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J Hamori

Publications and source records attributed to J Hamori.

At least 19 recordsLinked to original sources
PubMed2000

Distribution of Eisenia tetradecapeptide immunoreactive neurons in the nervous system of earthworms.

A detailed mapping of Eisenia-tetradecapeptide-immunoreactive neurons in the central and peripheral nervous system combined with quantitative morphological measurements was performed in Eisenia fetida and Lumbricus terrestris. In Eisenia, most labelled neurons were observed in the ganglia of the ventral cord (20.38% of the total cell number of the ganglion) and 15.67% immunoreactive cells occurred in the brain, while 6% of the neurons could be shown in the subesophageal ganglion. In the case of Lumbricus, most immunoreactive cells were found in the subesophageal ganglion (16.17%) and in the ventral ganglia (12.54%). The brain contained 122 ETP-immunoreactive cells (5.6%). The size of the immunoreactive cells varied between 35-75 microm. A small number of Eisenia-tetradecapeptide immunoreactive fibres were seen to leave the ventral ganglia via segmental nerves, and labelled processes could also be observed in the stomatogastric system and the body wall. Labelled axon branches originating from the segmental nerves formed an immunoreactive plexus both between the circular and longitudinal muscle layer and on the inner surface of the longitudinal muscle layer. This inner plexus was especially rich in the setal sac. Among the superficial epithelial cells the body wall contained a significant number of immunoreactive cells. Only a few Eisenia-tetradecapeptide immunoreactive neurons and fibres occurred in the stomatogastric ganglia. In the enteric plexus the number of immunoreactive neurons and fibres decreased along the cranio-caudal axis of the alimentary tract. Eisenia-tetradecapeptide immunoreactive cells were also present among the epithelial cells in the alimentary canal. Some of these cells resembled sensory neurons in the foregut, while others showed typical secretory cell morphology in the midgut and hindgut.

Animals↗
PubMed1996

Immunocytochemical visualization of the mGluR1a metabotropic glutamate receptor at synapses of corticothalamic terminals originating from area 17 of the rat.

Pre-embedding immunogold histochemistry was combined with Phaseolus vulgaris leucoagglutinin anterograde tract tracing in order to analyse the relationship between the subcellular localization of the GluR1a metabotropic glutamate receptors and the distribution of corticothalamic synapses in the dorsal lateral geniculate nucleus (dLGN) and the lateral posterior nucleus (LP) of the rat. The injection of the tracer into area 17 labelled two types of corticothalamic terminals: (i) the small boutons constituting the majority of the labelled fibres which form asymmetrical synapses both in the dLGN and LP; and (ii) the giant terminals typically participating in glomerulus-like synaptic arrangements and found exclusively in the lateral posterior nucleus. The small corticothalamic terminals often established synapses with mGluR1a-immunopositive dendrites, with immunometal particles concentrated at the periphery of their postsynaptic membranes. In contrast, the synapses formed by giant boutons in the lateral posterior nucleus were always mGluR1a-immunonegative. We conclude that the corticothalamic fibres forming the small synaptic terminals are the most likely candidates for the postulated mGluR-mediated modulation of visual information flow by corticothalamic feedback mechanisms.

Animals↗
PubMed1990

Morphological plasticity of postsynaptic neurones in reactive synaptogenesis.

Partial deafferentation of certain brain regions (septal nuclei, hippocampus, etc.) in adult animals results (1) in the disappearance of degenerating axon terminals and (2) in the short-term persistence of vacant postsynaptic sites. These postsynaptic sites have been shown to be re-supplied by sprouted axon terminals of intact axons. This paper will demonstrate that, in brain regions (e.g. cerebellar cortex, lateral geniculate nucleus) where axonal sprouting of local elements or of persisting afferent axons is negligible or absent, synaptic reorganization involves the active participation of postsynaptic dendritic and somatic elements of surviving local nerve cells. Synaptic regeneration can be demonstrated by morphological means both in developing and in adult central nervous system. The dendrites may show two types of response to deafferentation: (1) the formation of presynaptic specializations along their otherwise 'classical' postsynaptic membrane (the axonization of dendrites) resulting in the formation of new, dendrodendritic synapses, and (2) the 'adaptive' (structural) reduction in size ('atrophy') of the denervated nerve cell dendritic arborization, leading to a relative increase in density of the surviving (though non-sprouting) afferent axon terminals. In both cases a partial functional recovery can be demonstrated.

Animals↗
PubMed1990

Morphological plasticity of dendrites in adult brain.

Deafferentation of certain brain regions in adult animals results in (1) the disappearance of degenerating axon terminals and (2) in the temporary persistence of vacant postsynaptic sites. These postsynaptic sites were shown to be re-supplied by sprouted axon terminals of intact axons. It is described in this paper, that in brain regions (e.g. cerebellar cortex, lateral geniculate nucleus) where axonal sprouting of local elements or of persisting afferent axons is negligible or absent, synaptic reorganization occurs via the active participation of postsynaptic dendritic and somatic elements of surviving local nerve cells. The dendrites may develop two types of reaction upon deafferentation (1) formation of presynaptic specializations along their otherwise "classical" postsynaptic membrane, resulting in the formation of new, dendro-dendritic synapses and (2) the "adaptive" (structural) reduction in size of denervated nerve cell dendritic arbor, leading to a relative increase in density of the surviving (though non-sprouting) afferent axon terminals. A partial functional recovery in both cases is also demonstrated.

Afferent Pathways↗
PubMed1988

The orientation of interneurones in the dorsal lateral geniculate nucleus of the rat: a quantitative study.

The orientation of the processes of 60 Golgi-impregnated interneurones in the rat dorsal lateral geniculate nucleus (dLGN) was studied quantitatively. A statistical analysis of the orientation of 238 interneuronal processes (dendrites and axon-like processes) showed that they were aligned preferentially along a dorsoventral axis through the dLGN and were predominantly oriented parallel with the outlying optic tract. Computer reconstructions of two of the Golgi-impregnated dLGN interneurones and their subsequent 3-dimensional computer rotations showed that their processes ramified in long columnar-shaped territories aligned dorsoventrally. There was little extension of these processes along the rostrocaudal axis of the nucleus. The data of this investigation provide evidence that the processes of 'inhibitory' interneurones in the rat dLGN are predominantly aligned along the dorsoventral axis, parallel with both the optic tract and with the afferent and efferent fibre tracts coursing through the nucleus.

Animals↗
PubMed1987

Alteration of mouse cerebellar circuits following methylazoxymethanol treatment during development: immunohistochemistry of GABAergic elements and electron microscopic study.

Methylazoxymethanol (MAM) injected postnatally affects cerebellar development in mice. A single injection at the fifth postnatal day produces hypogranular cerebella whereas a single injection at birth produces, in addition, a disorderly cytoarchitecture of the folium and alteration of Purkinje cell positioning (Bejar et al.: Exp. Brain Res. 57:279-285, '85). In the present study we have used immunohistochemistry with anti-GABA immune serum and electron microscopy to further characterize these alterations. In addition to the already-described nonoccupied dendritic spines of Purkinje cells both in mice injected the day of birth and or at the fifth postnatal day, we have observed, in animals injected at birth, the absence of pericellular baskets around Purkinje cells and the presence of heterologous synapses between mossy fibres and Purkinje cell dendrites. These heterologous synapses apparently disappear after postnatal day 20. By using an appropriate timing of MAM injection, different types of hypogranular cerebella, phenocopies of different mutants, can be obtained in large enough number to carry out extensive biochemical studies at each developmental age.

Animals↗
PubMed1987

A quantitative study of morphological reorganization following chronic optic deafferentation in the adult cat dorsal lateral geniculate nucleus.

Neuronal and synaptic reorganization in the lateral geniculate nucleus (dLGN) of adult cats following chronic visual deafferentation has been investigated with the aid of GABA immunocytochemistry and quantitative electron microscopy. The main purpose of this study was to establish the morphological counterpart of the functional plasticity of dLGN relay cells after total visual deafferentation (Eysel: Brain Res. 166:259-271, '79). The results provide evidence that the regained excitability of relay cells is not the result of disinhibition (caused hypothetically by the selective loss of GABAergic cells) since the proportion of GABA-positive and GABA-negative cells as well as the inhibitory synaptic density did not change. The alternative suggestion that the enhanced excitability could be the result of compensatory axonal sprouting by corticothalamic fibers had also to be dropped: the absolute number of corticothalamic axons to the deafferented dLGN remains unchanged. Because of shrinkage of the dendritic trees of dLGN neurons, however, the density of cortical synaptic input at dLGN cells becomes elevated by almost 60%. It is suggested that the regained excitability of relay neurons is the consequence of the combined effects of adaptive (structural) reduction in size ("atrophy") of retinally denervated nerve cells, and, as a consequence, increase of input resistance, reduced shunting effects, and relative increase in density of the excitatory cortical input per neuron.

Animals↗
PubMed1986

GABA-immunoreactive neurons in the rat cerebellum: a light and electron microscope study.

An antibody raised against gamma - amino-butyric acid (GABA) coupled to bovine serum albumin with glutaraldehyde (Hodgson et al: J. Histochem. Cytochem. 33:229-239, '85) was used to localise immunocytochemically the presumptive GABAergic neuronal elements in the cerebellar cortex of the adult rat. employing the unlabelled antibody enzyme method with pre- and post-embedding immunocytochemical procedures, the following cellular structures were observed to be GABA-immunopositive in both the light and electron microscopes: the somata, dendrites, and axonal processes (including axon terminals) of stellate, basket, and Golgi neurons. In immunopositive neuronal somata and dendrites, the reaction product was found to be associated with all intracellular organelles and with the postsynaptic densities of synaptic junctions. Specific GABA-like immunoreactivity was also seen around outer mitochondrial membranes, microtubules, and neurofilaments, and coating synaptic vesicles in presynaptic axon terminals. In the pre-embedding procedure with dilutions of the antiserum between 1:1,000 and 1:2,000, the perikarya and dendrites of Purkinje cells were GABA-immunonegative, whereas at an antiserum dilution of 1:500 the somata of Purkinje cells were mildly GABA-immunoreactive. Purkinje cell axon terminals in the infra- and supraganglionic plexuses and in the deep cerebellar nuclei were always strongly immunopositive. Neuroglia were invariably GABA-immunonegative, as were the dendrites, axons (parallel fibres), and somata of granule cells. Mossy fibre and climbing fibre afferents were also immunonegative. The pattern of immunoreactivity obtained with this antiserum directed against the inhibitory neurotransmitter GABA was found to resemble closely the immunocytochemical distribution of GABA and of the GABA-synthesizing enzyme glutamic acid decarboxylase (GAD) as reported previously in other immunocytochemical investigations (Oertel et al. and Wu et al: Cytochemical Methods in Neuroanatomy. New York: A. R. Liss, '82; Seguela et al: Neuroscience 16:865-874, '85; Mugnaini and Oertel: GABA and Neuropeptides in the CNS. Handbook of Chemical Neuroanatomy, Vol. 4, Part I. Amsterdam: Elsevier, '85.

4-Aminobutyrate Transaminase↗
PubMed1986

gamma-Aminobutyric acid immunoreactivity in mouse barrel field: a light microscopical study.

The barrel field of the mouse somatosensory cortex (SmI) was investigated immunocytochemically using an antiserum against the inhibitory neurotransmitter gamma-aminobutyric acid (GABA). GABA-immunopositive cells and processes are grouped largely in the barrel side, whereas the barrel hollow is only weakly immunostained. The GABA-immunopositive cells have an ellipsoidal appearance similar to that of non-pyramidal class II barrel neurones described previously in Golgi impregnation studies of the mouse and rat barrel field.

Animals↗
PubMed1985

GABA-immunoreactive neurons in the rat dorsal lateral geniculate nucleus: light microscopical observations.

The dorsal lateral geniculate nucleus (dLGN) of the rat was investigated immunocytochemically using an antiserum against the inhibitory neurotransmitter gamma-aminobutyric acid (GABA). The appearance of GABA-immunopositive dendrites, dendritic appendages, and the size and shape of neuronal somata closely resembled the putative intrinsic neurons described previously in Golgi-impregnation studies of the rat dLGN.

Animals↗
PubMed1985

[Histological changes in the somatosensory thalamus after unilateral coagulation of vibrissa follicles of the muzzle of the newborn mouse].

Light microscopic study of the thalamic ventro-basal complex (VB), after unilateral coagulation of vibrissae follicles in newborn mouse, revealed an excess of neuronal perikarya on the controlateral "deafferented" side as compared to the normal side. The higher density of nerve cells was confined to the vibrissal relay in the medial part of VB nucleus (VBm), whereas the cell number in the non vibrissal-lateral part of this nucleus (VB1) remained on the control level. Electron microscopic investigation of the thalamic vibrissal relay has shown signs of a modified synaptogenesis on the "deafferented" side: (a) the number of specific afferents has diminished and in contrast to the normal side, most of the specific sensory terminals contain small spheroid synaptic vesicles and (b) the number of axon terminals with ovoid pleomorphic vesicles has been doubled.

Afferent Pathways↗