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PubMed2000

Ultrastructural characteristics and conduction velocity of olfactory receptor neuron axons in the olfactory marker protein-null mouse.

Olfactory receptor neuron (ORN) axon diameters and the conduction velocity of the compound action potential along ORN axons were studied in olfactory marker protein (OMP)-null mice and genotypically matched controls. The compound action potential was distinguished from postsynaptic field potentials by its shorter latency, its persistence following application of cobalt or kynurenic acid that blocked postsynaptic responses, and its ability to follow paired-pulse stimulation at 300 Hz. Blockade of the postsynaptic field responses by kynurenic acid indicates that in the mouse, as in the rat, glutamate is the olfactory nerve transmitter. The mean conduction velocity of ORNs in wild-type control mice was 0. 47+/-0.19 (S.E.M.) m/s (n=5), similar to the conduction velocity reported for other mammals. The mean diameter of ORN axons in control mice was 0.202+/-0.005 and 0.261+/-0.006 microm in the OMP-null mice. This increase in fiber diameter in the OMP-nulls predicts an increase in impulse conduction velocity. However, the mean conduction velocity of OMP-null mice, 0.38+/-0.03 m/s (n=6), was not significantly different from control (P>0.1). The conduction velocity predicted by the increase in fiber diameter in OMP-null mice was within the 95% confidence interval of the measured value. Thus, OMP-null ORNs are normal with respect to the conduction velocity of their axons. The number of axodendritic synapses in the glomeruli of OMP-null mice is higher than in congenic wild-type mice.

Action Potentials↗
PubMed2005

Seasonal meningoencephalitis in Holstein cattle caused by Naegleria fowleri.

Primary amoebic meningoencephalitis is a fulminant infection of the human central nervous system caused by Naegleria fowleri, a free-living amoeba that thrives in artificially or naturally heated water. The infection usually is acquired while bathing or swimming in such waters. The portal of entry is the olfactory neuroepithelium. This report describes fatal meningoencephalitis caused by N. fowleri in Holstein cattle that consumed untreated surface water in an area of California where summer temperatures at times exceed 42 degrees C. In the summers of 1998 and 1999, severe multifocal necrosuppurative hemorrhagic meningoencephalitis was observed in brain samples from nine 10-20-month-old heifers with clinical histories of acute central nervous system disease. Olfactory lobes and cerebella were most severely affected. Lesions were also evident in periventricular and submeningeal neuropil as well as olfactory nerves. Naegleria fowleri was demonstrated by immunohistochemistry in brain and olfactory nerve lesions and was isolated from one brain. Even though cultures of drinking water did not yield N. fowleri, drinking water was the likely source of the amoeba. The disease in cattle closely resembles primary amoebic meningoencephalitis in humans. Naegleria meningoencephalitis should be included among differential diagnoses of central nervous system disease in cattle during the summer season in areas with high ambient temperatures.

Amebiasis↗
PubMed1980

[Activation of afferent pathways and of control frog olfactory bulb and extracellular field potentials].

It has been recorded the extracellular field potentials of the frog's olfactory bulb produced by electrical stimulation of the commissura anterior and small branches of the olfactory nerve. The activation of the commissural system obtain a positive, long-lasting field potential generated at the soma of the granular cells. The olfactory nerve stimulation produce also a positive surface wave bath at the end of bulbar reply: this effect can be attributed to the activation of the bulbar component of commissural system at the NOA. The recognizable electrical effects of the commissural system allow to make clear the sources of the extracellular field potentials in the bulbar neuronal circuits.

Action Potentials↗
PubMed2001

Ephaptic interactions in the mammalian olfactory system.

Ephaptic coupling refers to interactions between neurons mediated by current flow through the extracellular space. Ephaptic interactions between axons are considered negligible, because of the relatively large extracellular space and the layers of myelin that separate most axons. By contrast, olfactory nerve axons are unmyelinated and arranged in tightly packed bundles, features that may enhance ephaptic coupling. We tested the hypothesis that ephaptic interactions occur in the mammalian olfactory nerve with the use of a computational approach. Numerical solutions of models of axon fascicles show that significant ephaptic interactions occur for a range of physiologically relevant parameters. An action potential in a single axon can evoke action potentials in all other axons in the fascicle. Ephaptic interactions can also lead to synchronized firing of independently stimulated axons. Our findings suggest that ephaptic interactions may be significant determinants of the olfactory code and that such interactions may occur in other, similarly organized axonal or dendritic bundles.

Action Potentials↗
PubMed1985

Membrane specializations of neuritic growth cones in vivo: a quantitative IMP analysis.

The internal structure of the membranes of axonal and Schwann cell growth processes was examined by freeze-fracture in the growing olfactory nerve, a simple in vivo system consisting of a homogeneous neuronal population. Excision of the mature nerve of adult bullfrogs provides well-synchronized primary neuritic outgrowth that is highly enriched in growth cones at its distalmost segment. The extreme uniformity of olfactory axons in terms of their diameter and their intramembrane particle (IMP) composition permits clear identification of the cellular origin of the growth cone structures observed in replicas. In vivo, growth cones of the olfactory nerve appear as irregularly shaped enlargements of the distal tip; filopodia are only infrequently exposed by the fracture plane. Axonal and Schwann cell growth cones are distinguished by 1) the larger size of the Schwann cell growth cone and the smaller diameter of its attached processes, and 2) the distinct differences in IMP composition of Schwann cell and axonal growth cones and cell processes. Schwann cell growth cones display a uniformly high IMP density on their P-face leaflet, with the exception of circumscribed moundlike protrusions that are relatively free of IMPs. In contrast, axonal growth cones display sharp regional variation in IMP density on their P-face: broad regions almost devoid of IMPs are interspersed with zones of high IMP density. Cytotic profiles occur within high IMP density zones located, most often, at the base of the axonal growth cone. A comparison of IMP size histograms of both high and low-density regions of axonal growth cones and that of the neighboring distal shaft of the axon indicates a strict partitioning of membrane components between these two regions. The IMP profile of the axonal growth cone, notable for its relative enrichment in large-diameter particles, suggests that IMP components of the growth cone are delivered to the distal tip by a mechanism that is distinct from the lateral diffusion process described for particles of the growing axon's shaft [cf. Small and Pfenninger, 1984]. The IMP profile of the concave P-face leaflet of the internal vesicles found clustered at the base of the growth cone is more similar in composition to the profile of the neuronal shaft than that of the growth cone.

Animals↗
PubMed1996

Joint migration of gonadotropin-releasing hormone (GnRH) and neuropeptide Y (NPY) neurons from olfactory placode to central nervous system.

The olfactory epithelium in vertebrates generates the olfactory sensory neurons and several migratory cell types. Prominent among the latter are the gonadotropin-releasing hormone (GnRH) neurons that differentiate within the olfactory epithelium during embryogenesis and migrate along the olfactory nerve to the central nervous system. We initiated studies to characterize additional neuronal phenotypes of olfactory epithelial derivation. Neuropeptide Y (NPY) neurons are functionally related to the reproductive axis, modulating the release of GnRH and directly enhancing GnRH-induced luteinizing hormone (LH) secretion from gonadotrophs. We demonstrate that a population of migratory NPY neurons originates within the olfactory epithelium of the chick. At stage 25, NPY-positive fibers, but not cells, were detected in the epithelium and the nerve. By stages 28-34, NPY neurons and processes were present in the olfactory epithelium, olfactory nerve, and at the junction of the olfactory nerve and forebrain. In these regions the number of NPY neurons increased until stage 30 and then declined as development progressed. Electron microscopic immunocytochemistry confirmed the neuronal phenotype of the NPY-positive cells. The origin and migratory nature of some of these NPY cells was confirmed by double-label immunocytochemical detection of NPY and GnRH. A large percentage of the NPY-cells coexpressed the GnRH peptide. Between stages 28 and 34 single- and double-labeled NPY and GnRH neurons were found side by side along the GnRH migratory route emanating from the nasal epithelium, along the olfactory nerve, and into the ventral forebrain. These data suggest that an NPY population originates in the olfactory epithelium and migrates into the central nervous system during embryogenesis. By stage 42, no NPY/GnRH double-labeled cells were detected.

Animals↗
PubMed1981

Analysis of synaptic potentials in mitral cells in the isolated turtle olfactory bulb.

1. The synaptic responses of mitral cells have been analysed in intracellular recordings from the isolated olfactory bulb of the turtle. 2. The response of a mitral cell to a single volley in the lateral olfactory tract consisted of and antidromic impulse and a complex hyperpolarizing potential that had the properties of an inhibitory post-synaptic potential. The inhibitory response consisted of two successive components I1 and I2, followed by a prolonged hyperpolarization. 3. High-gain recordings revealed miniature hyperpolarizing potentials during the I1 and I2 responses. Both the miniature potentials and the I1 and I2 responses were increased in amplitude by depolarizing injected currents, and decreased and reversed in polarity by hyperpolarizing currents. The input conductance was increased during the I2 component. In some cells the I1 and I2 components, recorded with micropipettes filled with potassium acetate or potassium citrate, were depolarizing. 4 A single orthodromic volley in the olfactory nerves elicited a complex depolarizing-hyperpolarizing potential in mitral cells. The depolarization consisted of two successive components, E1 and E2. The hyperpolarization consisted of two successive components, I1 and I2, followed by a prolonged hyperpolarization. 5. The depolarizing components had the properties of excitatory post-synaptic potentials. They decreased in amplitude with depolarizing current injection and increased with hyperpolarizing injection. The hyperpolarizing components resembled the I1 and I2 components of the tract-evoked responses in their timing and properties. 6. It is postulated that the E1 component reflects the initial excitation by olfactory nerve terminals of the mitral cell dendritic tufts in the olfactory glomeruli. The I1 component is postulated to arise from dendrodendritic synaptic input mediated by interneurones, mainly granule cells. The E2 and I2 components are likely to arise mainly from intrinsic synaptic circuits within the olfactory bulb.

Animals↗
PubMed1980

Effects of carnosine on olfactory bulb EEG, evoked potentials and DC potentials.

Carnosine is a dipeptide found in great quantities in the primary olfactory nerve and has been suggested to be the neurotransmitter of the olfactory receptor axons. The aim of the present study was to describe some of its electrophysiological actions in the olfactory bulb (OB) of rabbits under anesthesia. Carnosine as a 10% solution in amounts of 2-5 microliter was injected to the OB at the level of the glomerular layer by means of a pipette attached to a Hamilton syringe. Average evoked potentials (AEPs) on the stimulation of the lateral olfactory tract (LOT-AEP), electroencephalographic (EEG) activity and slow potential (DC) recordings were obtained. The LOT-AEPs were analyzed by fitting damped sine waves to them. The parameters of amplitude, frequency, decay rate, phase and rise rate were measured and statistically compared to the values obtained prior to the carnosine injection. An increase in frequency and decreases in the phase and the decay rate of the AEP were found. Carnosine also produced a sustained oscillation in the EEG and a surface negative, deep positive shift in the DC recording. The changes were maximal within the first minute after injection and lasted 2-7 min. Tyrodes' solution, which was used as the carnosine vehicle, did not produce any changes, nor did beta-alanine, which is one of the constituents of carnosine, at equivalent osmotic concentrations. It is concluded that carnosine has an excitatory action on the mitral/tufted cells, and that this effect is obscured by a secondary increase in granule cell (inhibitory) activity.

Animals↗
PubMed1989

Olfactory receptor cells: immunocytochemistry for nervous system-specific proteins and re-evaluation of their precursor cells.

The immunohistochemical localization of nervous system-specific proteins and cytokeratin in the olfactory mucosa is described mainly in humans and guinea pigs. Immunoreactivity for neuron-specific enolase (NSE) was demonstrated in olfactory receptor cells including their dendrite and axon. Immunoreactivity for neurofilament protein (NFP) was contained in the dendrite and perikaryon of the olfactory cells, but not in the axon. Immunoreactivity for spot-35 protein, a kind of neuron-specific proteins was selectively localized in several flask-shaped cells of the olfactory epithelium only in the guinea pig. These spot-35 protein-positive cells were suspected of being microvillar cells, considered the second type of receptor cells dispersed in the olfactory epithelium. Immunoreactivity for glia-specific S-100 protein was demonstrated in the Bowman's glands as well as Schwann cells associated with the olfactory nerves in the lamina propria. Supporting cells were not immunolabelled with any antisera against nervous system-specific proteins. Cytokeratin, a useful marker for epithelial cells, was expressed exclusively in basal cells. Axotomy of olfactory nerves induced the disappearance of the olfactory receptor cells with NSE immunoreactivity 3 days after the operation. Regenerating cells showing NSE immunoreactivity were first recognized in the lower portion of the epithelium within 7 days. The epithelium was completely repaired 3-4 weeks later and came to contain many NSE-reactive mature receptor cells. Bromodeoxyuridine (BrdU), administered during regeneration of the olfactory epithelium, was immunohistochemically detected in the cells of the layer above the basal cell layer, but not in the latter itself. This result does not support the general contention that the receptor cells originate from the basal cells.

Animals↗
PubMed1980

Developmental history of nervus terminalis in embryos of insectivorous bats.

Insectivorous bat embryos (Tadarida and Myotis) ranging from 6- to 16-mm C-R length were examined for the presence of the nervus terminalis. These embryos have no vomeronasal nerve with which the nervus terminalis could be confused. The nerve and associated ganglion cells first appear in the 7-mm embryo. As the embryo ages, a gradual increase in nerve size and ganglion cell numbers occurs. In the 13-mm embryo, nerve size and ganglion cell numbers are reduced, and in older embryos both nerve and cells are absent, as in the adult. The ganglion cells arise as clusters from the nasal septal epithelium. The largest number of cell clusters occurs in the 10.5-mm embryo. Their number then decreases and none are present in embryos of 13-mm and longer. These cells migrate centrally along the course of the nerve which accompanies the olfactory nerve from the nasal cavity roof to a level just caudal to the olfactory bulb, where the nervus terminalis turns dorsalward along the medial telencephalic wall surface. Except in the youngest and oldest embryos the nervus terminalis, where present, divides into two or three branches to pierce the hemispheric wall, one usually entering the region of the nucleus olfactorious anterior, and the other(s), the region of the medial septal nucleus. In some cases, several ganglion cells are present along the intrahemispheric course of the nerve fibers. All ganglion cells resemble those in various sensory ganglia, and so, are probably also sensory neurons.

Animals↗
PubMed1986

A reinvestigation of the Gn-RH (gonadotrophin-releasing hormone) systems in the goldfish brain using antibodies to salmon Gn-RH.

The organization of Gn-RH systems in the brain of teleosts has been investigated previously by immunohistochemistry using antibodies against the mammalian decapeptide which differs from the teleostean factor. Here, we report the distribution of immunoreactive Gn-RH in the brain of goldfish using antibodies against synthetic teleost peptide. Immunoreactive structures are found along a column extending from the rostral olfactory bulbs to the pituitary stalk. Cell bodies are observed within the olfactory nerves and bulbs, along the ventromedial telencephalon, the ventrolateral preoptic area and the latero-basal hypothalamus. Large perikarya are detected in the dorsal midbrain tegmentum, immediately caudal to the posterior commissure. A prominent pathway was traced from the cells located in the olfactory nerves through the medial olfactory tract and along all the perikarya described above to the pituitary stalk. In the pituitary, projections are restricted to the proximal pars distalis. A second immunoreactive pathway ascends more dorsally in the telencephalon and arches to the periventricular regions of the diencephalon. Part of this pathway forms a periventricular network in the dorsal and posterior hypothalamus, whereas other projections continue caudally to the medulla oblongata and the spinal cord. Lesions of the ventral preoptic area demonstrate that most of the fibers detected in the pituitary originate from the preoptic region.

Animals↗
PubMed2001

Smelling of odorous sex hormone-like compounds causes sex-differentiated hypothalamic activations in humans.

The anatomical pathways for processing of odorous stimuli include the olfactory nerve projection to the olfactory bulb, the trigeminal nerve projection to somatosensory and insular cortex, and the projection from the accessory olfactory bulb to the hypothalamus. In the majority of tetrapods, the sex-specific effects of pheromones on reproductive behavior is mediated via the hypothalamic projection. However, the existence of this projection in humans has been regarded as improbable because humans lack a discernable accessory olfactory bulb. Here, we show that women smelling an androgen-like compound activate the hypothalamus, with the center of gravity in the preoptic and ventromedial nuclei. Men, in contrast, activate the hypothalamus (center of gravity in paraventricular and dorsomedial nuclei) when smelling an estrogen-like substance. This sex-dissociated hypothalamic activation suggests a potential physiological substrate for a sex-differentiated behavioral response in humans.

Adult↗
PubMed2001

[The avian peripheral olfactory system: model for study of apoptosis and cellular regeneration].

UNLABELLED: A reliable model, usable in vitro and in vivo, is necessary for analysis of processes engaged during cell death, regeneration and differentiation. The peripheral olfactory system is an attractive model for studying these processes through its dynamic neurogenesis that occurs continually throughout the lifetime. STUDY AIM: The aim of this study was the analysis of these processes on an animal model. MATERIAL AND METHODS: We performed axotomy of the nerve olfactory on young animals and chicken embryos E17. Then we infused IGF-I (insulin-like growth factor-I) in the lesioned site. Death, regeneration and differentiation of cells were studied by immunocytology. RESULTS: After hatching, the section of the olfactory nerve induced a rapid neuronal apoptosis at the 24th hour followed by a wave of mitosis 24 hours later. In prenatal stages, the response to the axotomy was rather similar to a dedifferentiation. In postnatal stages, the IGF-I infusion at the lesioned site had a triple function: survival of mature neurons, maintenance of differentiation and stimulation of mitosis. The neoneurogenesis, which occurred from neuronal stem cells would depend on the maturation and environment of the olfactory neurons protected from apoptosis by IGF-I. CONCLUSION: The avian olfactory epithelium is a good model for analysis of cell death, regeneration and differentiation. The capacity of these neuronal stem cells to dedifferentiate makes then more primitive than the pluripotent cells, closer to totipotent embryonic stem cells.

Animals↗
PubMed1984

Fiber systems in the olfactory bulb and cortex: a study in adult and developing rats, using the timm method with the light and electron microscope.

The structure of the olfactory bulb and cortex of rats is described using the Timm method, in which endogenous transition or "heavy" metals are precipitated with sulfide and then stained with silver. With the light microscope, two types of staining, a fine, "colored" reaction and a coarse, "granular" reaction, are found in the neuropil of the adult forebrain; neuronal somata, fiber tracts, and some specific areas of the neuropil are almost unstained. With the electron microscope the Timm method consists of small silver granules, which are associated with axon terminals. These granules are located over the external surface of the presynaptic membrane, facing the synaptic cleft, and over synaptic vesicles, especially the internal surface of the vesicle membrane. This localization suggests that the reactive metals are related to a membrane component which is recycled during secretion of synaptic transmitters. The colored and granular reactions seen with the light microscope appear to be correlated with different intensities of staining of different types of axon terminals. The full extent of the olfactory cortex can be delineated by a bilaminar staining pattern in layer I, which coincides with the pattern of termination of fiber systems to the cortex demonstrated by axonal tracing experiments. The superficial part of layer I is very palely stained; this corresponds precisely to layer Ia, the zone of termination of fibers from the olfactory bulb. In contrast, the deep part of the layer is stained with an intense colored reaction; this corresponds precisely to layer Ib, the zone of termination of the major association fiber system within the olfactory cortex. A prominent granular reaction, which does not correspond to any known long axon system, is found in all layers of the cortex, although it is concentrated at the superficial edge of layer Ib and in layer II. Variations in staining in the several subdivisions of the olfactory cortex are illustrated and described. In the olfactory bulb, the most prominent staining is a relatively fine, granular reaction in the glomerular formations, which apparently corresponds to the olfactory nerve terminals. In immature rats, the Timm method stains the neuropil throughout the olfactory system, although the patterns and quality of staining differ from that found in adults. Before birth, the best-differentiated reaction is seen in glomeruli of the olfactory bulb and correlates well with the pattern of olfactory nerve ingrowth.(ABSTRACT TRUNCATED AT 400 WORDS)

Aging↗
PubMed1992

Nerve growth factor receptor and the transplanted rat olfactory bulb.

Nerve growth factor receptor (NGFR) in the rat olfactory system is developmentally regulated, localizing to the olfactory nerve (ON) in the young rat, and to the olfactory bulb (OB) glomeruli in the adult (Vickland et al. 1991. Brain Res., in press). This pattern of immunoreactivity (IR) may indicate the state of axon growth in the young ON and synaptogenesis in the adult glomeruli. Additional experiments in our laboratory involving lesions to the ON in adult rats have shown a recapitulation of the developmental pattern of expression: NGFR-IR is again found along the ON. Longer survival times after lesioning show the reexpression of the adult pattern of NGFR-IR. This phenomenon was further explored in a transplant (TX) model to determine the changes in NGFR-IR in both the host and TX tissue. A fetal OB labeled with [3H]thymidine is placed into the space created by the removal of the OB of a neonatal rat. After survival times of 1, 2, 8, and 13 weeks, the host animal is sacrificed and the OB TX is processed using monoclonal antibody 192 IgG for NGFR. The host ON shows strong NGFR-IR in TX of 1- and 2-week survival times. In TX survival times of 8 weeks or more, NGFR-IR is observed in glomerulus-like structures. All of these glomerulus-like structures are near groups of neurons in the TX tissue, indicating that they may be functional, with appropriate synapses. Therefore, even though the adult pattern of NGFR-IR takes longer to become established than in normal rats, we have demonstrated that this pattern does so in the TX OB model.

Animals↗
PubMed1992

The bilateral bulbar projections of the primary olfactory neurons in the frog.

Whether or not the frog olfactory neuroreceptor cells project bilaterally to the olfactory bulb is still a debated question. We therefore decided to ascertain whether bilateral projections of the primary olfactory input exist and if so to investigate their extent. Reproducible extracellular bilateral bulbar potentials were recorded in the frog following electrical stimulation of dorsal or ventral olfactory nerve bundles. The general features of the contralateral evoked responses were very similar to those of the ipsilateral response. The contralateral response disappeared after transection of the rostral part of the olfactory interbulbar adhesion but not following transection of the habenular or anterior commissures. Horseradish peroxidase labelling showed that the fiber terminations of the olfactory nerve bundle was not restricted to the ipsilateral olfactory bulb but included the medial aspects of the contralateral bulb. The intertelencephalic sections increased the magnitude of the ipsilateral evoked responses. Olfactory bulb isopotential maps revealed a rough topographical correspondence between the olfactory neuroepithelium and bulb along the medio-lateral axis as well as along the dorso-ventral axis. In addition, a projection of the medial and central part of the olfactory sac to the medial part of the contralateral olfactory bulb through the interbulbar adhesion was confirmed. These findings suggest first, that the fibers from the neuro-receptors located in either the ventral or the dorsal olfactory mucosae project to both olfactory bulbs, and second, that the left and right bulbs exert a constant inhibition on each other via the habenular commissure.

Animals↗
PubMed1977

Aging of the rat olfactory bulb: growth and atrophy of constituent layers and changes in size and number of mitral cells.

A quantitative study of the rat olfactory bulb during aging was carried out by directly measuring or calculating the following parameters at 3, 12, 24, 27, and 30 months: The volume of the glomerular, external plexiform, and internal granular layers, a relative measure of the size of the olfactory nerve layer, the mean volume of mitral cell nuclei and perikarya, a relative measure of the mean volume of the mitral cell dendritic tree as well as the total length and mean cross-sectional area of its constituent dendrites, and number of mitral cells. In addition, measurements of the size and number of mitral cells in the accessory olfactory bulb were performed. Data were analyzed with analysis of variance, multiple range tests for differences means at the various ages, and simple, partial, and multiple product-moment correlations. From 3 to 24 months a linear increase of approximately 50% occurs in all layers of the olfactory bulb. During this time the mean perikaryal volume and dendritic volume of mitral cells increases, also in a linear fashion, approximately 100%. No significant change occurs in the number of mitral cells. From 24 to 30 months a significant decrease occurs in the volume of the layers. Although the total volume of mitral cell dendritic trees decreases slightly from 24 to 27 months, the volume of individual mitral cell dendritic treess, as well as perikaryal and nuclear size, increases sharply during this period, apparently in compensation for a sharp decrease in the number of mitral cells which occurs at this time. From 27 to 30 months no further decrease in mitral cell number occurs, but the size of mitral cell perikarya, and especially dendritic trees, decreases sharply. The coordinated increase in olfactory bulb size from 3 to 24 months appears to be a comtinuation into adult life of earlier postnatal increases. The atrophy from 24 to 30 months appears not to be associated with peripheral rhinitis, since the glomerular and olfactory nerve layers do not show greater atrophy than the other layers, and atrophy also occurs in the accessory olfactory bulb, which is supplied by nerves from the vomeronasal organ, a structure not normally subject to rhinitis.

Aging↗
PubMed2006

Subdivision of the accessory olfactory bulb in the Japanese common toad, Bufo japonicus, revealed by lectin histochemical analysis.

Lectin binding patterns in the olfactory bulb of the Japanese common toad, Bufo japonicus, were examined using 21 types of lectin. Ten out of 21 lectins, WGA, s-WGA, LEL, STL, DBA, VVA, SJA, RCA-I, PNA, and PHA-L, stained the olfactory nerve, the glomeruli in the main olfactory bulb (MOB), the vomeronasal nerve, and the glomeruli in the accessory olfactory bulb (AOB). The binding patterns of LEL, STL, DBA, and PHA-L subdivided AOB glomeruli into rostral and caudal regions, where LEL, STL, and DBA stained the rostral region more intensely than the caudal region, and PHA-L had the opposite effect. Another lectin, BSL-I, stained both AOB glomeruli and the vomeronasal nerve, but not MOB glomeruli or the olfactory nerve. This is the first report of histological subdivision in the AOB of an amphibian, which suggests that the AOB development in Bufo may be unique.

Adaptation, Physiological↗