Abstract
Infant rats are born with a functional olfactory system ([Guthrie & Gall, 1999]). Within the first days of their life they begin to approach the odor of their mother in preference to the odor of a virgin female ([Leon & Moltz, 1971]). These preferences can be seen when the pups are placed in an apparatus designed to allow them to approach one of two areas on the basis of odor cues alone. Such a preference also can be induced when the natural situation is mimicked experimentally by pairing a nonmaternalodor (such as peppermint extract) with tactile stimulation of the kind that a mother might impose on her pups ([Coopersmith & Leon, 1984]). These data indicate that pups acquire their preference for the mother’s odor postnatally, rather than being born with that ability. In addition, the individuality of the odor of one mother compared to another is due to differences in their diet; mothers with identical diets are equally approached by their pups ([Leon, 1975])
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Alkasab, T. K., Bozza, T. C., Cleland, T. A., Dorries, K. M., Pearce, T. C., White, J., & Kauer, J. S. (1999). Characterizing complex chemosensors: information-theoretic analysis of olfactory systems. Trends in Neurosciences, 22, 102–108
Astic, L., & Cattarelli, M. (1982). Metabolic mapping of functional activity in the rat olfactory system after a bilateral transection of the lateral olfactory tract. tram Research, 245, 17–25
Astic, L. & Sacier, D. (1986). Anatomical mapping of the neuroepithelial projection to the olfactory bulb in the rat. Brain Research Bulletin, 16, 445–454
Axel, R. (1995). The molecular logic of smell. Scientific American, 273, 154–159
Bell, G. A., Laing, D. G., & Panhuber, H. (1987). Odour mixture suppression: Evidence for a peripheral mechanism in human and rat. Brain Research, 426, 8–18
Bozza, T. C., & Kauer,J. S. (1998). Odorant response properties of convergent olfactory receptor neurons. Journal of Neuroscience, 18, 4560–4569
Buck, L. B. (1996). Information coding in the vertebrate olfactory system. Annual Review of Neuroscience, 19, 517–544
Buck, L. B., & Axel, R. (1991) A novel multigene family may encode odorant receptors: A molecular basis for odor recognition. Cell, 65, 175–187
Buonviso, N., & Chaput, M. A. (1990). Response similarity to odors in olfactory bulb output cells presumed to be connected to the same glomerulus: Electrophysiological study using simultaneous single-unit recordings. Journal of Neurophysiology, 63, 447–454
Cain, W. S. (1979). To know with the nose: Keys to odor identification. Science, 203, 467–470
Cain, W. S., & Potts, B. C. (1996). Switch and bait: Probing the discriminative basis of odor identification via recognition memory. Chemical Senses, 21, 35–44
Chess, A., Simon, I., Cedar, H., & Axel, R. (1994). Allelic inactivation regulates olfactory receptor gene expression. Cell, 78, 823–834
Cinelli, A. R., Hamilton, K. A., Kauer, J. S. (1995). Salamander olfactory bulb neuronal activity observed by video rate, voltage-sensitive dye imaging. III. Spatial and temporal properties of responses evoked by odorant stimulation. Journal of Neurophysiology, 73, 2053–2071
Clyne, P. J., Warr, C. G., Freeman, M. R., Lessing, D., Kim, J., & Carlson, J. R. (1999). A novel family of divergent seven-transmembrane proteins: Candidate odorant receptors in Drosophila. Neuron, 22, 327–338
Cometto-Muñiz, J. E., Cain, W. S., & Abraham, M. H. (1998). Nasal pungency and odor of homologous aldehydes and carboxylic acids. Experimental Brain Research, 118, 180–188
Coopersmith, R., & Leon, M. (1984). Enhanced neural response to familiar olfactory cues. Science, 225, 849–851
Coopersmith, R., & Leon, M. (1986). Enhanced neural response by adult rats to odors experienced early in life. Brain Research, 371, 400–403
Coopersmith, R., Henderson, S. R., & Leon, M. (1986). Odor specificity of the enhanced neural response following early odor experience in rats. Developmental Brain Research, 27, 191–197
Dean, P. M. (1987). Molecular foundations of drug—receptor interaction Cambridge: Cambridge University Press
Dickinson, T. A., White, J., Kauer, J. S., Sc Walt, D. R. (1998). Current trends in ‘artificial-nose’ technology. Trends in Biotechnology, 16, 250–258
Do, J. T., Sullivan, R. M., & Leon, M. (1988). Behavioral and neural correlates of postnatal olfactory conditioning: II. Respiration during conditioning. Developmental Psychobiology, 21, 591–600
Domes, K. M. (1998). Olfactory coding: Time in a model. Neuron, 20, 7–10
Dôving, K. B. (1966). An electrophysiological study of odour similarities of homologous substances. Journal of Psychology, 186, 97–109
Eisthen, H. L. (1997). Evolution of vertebrate olfactory systems. Brain Behavior and Evolution, 50, 222–233
Firestein, S., Picco, C., & Menini, A. (1993). The relation between stimulus and response in olfactory receptor cells of the tiger salamander. Journal of Physiology, 468, 1–10
Freeman W. J., & Skarda, C. A. (1985). Spatial EEG patterns, non-linear dynamics and perception: The neo-Sherringtonian view. Brain Research, 357, 147–175
Friedrich, R. W., & Korsching, S. I, (1997). Combinatorial and chemotopic odorant coding in the zebrafish olfactory bulb visualized by optical imaging. Neuron, 18, 737–752
Galizia, C. G., Menzel, R., & Holldobler, B. (1999). Optical imaging of odor-evoked glomerular activity patterns in the antenna] lobes of the ant Camponotus rufipes. Naturwissenschaften, 86, 533–537
Galizia, C. G., Sachse, S., Rappert, A., & Menzel, R. (1999). The glomerular code for odor representation is species specific in the honeybee Apis mellifera. Nature Neuroscience,2, 473–478
Guthrie, K. M., & Gall, C. (1995). Functional mapping of odor-activated neurons in the olfactory bulb. Chemical Senses, 20, 271–282
Guthrie, K. M., & Gall, C. (1999). Functional mapping of the developing olfactory bulb. 21st Annual Meeting of the Association for Chemoreception Sciences (AChemS), Abstracts, p. 17
Guthrie, K. M., Anderson, A. J., Leon, M., & Gall, C. (1993). Odor-induced increases in c foc mRNA expression reveal an anatomical unit for odor processing in olfactory bulb. Proceedings of the National Academy of Sciences of the USA, 90, 3329–3333
Haberly L. B., & Bower, J. M. (1989). Olfactory cortex: Model circuit for study of associative memory? Trends in Neuroscience, 12, 258–264
Haberly L. B., & Price, J. L. (1977). The axonal projection patterns of the mitral and tufted cells of the olfactory bulb in the rat. Brain Research,129, 152–157
Imamura, K., Mataga, N., & Mori, K. (1992). Coding of odor molecules by mitral/tufted cells in rabbit olfactory bulb. I. Aliphatic compounds. Journal of Neurophysiology, 68, 1986–2002
Joerges, J., Kintner, A., Galizia, C. G., & Menzel, R. (1997). Representations of odours and odour mixtures visualized in the honeybee brain. Nature, 387, 285–288
Johnson, B. A., & Leon, M. (1996). Spatial distribution of [14C] 2-deoxyglucose uptake in the glomerular layer of the rat olfactory bulb following early olfactory preference learning. Journal of Comparative Neurology, 376, 557–566
Johnson, B. A., & Leon, M. (2000) Modular glomerular representations of odorants in the rat olfactory bulb: The effects of stimulus concentration. Journal of Comparative Neurology, 426, 496–509
Johnson, B. A., Woo, C. C., Duong, H., Nguyen, V., & Leon, M. (1995). A learned odor evokes an en-hanced Fos-like glomerular response in the olfactory bulb of young rats. Brain Research,699,192–200
Johnson, B. A., Woo, C. C., & Leon, M. (1998). Spatial coding of odorant features in the glomerular layer of the rat olfactory bulb. Journal of Comparative Neurology, 393, 457–471
Johnson, B. A., Woo, C. C., Hingco, E. E., Pham, K. L., & Leon, M. (1999). Multidimensional chemotopic responses to n-aliphatic acid odorants in the rat olfactory bulb. Journal of Comparative Neurology, 409, 529–548
Jourdan, F., Duveau, A., Astic, L., & Holley, A. (1980). Spatial distribution of [14C12-deoxyglucose uptake in the olfactory bulbs of rats stimulated with two different odours. Brain Research, 188, 139–154
Katoh, K., Koshimoto, H., Tani, A., & Mori, K. (1993). Coding of odor molecules by mitral/tufted cells in rabbit olfactory bulb. II. Aromatic compounds. Journal of Neurophysiology, 70, 2161–2175
Kauer, J. S. (1987). Coding in the olfactory system. In T. E. Finger & W. S. Silder (Eds.), Neurobiology of taste and smelt (pp. 205–231). New York: Wiley
Kauer, J. S., & Cinelli, A. R. (1993). Are there structural and functional modules in the vertebrate olfactory bulb? Microscopy Research and Technique, 24, 157–167
Krautwurst D., Yau, K. W., & Reed, R. R (1998). Identification of ligands for olfactory receptors by functional expression of a receptor library. Cell, 95, 917–926
Laska, M, & Teubner, P. (1998). Odor structure-activity relationships of carboxylic acids correspond between squirrel monkeys and humans. American Journal of Physiology, 274, R1639–R1645
Laurent, G. (1997). Olfactory processing: Maps, time and codes. Current Opinion in Neurobiology, 7, 547–553
Laurent, G., & Naraghi, M. (1994). Odorant-induced oscillations in the mushroom bodies of the locust. Journal of Neuroscience, 14, 2993–3004
Laurent, G., Wehr, M., & Davidowitz, H. (1996). Temporal representations of odors in an olfactory network. Journal of Neuroscience, 16, 3837–3847
Leon, M. (1975). Dietary control of maternal pheromone in the lactating rat. Physiology and Behavior, 14, 311–319
Leon, M. (1987). Plasticity of olfactory output circuits related to early olfactory learning. Trends in Neurosciences, 10, 434–438
Leon, M., & Moltz, H. (1971). Maternal pheromone: Discrimination by preweanling albino rats. Physiology and Behavior, 7, 265–267
Lu, X.-C. M., & Slotnick, B. M. (1994). Recognition of propionic acid vapor after removal of the olfactory bulb area associated with high 2-DG uptake. Brain Research,639, 26–32
Lu, X.-C. M., & Slotnick, B. M. (1998). Olfaction in rats with extensive lesions of the olfactory bulbs: Implications for odor coding. Neuroscience,84, 849–866
Macrides, F., & Davis, B.J. (1983). The olfactory bulb. In P. C. Emson (Ed.), Chemical neuroanatomy (pp. 391–426). New York: Raven Press
Malnic, B., Hirono, J., Sato, T, & Buck, L. (1999). Combinatorial receptor codes for odors. Cell, 96, 713–723
Matsutani, S., & Leon, M. (1993). Elaboration of glial cell processes in the rat olfactory bulb associated with early learning. Brain Research,613, 317–320
McCollum, J. F., Woo, C. C., & Leon, M. (1997). Granule and mitral cell densities are unchanged following early olfactory preference training. Developmental Brain Research, 99, 118–120
Michel, W. C., & Ache, B. W. (1994). Odor-evoked inhibition in primary olfactory receptor neurons. Chemical Senses, 19, 11–24
Mombaerts, P., Wang, E, Dulac, C., Chao, S. K., Nemes, A., Mendelsohn, M., Edmonson, J., & Axel, R. (1996a). Visualizing an olfactory sensory map. Cell, 87, 675–686
Mombaerts, P., Wang, F., Dulac, C., Chao, S. K., Nemes, A., Mendelsohn, M., Edmonson, J., & Axel, R. (1996b). The molecular biology of olfactory perception. Cold Spring Harbor Symposium on Quantitative Biology, 61, 135–145
Mori, K. (1987). Membrane and synaptic properties of identified neurons in the olfactory bulb. Progress in Neurobiology, 29, 275–320
Mori, K., & Yoshihara, Y. (1995). Molecular recognition and olfactory processing in the mammalian olfactory system. Progress in Neurobiology, 45, 585–619
Mori, K., Mataga, N., & Imamura, K. (1992). Differential specificities of single mitral cells in rabbit olfactory bulb for a homologous series of fatty acid odor molecules. Journal of Neurophysiology, 67, 786–789
Motokizawa, F. (1996). Odor representation and discrimination in mitral/tufted cells of the rat olfactory bulb. Experimental Brain Research, 112, 24–34
Nieuwenhuys, R. (1967). Comparative anatomy of olfactory centres and tracts. In Y. Zotterman (Ed.), Progress in brain research (pp. 1–64). New York: Elsevier
Ottoson, D. (1958). Studies on the relationship between olfactory stimulating effectiveness and physicochemical properties of odorant compounds. Acta Physiologica Scandanavica, 43, 167–181
Puche, A., Aroniadou-Anderjaska, V., & Shipley, M. (1998). Olfactory bulb-olfactory cortex slices in the study of central olfactory CNS circuits. Society for Neuroscience Abstracts, 34, 1885
Ressler, K. J., Sullivan, S. L., & Buck, L. B. (1994). Information coding in the olfactory system: Evidence for a stereotyped and highly organized epitope map in the olfactory bulb. Cell, 79, 1245–1255
Royet, J. P., Sicard, G., Souchier, C., & Jourdan, F. (1987). Specificity of spatial patterns of glomerular activation in the mouse olfactory bulb: Computer-assisted image analysis of 2deoxyglucose auto-radiograms. Brain Research, 417, 1–11
Rubin, B. D., & Katz, L. C. (1999). Optical imaging of odorant representations in the mammalian olfactory bulb. Neuron, 23, 499–511
Sallaz, M., & Jourdan, F. (1993). C-fos expression and 2-deoxyglucose uptake in the olfactory bulb of odour-stimulated awake rats. NeuroReport,4, 55–58
Sato, T., Hirono, J., Tonoike, M., & Takebayashi, M. (1994). Tuning specificities to aliphatic odorants in mouse olfactory receptor neurons and their local distribution. Journal of Neurophysiology, 72, 2980–2989
Shepherd, G. M. (1991). Computational structure of the olfactory system. In J. Davis and H. Eichenbaum (Eds.), Olfaction as a model system for computational neuroscience (pp. 3–41).Cambridge, MA: MIT Press
Shepherd, G. M. (1994). Discrimination of molecular signals by the olfactory receptor neuron. Neuron, 13, 771–790
Slotnick, B. M., Graham, S., Laing, D. G., & BeIl, G. A. (1987). Detection of propionic acid vapor by rats with lesions of olfactory bulb areas associated with high 2-DG uptake. Brain Research, 417, 343–346
Slotnick, B. M., Panhuber, H., Bell, G. A., & Laing, D. G. (1989). Odor-induced metabolic activity in the olfactory bulb of rats trained to detect propionic acid vapor. Brain Research, 500, 161–168
Slotnick, B. M., Bell, G. A., Panhuber, H., & Laing, D. G. (1997). Detection and discrimination of proplonic acid after removal of its 2-DG identified major focus in the olfactory bulb: A psychophysical analysis. Brain Research, 762, 89–96
Stevens, D. A., & O’Connell, R. J. (1995). Enhanced sensitivity to androstenone following regular exposure to pemenone. Chemical Senses, 20, 413–419
Stewart, W. B., Kauer, J. S., & Shepherd, G. M. (1979). Functional organization of rat olfactory bulb analyzed by the 2-deoxyglucose method. Journal of Comparative Neurology, 185, 715–734
Stopfer, M., Bhagavan, S., Smith, B. H., & Laurent, G. (1997) Impaired odour discrimination on de-synchronization of odour-encoding neural assemblies. Nature, 390, 70–74
Sullivan, R. M., & Leon, M. (1986). Early olfactory learning induces an enhanced olfactory bulb response in young rats. Developmental Brain Research, 27, 278–282
Sullivan, R. M., & Wilson, D. A. (1991). Neural correlates of conditioned odor avoidance in infant rats. Behavioral Neuroscience, 103, 307–312
Sullivan, R. M., Wilson, D. A., Kim, M. H., & Leon, M. (1988). Behavioral and neural correlates of postnatal olfactory conditioning: I. Effect of respiration on conditioned neural responses. Physiology and Behavior, 44, 85–90
Sullivan, R M., Wilson, D. A., & Leon, M. (1989). Norepinephrine and learning-induced plasticity in infant rat olfactory system. Journal of Neuroscience, 9, 3998–4006
Sullivan, R. M., Wilson, D. A., Wong, R., Correa, A., & Leon, M. (1990). Modified behavioral and olfactory bulb responses to maternal odors in preweanling rats. Developmental Brain Research, 53, 243–247
Sullivan, S. L., & Dyer, L. (1996). Information processing in mammalian olfactory system. Journal of Neurobiology, 30, 20–36
Tsuboi, A., Yoshihara, S., Yamazaki, N., Kasai, H., Asai-Tsuboi, H., Komatsu, M., Serizawa, S., Ishii, T., Matsuda, Y., Nagawa, F., & Sakano, H. (1999). Olfactory neurons expressing closely linked and homologous odorant receptor genes tend to project their axons to neighboring glomeruli on the olfactory bulb. Journal of Neuroscience, 19, 8409–8418
Vassar, R., Chao, S. K, Sitcheran, R., Nuñez, J. M., Vosshall, L. B., & Axel, R. (1994). Topographic organization of sensory projections to the olfactory bulb. Cell; 79, 981–991
Vickers, N. J., & Christensen, T. A. (1998). A combinatorial model of odor discrimination using a small array of contiguous, chemically defined glomeruli. Annals of the New York Academy of Sciences, 855, 514–516
Vosshall, L. B., Amrein, H., Morozov, P. S., Rzhetsky, A., & Axel, R. (1999). A spatial map of olfactory receptor expression in the Drosophila antenna. Cell, 96, 725–736
Wang, H.-W., Wysocki, C. J., & Gold, G. H. (1993). Induction of olfactory receptor sensitivity in mice. Science, 260, 998–1000
Wang, E, Nemes, A., Mendelsohn, M., & Axel, R. (1998). Odorant receptors govern the formation of a precise topographic map. Cell, 93, 47–60
Wehr, M., & Laurent, G. (1996). Odour encoding by temporal sequences of firing in oscillating neural assemblies. Nature, 384, 162–166
Wilson, D. A., & Leon, M. (1988). Spatial patterns of olfactory bulb single-unit responses to learned olfactory cues in young rats. Journal of Neurophysiolcgy, 59, 1770–1782
Wilson, D. A., Sullivan, R. M., & Leon, M. (1987). Single-unit analysis of postnatal olfactory learning: Modified olfactory bulb output response patterns to learned attractive odors. Journal of Neuroscience, 7, 3154–3162
Woo, C. C., & Leon, M. (1991). Increase in a focal population ofjuxtaglomerular cells in the olfactory bulb associated with early learning. Journal of Comparative Neurology, 305, 49–56
Woo, C. C., & Leon, M. (1995a). Distribution and development of beta-adrenergic receptorsinthe rat olfactory bulb. Journal of Comparative Neurology, 352, 1–10
Woo, C. C., & Leon, M. (1995b). Early olfactory enrichment and deprivation both decrease fl-adrenergic receptor density in the main olfactory bulb of the rat. Journal of Comparative Neurology, 360, 634–642
Woo, C. C., Coopersmith, R., & Leon, M. (1987). Localized changes in olfactory bulb morphology associated with early olfactory learning. Journal of Comparative Neurology, 263, 113–125
Woo, C. C., Oshita, M. H., & Leon, M. (1996). A learned odor decreases the number of Fos-immunopositive granule cells in the olfactory bulb of young rats. Brain Research,716, 149–156
Wysocki, C. J, Dorries, K. M., & Beauchamp, G. K (1989). Ability to perceive androstenone can be acquired by ostensibly anosmic people. Proceedings of the National Academy of Sciences of the USA, 86, 7976–7978
Yokoi, M., Mori, K, & Nakanishi, S. (1995). Refinement of odor molecule tuning by dendrodendritic synaptic inhibition in the olfactory bulb. Proceedings of the National Academy of Sciences of the USA, 92, 3371–3375
Youngentob, S. L., & Kent, P E (1995). Enhancement of odorant-induced mucosal activity patterns in rats trained on an odorant identification task. Brain Research, 670, 82–88
Zhao, H., Ivic, L, Otaki, J. M., Hashimoto, M., Mikoshiba, K, & Firestein, S. (1998). Functional expression of a mammalian odorant receptor. Science, 279, 237–242
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Johnson, B.A., Leon, M. (2001). Spatial Coding in the Olfactory System. In: Blass, E.M. (eds) Developmental Psychobiology. Handbook of Behavioral Neurobiology, vol 13. Springer, Boston, MA. https://doi.org/10.1007/978-1-4615-1209-7_3
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