Olfaction and neurogenesis in the olfactory epithelium

Anosmia was experimentally produced in strain C57BL/6 laboratory mice by treatment with 1% zinc sulfate solution. Structural and functional changes taking place in the olfactory epithelium were investigated during this process and during reinstatement of olfaction. Isoamyl acetate, butyl acetate, and substances present in murine urine were used as olfactory stimuli. Response to these odorants was found to recover from zinc sulfate action at different rates. The highest (both relative and absolute) daily rise in amplitude response was that induced by isoamyl acetate and butyl acetate and lowest in the case of odors of biological origin. Response to olfactory stimuli recovered most rapidly in the areas of the epithelium where maximum response to the same stimuli had been seen in intact animals."Biopharmautomatica" Combined Research and Production Unit, Gor'kii. Translated from Neirofiziologiya, Vol. 22, No. 4, pp. 500–506, July–August, 1990.     

Spatial distribution of electrical response in the mouse olfactory epithelium

Response from different areas of the olfactory epithelium was investigated in laboratory mice of two genetically pure strains (AKR and C57BL/6) to stimulation by isovaleric acid and isoamylacetate using electroolfactographic recording techniques. Apparently, genetically determined spatio-functional heterogeneity was found in the olfactory epithelium of these laboratory animals. Regions of greatest response to the action of the two different substances, although spatially distinct, could partially overlap; their position remained unchanged by altering the concentration of the test substances.Institute of Applied Mathematics and Cybernetics, N. I. Lobachevskii University, Gor'kii. Translated from Neirofiziologiya, Vol. 20, No. 5, pp. 597–602, September–October, 1988.     

Morphofunctional research into the mouse olfactory organ following the action of zinc sulfate

Correlations between morphological and functional changes occurring in the olfactory epithelium after treatment with various concentrations of zinc sulfate were investigated during experiments on mice. Electroolfactogram recordings (EOG) and epithelium morphometry showed that the intensity of damaging effects and the speed of regenerative processes at work in the epithelium are concentration-dependent. Amplitude of EOG and thickness of the olfactory epithelium have almost reached their normal level by the first month after olfactory epithelium treatment with a 1% zinc sulfate solution, while recuperative processes have only just started during this period when higher concentrations were used. It was noted that the capacity for generating EOG recovered well after processes of structural recovery in the olfactory epithelium and that application of higher concentrations of zinc sulfate (3 and 5%) increased the amount by which rise in EOG amplitude lagged behind thickening of the epithelium compared with the 1% solution.Research Institute of Applied Mathematics and Cybernetics, N. I. Lobachevskii University, Gor'kii. Translated from Neirofiziologiya, Vol. 19, No. 6, pp. 796–802, November–December, 1987.     

Electroolfactogram study of the unilaterally axotomized frog

Changes of amplitude in the electroolfactogram (EOG) were investigated following unilateral section of the olfactory nerve. A reduction in EOG amplitude was observed during the first two weeks after the operation; electrical activity gradually began to return to normal and reached 80–100% of control level for trial substances by the end of the third week. Complete disappearance of EOG over the entire surface of the olfactory organ was not observed in any of the animals. A reduction in EOG amplitude was also noted on the unoperated side of the olfactory organ. These changes were less pronounced: the decrease in electrical response level began at a later stage, while complete recovery in amplitude was achieved sooner. Findings showed that EOG amplitude changed at different rates in different areas of the olfactory epithelium; it decreased sooner and began to recover at a later stage in the caudal than in the centromedial portion of the olfactory organ.Institute of Applied Mathematics and Cybernetics, N. I. Lobachevskii University, Gor'kii. Translated from Neirofiziologiya, Vol. 18, No. 5, pp. 603–610, September–October, 1986.     

Electrophysiological evidence for detection and discrimination of pheromonal bile acids by the olfactory epithelium of female sea lampreys (<Emphasis Type="Italic">Petromyzon marinus</Emphasis>)

Electro-olfactograms were used to determine sensitivity and specificity of olfactory organs of female sea lampreys (Petromyzon marinus) to four bile acids: 3-keto petromyzonol sulfate and 3-keto allocholic acid from spermiating males and petromyzonol sulfate and allocholic acid from larvae. Spermiating male bile acids are thought to function as a mating pheromone and larval bile acids as a migratory pheromone. The response threshold was 10^–12 mol l^–1 for 3-keto petromyzonol sulfate and 10^–10 mol l^–1 for the other bile acids. At concentrations above 10^–9 mol l^–1, the sulfated bile acids showed almost identical potency, as did the non-sulfated bile acids. The two sulfated bile acids were more potent than the two non-sulfated ones. In addition, 3-keto petromyzonol sulfate and water conditioned with spermiating males induced similar concentration-response curves and response thresholds. Cross-adaptation experiments demonstrated that the sulfated and non-sulfated bile acids represent different odors to the olfactory epithelium of females. Further exploration revealed that 3-keto petromyzonol sulfate represents a different odor than petromyzonol sulfate, while 3-keto allocholic acid and allocholic acid represent the same odor. Results indicate that male-specific bile acids are potent and specific stimulants to the female olfactory organ, supporting the previous hypothesis that these bile acids function as a pheromone.Abbreviations 3kACA 3-keto allocholic acid - 3kPZS 3-keto petromyzonol sulfate - ACA allocholic acid - ANOVA analysis of variance - ELISA enzyme-linked immunosorbent assay - EOG electro-olfactogram - PIR percent initial response - PZS petromyzonol sulfate - SMW spermiating male washings     

The influence of early odour experience on the neural response of the olfactory bulb in laboratory mice

Summary In mice (strain NMRI) the influence of olfactory rearing conditions on the ontogenetic development of the bulbar electroencephalogram (EEG) was investigated.The cages of control animals were perfused continually with filtered air, whereas in the three experimental groups geraniol was added to the atmosphere at different times (group G_0–13, from birth till day 13; group G_0–6, from birth till day 6; group G_6–12, from day 6 till day 12). At various ages the EEG of the bulbus olfactorius was studied by means of permanently implanted tungsten electrodes, and the neural response to nest odour and geraniol (10^–2 vol. %) was recorded.No differences were found between the groups regarding the overall development of the bulbar EEG, nor did the raising conditions affect the neural response to nest odour. However, in groups G_0–13 and G_6–12 a marked response to the odour of geraniol was recorded, while in the controls and the individuals that had experienced geraniol only during their first week of life, the bulbar response to this odourant did not differ from that obtained following stimulation with clean air. In the animals of group g_0–13, which were investigated as adults (day 70), the prominent geraniol response was still recordable 2 months after the last contact with the odour.These results indicate that odours experienced during a sensitive period in the nest evoke neuronal alterations in the olfactory system of the mouse that facilitate processing of a known odourant.     

Distribution and severity of spontaneous lesions in the neuroepithelium and Bowman’s glands in mouse olfactory mucosa: age-related progression

Age-related changes were examined in the distribution and severity of spontaneous lesions in the neuroepithelium and Bowman’s glands in mouse olfactory mucosa. The olfactory mucosa of female ICR mice at postnatal ages from 10 days to 16 months were investigated histologically by hematoxylin and eosin staining, high-iron diamine-Alcian blue (HID-AB) staining, and immunohistochemistry for olfactory marker protein (OMP), βIII tubulin (βIIIT), and Ki67. The lesions in the neuroepithelium and Bowman’s glands were quantitatively assessed by morphometric analyses of sections stained with anti-OMP antibody or HID-AB. The first appearance of neuroepithelial abnormality was observed in the dorsomedial portion of the olfactory mucosa in 5-month-old mice. The distribution and severity of lesions progressed with increasing age. In mildly affected epithelium in which OMP-positive olfactory receptor neurons (ORNs) were present but in smaller amounts, the numbers of βIIIT-positive and Ki67-positive neuroepithelial cells tended to be increased, indicating that neurogenesis was upregulated in these areas. In contrast, severely affected epithelium in which OMP-positive ORNs were virtually absent showed high variability in the numbers of βIIIT- and Ki67-positive cells among the areas examined, probably reflecting differences in the capacity of the basal cells remaining in the affected area to generate new neuronal cells. Histological analysis with HID-AB revealed that spontaneous lesions in Bowman’s glands also occurred in aged mouse olfactory mucosa. Lesions in the neuroepithelium and underlying Bowman’s glands tended to be spatially co-localized, suggesting a close association between pathogeneses in these two structures. Moreover, lesions in Bowman’s glands were associated with changes in the biochemical composition of mucus on the olfactory mucosa. This information should prove useful in improving the understanding of the pathogenetic mechanisms underlying age-related changes in the peripheral olfactory system. This work was supported by grants from the Japanese Ministry of Education, Culture, Sports, Science, and Technology (nos. 14770886, 16790987 and 18799002; K. Kondo) and a grant from the Japanese Ministry of Health, Labour, and Welfare (Comprehensive Research on Aging and Welfare, no. H13-choju-012; K. Nibu).     

The microvillar cells of the olfactory epithelium in swine

Electron microscopic studies have been made on the olfactory porcine epithelium. Peculiarities of distribution of microvillar cells in the olfactory epithelium are described and their morphometric parameters are presented. It was shown that cells with long microvilli on their apex are located in the epithelium which covers the inner side of the perforated bone. Cells which have only microvillar enlargement on their apex were found on the external surface. Differential localization of microvillar cells in the olfactory epithelium indicates the existence of zones with different sensitivity. Reduction of the microvilli presumably is associated with active work or with ageing of a cell, and may correspond to those zones of the olfactory epithelium which possess different sensibilization.     

Receptive fields of second-order neurons in the olfactory bulb of the hamster

Electrical stimulation of nerve fibers emerging from different positions of the olfactory epithelium was used to determine the receptive fields for 52 olfactory bulb neurons in the hamster. The responses of olfactory bulb neurons were recorded extracellularly with metal-filled micropipettes. Suprathreshold stimuli (500 microA) were applied to each of eight standard epithelial positions spaced approximately 250 microns apart, and the position, or positions, which, when stimulated, produced a response in the bulb were taken as an index of the neuron's receptive field. The results indicate that most bulb neurons have very localized receptive fields limited to only one or two stimulating positions. Furthermore, there was a statistically significant correlation between the location of a neuron's receptive field in the olfactory epithelium and the recording depth of the neuron in the olfactory bulb (Spearman rank correlation coefficient, rs, 0.67, P < 0.001). These findings demonstrate that in the mammalian olfactory system there exists a topographical projection of input from localized regions in the epithelium onto the second-order neurons in the olfactory bulb.     

Subcellular aging markers of retinal pigment epithelium in Japanese quail Coturnix japonica

Age-related changes of retinal pigment epithelium of the Japanese quail, which at present is a promising experimental model of accelerated aging, were studied by electron microscopy using morphometric analysis. It was established that, along with accumulation of lipofuscin granules and ultrastructural changes of the Bruch’s membrane, changes in the shape of nuclei and mitochondria (increase in the portion of ring-shaped and dumbbell-like mitochondria), decrease in the amount of myeloid bodies, and disorganization of basal infoldings are also aging markers of retinal pigment epithelium.     

Effects of reversible nare occlusion on the development of the olfactory epithelium in the rabbit nasal septum

Summary To investigate environmental influences on the development of the olfactory epithelium, semi-thin sections were taken from the nasal septum of newborn and 30-dayold rabbits; the epithelial thickness and the number of olfactory knobs, supporting cells, dark basal cells, and receptor cells were compared. During normal development, a marked increase in epithelial thickness was found, largely because of an increase in the number of receptor cells. Whereas unilateral nare occlusion on day 1 resulted in 10% fewer receptor cells and 25% fewer knobs on the deprived side by day 30, nare occlusion either up to or after day 5 had little effect, and even temporary reopening from days 6–7 was sufficient to stimulate receptor-cell development on the occluded side. Although in these latter cases, a slight deprivation effect of 6% was still found in the number of receptor-cell nuclei, there was no longer a significant difference in the number of knobs between the open and closed sides. Thus, whereas exposure to the environment during the first days of life appears to be sufficient to stimulate sustained growth, the deprived epithelium may retain the capacity to respond to such cues beyond this time. However, as nare occlusion also had an effect on the respiratory epithelium and nasal lymphatic tissue, the nature of the cues stimulating receptor-cell development, whether olfactory or non-olfactory, is not yet clear.     

An investigation of the role of dopamine in the antennal lobes of the honeybee,Apis mellifera

Summary The effects of dopamine applied to the antennal lobes of the honeybee are investigated using the proboscis conditioning paradigm (Kuwabara 1957). The percentage of bees responding to a conditioned olfactory stimulus after a single conditioning trial is reduced significantly by the application of dopamine (10^–6 M) to the antennal lobes of the bee brain. Reduction in response levels is significantly smaller in bees conditioned to the olfactory stimulus in multiple conditioning trials prior to treatment with dopamine. The effects of dopamine on the percentage of bees responding to a conditioned olfactory stimulus are blocked by the butyrophenone, haloperidol (10^–5 M). The possible role of dopaminergic interneurones in the antennal lobes of the bee brain is discussed.     

Feinstruktur des Riechepithels von Calamoichthys calabaricus J. A. Smith (Pisces,Brachiopterygii)

Zusammenfassung Die vorliegende Untersuchung befaßt sich mit der Feinstruktur der Riechfalten von Calamoichthys calabaricus unter besonderer Berücksichtigung des Riech- und Flimmerepithels. — Das Flimmerepithel ist aus 3 Zelltypen aufgebaut: Flimmerzellen, wenigen Stützzellen und Basalzellen. Die Flimmerzellen sind mitochondrienreich und tragen bis zu 160 Flimmerhärchen pro Zelle. Diese Kinocilien besitzen an ihren Basalkörpern Zilienwurzeln, von denen ein Teil ins Zellinnere bis in Kernnähe zieht, während der andere Teil parallel zur Oberfläche verläuft und benachbarte Basalapparate verbindet. — Auch das Riechepithel, das gegen das Flimmerepithel scharf abgesetzt ist, besteht aus 3 Zelltypen: Rezeptoren, Stützzellen und Basalzellen. Die Rezeptoren haben eine einheitliche Gestalt und Struktur. Sie sind schlank keulenförmig und überragen mit einer kleinen Vesicula olfactoria die Epitheloberfläche. Seitlich sitzen an der Vesicula — unter konstant 25–27° Ablenkung von der Senkrechten — in der Regel 12 sensorische Cilien, die alle auf gleicher Höhe entspringen. Basal setzt sich das Rezeptorperikaryon in ein Axon fort. Die Axone mehrerer Rezeptoren vereinigen sich noch innerhalb des Epithels zu Bündeln, die durch die Basalmembran ins Bindegewebe ziehen. Die stark osmiophilen Stützzellen des Riechepithels durchziehen das Riechepithel von der Basalmembran bis zur Epitheloberfläche und tragen einzelne Cilien. Der verbreiterte Apikalteil der Stützzellen enthält zahlreiche Schleimvesikel, die auf eine sezernierende Funktion dieser Zellen hinweisen. Die präparative Behandlung von Riechepithelien wird kritisch diskutiert.

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Ultrastructure of the olfactory epithelium of Calamoichthys calabaricus J. A. Smith (Pisces, Brachiopterygii)

Summary The ciliary epithelium of the olfactory folds in Calamoichthys calabaricus is composed of ciliary cells, supporting cells, and basal cells. All ciliary cells contain numerous mitochondria and bear up to 160 kinocilia. Some rootlets of the basal bodies of the kinocilia, project towards the nucleus, while others run parallel to the epithelial surface and connect with neighbouring basal bodies. Ciliary and olfactory epithelia are separated from each other. — The olfactory epithelium contains olfactory receptor cells, supporting cells, and basal cells. The club shaped olfactory receptor cells have a uniform ultrastructure. The terminal portions of the olfactory dendrites form small olfactory vesicles which are seen above the olfactory surface. 12 sensory cilia project constantly to the more basal portion of the olfactory vesicles, each cilium forming a 25–27° angle with the vertical cell axis. Basally, an axon originates from each olfactory receptor cell. Axons from a number of olfactory receptor cells may combine to form bundles within the epithelium. The supporting cells of the olfactory epithelia are strongly osmiophilic. Supporting cells occur in all parts of the olfactory epithelium and bear few cilia. Numerous mucous vesicles, located within the apical region of the supporting cells, probably have a secretory function.

Mit Unterstützung durch die Deutsche Forschungsgemeinschaft.     

Olfaction in Three Genetic and Two MPTP-Induced Parkinson’s Disease Mouse Models

Various genetic or toxin-induced mouse models are frequently used for investigation of early PD pathology. Although olfactory impairment is known to precede motor symptoms by years, it is not known whether it is caused by impairments in the brain, the olfactory epithelium, or both. In this study, we investigated the olfactory function in three genetic Parkinson’s disease (PD) mouse models and mice treated with MPTP intraperitoneally and intranasally. To investigate olfactory function, we performed electro-olfactogram recordings (EOGs) and an olfactory behavior test (cookie-finding test). We show that neither a parkin knockout mouse strain, nor intraperitoneal MPTP treated animals display any olfactory impairment in EOG recordings and the applied behavior test. We also found no difference in the responses of the olfactory epithelium to odorants in a mouse strain over-expressing doubly mutated α-synuclein, while this mouse strain was not suitable to test olfaction in a cookie-finding test as it displays a mobility impairment. A transgenic mouse expressing mutated α-synuclein in dopaminergic neurons performed equal to control animals in the cookie-finding test. Further we show that intranasal MPTP application can cause functional damage of the olfactory epithelium.     

Complex action potentials of secondary neurons of the rat olfactory bulb

Complex action potentials arising spontaneously or evoked by stimulation of the lateral olfactory tract in secondary neurons of the rat olfactory bulb were recorded. The amplitude and duration of the complex potentials varied depending on synchronization of onset of the individual components (of which more than four were distinguished) and their combination. It is suggested that complex potentials were recorded in cases when the electrode was located in the region of the junction between spike-generating zones (the branching node of the dendrite, the junction of the soma with the dendrites and axon). It is concluded that there are numerous generating zones in the dendrites of the secondary olfactory neurons. Evoked action potentials appeared after the following latent periods: first, about 1 msec; second, about 2 msec; and third, about 3 msec. The results of the analysis showed that the antidromic response appeared after the shortest latent period. These results are evidence of the existence of considerable and varied representation of excitatory synapses in secondary neurons (besides the excitatory input in the olfactory glomeruli).M. B. Lomonosov Moscow State University. Translated from Neirofiziologiya, Vol. 8, No. 6, pp. 575–582, November–December, 1976.     

Heme oxygenase-2 and nitric oxide synthase immunoreactivity of bovine olfactory receptor neurons and a comparison with the distribution of NADPH-diaphorase staining

It has recently been suggested that, in addition to nitric oxide (NO), carbon monoxide (CO) is an important gaseous messenger which might be involved in vertebrate olfactory transduction because its effects include activation of guanylyl cyclase and the formation of cGMP. As there is no information regarding the presence of heme oxygenase-2 – the constitutive isoform of the heme oxygenase system – in olfactory neurons of non-rodent species, we have investigated the distribution pattern of heme oxygenase-2 in the olfactory epithelium of the bovine, a representative of macrosmatics. Localization of nicotinamide adenine dinucleotide phosphate-diaphorase (NADPH-d) activity of the olfactory epithelium was compared with heme oxygenase-2 and NO synthase (NOS) immunoreactivities in order to obtain possible hints at functional significance. NADPH-d activity was particularly intense in apical dendrites of receptor neurons. It was also found in Bowman glands and intraepithelial duct cells. Less intense, discrete NADPH-d activity was present also at intermediate and basal levels of the olfactory epithelium, corresponding to the layer of receptor neuron somata and basal cells. While heme oxygenase-2 activity mainly occured in neuronal perikarya, a very intense NOS immunoreactivity, exclusively for the inducible isoform, was detected in the apical dendrites. Ultrastructurally, NADPH-d histochemistry showed distinct labelling of membranes, in particular of endoplasmic reticulum, mitochondria and nucleus. The coincident localization of the moderate NADPH-d activity and heme oxygenase-2 immunoreactivity in receptor cell perikarya suggest a functional association between NADPH-cytochrome P450 reductase and heme oxygenase-2. In contrast, dendritic localization of NADPH-d activity is topically and possibly functionally related to the presence of the inducible isoform of NOS. The results suggest that both CO and NO may be generated in bovine receptor neurons and thus involved in odorant stimulation. Based on immunocytochemical localization of synthesizing enzymes, NO might be regarded as a direct regulator of transduction related processes while CO might act as a modulator of the initial signal.     

Response of the hammerhead shark olfactory epithelium to amino acid stimuli

Sharks and rays are highly sensitive to chemical stimuli in their natural environment but several hypotheses predict that hammerhead sharks, with their expanded head and enlarged olfactory epithelium, have particularly acute olfactory systems. We used the electro-olfactogram (EOG) technique to compare the relative response of the scalloped hammerhead shark (Sphyrna lewini) olfactory epithelium to 20 proteinogenic amino acids and determine the sensitivity for 6 amino acids. At micromolar concentrations, cysteine evoked the greatest EOG response which was approximately twice as large as that of alanine. The weakest response was obtained for proline followed by aspartic acid and isoleucine. The olfactory epithelium showed adaptation to sequential stimulation, and recovery was related to the inter-stimulus time period. Estimated EOG response thresholds were in the sub-nanomolar range for both alanine (9.2 × 10⁻¹¹ M) and cysteine (8.4 × 10⁻¹⁰ M) and in the micromolar range for proline and serine. These thresholds from 10⁻¹⁰ to 10⁻⁶ M for the scalloped hammerhead shark are comparable or lower than those reported for other teleost and elasmobranch species. Future work should focus on binary and more complex compounds to test for competition and cross-adaptation for different classes of peripheral receptors, and their responses to molecules found in biologically relevant stimuli.     

Ca2+-Activated Cl? Channels of the ClCa Family Express in the Cilia of a Subset of Rat Olfactory Sensory Neurons

The Ca²⁺-activated Cl⁻ channel is considered a key constituent of odor transduction. Odorant binding to a specific receptor in the cilia of olfactory sensory neurons (OSNs) triggers a cAMP cascade that mediates the opening of a cationic cyclic nucleotide-gated channel (CNG), allowing Ca²⁺ influx. Ca²⁺ ions activate Cl⁻ channels, generating a significant Cl⁻ efflux, with a large contribution to the receptor potential. The Anoctamin 2 channel (ANO2) is a major constituent of the Cl⁻ conductance, but its knock-out has no impairment of behavior and only slightly reduces field potential odorant responses of the olfactory epithelium. Likely, an additional Ca²⁺-activated Cl⁻ channel of unknown molecular identity is also involved. In addition to ANO2, we detected two members of the ClCa family of Ca²⁺-activated Cl⁻ channels in the rat olfactory epithelium, ClCa4l and ClCa2. These channels, also expressed in the central nervous system, may correspond to odorant transduction channels. Whole Sprague Dawley olfactory epithelium nested RT-PCR and single OSNs established that the mRNAs of both channels are expressed in OSNs. Real time RT-PCR and full length sequencing of amplified ClCa expressed in rat olfactory epithelium indicated that ClCa4l is the most abundant. Immunoblotting with an antibody recognizing both channels revealed immunoreactivity in the ciliary membrane. Immunochemistry of olfactory epithelium and OSNs confirmed their ciliary presence in a subset of olfactory sensory neurons. The evidence suggests that ClCa4l and ClCa2 might play a role in odorant transduction in rat olfactory cilia.     

Cell Adhesion Molecules and the Migration of LHRH Neurons during Development

During embryogenesis, LHRH neurons arise in the olfactory epithelium, migrate along the olfactory nerve, and enter the forebrain. We have examined the distribution of several cell adhesion molecules (CAMs) in the developing chick olfactory system and brain to determine whether differential distributions of these adhesion molecules might be important in pathway choices made by migrating LHRH neurons. Single- and double-label immunocytochemical studies indicated that high levels of N-CAM and N-cadherin were expressed throughout the olfactory epithelium and not restricted to the medial half of the olfactory epithelium where most of the LHRH neurons originate. Further, high levels of N-CAM, Ng-CAM, and N-cadherin were uniformly expressed throughout the entire olfactory nerve while migrating LHRH neurons were confined to the medial half of the nerve. However, once LHRH neurons reach the brain, they migrate dorsally and caudally, tangential to the medial surface of the forebrain, along a region enriched in N-CAM and Ng-CAM. After this first stage of migration within the brain, LHRH neurons migrate laterally. At this stage, there is no correlation between the intensity of N-CAM and Ng-CAM immunostaining and the location of LHRH neurons. These results suggest that N-CAM, Ng-CAM, and N-cadherin do not play a guiding role in LHRH neuronal migration through the olfactory epithelium and olfactory nerve but that migrating LHRH neurons may follow a "CAM-trail" of N-CAM and Ng-CAM along the medial surface of the forebrain.     

Odorant Metabolism Catalyzed by Olfactory Mucosal Enzymes Influences Peripheral Olfactory Responses in Rats

A large set of xenobiotic-metabolizing enzymes (XMEs), such as the cytochrome P450 monooxygenases (CYPs), esterases and transferases, are highly expressed in mammalian olfactory mucosa (OM). These enzymes are known to catalyze the biotransformation of exogenous compounds to facilitate elimination. However, the functions of these enzymes in the olfactory epithelium are not clearly understood. In addition to protecting against inhaled toxic compounds, these enzymes could also metabolize odorant molecules, and thus modify their stimulating properties or inactivate them. In the present study, we investigated the in vitro biotransformation of odorant molecules in the rat OM and assessed the impact of this metabolism on peripheral olfactory responses. Rat OM was found to efficiently metabolize quinoline, coumarin and isoamyl acetate. Quinoline and coumarin are metabolized by CYPs whereas isoamyl acetate is hydrolyzed by carboxylesterases. Electro-olfactogram (EOG) recordings revealed that the hydroxylated metabolites derived from these odorants elicited lower olfactory response amplitudes than the parent molecules. We also observed that glucurono-conjugated derivatives induced no olfactory signal. Furthermore, we demonstrated that the local application of a CYP inhibitor on rat olfactory epithelium increased EOG responses elicited by quinoline and coumarin. Similarly, the application of a carboxylesterase inhibitor increased the EOG response elicited by isoamyl acetate. This increase in EOG amplitude provoked by XME inhibitors is likely due to enhanced olfactory sensory neuron activation in response to odorant accumulation. Taken together, these findings strongly suggest that biotransformation of odorant molecules by enzymes localized to the olfactory mucosa may change the odorant’s stimulating properties and may facilitate the clearance of odorants to avoid receptor saturation.