PubMed Health⌕ Search

SEARCH · PubMed Health

Results for “OLFACTORY NERVE”

Explore indexed PubMed citations for clinical trials, systematic reviews and public health research. Read source abstracts and follow each citation to its original PubMed record.

Quote a phrase for an exact phrase match. Source license links do not imply unrestricted reuse.

At least 1,423 records · Page 79Linked to original sources

Increase in efflux of inorganic phosphate during electrical activity in small non-myelinated nerve fibres.

1. The movements of labelled phosphate were measured in garfish olfactory and in rabbit vagus nerves at rest and during activity. 2. In garfish olfactory nerve kept in solutions with 120 mM-sodium and 0.2 mM-phosphate the fractional loss of 32P was 9.82 X 10(-4) min-1. Lowering the sodium concentration of the washing fluid decreased the efflux; lowering the phosphate produced a transient increase with subsequent return towards the efflux in 0.2 mM-phosphate. 3. Stimulation at 0.50 sec produced an extra fractional loss of 12 X 10(-6) impulse-1. At 1/sec the effect was larger; at 5/sec it was about the same as at 0.5/sec. 4. After stimulation the effect of activity disappeared exponentially with a time constant of 4.4 min. 5. Lowering the sodium decreased the extra efflux with stimulation, whereas changing the phosphate concentration did not much affect the extra efflux. 6. In rabbit vagus nerve kept in 154 mM-sodium and 0.2 M-phosphate the fractional loss of 32P was 4.91 X 10(-4) min-1. Lowering the sodium or the phosphate decreased the resting efflux. 7. Stimulation of the vagus nerve at 15/sec produced an extra fractional loss of 0.87 X 10(-6) impulse-1. 8. The extra efflux with stimulation seems to result predominantly from an increase in intracellular inorganic phosphate resulting from increased break-down of ATP after activity.

Action Potentials↗

ELECTRICAL RESPONSE AND GROWTH OF OLFACTORY CILIA OF THE OLFACTORY EPITHELIUM OF THE NEWT IN WATER AND ON LAND.

A correlation between the length of the olfactory cilia and the electrical activity of the olfactory epithelium was studied in newts living in water and on land. The olfactory cilia grew when newts were transferred onto land. The cilia in the olfactory bud became longest in 108 hours after the transfer and then became shorter, while those in the interstitium only gradually elongated. Slow potentials were evoked in the epithelium by the application of odorous fluids but not by odorous vapors for 20 hours after the transfer. Thereafter, the slow potential began to appear in response to odorous vapors and reached maximal magnitude between 60 and 70 hours after the transfer, while it was not evoked by odorous fluids in this period. In the later stage, the slow potential to odorous vapors decreased in magnitude and disappeared 120 hours after the transfer, while it began to reappear in response to odorous fluids. When these changes in the slow potential were compared with those in the cilium, a discrepancy was found between the period of maximal potential magnitude and that of maximal cilium length.

Animals↗

Fine structural aspects of secretion and extrinsic innervation in the olfactory mucosa.

The mucus at the surface of the olfactory mucosa constitutes the milieu in which perireceptor events associated with olfactory transduction occur. In this review, the ultrastructure of olfactory mucus and of the secretory cells that synthesize and secrete olfactory mucus in the vertebrate olfactory mucosa is described. Bowman's glands are present in the olfactory mucosa of all vertebrates except fish. They consist of acini, which may contain mucous or serous cells or both, and ducts that traverse the olfactory epithelium to deliver secretions to the epithelial surface. Sustentacular cells are present in the olfactory epithelium of all vertebrates. In fish, amphibia, reptiles, and birds, they are secretory; in mammals, they generally are considered to be "non-secretory," although they may participate in the regulation of the mucous composition through micropinocytotic secretion and uptake. Goblet cells occur in the olfactory epithelium of fish and secrete a mucous product. Secretion from Bowman's glands and vasomotor activity in the olfactory mucosa are regulated by neural elements extrinsic to the primary olfactory neurons. Nerve fibers described in early anatomical studies and characterized by immunohistochemical studies contain a variety of neuroactive peptides and have several targets within the olfactory mucosa. Ultrastructural studies of nerve terminals in the olfactory mucosa have demonstrated the presence of adrenergic, cholinergic and peptidergic input to glands, blood vessels, and melanocytes in the lamina propria and of peptidergic terminals in the olfactory epithelium. The neural origins of the extrinsic nerve fibers and terminals are the trigeminal, terminal, and autonomic systems.

Animals↗

Evidence for a role of the chemorepellent semaphorin III and its receptor neuropilin-1 in the regeneration of primary olfactory axons.

To explore a role for chemorepulsive axon guidance mechanisms in the regeneration of primary olfactory axons, we examined the expression of the chemorepellent semaphorin III (sema III), its receptor neuropilin-1, and collapsin response mediator protein-2 (CRMP-2) during regeneration of the olfactory system. In the intact olfactory system, neuropilin-1 and CRMP-2 mRNA expression define a distinct population of olfactory receptor neurons, corresponding to immature (B-50/GAP-43-positive) and a subset of mature (olfactory marker protein-positive) neurons located in the lower half of the olfactory epithelium. Sema III mRNA is expressed in pial sheet cells and in second-order olfactory neurons that are the target cells of neuropilin-1-positive primary olfactory axons. These data suggest that in the intact olfactory bulb sema III creates a molecular barrier, which helps restrict ingrowing olfactory axons to the nerve and glomerular layers of the bulb. Both axotomy of the primary olfactory nerve and bulbectomy induce the formation of new olfactory receptor neurons expressing neuropilin-1 and CRMP-2 mRNA. After axotomy, sema III mRNA is transiently induced in cells at the site of the lesion. These cells align regenerating bundles of olfactory axons. In contrast to the transient appearance of sema III-positive cells at the lesion site after axotomy, sema III-positive cells increase progressively after bulbectomy, apparently preventing regenerating neuropilin-1-positive nerve bundles from growing deeper into the lesion area. The presence of sema III in scar tissue and the concomitant expression of its receptor neuropilin-1 on regenerating olfactory axons suggests that semaphorin-mediated chemorepulsive signal transduction may contribute to the regenerative failure of these axons after bulbectomy.

Age Factors↗

The terminal nerve ganglion cells project to the olfactory mucosa in the dwarf gourami.

Single- and double-label immunocytochemical studies were conducted using antisera to salmon gonadotropin-releasing hormone (sGnRH) and molluscan cardioexcitatory peptide (FMRFamide) to determine whether terminal nerve ganglion cells project to the olfactory mucosa in the dwarf gourami, Colisa lalia. Both peptides were present in terminal nerve ganglion perikarya and fibers in brain and nasal cavity. Labeled fibers were present in the olfactory nerve and could be traced to the olfactory mucosa. All terminal nerve ganglion cells contained both sGnRH and FMRFamide-like peptides. This study suggests that the terminal nerve ganglion cells can influence both brain and chemoreceptive structures.

Animals↗

An in vitro evaluation of the effects of local magnetic-susceptibility-induced gradients on anisotropic water diffusion in nerve.

It has been suggested that the anistropy of the water-diffusion coefficient measured in nerve and in white matter could arise from locally anisotropic background gradients induced by the static field, B0. By utilizing 1) pulse sequences, which minimize the effects of background gradients, and 2) changes in sample orientation, which would maximize the change in the magnitude of these gradients if present, it is shown that in four excised nerves the background gradients do not play a measurable role in the anisotropy of the water-diffusion coefficient at a field strength of 2.35 T. The excised nerves evaluated were the olfactory, trigeminal, and optic nerves of the garfish and the sciatic nerve of the frog.

Animals↗