activity of SDH and MAO, with the exception of the primordium hippocampi of Jansen. Finally, (1) two groups of continuous areas of AChE activity are found conspicuously in the telencephalon; one group consists of layers 3, 4, and 5, and the other consists of the ventral part of the primordium hippocampi, the lateral part of the pars ventralis thalami, and the nucleus tuberculi posterior. These two groups may play a correlative role between the visceral and somatic areas and the cholinergic mechanisms. (2) It seems that the forebrain, especially in the hypothalamus, is poorly differentiated. Furthermore, (3) a comparison with other nonmammalian brains is made from the viewpoint of the chemoarchitectonics.

Acetylcholinesterase↗
PubMed1980

A new tectal afferent nucleus of the infrared sensory system in the medulla oblongata of Crotaline snakes.

The existence of an infrared sensory neuron group with ascending fibers which directly reach the optic tectum in Crotaline snakes was confirmed with three methods. (1) With the retrograde horseradish peroxidase (HRP) method, labeled neurons were not found within the nucleus descendens lateralis nervi trigemini (DLV), but in an unnamed cell group located immediately ventral to the DLV of the contralateral side at the transitional portion between the nucleus oralis (DVo) and the nucleus interpolaris (DVi). This unnamed cell group, which was seen only in the Crotalinae, was provisionally called the 'new nucleus'. (2) Normal brain series of 15 species were stained by the methods of Bodian-Otsuka, Klüver-Barrera and Nissl staining to compare the cytoarchitecture of the medulla oblongata. The 'new nucleus' was found only in species belonging to the Crotalinae. This nucleus was situated in fiber tracts which appeared to correspond to the lemniscus spinalis and tractus spino-cerebellaris of the reptilian medulla oblongata, and contained medium-sized multipolar or fusiform neurons. (3) In an electrophysiological study 16 single units responding unimodally to an infrared stimulus were recorded. Three of these recording sites were determined with Pontamine sky blue marking to be near or within the 'new nucleus'.

Animals↗
PubMed1979

Comparative study on the teleostean optic tectum. Lamination and cytoarchitecture.

Seventy-five species of teleosts were studied by a modified Bodian and the Golgi-Cox method to clarify certain relationship between habits and laminar formation in the optic tectum. The optic tectum of all species studied was divided into four layers (SM, 20 + SFGS, SGC + SAC and SPV) depending upon fiber connections with other areas, and the relative thickness of each layer was measured. All animals were classified into 8 groups (thick SM, thin SM, thick SO + SFGS, thin SO + SFGS, thick SGC + SAC, thick SPV, thin SPV and standard) based on relative thickness of each layer. The thick SM group has the large torus longitudinalis. The SO + SFGS group comprises diurnal, especially visually active fishes. As relative thickness of surface layers (SM and SO + SFGS) increases, the absolute value of whole layers becomes large. Aniamls with large relative thickness of the deepest layer (SPV) show the thin optic tectum. Seven types of cells, (a) pyramidal cell, (b) fusiform cell, (c) periventricular cell, (d) pyriform cell, (e) large multipolar cell, (f) horizontal cell and (g) small multipolar cell, were classified in Golgi-Cox preparations, and the extent of dendritic arborization was compared among the groups in relation to the thickness of each layer. Dendritis of pyramidal, fusiform and preiventricular neurons show varoius extents of arborization in proportion to thickness of layers where branch out. Other types of neuron do not conspicously vary in different groups. Animals belonging to the thick SPV group show poor dendritic arborization in all types of cells. These results were discussed from the ecological standpoint.

Animals↗
PubMed1978

Afferent and efferent fiber connections of the carp torus longitudinalis.

The efferent and afferent pathways of the carp torus longitudinalis were studied by means of degeneration and retrograde HRP methods. Efferent projections were only seen in the most superficial layer of the ipsilateral optic tectum (stratum fibrosum marginale). Afferent pathways to the torus longitudinalis were found to originate mainly in the valvula cerebelli. Degenerating fibers course in the tractus mesencephalocerebellaris posterior within the valvula, and join the tractus mesencephalocerebellaris anterior in the tegmentum. The fibers which ascend in the tract gradually invade the optic tectum through which they are distributed to the torus longitudinalis. The remaining fibers pass through the posterior commissure and terminate in the torus longitudinalis at the rostral end of the tract. Degenerating terminals were also seen in the torus longitudinalis when lesions were made in the optic tectum, tectal commissure, torus semicircularis, and in the area between the valvula and the corpus cerebelli. The possibility of projections from these areas is discussed depending upon the results of the retrograde HRP method.

Animals↗
PubMed1977

Synaptic organization of the nucleus rotundus in some teleosts.

Synaptic organization of the nucleus rotundus was studied with the electron microscope in three teleost species belonging to the same order. In spite of the different histological organization (non-laminated, incompletely laminated, and laminated), the same kinds of axon terminals (S and F) are observed in all species. A fibrous layer which is clearly formed only in the laminated nucleus is composed of F1 terminals and dendrites from a layer of small cells. The same kind of synapses formed between F1 terminals and dendrites of small cells are also found among glomeruli in the non-laminated and incompletely laminated nuclei. The main constituents of glomeruli are S and F2 terminals and dendrites of large cells in the non-laminated and incompletely laminated nuclei, and are S terminals and star-like structures which correspond to the tips of the dendrites of large cells in the laminated nucleus. The star-like structure contains numerous mitochondria and clusters of small polymorphic vesicles. Some of the vesicles aggregate at thickened cell membranes of the structure as in presynaptic dendrites.

Animals↗