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Computation of frequency-to-spatial transform by olfactory bulb glomeruli

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Abstract

A physiological simulation of 2.5% of the input and inhibitory neurons and 25% of the primary mitral/tufted cells in a single mammalian olfactory bulb glomerulus was constructed. This physiological simulation used the integrate-and-fire paradigm with realistic activation curves and synaptic delays. The dendritic integration incorporated non-linear interactive effects of individual cell excitatory and inhibitory post-synaptic potentials (PSPs) from both axodendritic and dendrodendritic synaptic contacts. Refractory periods for granule-cell inhibition of mitral/tufted cell activity lead to relatively fixed-frequency rhythmic activity in the glomerulus, independent of the input frequency from the olfactory nerve. Though the frequency of mitral/ tufted cell firing in bulb was approximately independent of input frequency, the number of cells active in the glomerulus was a roughly-linear function of input frequency to the glomerulus, indicating the mechanism's ability to function as a frequency-to-spatial encoder.

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References

  • Adrian ED (1950) The electrical activity of the mammalian olfactory bulb. Electroencephalogr Clin Neurophysiol 2:377–388

    Google Scholar 

  • Allison AC (1953) The morphology of the olfactory system in the vertibrates. Biol Rev 28:195–244

    Google Scholar 

  • Ambros-Ingerson J, Granger R, Lynch G (1990) Simulation of paleocortex performs hierarchical clustering. Science 247:1344–1348

    Google Scholar 

  • Antón PS (1991) Simulations of information processing, control, and plasticity effects in the olfactory bulb. Ph. D. Thesis, University of California, Irvine

    Google Scholar 

  • Castellucci VF (1985) The chemical senses: taste and smell. In: Kandel ER, Schwartz JH (eds) Principles of neural science, 2nd edn. Elsevier, New York Amsterdam Oxford, pp 409–425

    Google Scholar 

  • DeVries H, Stuiver M (1961) The absolute sensitivity of the human sense of smell. In: Rosenblith WA (ed) Sensory communication. MIT Press, Cambridge

    Google Scholar 

  • Eisenberg J, Freeman WJ, Burke B (1989) Hardware architecture of a neural network model simulating pattern recognition by the olfactory bulb. Neural Networks 2:315–325

    Google Scholar 

  • Freeman WJ (1987) Simulations of chaotic EEG patterns with a dynamic model of the olfactory system. Biol Cybern 56:139–150

    Google Scholar 

  • Freeman WJ, Schneider W (1982) Changes in spatial patterns of rabbit olfactory EEG with conditioning to odors. Psychophysiology 19:44–56

    Google Scholar 

  • Getchell TV (1986) Functional properties of vertebrate olfactory receptor neurons. Physiol Rev 66:772–818

    Google Scholar 

  • Getchell TV, Shepherd GM (1978) Responses of olfactory receptor cells to step pulses of odour at different concentrations in the salamander. J Physiol 282:521–540

    Google Scholar 

  • Granger R, Ambros-Ingerson J, Staubli U, Lynch G (1990a) Memorial operation of multiple, interacting simulated brain structures. In: Gluck M, Rummelhart D (eds) Neuroscience and connectionist theory. Lawrence Erlbaum Associates, Hillsdale, pp 95–129

    Google Scholar 

  • Granger R, Ambros-Ingerson J, Antón P, Lynch G (1990b) Unsupervised perceptual learning: a paleocortical model. In: Hanson SJ, Olson CR (eds) Connectionist modeling and brain function: the developing interface. MIT Press, Cambridge, pp 105–131

    Google Scholar 

  • Jack JJB, Noble D, Tsien RW (1975) Electric current flow in excitable cells. Clarendon Press, Oxford

    Google Scholar 

  • Koch C, Poggio T (1987) Biophysics of computation: neurons, synapses, and membranes. In: Edelman GM, Gall WE, Cowan WM (eds) Synaptic function. Wiley, New York, pp 637–697

    Google Scholar 

  • Kuffler SW, Nicholls JG, Martin AR (1984) From neuron to brain. Sinauer, Sunderland

    Google Scholar 

  • Li Z, Hopfield JJ (1989a) Modeling the olfactory bulb and its neural oscillatory processings. Biol Cybern 61:379–392

    Google Scholar 

  • Li Z, Hopfield JJ (1989b) Modeling the olfactory bulb—coupled nonlinear oscillators. In: Touretzky DS (ed) Advances in neural information processing systems I. Morgan Kaufmann, San Mateo, pp 402–409

    Google Scholar 

  • Macrides F, Schneider SP (1982) Laminar organization of mitral and tufted cells in the main olfactory bulb of the adult hamster. J Comp Neurol 208:419–430

    Google Scholar 

  • Mori K (1987) Membrane and synaptic properties of identified neurons in the olfactory bulb. Prog Neurobiol 29:275–320

    Google Scholar 

  • Mori K, Takagi SF (1978a) An intracellular study of dendrodendritic inhibitory synapses on mitral cells in the rabbit olfactory bulb. J Physiol 279:569–588

    Google Scholar 

  • Mori K, Takagi SF (1978b) Activation and inhibition of olfactory bulb neurons by anterior commissure volleys in the rabbit. J Physiol 279:589–604

    Google Scholar 

  • Mori K, Kishi K, Ojima H (1983) Distribution of dendrites of mitral, displaced mitral, tufted, and granule cells in the rabbit olfactory bulb. J Comp Neurol 219:339–355

    Google Scholar 

  • Nowycky MC, Mori K, Shepherd GM (1981) Blockage of synaptic inhibition reveals long-lasting synaptic excitation in isolated turtle olfactory bulb. J Neurophysiol 46:649–658

    Google Scholar 

  • Onoda N, Mori K (1980) Depth distribution of temporal firing patterns in olfactory bulb related to air-intake cycles. J Neurophysiol 44:29–39

    Google Scholar 

  • Orona E, Rainer EC, Scott JW (1984) Dendritic and axonal organization of mitral and tufted cells in the rat olfactory bulb. J Comp Neurol 226:346–356

    Google Scholar 

  • Rall W (1962) Theory of physiological properties of dendrites. Ann NY Acad Sci 96:1071–1092

    Google Scholar 

  • Rall W, Shepherd GM, Reese TS, Brightman MW (1966) Dendrodendritic synaptic pathway for inhibition in the olfactory bulb. Exp Neurol 14:44–56

    Google Scholar 

  • Roman FU, Staubli U, Lynch G (1987) Evidence for synaptic potentiation in a cortical network during learning. Brain Res 418:221–226

    Google Scholar 

  • Schneider SP, Scott JW (1983) Orthodromic response properties of rat olfactory bulb mitral and tufted cells correlate with their projection patterns. J Neurophysiol 50:358–378

    Google Scholar 

  • Schoenfeld TA, Macrides F (1984) Topographical organization of connections between the main olfactory bulb and pars externa of the anterior olfactory nucleus in the hamster. J Comp Neurol 227:121–135

    Google Scholar 

  • Shepherd GM (1972) Synaptic organization of the mammalian olfactory bulb. Physiol Rev 52:864–917

    Google Scholar 

  • Shepherd GM (1979) The synaptic organization of the brain, 2nd edn. Oxford University Press, New York Oxford

    Google Scholar 

  • Tuckwell HC (1988) Introduction to theoretical neurobiology, vol 1. Cambridge University Press, Cambridge

    Google Scholar 

  • Vodyanoy V (1988) Molecular sensor based on olfactory transduction. In: Hong FT (ed) Molecular electronics: biosensors and biocomputers. Plenum Press, New York London, pp 317–28

    Google Scholar 

  • Wellis DP, Scott JW (1990) Intracellular responses of identified rat olfactory bulb interneurons to electrical and odor stimulation. J Neurophysiol 64:932–947

    Google Scholar 

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Antón, P.S., Lynch, G. & Granger, R. Computation of frequency-to-spatial transform by olfactory bulb glomeruli. Biol. Cybern. 65, 407–414 (1991). https://doi.org/10.1007/BF00216975

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