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Query: UNIPROT:P50583 (asymmetrical)
 12,197 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

GABAergic neuronal profiles in the supraoptic nucleus of the rat were immunohistochemically identified by using a purified GABA antibody with the peroxidase-antiperoxidase method. The localization of GABA-like immunoreactivity in nerve terminals on the neurosecretory neurons was examined electron microscopically. A few small GABAergic neurons were found inside the supraoptic nucleus while only a very few medium-sized ones were detected in the perinuclear zone. Intrinsic, non-GABAergic small neurons covered by GABAergic neuropil were also detected. The neuropil with GABAergic axo-somatic synapses evenly encompassed unlabeled neurosecretory perikarya throughout the supraoptic nucleus. The GABAergic system seems to inhibit both vasopressin and oxytocin cells. In this area, glia cells showed clear outlines of unlabeled somata around counter-stained nuclei. Blood capillaries in the supraoptic nucleus were only slightly covered with a GABAergic neuropil. Electron microscopic observations demonstrated the presence of GABAergic axo-somatic symmetrical and axo-dendritic asymmetrical synapses on the neurosecretory neurons. GABA-like immunoreactivity was localized on the membranes of microtubules and synaptic vesicles, on the external membranes of the mitochondria, and on the inner leaf of the presynaptic sites. Numerous pairs of non-immunoreactive synapses were arranged along these immunoreactive synapses.
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PMID:Immunohistochemical studies on the GABAergic system in the rat supraoptic nucleus using the PAP method with an application of electron microscopy. 355 72

Retinorecipient regions of the ventral lateral geniculate nucleus of the thalamus and the superior colliculus of the midbrain are linked by reciprocal axonal projections. In this study we have investigated the ultrastructural characteristics, the distribution, and the postsynaptic targets of the terminals of axons projecting to the ventral lateral geniculate nucleus from the superior colliculus. Horseradish peroxidase was injected into the superior colliculi of adult albino rats, and the Hanker-Yates method was used to visualize anterogradely and retrogradely transported peroxidase in the ventral lateral geniculate nuclei 24 hours following the injection. Labelled terminals were found in the lateral and ventrolateral parts of the external division of the ipsilateral ventral lateral geniculate nucleus. The labelled terminals were confined to areas of simple, nonglomerular neuropil. They were 0.45-1.5 micron in diameter; contained small, dark mitochondria and spherical synaptic vesicles; and established Gray type I (asymmetrical) synaptic contacts with the dendritic shafts, dendritic spines, and occasionally cell bodies of cells with the ultrastructural characteristics of projection cells. A few labelled terminals established synaptic contact with retrogradely labelled cells. Thus, in the rat, the projection from the superior colliculus gives rise to a uniform population of axon terminals in the nonglomerular neuropil of the lateral portion of the ventral lateral geniculate nucleus, which synapse with, and are probably excitatory to, geniculocollicular and other projection cells.
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PMID:Ultrastructural organisation of the projection from the superior colliculus to the ventral lateral geniculate nucleus of the rat. 357 17

The synaptic organization of three kinds of afferent projections in the feline anterior pretectal nucleus (PTA) was analyzed by a combination of the degeneration and retrograde transport of horseradish peroxidase (HRP) techniques, along with that of the degeneration and anterograde transport of HRP techniques. Retrograde labeling of PTA neurons was performed by injections of HRP in the dorsal accessory olivary nucleus (DAO). Three kinds of afferent sources of the PTA--the cerebral motor cortex, the anterior interpositus nucleus of the cerebellum, and the gracile nucleus--were subjected to electrolysis, suction, or injection of kainic acid or HRP for identification of axon terminals of each system. Axon terminals of these different afferent sources identified by degeneration or anterograde HRP transport techniques showed similar morphological features: They were relatively large (1-6.5 microns in diameter), contained round or ovoid synaptic vesicles, and made asymmetrical synaptic contacts. When the degeneration study was combined with the retrograde HRP transport technique, some degenerating terminals from the motor cortex, anterior interpositus, or gracile nuclei were found to synapse directly with HRP-labeled dendrites or somata of the PTA neurons projecting to the DAO. Each combination of the degeneration and anterograde HRP transport techniques revealed the fact that neither degenerating nor HRP-labeled terminals were found to synapse with the same neuronal structure. These observations indicate that the PTA neurons relay afferent inputs from three different sources directly to the DAO, and that there is a possibility of parallel processing rather than convergence of three different afferent systems via the PTA to the DAO.
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PMID:An ultrastructural analysis of afferent terminals to the anterior pretectal nucleus in the cat. 358 60

The synaptic organization of the feline entopeduncular nucleus was studied electron microscopically. After horseradish peroxidase injections into the ventral anterior and ventral lateral nuclear complex of the thalamus, normal axon terminals synapsing with entopedunculothalamic projection neurons were classified into four types on the basis of the size and shape of synaptic vesicles in them, and types of the postsynaptic membrane differentiation. Type I and type II axon terminals were characterized by symmetrical synaptic contacts, and large ovoid or small ovoid synaptic vesicles, respectively. Type II axon terminals were further classified into two subtypes as to their sizes: one was small (IIa), the other large (IIb). Type III and type IV axon terminals were characterized by asymmetrical synaptic contacts, and large ovoid or small ovoid synaptic vesicles, respectively. To determine the origin of each type of terminal, electrolytic lesions of the caudate nucleus or the subthalamic nuclear region were combined with horseradish peroxidase injections into the thalamus or the subthalamic nuclear region. After electrolytic lesions of the caudate nucleus, degeneration was seen in type I axon terminals contacting entopedunculothalamic projection neurons. Following electrolysis or horseradish peroxidase injection into the subthalamic nuclear region, type IIa and type IV axon terminals showed degenerations or horseradish peroxidase labelling. Such terminals also synapsed with entopedunculothalamic projection neurons. It was demonstrated that these projection neurons relay the striatal or subthalamic inputs directly to the thalamus. After horseradish peroxidase injection into the thalamus, many labelled type II axon terminals were observed to synapse with entopedunculothalamic projection neurons. Type III axon terminals were left unchanged throughout these experiments. In addition, the entopeduncular neuron was observed to receive convergent inputs from both the caudate nucleus and probably the subthalamic nucleus. Axoaxonal synapses were also found to be involved in the synaptic triad. These results indicate that type I axon terminals originate from the caudate nucleus, part of type IIa and type IV axon terminals originate from the subthalamic nucleus or caudal to the subthalamic nuclear region, and part of type IIa and type IIb terminals come from intrinsic axon collaterals.
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PMID:Synaptic organization of the cat entopeduncular nucleus with special reference to the relationship between the afferents to entopedunculothalamic projection neurons: an electron microscope study by a combined degeneration and horseradish peroxidase tracing technique. 360 Oct 64

This anterograde horseradish peroxidase study examines the morphology and synaptic connections of a population of primary axons which terminate in the dorsal one-half of the border zone (BZ) of rat trigeminal nucleus oralis. Unmyelinated parent fibers in the spinal V tract enter BZ directly and each terminate by continuing as a sparsely branched, long caudally directed strand containing several axonal endings. Primary endings lie in glomeruli where each forms an asymmetrical synapse on a central dendrite. Other glomerular components include two types of non-primary endings. One contains flattened synaptic vesicles, and forms a symmetrical synapse on either the primary ending or the central dendrite, while the other contains pleomorphic synaptic vesicles and establishes a symmetrical synapse on the central dendrite.
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PMID:Morphology and synaptic connections of unmyelinated primary axons in the border zone of rat trigeminal nucleus oralis. 377 35

The anterograde transport of horseradish peroxidase (HRP) was used to examine the morphology and synaptic connections of a morphologically distinct group of small-diameter primary trigeminal axons that arborize throughout the border zone (BZ) of rat trigeminal nucleus oralis. Thinly myelinated parent branches (0.75-1.5 micron in diameter) descending in the spinal V tract (SVT) were seen to issue medially directed collaterals that entered BZ, where they branched and eventually terminated by giving rise to thin terminal strands characterized by several relatively widely spaced axonal endings. Based on the size and morphology of the parent branches in SVT, in the root entry zone, and in the sensory root of the trigeminal nerve, these primary axonal (P) endings are considered to be derived from small-diameter myelinated primary trigeminal axons (SDMA). The P endings measured 1-2 micron in diameter and contained numerous agranular spherical (40-60 nm) synaptic vesicles. In the BZ neuropil, most P endings lay in glomeruli, where each formed at least one asymmetrical axodendritic synapse on a dendritic shaft. It is at these synapses that this group of primary axons is thought to transfer its input directly to the dendritic arbors of BZ neurons. A small (0.5-1.5 micron) axonal (F) ending filled with flattened synaptic vesicles (29 X 60 nm) was observed to form at least one symmetrical to intermediate axoaxonic synapse on the P ending, as well as at least one axodendritic synapse on the same dendritic shaft receiving the primary input. Some F endings only contacted dendritic shafts. In view of their symmetrical to intermediate synaptic contacts, F endings are thought to belong to axons derived from at least one source that can inhibit or diminish the firing rate of BZ neurons in response to SDMA input. This would be accomplished either postsynaptically through the axodendritic synapses on the dendritic shafts, and/or presynaptically through the axoaxonic synapses on the P endings.
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PMID:Morphology and synaptic connections of small myelinated primary trigeminal axons arborizing among neurons in the border zone of rat trigeminal nucleus oralis. 380 36

This study demonstrates the termination of ascending tract of Deiters' (ATD) axons on ipsilateral medial rectus (MR) motoneurons. Horseradish peroxidase (HRP) was iontophoretically injected into ATD axons which were recorded in the MR motoneuron pool of the oculomotor nucleus. MR motoneuron cell bodies were identified by retrograde transport of HRP injected into MR muscles in the orbit. ATD axons were identified by Type I responses to horizontal rotation, monosynaptic responses on stimulation of the ipsilateral labyrinth, and no response on contralateral labyrinth or contralateral abducens nucleus or on ipsilateral MR nerve stimulation. Light microscopic examination showed the main stem axons to be lateral to the medial longitudinal fasciculus, and terminal boutons were in contact with ipsilateral identified MR motoneurons (Furuya and Markham: Exp. Brain Res. 43: 289-303, 1981). Light microscopy and semi-thin sections showed boutons of ATD in contact with identified MR motoneuron cell bodies and proximal dendrites. The electron micrographs (EM) showed the HRP-injected ATD axons have synapses on MR motoneurons. ATD boutons made axosomatic and axodendritic synapses on MR motoneurons. The boutons contained numerous spheroidal synaptic vesicles. Several examples showed clear asymmetrical post-synaptic membrane specialization. This confirms the synaptic connection between horizontal canal activated elements in the ATD and MR motoneurons.
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PMID:Synaptic connections of horizontal canal mediated ascending Deiters tract axons on medial rectus motoneurons in cat. 382 46

The fine structure of retrogradely labelled neurons in the nucleus ambiguus (NA) has been examined in cat and monkey (Macaca fascicularis) following injections of horseradish peroxidase (HRP) into the vagus nerve. Many retrogradely labelled neurons were observed in the NA although unlabelled neurons were also present within the boundaries of the NA as identified by the distribution of retrogradely labelled cells. In both species a wide range of sizes of labelled neurons (20-60 microns in long axis) was observed from rostral to caudal levels of the NA. Large labelled neurons were generally oval or spindle-shaped while smaller neurons were oval in cross-section. Unlabelled neurons observed among labelled NA neurons tended to be smaller on average than the labelled neurons and ranged in size from 15 to 30 microns in long axis. The unlabelled neurons typically had nuclei which were more invaginated than those of the labelled neurons. Quantitative analyses of the synaptic organization in the NA revealed high proportions of terminals containing round vesicles and making asymmetrical or symmetrical contact with the somata in both monkey and cat. Terminals containing pleomorphic vesicles and making symmetrical contact with somata were slightly less numerous. Retrogradely labelled neurons exhibited a positive correlation between the size of neuron and density of synapses on the surface. There tended to be a greater synaptic density on monkey NA neurons than on cat NA neurons of comparable size.
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PMID:Ultrastructural studies of the nucleus ambiguus in cat and monkey following injection of HRP into the vagus nerve. 383 Dec 47

Injections of horseradish peroxidase (HRP) or wheat-germ agglutinin-horseradish peroxidase (WGA-HRP) into the nucleus reticularis parvocellularis (RPc) produced anterograde labeling of axon terminals within the hypoglossal nucleus. Based on morphological parameters of vesicle population, membrane specializations, and postsynaptic articulations, two types of axon terminals derived from neurons in RPc end on hypoglossal neurons. More than half of the terminals contained spherical vesicles (S-type), established asymmetrical membrane specializations and contacted proximal and medium-sized dendrites. The remaining labeled terminals had flattened vesicles (F-type), symmetrical membrane densities and apposed medium and small dendrites. The morphological differences expressed in the two types of terminals may reflect physiological and/or pharmacological differences in the action of RPc neurons on motoneurons in the hypoglossal nucleus.
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PMID:The ultrastructural identification of reticulo-hypoglossal axon terminals anterogradely labeled with horseradish peroxidase. 383 52

The projections from the deep cerebellar nuclei and the sensorimotor cortex to the red nucleus were studied in the rat using anterograde transport of horseradish peroxidase conjugated with wheat germ agglutinin (HRP-WGA). The anterogradely transported HRP-WGA was visualized ultrastructurally by using a modification of the tetramethylbenzidine (TMB) histochemical technique of Carson and Mesulam ('82). Following injection of HRP-WGA into the sensorimotor cortex, ultrastructural examination of anterograde labeling in the ipsilateral red nucleus revealed labeled synaptic terminals located on small-diameter dendrites of the parvocellular region. These terminals made asymmetrical contacts and contained round vesicles. HRP-WGA placement in the nucleus lateralis resulted in anterograde labeling of synaptic terminals which made asymmetrical contacts with small- to medium-sized dendrites of the parvocellular red nucleus. Similar placements in the nucleus interpositus gave rise to anterograde labeling of synaptic terminals which made asymmetrical contacts with somata and proximal dendrites of magnocellular neurons. In addition, retrograde labeling of magnocellular neurons was also observed following HRP-WGA placements in the nucleus interpositus. Anterogradely labeled interpositorubral synaptic terminals were located on retrogradely labeled rubrocerebellar neurons. The rat red nucleus thus receives topographically organized afferents which are characterized by their specificity in location at the cellular level.
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PMID:An HRP-TMB ultrastructural study of rubral afferents in the rat. 384 Jan 84


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