Biomedical subjects

R Kishida

Publications and source records attributed to R Kishida.

At least 19 recordsLinked to original sources

PubMed1992

Visual and infrared input to the same dendrite in the tectum opticum of the python, Python regius: electron-microscopic evidence.

In snakes with infrared receptors, the optic tectum receives input from both the visual and the infrared senses. We investigated the infrared and optic fiber terminations in the tectum with a combination of horseradish peroxidase and degeneration labeling. In addition to synapses by visual and infrared fibers onto individual neurons, we were able to observe for the first time visual and infrared synapses on one and the same dendrite.

Animals↗

PubMed1991

Afferent and efferent projections of the glossopharyngeal-vagal nerve in the hagfish.

Anterograde and retrograde transport of horseradish peroxidase was used to examine the afferent and efferent projections of the glossopharyngeal-vagal nerve in the hagfish Eptatretus burgeri. Anterogradely labeled ganglion cells are scattered in the glossopharyngeal-vagal nerve trunk, in the saccular ganglion, and in the brainstem. Afferent fibers of the glossopharyngeal-vagal nerve terminate in both the vagal lobe and the fasciculus communis. Close observation showed no morphological differentiation between these two structures, indicating that they are not separate entities, but a single, continuous structure that is homologous with the nucleus and tractus solitarius of other vertebrates. The median part of this structure (the commissura infima) is displaced more rostrally than the same part of the solitary nucleus in many other vertebrates. Some of the afferent fibers invade the ventral portion of the trigeminal sensory nucleus, which receives the maxillo-mandibular nerve fibers, and terminate there. Our study showed that the hagfish has only one nucleus in the vagal motor system, i.e., the vagal motor nucleus, which contains both parasympathetic and branchiomotor neurons. The dendrites of the vagal motor neurons in the hagfish are more highly developed than those in other vertebrates. This suggests that the motor reflex arc of the glossopharyngeal-vagal nerve in hagfishes may be simpler than in other vertebrates.

Afferent Pathways↗

PubMed1990

Organization of the primary projections of the lateral line nerves in the lamprey Lampetra japonica.

The lateral line sensory system of Lampetra japonica is innervated by the anterior and posterior lateral line nerves. The anterior lateral line nerve innervates all electroreceptors throughout the body and mechanoreceptors of the head. The posterior lateral line nerve innervates trunk mechanoreceptors. The anterior lateral line nerve consists of two ganglia (anterior lateral line and intracapsular) and four major peripheral branches (superficial ophthalmic, buccal, hyomandibular, and recurrent nerves). The posterior lateral line nerve has one posterior lateral line ganglion and one peripheral branch. The location and central projection patterns of the primary sensory neurons of these branches of the lateral line nerves were studied with the aid of horseradish peroxidase labeling. The ganglion cells of the buccal nerve were found in the rostral half, and those of the hyomandibular nerve were found in the caudal half of the medial part of the anterior lateral line ganglion. The lateral part of the anterior lateral line ganglion contains ganglion cells of the recurrent nerve and the superficial ophthalmic nerve. The rostral half of the intracapsular ganglion contains ganglion cells of the recurrent, hyomandibular, and buccal nerves. The ganglion cells of the posterior lateral line nerve were found in the posterior lateral line ganglion. The buccal nerve afferents terminated mainly in the lateral part of the ipsilateral mechanoreceptive medial nucleus. The peripheral part of the electroreceptive dorsal nucleus also received several afferents. The hyomandibular afferents terminated ipsilaterally in the central part of the medial nucleus and in the dorsolateral part of the dorsal nucleus. Some afferents of the hyomandibular nerve ascended and descended in the descending nucleus of the trigeminal nerve near its dorsal margin. The ventral nucleus, the primary nucleus of the VIIIth nerve, received a few fibers of the buccal and hyomandibular nerves. In the recurrent nerve, the fibers of the lateral part of the anterior lateral line ganglion terminated throughout the entire dorsal nucleus, and the fibers of the intracapsular ganglion projected to the dorsolateral part of the nucleus. The afferents of the posterior lateral line nerve terminated in the medial part of the ipsilateral medial nucleus and in the lateral part of the contralateral medial nucleus. In the cerebellar area, afferents of the anterior lateral line nerve were located laterally to those of the posterior lateral line nerve. Several fibers terminated in some branchiomotor nuclei, the cerebellar crest, and the dorsal gray near the obex level. No efferent cell bodies were found in the place where efferent neurons of the VIIIth nerve have been previously reported.

Afferent Pathways↗

PubMed1989

Afferent and efferent projections of the VIIIth cranial nerve in the lamprey Lampetra japonica.

Anterograde and retrograde transport of horseradish peroxidase was used to examine the afferent and efferent projections of the VIIIth cranial nerve in the lamprey Lampetra japonica. Ganglion cells of the VIIIth nerve are classified into three types on the basis of their morphology. The central processes of these ganglion cells enter the medulla in two groups: the anterior group (mostly thick fibers) and the posterior group (mostly thin fibers). Afferent fibers mainly terminate within the ipsilateral ventral and octavomotor nuclei of the octavolateralis area and within the granular and molecular layer of the cerebellum. Some fibers terminate in the contralateral cerebellum, the medial and dorsal nuclei of the octavolateralis area, the descending nucleus of the trigeminal nerve, some cranial motor nuclei, and the lateral octavus nucleus, which has not been described previously. This small nucleus is located beneath the descending nucleus of the trigeminal nerve near the obex. Within the ventral nucleus, thin fibers occupy the dorsal part and thick fibers occupy the ventral part. The basic projection pattern of the primary afferents of the VIIIth nerve in the lampreys was similar to that of gnathostome fishes that have been studied to date. Cell bodies of the efferent vestibular neurons are located between the ipsilateral trigeminal motor nucleus and the facial motor nucleus. The lateral location of these cell bodies differs from that of all other fish species that have been studied.

Animals↗

PubMed1989

Substance P immunoreactivity in the vagal nerve of mice.

After horseradish peroxidase was applied to the main trunk of the mouse vagal nerve, anterogradely labeled cells in the vagal ganglia and fibers in the solitary complex, and retrogradely labeled cells in the dorsal motor nucleus and the ambiguous nucleus were observed. Most of the cells in the nodose ganglion were labeled, but only a few cells in the jugular ganglion were labeled. Heavily labeled nerve terminals and fibers were found in 3 areas in the solitary nucleus: i.e., the lateral half of the medial nucleus, the ventrolateral nucleus, and the commissural nucleus. There was only weak labeling in the dorsolateral nucleus, ventral nucleus, and intermediate nucleus. Substance P immunoreactive neurons in the vagal ganglia were found in the jugular ganglion and the dorsal part of the nodose ganglion, but not in the ventral part of the nodose ganglion. Substance P immunoreactivity in the solitary nucleus was moderate in the commissural nucleus and the intermediate nucleus, but was lacking or very weak in the lateral half of the medial nucleus, ventral nucleus, dorsolateral nucleus, and ventrolateral nucleus. We conclude that most substance P containing fibers in the main trunk of the vagal nerve project centrally to the commissural nucleus and peripherally to some of the thoracic viscera.

Animals↗

PubMed1988

Somatotopic organization of the primary sensory trigeminal neurons in the hagfish, Eptatretus burgeri.

Primary sensory trigeminal projections were investigated in the hagfish following application of horseradish peroxidase (HRP) to the sensory branches. In our control preparations we were able to distinguish five sensory ganglia and their respective nerves. HRP application confirmed the almost exclusive relation of each of these nerves to their respective ganglia, with very little overlap. In normal frontal sections of the medulla oblongata, five columns of fibers surrounded by neuronal cell bodies could be clearly distinguished, but the number is probably fortuitous, for there was no one-on-one relationship with the five trigeminal ganglia. From their peripheral connections, we surmised that columns 1 and 3 handle general cutaneous sensation, columns 2, 4, and 5 handle taste sensation, and column 5 handles general mucous cutaneous sensation conveyed by utricular ganglion cells. Dorsally located columns received projections from nerves with dorsal peripheral connections, and more ventrally located columns received projections from nerves with ventral peripheral connections. This relation is the reverse of that seen in other vertebrates.

Afferent Pathways↗

PubMed1988

Substance P-like immunoreactivity in the trigeminal sensory nuclei of an infrared-sensitive snake, Agkistrodon blomhoffi.

With the peroxidase-antiperoxidase immunohistochemical method we ascertained the presence of substance P-like immunoreactivity (SPLI) in fibers and cell bodies of the trigeminal sensory system of the pit viper, Agkistrodon blomhoffi. There are a few SPLI fibers each in the principal sensory nucleus and the main neuropil of the lateral descending nucleus (i.e., the infrared sensory nucleus); a moderate number in the descending nucleus; and a large number in the caudal subnucleus, the medial edges of the interpolar subnucleus, and the marginal neuropil of the lateral descending nucleus. About 30% of the cell bodies in the ophthalmic and maxillo-mandibular ganglia show SPLI, and of the two craniocervical ganglia, the proximal ganglion has many more cells with SPLI than the distal ganglion. The SPLI distribution in the common trigeminal sensory system is similar to that of mammals, and suggests that the function of this system is also similar. In the infrared that the function of this system is also similar. In the infrared sensory system, the differing distribution in the main and marginal neuropils suggests separate functions for these two structures in the system.

Afferent Pathways↗

PubMed1988

Giant lateral-line afferent terminals in the electroreceptive dorsal nucleus of lampreys.

In HRP studies of the lateral line nerve in lampreys, the dorsal nucleus of the area octavolateralis received projections mainly from the recurrent branch of the anterior lateral line nerve. Furthermore, the recurrent branch projected exclusively to the dorsal nucleus. Besides the common type (1-3 micron) of nerve terminals, a hitherto unreported type of giant (10-30 micron) nerve terminal was found aggregated at the rostral and caudal ends of the nucleus. Since the dorsal nucleus mediates electroreception in lampreys, we conclude that the giant terminals are very probably the terminals of the electroreceptive primary fibers.

Animals↗

PubMed1988

Substance P-like immunoreactivity in the central retinal artery of the rabbit.

Substance P-like immunoreactive nerve fibers were identified in the central retinal artery of the rabbit using the peroxidase-antiperoxidase method. The fibers were seen to encircle the central retinal artery throughout its course in the main trunk of the optic nerve. No labeled fibers were seen in the central retinal vein or in the retinal blood vessels. It appears, therefore, that the central retinal artery and the retinal blood vessels are innervated by different nerve systems: the central retinal artery by one of the peripheral nerves, and the retinal vessels by the central nervous system.

Animals↗

PubMed1987

Organization of sensory and motor nuclei of the trigeminal nerve in lampreys.

Anterograde and retrograde HRP transport were used to elucidate the primary central projections of the trigeminal nerve in a lamprey, Lampetra japonica, by application to the ophthalmic, apical, basilar, suborbital, and mandibular branches of the trigeminal nerve. (1) Most of the trigeminal and a few facial ganglion cells were labeled. The ganglion cells of each nerve were distributed in separate areas within their respective ganglia. (2) Some ipsilateral medullary and spinal dorsal cells were labeled after HRP application to the ophthalmic and apical nerves, but there was no contralateral labeling. (3) Most of the neurons of the trigeminal motor nucleus were labeled, and when the apical or the basilar nerve was labeled, in each case a cluster of small motor neurons was found ventrolateral to the classic motor nucleus. (4) Miscellaneous neurons were found scattered along the course of the descending trigeminal tract and nucleus in all cases except after application to the mandibular branch. The shape, size, and distribution patterns of these neurons were varied, and several characteristics indicated that they were sensory in nature. (5) In the rostral part of the medulla, sensory fibers of each nerve showed restricted localization within the descending trigeminal tract and nucleus. When compared to the distribution of the same fibers in the hagfish Eptatretus burgeri, another member of the cyclostomes, the distribution pattern in the lampreys studied was closer to the type seen in gnathostomes.

Animals↗

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↗

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↗