Gene/Protein Disease Symptom Drug Enzyme Compound
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Query: UNIPROT:P50583 (asymmetrical)
 12,197 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

The ultrastructure of the accessory olfactory bulb (AOB) of the bullfrog tadpole and adult was examined, and the main difference between tadpole and adult is that the latter is more compact and shows more synapses. Except for vomeronasal (VMN) glomeruli, the AOB is not highly organized, with mitral cell neurons scattered throughout the neuropil. VMN axon terminals form asymmetric synapses with mitral cell dendrites in glomeruli; in VMN axon terminals, dense-cored vesicles are seen along with the more abundant lucent vesicles 40-50 nm in diameter. Counts indicated that more than 90% of the dendro-dendritic synapses between mitral cells and presumed granule cells are of the asymmetrical type, and reciprocal asymmetrical-symmetrical synapses are not common. Lucent vesicles with round or slightly ellipsoidal profiles and less abundant dense-cored vesicles 60-90 nm in diameter are found in pre- and postsynaptic dendrites; sometimes the dense-cored vesicles lie against or near the presynaptic membrane. Microtubules were often seen to be closely associated with pre- and postsynaptic elements of dendro-dendritic synapses. The most characteristic feature of mitral cell bodies, apart from their large size, is an extensive Golgi system that may extend well into their major dendritic extensions. Dense-cored vesicles are associated with Golgi membranes, from which they probably originate. Centrioles are associated with the Golgi system, and some become basal bodies and give rise to cilia in some mitral cells.
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PMID:Vomeronasal and olfactory nerves of adult and larval bullfrogs: II. Axon terminations and synaptic contacts in the accessory olfactory bulb. 232 17

Nasal congestion associated with the common cold or allergy is associated with a decreased sensitivity of the sense of smell. This study was designed to detect any relationship between nasal resistance to airflow and the ability to detect odors presented to the nose. In particular we were interested to determine if the asymmetrical nasal resistance to airflow associated with the nasal cycle influenced nasal thresholds to menthol which is detected by trigeminal nerves and vanillin which is detected by olfactory nerves. Nasal resistance to airflow and the thresholds for L-menthol and vanillin were measured for each nasal passage in 17 normal volunteer subjects. Nasal resistance to airflow was asymmetrical due to the nasal cycle with a resistance on the high side of 0.94 +/- 0.15 Pa/cm3 s (mean +/- S.E. n = 17). and 0.48 +/- 0.04 Pa/cm3 s on the low side. The range of unilateral nasal resistances varied from 0.31-2.55 Pa/cm3 s. Despite these variations in nasal resistance to airflow no relationship was found between nasal resistance to airflow and thresholds for menthol or vanillin. Since threshold and nasal resistance are not related in normal subjects this may indicate that it is not the level of nasal congestion that affects the sense of smell in nasal infection and allergy, but some other factor related to the inflammatory response of the nasal mucosa.
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PMID:Olfactory and trigeminal thresholds and nasal resistance to airflow. 281 41

N-Nitrosomethylamylamine (NMAA) is a potent carcinogen in rodents with the esophagus as the principal target organ. The present study aims at an assessment of DNA methylation by NMAA in various rat tissues and an identification of cell populations actively involved in its bioactivation. Adult male F344 rats received a single i.p. dose of N-nitroso[methyl-14C]amylamine (0.1 mmol/kg). After 6 h organs were removed and the DNA was extracted, hydrolyzed in 0.1 M HCl, and subjected to radiochromatography on Sephasorb-HP. Highest levels of DNA alkylation were found in esophagus (798 mumol 7-methylguanine/mol mol guanine), followed by nasal epithelium (672 mumol) and liver (624 mumol). Trachea, lung, forestomach, and kidney had considerably lower levels of alkylation and in glandular stomach, spleen, and duodenum, values were close to the limit of detection. Specific target cell populations were identified autoradiographically and by immunohistochemistry using a rabbit antiserum to O6-methyldeoxyguanosine. In the esophagus, NMAA was selectively metabolized by the basal cells of the mucosa. In the respiratory tract, O6-methyldeoxyguanosine was almost exclusively present in the tracheal and bronchiolar epithelia. In the nasal cavity, labeled nuclei were found in both the olfactory and the respiratory epithelium and in the serous glands. Our studies indicate that NMAA and related asymmetrical nitrosamines are, in addition to liver, preferentially metabolized in tissues derived from the ventral entoderm, including the upper respiratory and gastrointestinal tract.
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PMID:Organ and cell specificity of DNA methylation by N-nitrosomethylamylamine in rats. 341 4

GABAergic neurons have been identified in the piriform cortex of the opossum at light and electron microscopic levels by immunocytochemical localization of GABA and the GABA-synthesizing enzyme glutamic acid decarboxylase and by autoradiographic visualization of high-affinity 3H-GABA uptake. Four major neuron populations have been distinguished on the basis of soma size, shape, and segregation at specific depths and locations: large horizontal cells in layer Ia of the anterior piriform cortex, small globular cells with thin dendrites concentrated in layers Ib and II of the posterior piriform cortex, and multipolar and fusiform cells concentrated in the deep part of layer III in anterior and posterior parts of the piriform cortex and the subjacent endopiriform nucleus. All four populations were well visualized with both antisera, but the large layer Ia horizontal cells displayed only very light 3H-GABA uptake, thus suggesting a lack of local axon collaterals or lack of high-affinity GABA uptake sites. The large, ultrastructurally distinctive somata of layer Ia horizontal cells receive a very small number of symmetrical synapses; the thin, axonlike dendrites of small globular cells are exclusively postsynaptic and receive large numbers of both symmetrical and asymmetrical synapses, in contrast to somata which receive a small number of both types; and the deep multipolar and fusiform cells receive a highly variable number of symmetrical and asymmetrical synapses on somata and proximal dendrites. Labeled puncta of axon terminal dimensions were found in large numbers in the neuropil surrounding pyramidal cell somata in layer II and in the endopiriform nucleus. Moderately large numbers of labeled puncta were found in layer I at the depth of pyramidal cell apical dendrites with greater numbers in layer Ia at the depth of distal apical segments than in layer Ib. High-affinity GABA uptake was demonstrated in the termination zone of the projection from the anterior olfactory nucleus to the anterior piriform cortex. Cell bodies of origin of this projection displayed heavy retrograde labeling with 3H-GABA. Matching neuropil and cellular labeling was demonstrated with the GABA-BSA antiserum but not with the GAD antiserum, thus suggesting that GABA is normally present in these cells but is taken up from the neuropil rather than synthesized. No comparable high-affinity GABA uptake was demonstrated in the association fiber systems that originate in the piriform cortex.(ABSTRACT TRUNCATED AT 400 WORDS)
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PMID:Distribution and ultrastructure of neurons in opossum piriform cortex displaying immunoreactivity to GABA and GAD and high-affinity tritiated GABA uptake. 343 76

Mitral cells of the olfactory bulb typically form reciprocal dendrodendritic synapses with anaxonic interneurons, granule cells, within a sublamina of the external plexiform layer. As a result of mitral cell loss in the murine mutant Purkinjie cell degeneration (PCD), subpopulations of these granule cells are denervated. The present report examines the capacity of these denervated interneurons to form new dendrodendritic microcircuits with a second population of olfactory bulb neurons, tufted cells. Quantitative ultrastructural assessments were made of the morphology and distribution of dendrodendritic circuits in the olfactory bulbs of normal heterozygous littermates and affected homozygous recessive PCD mice following mitral cell loss. There were no apparent morphological characteristics that distinguished the reciprocal synaptic connections formed by mitral cells from those formed by tufted cells. However, the segregation of mitral cell dendrodendritic circuits in the deep sublamina of the external plexiform layer (EPL) and tufted cell circuits in the superficial sublamina provided the basis for a comparative analysis of synaptic organization following mitral cell loss. Following mitral cell loss there was a significant reduction in the area occupied by characteristic mitral cell dendrites within the deep sublamina of the EPL. A slight but nonsignificant increase in the area occupied by granule cell spines was also observed. The number of synaptic appositions involving granule cells decreased slightly, the number involving tufted cells increased significantly in the mutant mice. This indicates that many granule cell spines survive denervation and establish new reciprocal dendrodendritic synapses at available sites on tufted cells. In both the control and mutant mice the ratios of symmetrical:asymmetrical dendrodendritic synapses closely approached 1. This demonstrates that not only do the denervated spines receive new afferent input from tufted cell dendrites, but they also establish the reciprocal efferent projection. These data are discussed in terms of the sublaminar organization of dendrodendritic microcircuits in the olfactory bulb and their capacity of plasticity and reorganization following pertubation.
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PMID:Plasticity of dendrodendritic microcircuits following mitral cell loss in the olfactory bulb of the murine mutant Purkinje cell degeneration. 355 82

The ultrastructure of differentiating rat presumptive olfactory bulb in organ culture was investigated with particular reference to mitral cell differentiation and formation of synapses. The presumptive olfactory bulb and olfactory mucosa were dissected en bloc from rat embryos on the fifteenth day of gestation and cultured for 7 days, after which the explants were examined by electron microscopy. The presumptive olfactory bulb had differentiated into a laminated structure with layers corresponding to the glomerular, external plexiform and mitral cell layers. Mitral-like cells were identified by their location and large cell size. Ultrastructural observations indicated that they were relatively well-differentiated. Their dendrites extended into the glomerular layer in which they were postsynaptic to incoming olfactory axons. The distal part of these dendrites frequently contained coated vesicles. Both asymmetrical and symmetrical synapses were found. The symmetrical synapses involved dendrodendritic contacts between periglomerular cells. Synapses in reciprocal arrangements were not observed in the organ cultures.
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PMID:Mitral cell differentiation and synaptogenesis of rat presumptive olfactory bulb in organ culture. 394 39

Recent claims to have demonstrated associative learning ability in Drosophila melanogaster raise questions about the adaptive significance of behavioral modifiability of this species. In a strain survey and a 9 X 9 half diallel cross study of olfactory discriminative avoidance conditioning, a low narrow heritability and strong directional dominance or heterosis controlling nonrandom phenotypic variation were found. Furthermore, the predicted inbreeding depression and asymmetrical response to bidirectional genetic selection were both observed. The genetic architecture revealed in these experiments is consistent with a close association between this conditioning phenotype and evolutionary fitness. Predictions from this interpretation to the nature of new mutations have been confirmed, and a possible role for conditioning in courtship behavior has been identified.
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PMID:Genetic architecture of olfactory discriminative avoidance conditioning in Drosophila melanogaster. 640

The rat olfactory tubercle was studied with the rapid Golgi method. Several distinct cell types were identified mainly on the basis of the size of their somata and the structure of their dendrites. The commonest neuron type in the tubercle is the medium-sized densely spined cell. The somata of these neurons occur chiefly in the dense cell and multiform layers. They also form the cell bridges that directly link the olfactory tubercle with the nucleus accumbens and caudate-putamen. Their dendritic trees exhibit a variety of shapes; some of them are spherical, some are bipolar, and others are asymmetrical. The axons project dorsally, deep into the multiform layer. En route they give off numerous collaterals. A large version of this cell type is the crescent cell. Other medium-sized neurons also have somata in the dense cell and multiform layers. They include the spindle cells, so named because of the shape of their cell bodies, and the medium-sized spine-poor neurons. Neither of these cell types has dendritic trees that are as highly branched as those of the medium-sized densely spined cells. There are three types of small cells; their somata occur primarily in the dense cell and molecular layers. The dwarf cells are near the pial surface, although their somata are included in the dense cell layer, and they have axons that resemble those of medium-sized densely spined cells. The radiate cells have numerous, relatively short, spine-free dendrites that extend out from the rounded somata in all directions. The small spine-rich cells look like miniature versions of the medium-sized densely spined neurons. They are frequently confined to the molecular layer. Large spine-poor neurons, with their cell bodies located in the dense cell and multiform layers, seem to be a heterogeneous cell group since there are subtle variations in the structure of their dendrites and the shape and extent of their dendritic trees. The large, moderately spined neurons are less common than the other large cells; their somata are found in all three layers. The granule cells of the islands of Calleja make up the most homogeneous cell group. They have only a few dendrites, and these are quite thin. Except for the medium-sized densely spined and dwarf cells, the axons of the different cell types were not very well impregnated. The different cell types in the tubercle are compared to cells in the nucleus accumbens, caudate-putamen, and globus pallidus.(ABSTRACT TRUNCATED AT 400 WORDS)
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PMID:Cell configurations in the olfactory tubercle of the rat. 649 Sep 70

The effect of severe zinc deficiency on the distribution of nine elements (potassium, phosphorus, sodium, magnesium, calcium, iron, zinc, copper and manganese) in brain regions (olfactory lobes, right and left hippocampi, cerebellum and the rest of the brain) has been studied. After male rats (30 days old) were fed a zinc-deficient diet for 28 days, the zinc concentration of most brain parts was similar to zinc-adequate control values. Olfactory lobe zinc, on the other hand, was slightly depressed. However, the levels of other metals were dependent on zinc nutriture. Zinc deficiency caused an elevation in copper concentrations in most brain parts. Restriction of food intake caused a similar increase in brain copper but generally the effect was less than with zinc deficiency. Levels of calcium, manganese, sodium and potassium, in certain brain regions, also appeared to be altered by the zinc status of an animal. Of the minerals examined, only zinc and copper displayed asymmetrical distribution between the right and left hippocampus, and severe zinc deficiency did not affect lateral distribution of these trace metals in the hippocampus. The data suggest the hypothesis that changes in brain metal content, associated with zinc deficiency, contribute to the behavioral abnormalities that occur.
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PMID:Severe zinc deficiency: effects on the distribution of nine elements (potassium, phosphorus, sodium, magnesium, calcium, iron, zinc, copper and manganese) in regions of the rat brain. 661 70

Terminals of olfactory bulb afferent (OB) and association (ASSN) fibers within the piriform cortex were characterized ultrastructurally. Identification was by electron microscopic (EM) autoradiography following injections of tritiated amino acids into the olfactory bulb and anterior piriform cortex. The results show that terminals of both fiber systems contain round vesicles and make asymmetrical synaptic contacts predominantly onto dendritic spines. Profiles with pleomorphic vesicles do not appear to be labeled from either site. Since there is strong evidence that both fiber systems generate excitatory postsynaptic potentials (EPSPs) in pyramidal cells, these results provide additional examples in the mammalian CNS of terminals with round vesicles and asymmetrical contacts that mediate an excitatory effect. Percentage density analysis and quantitative study of a large number of heavily labeled terminals revealed that while OB and ASSN terminals are similar in terms of vesicle shape and contact type, they differ in many morphological details including pre- and postsynaptic profile size, the packing density and distribution of synaptic vesicles, synaptic contact shape, and the presence of overlying neuroglial lamellae. However, large variations in appearance of different terminals of the same type are also present so that a small percentage of OB and ASSN terminals are indistinguishable morphologically in the absence of label. An important finding of the quantitative analysis is that spines contacted by lateral olfactory tract (LOT) terminals appear to be of two types based on a bimodal distribution in size and differences in morphology, while spines contacted by ASSN terminals appear to be of a single type. Comparison of these data with results from Golgi analysis indicates that ASSN terminals predominantly contact pyramidal cell spines while OB terminals contact both pyramidal and semilunar cell spines. Quantitative analysis of synaptic vesicles revealed that histograms of vesicle size for OB and ASSN terminals are virtually identical in shape, but peaks are slightly displaced (ASSN vesicles are 5% larger; significant with P less than .002). An analysis of the laminar distribution of OB and ASSN synaptic terminals revealed that while most OB terminals are segregated in layer Ia and most ASSN terminals in layer Ib, occasional OB terminals are observed up to approximately 50 micro deep to the Ia-Ib boundary and occasional ASSN terminals up to approximately 50 micro superficial to this boundary.
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PMID:Structure of the piriform cortex of the opossum. III. Ultrastructural characterization of synaptic terminals of association and olfactory bulb afferent fibers. 664 15


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