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 12,197 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

The morphology, ultrastructure and synaptic relationships of the cholinergic and non-cholinergic neurons in the medial septal nucleus (MS) and vertical limb of the diagonal band of Broca (VDB) in the basal forebrain of the rat were studied at the light and electron microscopic levels. The cholinergic neurons were localized immunocytochemically using a monoclonal antibody against choline acetyltransferase (ChAT). Morphometric and statistical analyses showed that ChAT-labelled cells presented a predominantly oval morphology in both nuclei. The sizes of the neurons were significantly larger in the VDB nucleus. Within the two nuclei, two populations of cholinergic neurons were differentiated. One of the large immunolabelled neurons presented deep indentations and prominent nucleoli in their non-immunoreactive nuclei. Their cytoplasm contained a well-organized endomembrane system composed of short cisternae of rough endoplasmic reticulum (RER). One or two lamellar bodies with a peculiar ultrastructure were frequently found intercalated in this system. The Golgi areas presented numerous coated vesicles, sequestration and multivesicular bodies, which was indicative of an intense metabolic activity in these cells. The second population of small immunolabelled neurons exhibited reduced cytoplasm with a poorly developed endomembrane system and apparent absence of lamellar bodies. The neighbouring non-immunolabelled neurons presented a different type of organization of the endomembrane system which was composed of scattered and loosely arranged elongated cisternae of RER and infrequent lamellar bodies, with a structure different from that seen in the large cholinergic neurons. We propose that the structural differences in composition of the endomembrane system and lamellar bodies observed in the three types of neurons in this study indicate different metabolic activities. Symmetrical and asymmetrical synaptic contacts were observed on somata and dendrites of labelled neurons, the latter being more frequent. ChAT-labelled axon boutons were never seen. The absence of immunolabelled axon terminals and the presence of immunolabelled myelinated axons leads us to suggest that the majority of neurons in these areas are of the long projecting type.
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PMID:Ultrastructural study of cholinergic neurons in the medial septal nucleus and vertical limb of the diagonal band of broca in the basal forebrain of the rat. 171 43

The subcellular morphology of the mesencephalic trigeminal (Me5) nucleus in the rat was studied by transmission electron microscopy. Most neurons in the thin rostral as well as in the major caudal part of Me5 appeared as large (40-50 microns), round- to ovoid-shaped unipolar cells. A few neurons (estimated 5%) appeared to be multipolar, usually bipolar. The Me5 neurons had a large, round, centrally located nucleus, and their cytoplasm was characterized by a dense network of lamellar granular endoplasmic reticulum, an abundant Golgi apparatus, many mitochondria and neurofilaments suggesting very active cells with a high rate of synthesis and axoplasmatic transport. Numerous small spinous processes covered the surface of the Me5 neurons. Clustering of 2 or 3 cells was accomplished by maculae, i.e. zones of gap junctions and close cell appositions. Boutons contacting the soma of Me5 neurons and boutons contacting large and small dendrites were defined as axosomatic and axodendritic synapses, respectively. Four types of synaptic boutons were distinguished: (1) S boutons, with round vesicles and asymmetrical as well as symmetrical synapses, (2) F boutons, with pleomorphic admixture of flattened and spherical vesicles and asymmetrical synapses, (3) P boutons, which resembled the F-type boutons but contained predominantly spherical vesicles and symmetrical synapses, and (4) G boutons, characterized by a heterogeneous population of vesicles. This description of the Me5 nucleus is particularly useful for future studies that attempt to correlate the structure of a particular synapse with its function.
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PMID:Ultrastructure of the rat mesencephalic trigeminal nucleus. 186 50

In an extension of our previous light microscopic observations, a type of neuron which shows GABA-like immunoreactivity was identified and described in the ectostriatal core of young domestic chicks, using pre- and postembedding electron microscopic immunocytochemistry. Large GABA immunopositive (GABA+) cells are characterized by an ovoidal or polygonal soma of 12-16 micron diameter, uniformly distributed nuclear chromatin, a prominent Golgi apparatus and an abundance of rough endoplasmic reticulum. In addition to axodendritic terminals, large GABA neurons receive numerous axosomatic synapses of both symmetrical and asymmetrical types covering a substantial part of their perikaryal surface. Axosomatic terminals with symmetrical junctions are usually immunoreactive to GABA whereas the boutons with asymmetrical synaptic specialization are immunonegative. GABA+ boutons also synapse with dendritic spine necks presumably belonging to projection neurons. These terminals usually contain loosely packed synaptic vesicles without any marked accumulation near the synaptic cleft. Large GABA+ terminals with densely packed vesicles were found to synapse with axon hillocks. Based on known descriptions of ectostriatal cytoarchitecture and synaptology, it is suggested that the GABA+ cells of chick ectostriatum represent inhibitory interneurons which may be equivalent to GABAergic non-pyramidal neuronal types of mammalian visual cortex. GABA+ axosomatic synapses afferent to large GABA cells are likely to form the structural basis for a disinhibitory mechanism in the avian ectostriatum.
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PMID:Large GABA cells of chick ectostriatum: anatomical evidence suggesting a double GABAergic disinhibitory mechanism. An electron microscopic immunocytochemical study. 186 87

In the present study, we examined the ultrastructure of striatal neurons containing neuropeptide Y (NPY) which were labeled by an immunohistochemical method using peroxidase-conjugated F(ab) fragments in the rat. Each of the 26 neurons identified had a deeply indented oval nucleus. The cytoplasm, which was mainly concentrated at the emergence of the dendrites, contained an abundant Golgi apparatus and a well-developed granular endoplasmic reticulum. Dendrites were poorly branched and rarely exhibited varicosities or dendritic spines. NPY-immunoreactive (Ir) axons were small in diameter and unmyelinated. These features corresponded to a subpopulation of striatal neurons classified as aspiny type IV in previous Golgi studies. Axon terminals forming symmetrical synapses were numerous on the NPY-Ir perikarya and proximal dendrites. On distal NPY-Ir dendrites, synaptic contacts were mainly of the asymmetrical type, suggesting that NPY neurons are contacted by at least 2 categories of afferent fibers. Several NPY-Ir axonal processes and boutons were found to form symmetrical synapses with dendrites, dendritic spines and perikarya belonging to spiny type neurons. These data were consistent with the view that NPY may act as a neurotransmitter of striatal interneurons. Moreover, the frequent observation of NPY axonal processes in the close vicinity of striatal vessels suggested that NPY might also play a role in the control of cerebral vasomotricity. Thirty hours after intranigral injection of 6-hydroxydopamine to induce a degeneration of nigrostriatal dopamine terminals, some characteristic degenerative boutons were observed in close apposition to NPY-Ir cell bodies, suggesting that NPY neurons are under a direct nigrostriatal dopaminergic influence.
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PMID:Ultrastructural features of NPY-containing neurons in the rat striatum. 270 86

The dorsal nucleus of the lateral lemniscus (DNLL) and its connections constitute one of the ascending auditory pathways to the inferior colliculus. One notable feature of this nucleus is the heavy commissural connections between DNLL on opposite sides of the midbrain. These commissural connections may have a significant impact on the ascending pathway. In this study, the fine structure of DNLL in the cat and its commissural connections were examined. Both anterograde and retrograde transport methods were used simultaneously at the EM level. Injections of 3H-leucine mixed with WGA-HRP were made in one DNLL. After axonal transport, EM autoradiographic methods were used to identify the anterogradely labeled axonal endings from the opposite DNLL. In the same location, retrogradely labeled neurons with crossed connections were identified with HRP histochemistry. Two types of axonal endings were found in DNLL, those with round synaptic vesicles forming asymmetrical synaptic junctions and those with pleomorphic vesicles and symmetrical synapses. Both types were equally common. However, only endings with pleomorphic vesicles were labeled after injections in the contralateral DNLL. The labeled endings from the opposite DNLL appeared to represent a homogeneous population, even though a number of variations in the 2 types of endings were found. Labeled endings were presynaptic to all parts of neurons in DNLL, but a large proportion of the synapses were on cell bodies and large dendrites. Two patterns of nuclear morphology and distribution of rough endoplasmic reticulum were identified and may represent different cell types. Examples of both cell types were observed to project to the contralateral side and received labeled synaptic endings. The major finding of this study is that the crossed connections between DNLL exhibit the morphology associated with inhibitory function. Since neurons in DNLL are thought to use GABA as a neurotransmitter, the crossed connections could provide inhibitory inputs to DNLL on each side. Since some neurons receive numerous axosomatic inputs from the contralateral DNLL and also project to the opposite side, they may participate in direct reciprocal, inhibitory connections between the nuclei. Crossed inhibitory connections in the DNLL pathway may be important in regulating the flow of ascending auditory information.
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PMID:An EM study of the dorsal nucleus of the lateral lemniscus: inhibitory, commissural, synaptic connections between ascending auditory pathways. 292 87

The fine structure of neurons containing human growth-hormone-releasing factor (hGRF) immunoreactivity located in the arcuate nucleus of the guinea pig was studied by means of the preembedding immunohistochemical technique. The perikaryon of labeled neurons was fusiform or ovoid; the nucleus was regular in shape and contained a prominent nucleolus. The main ultrastructural features of the hGRF-immunoreactive neurons were the presence of numerous labeled secretory granules (100-120 nm in diameter) and the abundance and the enlargement of the organelles involved in the synthesis of the peptides: a well-developed rough endoplasmic reticulum and a conspicuous Golgi apparatus. Synaptic inputs were observed on immunoreactive perikarya but, above all, on the labeled dendrites. The unstained presynaptic nerve endings most often contained only small clear vesicles and formed symmetrical contacts. In rare cases, the presynaptic terminals exhibited both small clear and large dense vesicles and constituted asymmetrical contacts. Immunoreactive nerve endings were also observed in this area: the synaptic boutons contained large, stained vesicles and small, unlabeled, clear vesicles. These axon terminals made synaptic contacts with unstained dendritic processes; the contacts were symmetrical. The results indicate that hGRF-immunoreactive neurons of the guinea pig arcuate nucleus present morphological features of neuroendocrine cells. Moreover, the presence of hGRF-labeled nerve endings in the arcuate nucleus itself suggests that a substance related to hGRF might be a neuromodulator, at least in this area.
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PMID:Fine structural studies of growth-hormone-releasing-factor (GRF)-immunoreactive neurons and their synaptic connections in the guinea pig arcuate nucleus. 310 66

A monoclonal antibody against choline acetyltransferase (ChAT), the acetylcholine synthesizing enzyme, was used to identify cholinergic neurons in the nucleus of the horizontal limb of the diagonal band of Broca at the light and electron microscopic levels. ChAT-labelled somata were fusiform, triangular or round in shape and varied considerably in size. Depending on the type of the cell, one to four dendrites emerged from the soma, but an axon could rarely be seen. The nuclei of most cells were round or oval, showed invaginations and displayed prominent nucleoli. The karyoplasm of the larger fusiform and triangular neurons contained abundant organelles including parallel arrays of granular endoplasmic reticulum. The synaptic input to labelled perikarya and proximal dendrites was sparse. It consisted chiefly of asymmetrical synaptic contacts, sometimes with postjunctional densities, but a few symmetrical synapses were also noted. ChAT-positive axon terminals were not identified which suggests that axon collaterals are rare within the nucleus of the horizontal limb of the diagonal band of Broca.
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PMID:Morphological characterization of cholinergic neurons in the horizontal limb of the diagonal band of Broca in the basal forebrain of the rat. 353 49

The Cuneiformis nucleus (Cu.n.) is a reticular nucleus of the mesencephalic tegmentum which is involved in several functions and particularly in locomotor activities. While the physiological properties and the nervous connections of the nucleus have been studied, there is no data about its ultrastructure. Therefore, we investigated this region in cat at the electron microscope and with morphoquantitative methods to clarify its ultrastructural organization and particularly the characteristics of its synaptic complex. The neurons are small and medium in size, with a high nucleo-cytoplasmic ratio and a modest rough endoplasmic reticulum organization. The neuropil is very extensive. Myelinated axons are very numerous. Dendritic profiles whose plasmalemma is almost completely covered by synaptic boutons are observed frequently. There are few somatic synapses; 81% have symmetrical junctions and 23% have round vesicles only. There are numerous synapses in the neuropil, 40% having asymmetrical junctions and 60% containing round vesicles only. The greater functional complexity indicated by the morphological data and the greater extension of the neuropil synapses with respect to that of the somatic ones, suggest that the neuropil is the main site of modulation and integration of the inputs to the nucleus. A highly significant statistical difference between the sizes of the somatic vesicles and those of the neuropil was found. This may point to the presence of distinct populations of vesicles, which may be correlated with the variety of substances (neurotransmitters, neuropeptides etc ...) found in the nucleus. The remarkable ultrastructural similarity between the Cu.n. and the periaqueductal gray matter is discussed.
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PMID:Ultrastructural study of the nucleus Cuneiformis in the cat. 365 29

Electron microscopic studies were conducted in the marginal zone (lamina I) in human fetuses ranging from 8-25 weeks of gestational age. At 8 weeks the neurons have indented nuclei and sparse organelles in the cytoplasm. The neuropil shows contacts between the axons and dendritic profiles. Some of them are well defined synapses with post synaptic thickening and agranular spherical vesicles in the presynaptic terminal. At 18 weeks compactly packed organelles with long cisternae of rough endoplasmic reticulum could be visualized in the neuronal cytoplasm. At 25 weeks the neurons have heterochromatin patches in the nuclei. Axosomatic, dendrodendritic, axoaxonic, symmetrical, asymmetrical and multisynaptic contacts with agranular and dense core vesicles are seen at different sequential age periods.
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PMID:Ultrastructure of marginal zone during prenatal development of human spinal cord. 380 86

The interrelationships of corticotropin-releasing factor (CRF) immunoreactive neuronal cell bodies and processes have been examined in the paraventricular nucleus (PVN) of adrenalectomized-dexamethasone treated rats. Antisera generated against ovine CRF (oCRF) were used in the peroxidase-anti-peroxidase-complex (PAP)-immunocytochemical method at both the light and electron microscopic levels. In this experimental model, a great number of CRF-immunoreactive neurons were detected in the parvocellular subdivisions of the PVN and a few scattered labelled parvocellular neurons were also observed within the magnocellular subunits. Characteristic features of immunolabeled perikarya included hypertrophied rough endoplasmic reticulum with dilated endoplasmic cisternae, well developed Golgi complexes and increased numbers of neurosecretory granules. These features are interpreted to indicate accelerated hormone synthesis as a result of adrenalectomy. Afferent fibers communicated with dendrites and somata of CRF-immunoreactive neurons via both symmetrical and asymmetrical synapses. Some neurons exhibited somatic appendages and these structures were also observed to receive synaptic terminals. Within both the PVN and its adjacent neuropil, CRF-immunoreactive axons demonstrated varicosites which contained accumulations of densecore vesicles. CRF-containing axons were observed to branch into axon collaterals. These axons or axon collaterals established axo-somatic synapses on CRF-producing neurons in the parvocellular regions of the PVN, while in the magnocellular area of the nucleus they were found in juxtaposition with unlabeled magnocellular neuronal cell bodies or in synaptic contact with their dendrites. The presence of CRF-immunoreactive material in presynaptic structures suggests that the neurohormone may participate in mechanisms of synaptic transfer. These ultrastructural data indicate that the function of the paraventricular CRF-synthesizing neurons is adrenal steroid hormone dependent. They also provide morphological evidence for the existence of a neuronal ultrashort feed-back mechanism within the PVN for the regulation of CRF production and possibly that of other peptide hormones contained within this complex.
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PMID:Evidence for local corticotropin releasing factor (CRF)-immunoreactive neuronal circuits in the paraventricular nucleus of the rat hypothalamus. An electron microscopic immunohistochemical analysis. 390 7


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