Trends in Neurosciences
Volume 26, Issue 2, February 2003, Pages 61-64
Journal home page for Trends in Neurosciences

Research Focus
From synchrony to sparseness

https://doi.org/10.1016/S0166-2236(02)00016-4Get rights and content

Abstract

The neurons in the antennal lobe of the locust had been shown to encode the identity of odorants using spatially distributed synchronized patterns of neural activity. Recent work describes how such neural patterns are detected. By using non-linear membrane properties, one set of target neurons, the Kenyon cells of the mushroom bodies, are able to act as coincidence detectors, sensitive to synchronized activity. In addition, the specific circuitry between the antennal lobe and the mushroom body refines the spatial–temporal selectivity of the Kenyon cells. In this process, the neural representation of odor identity is transformed from a dense spatial–temporal code into a sparse code.

Section snippets

Neural circuits and neural code in the locust olfactory system

The olfactory system of the locust has been a remarkable model system for the study of the neural code (Fig. 1). Odorants are first detected by 90 000 olfactory receptors distributed on each antenna of the animal. Odorant identity is encoded in the olfactory receptor neurons by their mean firing rates, with many neurons responding to any particular odor. This spatially distributed code is then transformed into the spatial–temporal code found in the antennal lobe. The 830 projection neurons of

Intermediate conclusion

Perez-Orive et al. have shown that the properties of the Kenyon cells and the circuitry between the antennal lobe and the mushroom bodies favor the detection of the synchronized spatial–temporal patterns that are generated in the antennal lobe, and that this tuning results in a drastic transformation of the code for odor identity. It would be difficult, therefore, to argue that the synchrony found in the antennal lobe and all of the specialized circuitry apparently designed to detect it is an

Sparse codes

Theoreticians have provided answers to the first question ever since the term sparse-coding was proposed to describe neural code. In one of the earlier formulations, David Field suggested that sparse codes are ultimately related to the statistics of natural stimulus ensembles [17]. It is presently believed that many of the relevant features within natural scenes produce high-order correlations between the points within an image (e.g. curved edges within an image influence three-point

Dense spatial–temporal codes

The second theoretical question is whether the dense spatial–temporal code that was found at the level of the antennal lobe in the locust is a necessary intermediate step to ultimately obtaining the sparse representation found in the mushroom bodies. The answer to that question remains more elusive. One could envisage circuitry that generates a sparse code directly from a spatially distributed representation of sensory information, in which the information is represented by mean rates. For

Conclusion

The dense spatial–temporal neural code found in the AL is a highly efficient combinatorial code that might be needed both for the encoding of a large ensemble of odors with a limited number of neurons and for the formation of short-term olfactory memories. The sparse code found in the MB represents odor identity in a synthetic fashion that could facilitate the formation of long-term associative memories. The circuitry in the olfactory system of the locust exploits the synchronicity found in the

Acknowledgements

I would like to thank W. Vinje, J. Gallant and S. Shaevitz for their helpful comments on the manuscript.

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