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K Shoumura

Publications and source records attributed to K Shoumura.

At least 19 recordsLinked to original sources

Marked miosis caused by deafferenting the oculomotor nuclear complex in the cat.

Animals show highly constricted pupils in certain conditions (e.g., coma). To know the anatomical basis for this miosis, mechanical separation of the oculomotor nuclear complex was done using four transections of the brain. Two frontal transections were placed rostral and caudal to the oculomotor nuclear complex. Two bilateral oblique transections were performed by aiming through the dorsal edge of the Edinger-Westphal nucleus at an angle of 50 degrees from the horizontal plane and vertical to the frontal plane. After the transections, we examined pupillary size for up to 2 weeks to exclude acute effects of deafferentiation. The transections were histologically examined. If the bilateral pupils were highly constricted after the transections, those pupils remained in the miotic state during the survival periods (4-14 days). The deafferented midbrain of the animals, which showed marked miosis, contained the intact oculomotor nuclear complex and nerves with the whole part of the midbrain ventral to them, but with only a small region dorsolateral to them. Given the previous finding that electrical microstimulation of the area ventral to the oculomotor nuclear complex and nerves has failed to elicit pupil constriction, our results suggest that the oculomotor nuclear complex itself could work as a generator for the strong activity of preganglionic pupilloconstrictor neurons.

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'In vivo perfusion Turnbull's reaction' for Fe(II) histochemistry in non-anoxic/non-ischemic and anoxic/ischemic cat brains.

We developed a simple but ingenious histochemical method, 'in vivo perfusion-Turnbull's reaction', for the visualization of non-heme Fe(II) of the brain; in situ release of Fe(2+) ions was coupled with formation of insoluble reaction product (Turnbull's blue) by in vivo perfusion of acid ferricyanide through the abdominal (non-anoxic/non-ischemic brain) or ascending (anoxic/ischemic brain) aorta in the deeply anesthetized adult cats. Frozen sections of the brain were treated according to the method of Nyguen-Legros et al. [12] to intensify Turnbull's reaction. The method revealed that cytoplasmic Fe(III) was reduced to Fe(II) in oligodendroglias in anoxic/ischemic (for 20 min) brains, and that Fe(II) was concentrated in the neuronal and glial cell nuclei regardless of the presence or absence of blood supply impairment.

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Intrastriatal targets of projection fibers from the central lateral nucleus of the rat thalamus.

We examined light and electron microscopically intrastriatal targets of projection fibers from the central lateral thalamic nucleus (CL), which is a major relay of cerebello-striatal projections. The study was done in the rat by combining the anterograde tract-tracing with immunohistochemistry for parvalbumin (PV); an anterograde tracer (biotin dextran amine: BDA) was injected into the CL. In the striatum, 91% of BDA-labeled axon terminals made asymmetrical synapses on PV immunonegative dendritic spines (assumed to be those of striatal projection neurons); only 0.5% of BDA-labeled axon terminals made synapses on PV immunopositive dendritic shafts. The remaining BDA-labeled axon terminals were in synaptic contact with PV immunonegative dendritic shafts. The results suggest that the cerebello-striatal projections through the CL predominantly access to striatal projection neurons, with only minor access to PV immunopositive (assumed to be GABAergic) interneurons in the striatum.

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A di-synaptic projection from the lateral cerebellar nucleus to the laterodorsal part of the striatum via the central lateral nucleus of the thalamus in the rat.

We have examined a cerebello-thalamo-striatal pathway from the lateral cerebellar nucleus (LCN) to the laterodorsal part of the striatum (LDS) through the central lateral nucleus (CL) using light and electron microscopy through the employment of a combination of anterograde and retrograde tracing techniques. Biotinylated dextran amine (BDA) was injected into the unilateral LCN, and used as an anterograde tracer. Cholera toxin B subunit (CTb), used for light microscopy, and wheat germ agglutinin-horseradish peroxidase (WGA-HRP), used for electron microscopy, were injected into the contralateral LDS as retrograde tracers. Light microscopic analysis showed a good overlap of the distribution of BDA-labeled axon terminals and CTb-labeled neurons in the middle third of the CL in both dorsoventral and rostrocaudal axes on the LDS injection side. Electron microscopy confirmed the presence of direct synaptic contacts between BDA-labeled terminals and WGA-HRP-labeled dendrites in the CL.

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Cornu Ammonis of the dog: a rudimentary CA2 field is only present in a small part of the dorsal division, and is absent in the ventral division of the cornu Ammonis.

The relationship between mossy fiber projections and cytoarchitecture was studied in the cornu Ammonis (CA) of three mongrel dogs and two Japanese white rabbits. Precise comparisons were accomplished by examining adjoining sections that were stained by two methods: 1) the Timm-Danscher method which stains for zinc, which is contained in high concentrations in the mossy fiber terminals, and 2) thionin staining of the Nissl substance, so that the mossy fiber projections and cytoarchitecture could be closely compared in each subdivision of the CA. There was a cytoarchitectonically transitional zone (TZ) between CA3 and CA1 in both dogs and rabbits. The TZ was composed of an intermingling of CA3-like large pyramidal cells and CA1-like small pyramidal cells. Across the dorso-ventral length of the rabbit CA, the mossy fiber projections emitted from the dentate granular cell layer extended as far as the distal border of CA3 toward the TZ but did not enter the TZ or CA1. The TZ of the rabbit was equivalent to CA2 of Lorente de Nó (1934), that was characterized by CA3-like large pyramidal cells which did not receive mossy fiber inputs. In the dorsal CA of the dog, the mossy fiber projections extended across the CA3/TZ border, as far as the most distal part of the TZ in one dog but only for a short distance in the other two dogs. That part of the TZ which did not receive mossy fiber projections corresponded with CA2. There were no mossy fiber projections to CA1. In the ventral CA of the dog, however, mossy fiber projections were more extensive than in the dorsal CA, extending across CA3/TZ as well as TZ/CA1 borders to enter the proximal part of CA1. These observations indicate that there is a distinct CA2 in the rabbit CA, and that a rudimentary CA2 is present only in a small part of the dorsal CA of the dog, whereas it is absent in the ventral CA.

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Lattice-like collagen fiber meshwork in the iris stroma of the cat: a possible mechanism to generate the tension directed towards the iris root which is required for pupillary dilatation in the sympathectomized eye.

NaOH digestion technique for collagen fiber dissection and scanning electron microscopy demonstrated a lattice-like meshwork in the anterior surface of the iris stroma of the cat. The mesh threads were made of collagen fibril bundles. In the constricted pupil, the meshes were square to rhomboid with the diagonals in the direction of the radius or circumference of the iris. In the dilated pupil, however, the meshes were strongly flattened rhomboid or ellipse with a longer diagnoal or axis in the circumferential direction. At the mesh corners facing the pupillary margin or the iris root, the collagen fibril bundles were strongly bent in the iris of the constricted pupil, while they were almost straight or slightly wavy in the iris of the dilated pupil. Accumulation of elasticity tension generated by this small distortion of the iris-mesh threads in the constricted pupil was considered to generate a tension directed towards the iris root, which is required for pupillary dilatation in the sympathectomized eye. On the posterior surface of the iris stroma, numerous thin pleats tightly woven with collagen fibrils traversed straightway through the radial length of the ciliary zone of the iris in both constricted and dilated pupils. The structural changes of these pleats in miosis and mydriasis were very small compared with the meshwork of the anterior aspect of the iris. Therefore, they were considered to work mainly as an iris skeleton.

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A di-synaptic projection from the superior colliculus to the head of the caudate nucleus via the centromedian-parafascicular complex in the cat: an anterograde and retrograde labeling study.

Centromedian-parafascicular (CM-Pf) complex of the thalamus receives inputs from the superior colliculus (SC). The CM-Pf neurons, in turn, project to the neostriatum. In order to establish a circuitry that the efferent terminals of SC neurons make direct synaptic contacts with thalamostriatal neurons in the CM-Pf complex, the anterograde tracer (biocytin) was injected into the unilateral SC and the retrograde tracer (wheat germ agglutinin conjugated to horseradish peroxidase, WGA-HRP) into the ipsilateral head of the caudate nucleus of the cat. The anterogradely labeled SC fibers and their terminals and retrogradely labeled CM-Pf neuronal elements were examined under light and electron microscope. At the light microscopic level, biocytin-labeled terminal-like varicosities were observed densely in the latero-dorsal part of the CM and the dorsal part of the Pf lateral to the fasciculus retroflexus. These varicosities were often in close proximity to HRP-labeled somata and dendrites of CM-Pf neurons. Electron microscopic analysis revealed that the biocytin-labeled synaptic boutons contained mainly round synaptic vesicles and established asymmetrical synaptic contacts with retrogradely labeled thalamostriatal neuronal elements, including perikarya, and small and large dendrites. In addition, anterogradely labeled terminals made synaptic contacts with unlabeled somata, small and large dendrites, and spines as well as profiles containing synaptic vesicles. These vesicle-containing profiles were considered to be pre-synaptic elements contacting on thalamostriatal neurons or the vesicle-containing dendrites of local circuit neurons. These results demonstrate that the neurons of the CM-Pf complex of the thalamus is involved in a di-synaptic tecto-striatal circuit.

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Anisocoria--a pupillary sign of hippocampal lesions: an experimental study in the cat by using neurotoxins.

Pupillary inequality developed after unilateral lesions of the hippocampal formation (HF) of the cat. Lesions were made by an injection of a small amount of colchicine, ibotenic acid or kainic acid. In all anisoric cats, the pupil on the side of the lesions was invariably smaller than its partner. Evident pupillary inequality developed in the cats with dorsal HF lesions. Although there was a considerable variation in the extent and the location of lesions among these cats, the involvement of the giganto-pyramidal CA 3-2 appeared very responsible for the development of the pupillary sign. However, an evidently anisoric cat hat a lesion affecting only the prosubiculum and the subiculum in the posterior part of the dorsal HF. Despite a large involvement of CA 3-2 with or without coincident injuries to CA1, the prosubiculum and the subiculum, only slight pupillary inequality developed following ventral HF lesions. Evident anisocoria in the cats with large dorsal HF lesions disappeared after bilateral cervical sympathectomy, implying that the asymmetry of sympathetic nervous activity might be critically involved in the development of the pupillary sign. The hippocampo-spinal pathway relayed by the lateral septal nucleus and, then, by the lateral hypothalamic area to terminate in the intermedio-lateral cell column of the spinal cord was considered to be most concerned with anisocoria caused by HF lesions.

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Cornu ammonis of the cat: lack of a separate field of CA2.

Close comparison of Timm or Nissl stained adjoining sections of the cat cornu Ammonis (CA) disclosed the lack of a separate CA2 field, which was defined as a field of CA characterized by giant pyramids similar to those of CA3 and by absence of mossy fiber inputs in mice, rats, monkeys and humans. In the cat CA, mossy fiber terminals stained by Timm's method filled the hilar region (CA4) of the dentate gyrus and extended through the stratum pyramidale and/or stratum lucidum of the giant pyramidal part of CA as far as the border with CA1, which was clearly delineated by sudden appearance of smaller pyramids. Thus, there was no separate giant pyramidal field devoid of mossy fiber inputs in the cat CA. Unlike other mammals, some parts of CA1 also received mossy fiber projections in the cat.

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Quantitative electromicroscope study of the oculomotor parasympathetic neurons projecting to the ciliary ganglion in cats: comparison of the synaptic (axon-somatic and axo-proximal dendritic) organization of anterior-dorsal and ventral cell groups.

The synaptic organization of the oculomotor parasympathetic preganglionic neurons (OPNs), labeled retrogradely after a horseradish peroxidase (HRP) injection into the ciliary ganglion, was studied in cats by electron microscopy. We divided the OPNs into two groups, anterior-dorsal (ADG) and ventral (VG) cell groups, based upon physiological studies in cats suggesting that accomodation-related OPNs are predominantly located anterior and dorsal to the somatic nuclei of the oculomotor nuclear complex (i.e., the anteromedian and Edinger-Westphal nuclei, and the ventral central gray area), while pupillo-constriction-related OPNs are predominantly located ventral to the somatic nuclei (i.e., the ventral tegmental area). The synaptic organization of these two groups was quantitatively compared, using a nested analysis of variance to determine statistical significance (P < 0.05). Partial reconstructions of the labeled somata and proximal dendrites were made from tracings of electron micrographs of every 2nd section in serial ultrathin sections that included the nucleolus or were adjacent to sections that included the nucleolus. The mean number of boutons of apposition on a reconstructed labeled soma of VG was significantly greater than that of ADG (mean +/- SD; ADG, 5.3 +/- 3.3; VG, 8.6 +/- 3.2). The mean synaptic density on a VG soma was significantly greater than on an ADG soma (mean +/- SD; ADG, 3.74 +/- 2.11 counts/100 microns2; VG, 6.30 +/- 1.99 counts/100 microns2). The mean synaptic covering ratio on a VG soma was significantly greater than on an ADG soma (mean +/- SD; ADG, 5.21 +/- 2.91%; VG, 10.14 +/- 3.76%). The mean estimated number of boutons of apposition on a VG soma was significantly greater than on an ADG soma (mean +/- SD: ADG, 53 +/- 36; VG, 100 +/- 48). Boutons were classified on the basis of the shape of their synaptic vesicles as S-type (containing spherical clear synaptic vesicles) or P-type (containing both flattened and spherical clear synaptic vesicles). The significantly greater than on an ADG soma (mean +/- SD; ADG, 0.31 +/- 0.20; VG, 0.67 +/- 0.18). The differences demonstrated in this study reinforce, morphologically, the assumption of functional localization of OPNs, and further allow us to estimate the relative characteristics of the synaptic organization of accommodation-related OPNs and pupillo-constriction-related OPNs.

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Functional and anatomical fiber analysis of the posterior commissure (PC) in the cat: evidence for PC fibers of which stimulation elicits non-oculosympathetic pupillary dilation.

Pupillary responses were studied by electrical stimulation of the posterior commissure (PC) and the nuclei of origin and termination of PC fibers in the cat. Prior to stimulation experiments, cervical sympathectomy was carried out to study the pupillary responses not mediated by the ocular sympathetic nerve. Pupillary responses were recorded by using an infrared pupillo-analyzing system. The stimulus consisted of a 5 s train of cathodal square wave (0.5 ms duration, 50 Hz) pulses. Stimulation of the PC evoked a pupillary response complex (PRC), which began with a rapid pupillary constriction after the latency of 210-317 ms. The threshold of constriction was 10 or 20 microA. Constriction reached its peak shortly after the onset of the stimulus, then the pupil gradually re-dilated (pupillary escape, PE) even though the stimulus was still lasting. The pupil gradually returned, after stimulus termination, to the size before stimulation in the cases with the pupil area before stimulation larger than 20 mm2. On the other hand, in the cases with smaller pupil area before stimulation (< 20 mm2), rapid constriction and PE were followed, after stimulus termination, by a large dilation (after-dilation, AD). The thresholds of PE and AD were 20 or 40 microA. Pupillary constriction was evoked with a large range of stimulus frequency (1-100 Hz). To evoke PE and AD, stimulus frequencies of 10 and 50 Hz were required respectively, and lower frequencies were ineffective. The peak latency of AD increased in proportion to the increase in stimulus frequency and intensity. Following horseradish peroxidase (dissolved in 5% alkyl-phenol ethylene oxide) injection into the pretectal region where fibers from the PC fan out, retrogradely labeled neurons occurred in many subthalamic, pretectal and midbrain nuclei on the other side. They were classified into three groups in terms of the pupillary response evoked by electrical stimulation; the pupillo-constrictory nuclei (PCNs) of which stimulation evoked constriction with the threshold of 20 microA, the pupillo-dilatory nuclei (PDNs) of which stimulation evoked dilation with the threshold of 20 or 10 microA, and other nuclei with higher thresholds of constriction or dilation. The PDNs were further, classified into two groups (Type 1 and Type 2 PDNs) according to the relationship between stimulus intensity and the peak latency of dilation.(ABSTRACT TRUNCATED AT 400 WORDS)

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Neural mechanisms of pupillary abnormality following thalamic lesions: experimental lesion and stimulation studies in cats, and consideration of pupillary findings in thalamic vascular lesions.

Neural mechanisms of the pupillary abnormality in thalamic lesions were experimentally studied in cats. Moderate to considerable anisocoria appeared after kainic acid lesions involving the medial thalamus. The pupil on the side of the lesion was larger than its partner. Only subtle or no pupillary inequality was produced by lateral thalamic lesions. Electrical stimulation of the midline and medial thalamus evoked dilation bilaterally in sympathectomized pupils. Thus, pupillary dilation produced by stimulation of the thalamus was shown to be mediated in part by the oculomotor parasympathetic nerve (OPN). There was no threshold difference between ipsilateral (ipsi) and contralateral (contra) pupils. However, amplitude of dilation was significantly larger in the contra pupil than in the ipsi, when stimulus was given to the pupillo-dilatory medial thalamic nuclei. In these, the mediodorsal, parataenial, central dorsal, paracentral (Pc), and parafascicular nuclei and the medial division of the medial pulvinar nucleus were included. Pupillary dilation mediated by the ocular sympathetic nerve (OSN) was investigated by stimulating Pc and comparing the ipsi-contra difference in the amplitude of dilation between sympathectomized and non-sympathectomized pairs of pupils. In contrast to the results in sympathectomized pairs, there was no ipsi-contra difference in the amplitude of dilation or it was larger in the ipsi pupil in non-sympathectomized pairs. From these, it was inferred that stimulation of Pc activated OSN ipsilaterally or bilaterally with ipsi dominance. It was concluded that the medial and midline thalamus exerts pupillo-dilatory effects through a set of neural mechanisms; 1) ipsi-dominant bilateral OPN inhibition, and 2) ipsi or ipsi-dominant bilateral OSN activation. Neural mechanisms of the pupillary abnormality in thalamic vascular lesions were also considered.

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Properties of the pupillary dilation produced by the humoral factor in the pupillary reflex dilation: an experimental study in the cat.

Physiopharmacological properties of the pupillary dilation produced by the humoral factor in the reflex pupillary dilation were studied in cats anesthetized with ketamine-HC1. Pupillary dilation produced by the humoral factor was separated from that produced by the neural mechanism, ie, sympathetic activation and parasympathetic inhibition, by atropinization of acutely sympathectomized pupil. To evoke the pupillary reflex dilation, the sciatic nerve was stimulated by using a bipolar electrode. The stimulus consisted of trains of 0.5 milliseconds duration rectangular pulses and was given for 5 seconds. The stimulus frequency was usually 50 Hz; high frequency stimuli were more effective to evoke pupillary dilation produced by the humoral factor. The pupillary dilation was recorded with an infrared pupillo-analyzing system. A long latency (about 6 seconds) and long peak latency (about 10 seconds) pupillary dilation was produced by the humoral factor. The threshold of pupillary dilation produced by the humoral factor was always higher than that produced by parasympathetic inhibition. The pupillary dilation produced by the humoral factor was not affected by local application and intravitreal injection of 10(-2) M propranolol-HC1 and 10(-2) M yohimbine-HC1. However, the dilation was markedly inhibited by intravitreal injection of 10(-2) M phenoxybenzamine-HC1 or local application of 10(-2) M bunazosin-HC1.

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Posterior commissural connections of area pretectalis and neighboring structures in cat, with special reference to pupilloconstrictory pathway via posterior commissure.

The overall distribution of posterior commissural connections of the area pretectalis and the neighboring structures was studied in the cat, by the methods of anterograde fiber degeneration and retrograde axonal transport of horseradish peroxidase (HRP). After a localized lesion was made within the posterior commissure, dense degenerated terminals were distributed in the most rostral part of the nucleus pretectalis posterior, the nucleus of posterior commissure, the interstitial nucleus of Cajal, and the central tegmental field. A medium amount of degenerated terminals were observed in the nucleus pretectalis anterior (pars reticularis), the dorsal part of the periaqueductal grey at its most rostral levels, the caudolateral parts of the nucleus pretectalis posterior and the nucleus of optic tract, the H field of Forel, parts of the somatic cell columns of the oculomotor nucleus and the trochlear nucleus. A small amount of degenerated terminals were seen in the ventromedial part of the caudal periaqueductal grey, the ventral lateral geniculate nucleus and the zona incerta. However, the amount of degenerated terminals was very small in the nucleus pretectalis medialis and the nucleus pretectalis olivaris. Following an HRP (dissolved in 5% alkyl-phenol ethylene oxide) injection into the unilateral area pretectalis where fibers of the posterior commissure fan out, retrogradely labeled cells were observed in all of the above described (posterior commissural fiber recipient) regions of the pretectal and neighboring structures, with the exception of the somatic cell columns of the oculomotor nucleus and the trochlear nucleus. The number of labeled cells appeared roughly proportional to the amount of degenerated terminals of the posterior commissural fibers described above with the apparent exception of the nucleus pretectalis anterior, pars reticularis, where only a few labeled cells were identified. The findings were discussed with special reference to the pupilloconstrictory pathway via the posterior commissure.

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Pupillary responses evoked by electrical stimulation of area pretectalis in cats.

Pupillary responses evoked by electrical stimulation of the area pretectalis and neighboring midbrain structures were studied in the cat. The pupillary responses evoked were recorded using an infrared pupilloanalyzing system. Bilateral pupillary constriction was evoked with a low threshold current intensity by stimulation of the nucleus pretectalis medialis, nucleus pretectalis olivaris, rostral part of the nucleus pretectalis posterior, the most rostral part of the periaqueductal grey and the nucleus of posterior commissure. Bilateral pupillary dilation was induced with a low threshold current intensity by stimulating the nucleus pretectalis anterior, caudal periaqueductal grey and the midbrain tegmentum. The effects of changing stimulus intensity and stimulus frequency were also studied.

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Pupillo-motor areas in the rabbit visual cortex.

Pupillo-motor areas in the visual cortex of the rabbit were studied. Electrical stimulation of the rabbit visual cortex induced pupillary constriction or dilation. The low threshold area (0.5-1.0 mA) for pupillary dilation was in the form of a narrow band extending rostro-caudally along the boundary between the striate cortex (VI) and the occipital cortex (VII), where the binocular area of the visual field is represented. The pupillo-constrictory cortical points were also identified in the caudal part of the splenial gyrus (lateral part) and the pupillo-dilator points in the rostral part of the gyrus (lateral part).

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Afferents to the cortical pupillo-constrictor areas of the cat, traced with HRP.

Afferents of the cortical pupillo-constrictor areas (PCAs) of the cat were studied using the horseradish peroxidase method. PCAs receive heavy cortical inputs from areas 7, 19, 21, the lateral suprasylvian area, the splenial visual area, and subcortically from the claustrum, the intralaminar nuclei, the pulvinar-lateral posterior nuclear complex.

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