scholarly journals Effect of intervening lesions on amino acid distributions in rat olfactory cortex and olfactory bulb.

1980 ◽  
Vol 28 (11) ◽  
pp. 1157-1169 ◽  
Author(s):  
D A Godfrey ◽  
C D Ross ◽  
J A Carter ◽  
O H Lowry ◽  
F M Matschinsky

Levels of the proposed neurotransmitter amino acids glutamate, aspartate, gamma-aminobutyric acid (GABA), and glycine were measured within the layered structures of the olfactory bulb and olfactory cortex following unilateral transections of the lateral olfactory tract or of virtually all fiber tracts of the olfactory peduncle. Distributions of the amino acids on both lesion and control sides were examined and compared by means of a mapping procedure. The results suggest: 1) Glutamate and aspartate are specifically associated with mitral (and presumably also tufted) cell axons and terminals in the piriform cortex. The distribution of aspartate in the olfactory bulb is further suggestive of a specific association of aspartate with mitral cell dendrites and somata. 2) Glutamate might be specifically associated with some centrifugal fibers traveling to the olfactory bulb in or near the anterior commissure. 3) GABA might be specifically related to some certrifugal fibers to the olfactory bulb in addition to its prominent association with granule cells of the bulb. 4) Glycine is unlikely to play a prominent neurotransmitter role in either the olfactory bulb or olfactory cortex.

2007 ◽  
Vol 97 (4) ◽  
pp. 3136-3141 ◽  
Author(s):  
Thomas Heinbockel ◽  
Kathryn A. Hamilton ◽  
Matthew Ennis

In the main olfactory bulb, several populations of granule cells (GCs) can be distinguished based on the soma location either superficially, interspersed with mitral cells within the mitral cell layer (MCL), or deeper, within the GC layer (GCL). Little is known about the physiological properties of superficial GCs (sGCs) versus deep GCs (dGCs). Here, we used patch-clamp recording methods to explore the role of Group I metabotropic glutamate receptors (mGluRs) in regulating the activity of GCs in slices from wildtype and mGluR−/− mutant mice. In wildtype mice, bath application of the selective Group I mGluR agonist DHPG depolarized and increased the firing rate of both GC subtypes. In the presence of blockers of fast synaptic transmission (APV, CNQX, gabazine), DHPG directly depolarized both GC subtypes, although the two GC subtypes responded differentially to DHPG in mGluR1−/− and mGluR5−/− mice. DHPG depolarized sGCs in slices from mGluR5−/− mice, although it had no effect on sGCs in slices from mGluR1−/− mice. By contrast, DHPG depolarized dGCs in slices from mGluR1−/− mice but had no effect on dGCs in slices from mGluR5−/− mice. Previous studies showed that mitral cells express mGluR1 but not mGluR5. The present results therefore suggest that sGCs are more similar to mitral cells than dGCs in terms of mGluR expression.


1970 ◽  
Vol 7 (3) ◽  
pp. 631-651
Author(s):  
J. L. PRICE ◽  
T. P. S. POWELL

A description is given of the mitral and short axon cells of the olfactory bulb of the rat from Golgi material examined with the light microscope and from material examined with the electron microscope. The mitral cells are large neurons with primary and secondary dendrites which both extend into the overlying external plexiform layer, although only the primary dendrite enters the glomerular formations. No predominant antero-posterior orientation of the secondary dendrites has been found. Within the glomeruli the mitral cell dendrites are in synaptic contact with the olfactory nerves and also with the periglomerular cells, but elsewhere the only synapses on the mitral cells are the ‘reciprocal synapses’ with the granule cells. Synaptic-type vesicles are found in all parts of the mitral cells, including the axon initial segments; they appear to be especially concentrated in the distal portions of the dendrites. Several types of short axon cells have been found in the granule cell layer in Golgi-impregnated material. Their cell bodies can also be distinguished with the electron microscope, and from previous work it is probable that the axons of at least some of these cells form flattened-vesicle symmetrical synapses upon the granule cells.


2014 ◽  
pp. 133-160 ◽  
Author(s):  
Shin Nagayama ◽  
Kei M. Igarashi ◽  
Hiroyuki Manabe ◽  
Kensaku Mori

2021 ◽  
pp. 851-861
Author(s):  
Kelly D. Flemming

This chapter briefly repeats key anatomic characteristics and then reviews clinical disorders affecting each cranial nerve in addition to the brainstem. More specifically, this chapter covers cranial nerves I, V, VII, and IX through XII plus the brainstem. The olfactory nerve is a special visceral afferent nerve that functions in the sense of smell. The axons of the olfactory receptor cells within the nasal cavity extend through the cribriform plate to the olfactory bulb. These olfactory receptor cell axons synapse with mitral cells in the olfactory bulb. Mitral cell axons project to the primary olfactory cortex and amygdala. The olfactory cortex interconnects with various autonomic and visceral centers.


1993 ◽  
Vol 69 (6) ◽  
pp. 1948-1965 ◽  
Author(s):  
U. S. Bhalla ◽  
J. M. Bower

1. Detailed compartmental computer simulations of single mitral and granule cells of the vertebrate olfactory bulb were constructed using previously published geometric data. Electrophysiological properties were determined by comparing model output to previously published experimental data, mainly current-clamp recordings. 2. The passive electrical properties of each model were explored by comparing model output with intracellular potential data from hyperpolarizing current injection experiments. The results suggest that membrane resistivity in both cells is nonuniform, with somatas having a substantially lower resistivity than the dendrites. 3. The active properties of these cells were explored by incorporating active ion channels into modeled compartments. On the basis of evidence from the literature, the mitral cell model included six channel types: fast sodium, fast delayed rectifier (Kfast), slow delayed rectifier (K), transient outward potassium current (KA), voltage- and calcium-dependent potassium current (KCa), and L-type calcium current. The granule cell model included four channel types: rat brain sodium, K, KA, and the non-inactivating muscarinic potassium current (KM). Modeled channels were based on the Hodgkin-Huxley formalism. 4. Representative kinetics for each of the channel classes above were obtained from the literature. The experimentally unknown spatial distributions of each included channel were obtained by systematic parameter searches. These were conducted in two ways: large-scale simulation series, in which each parameter was varied in turn, and an adaptation of a multidimensional conjugate gradient method. In each case, the simulated results were compared wtih experimental data using a curve-matching function evaluating mean squared differences of several aspects of the simulated and experimental voltage waveforms. 5. Systematic parameter variations revealed a single distinct region of parameter space in which the mitral cell model best fit the data. This region of parameter space was also very robust to parameter variations. Specifically, optimum performance was obtained when calcium and slow K channels were concentrated in the glomeruli, with a lower density in the soma and proximal secondary dendrites. The distribution of sodium and fast potassium channels, on the other hand, was highest at the soma and axon, with a much lighter distribution throughout the secondary dendrites. The KA and KCa channels were also concentrated near the soma. 6. The parameter search of the granule cell model was much less restrained by experimental data. Several parameter regimes were found that gave a good match to the data.(ABSTRACT TRUNCATED AT 400 WORDS)


1970 ◽  
Vol 7 (1) ◽  
pp. 157-187
Author(s):  
J. L. PRICE ◽  
T. P. S. POWELL

An experimental investigation has been made of the site and mode of termination of the 3 groups of afferent fibres to the olfactory bulb which come from more caudal parts of the cerebral hemisphere. Lesions have been placed in the relevant parts of the brain of the rat and the resulting degeneration of axon terminals in the olfactory bulb studied with the electron microscope. All 3 groups of these extrinsic afferent fibres end in asymmetrical synapses upon the granule cells, and they have a differential termination upon its various processes. The possibility that these fibres also end upon other cells in the bulb (particularly the short-axon and periglomerular cells) cannot be excluded. The centrifugal fibres end upon gemmules in the deep half of the external plexiform layer only; no degenerating terminals were found in relation to the glomeruli although degenerating centrifugal axons are present here. The fibres of the anterior commissure terminate upon spines and varicosities of the deep dendrites and upon somatic spines of the granule cells. After lesions of the anterior olfactory nucleus, degenerating terminals were found in the ipsilateral olfactory bulb, which could not be ascribed to the centrifugal fibres or to the fibres of the anterior commissure, as they ended upon the spines of peripheral processes in the granule cell layer, and upon gemmules in the superficial as well as in the deep half of the external plexiform layer. It is proposed that these terminals are those of the axon collaterals from the ipsilateral anterior olfactory nucleus. The axons which form symmetrical synapses, and many which form asymmetrical synapses, do not degenerate even after a lesion immediately behind the olfactory bulb, and are therefore intrinsic to the bulb. It is suggested that the axons which are associated with symmetrical synapses are those of the short-axon cells, and the asymmetrical synapses are formed by the axon collaterals of the mitral and tufted cells.


1970 ◽  
Vol 7 (1) ◽  
pp. 125-155
Author(s):  
J. L. PRICE ◽  
T. P. S POWELL

The synapses related to the granule cells of the olfactory bulb of rat brain have been studied in aldehyde-fixed material. The synapses can be divided into three classes: (1) those which have asymmetrical synaptic membrane thickenings and spheroidal synaptic vesicles; (2) those with symmetrical synaptic thickenings and flattened vesicles; and (3) the reciprocal synapses, one half of which (from mitral to granule cell) has an asymmetrical synaptic thickening associated with spheroidal vesicles, while the other half (from granule to mitral cell) has a symmetrical synaptic thickening and flattened vesicles. Qualitative observations, supported by preliminary quantitative measurements, suggest that it may be possible to divide both the spheroidal and flattened-vesicle types into two further varieties, on the basis of size, The smaller variety of spheroidal vesicles is found in most axon terminals, while the larger spheroidal vesicles are present in mitral cell dendrites and in some of the axon terminals. The flattened vesicles associated with symmetrical synapses which are oriented on to the granule cells are smaller than the spheroidal vesicles, but the flattened vesicles in the spines and gemmules of the granule cells are the same size or larger than the spheroidal vesicles. The division of flattened vesicles into two sizes is supported by statistical analysis of measurements of these vesicles, but because of difficulty in identifying the axon terminals with asymmetrical synapses there is no quantitative evidence for such a division of spheroidal vesicles. The asymmetrical synapses are found predominantly on spines, gemmules, and dendritic varicosities, although they are occasionally present on shafts of dendrites and on the cell somata. The symmetrical synapses are almost completely restricted to the shafts of the peripheral processes and the deep dendrites, and to the cell somata; only very rarely are synapses of this type found on spines, and then always in conjunction with an asymmetrical synapse.


1998 ◽  
Vol 79 (1) ◽  
pp. 137-142 ◽  
Author(s):  
Hiromasa Kitazawa ◽  
Takeshi Yagi ◽  
Tsuyoshi Miyakawa ◽  
Hiroaki Niki ◽  
Nobufumi Kawai

Kitazawa, Hiromasa, Takeshi Yagi, Tsuyoshi Miyakawa, Hiroaki Niki, and Nobufumi Kawai. Abnormal synaptic transmission in the olfactory bulb of Fyn-kinase–deficient mice. J. Neurophysiol. 79: 137–142, 1998. We studied synaptic transmission in the granule cells in the olfactory bulb of the homozygous Fyn (a nonreceptor type tyrosine kinase)-deficient ( fyn z/ fyn z) and heterozygous Fyn-deficient (+/ fyn z) mice by using slice preparations from the olfactory bulb. Stimulation to the lateral olfactory tract and/or centrifugal fibers to the olfactory bulb evoked field excitatory postsynaptic potentials (fEPSPs) in the granule cells. In +/ fyn z mice, fEPSPs were augmented by bicuculline, a γ-aminobutyric acid (GABAA) antagonist and picrotoxin, whereas fEPSPs in fyn z/ fyn z mice were much less sensitive to bicuculline and picrotoxin. Application of d-2-amino-5-phosphonopentanoic acid had no effect but 6-cyano-7-nitroquinoxaline-2,3-dione produced almost complete block of fEPSPs in both +/ fyn z mice and fyn z/ fyn z mice. (1S, 3R)-1-aminocyclo-pentane-1.3-dicarboxylate, an agonist of metabotropic glutamate receptors caused a similar depression of fEPSPs in both +/ fyn z and fyn z/ fyn z mice. In +/ fyn z mice tetanic stimulation to the lateral olfactory tract and/or centrifugal fibers induced N-methyl-d-aspartate (NMDA)-dependent long-term potentiation (LTP) of fEPSPs, whereas LTP was impaired in fyn z/ fyn z mice. Our results demonstrate altered functions of GABAA and NMDA receptors in the olfactory system of Fyn-deficient mice.


2020 ◽  
Author(s):  
Sara Zeppilli ◽  
Tobias Ackels ◽  
Robin Attey ◽  
Nell Klimpert ◽  
Kimberly D. Ritola ◽  
...  

AbstractProjection neurons (PNs) in the mammalian olfactory bulb (OB) receive direct input from the nose and project to diverse cortical and subcortical areas. Morphological and physiological studies have highlighted functional heterogeneity, yet no molecular markers have been described that delineate PN subtypes. Here, we used viral injections into olfactory cortex and fluorescent nucleus sorting to enrich PNs for high-throughput single nucleus and bulk RNA deep sequencing. Transcriptome analysis and RNA in situ hybridization identified three mitral and five tufted cell populations with characteristic transcription factor network topology and cell adhesion and excitability-related gene expression. Finally, by integrating bulk and snRNA-seq data we propose that different mitral cell populations selectively project to different regions of olfactory cortex. Together, we have identified potential molecular and gene regulatory mechanisms underlying PN diversity and provide new molecular entry points into studying the diverse functional roles of mitral and tufted cell subtypes.


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