Author:
Cleland Thomas A,Sethupathy Praveen
Abstract
Abstract
Background
Contrast enhancement within primary stimulus representations is a common feature of sensory systems that regulates the discrimination of similar stimuli. Whereas most sensory stimulus features can be mapped onto one or two dimensions of quality or location (e.g., frequency or retinotopy), the analogous similarities among odor stimuli are distributed high-dimensionally, necessarily yielding a chemotopically fragmented map upon the surface of the olfactory bulb. While olfactory contrast enhancement has been attributed to decremental lateral inhibitory processes among olfactory bulb projection neurons modeled after those in the retina, the two-dimensional topology of this mechanism is intrinsically incapable of mediating effective contrast enhancement on such fragmented maps. Consequently, current theories are unable to explain the existence of olfactory contrast enhancement.
Results
We describe a novel neural circuit mechanism, non-topographical contrast enhancement (NTCE), which enables contrast enhancement among high-dimensional odor representations exhibiting unpredictable patterns of similarity. The NTCE algorithm relies solely on local intraglomerular computations and broad feedback inhibition, and is consistent with known properties of the olfactory bulb input layer. Unlike mechanisms based upon lateral projections, NTCE does not require a built-in foreknowledge of the similarities in molecular receptive ranges expressed by different olfactory bulb glomeruli, and is independent of the physical location of glomeruli within the olfactory bulb.
Conclusion
Non-topographical contrast enhancement demonstrates how intrinsically high-dimensional sensory data can be represented and processed within a physically two-dimensional neural cortex while retaining the capacity to represent stimulus similarity. In a biophysically constrained computational model of the olfactory bulb, NTCE successfully mediates contrast enhancement among odorant representations in the natural, high-dimensional similarity space defined by the olfactory receptor complement and underlies the concentration-independence of odor quality representations.
Publisher
Springer Science and Business Media LLC
Subject
Cellular and Molecular Neuroscience,General Neuroscience
Reference126 articles.
1. Mori K, Shepherd GM: Emerging principles of molecular signal processing by mitral/tufted cells in the olfactory bulb. Semin Cell Biol. 1994, 5 (1): 65-74. 10.1006/scel.1994.1009.
2. Aungst JL, Heyward PM, Puche AC, Karnup SV, Hayar A, Szabo G, Shipley MT: Centre-surround inhibition among olfactory bulb glomeruli. Nature. 2003, 426 (6967): 623-629. 10.1038/nature02185.
3. Hayar A, Karnup SV, Shipley MT, Ennis M: Olfactory bulb glomeruli: external tufted cells intrinsically burst at theta frequency and are entrained by patterned olfactory input. J Neurosci. 2004, 24 (5): 1190-1199. 10.1523/JNEUROSCI.4714-03.2004.
4. Cleland TA, Linster C: Central olfactory processing. Handbook of olfaction and gustation, 2nd ed. Edited by: Doty RL. 2003, New York , Marcel Dekker, 165-180.
5. Shipley MT, McLean JH, Ennis M: Olfactory system. The rat nervous system. Edited by: Paxinos G. 1995, San Diego , Academic Press, 899-928. 2nd
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