Letters to Nature

Nature 395, 693-698 (15 October 1998) | doi:10.1038/27201; Received 5 June 1998; Accepted 10 August 1998

Who reads temporal information contained across synchronized and oscillatory spike trains?

Katrina MacLeod1, Alex Bäcker1 and Gilles Laurent1

  1. California Institute of Technology, Division of Biology 139-74, Pasadena, California 91125, USA

Correspondence to: Gilles Laurent1 Correspondence and requests for materials should be addressed to G.L.
(e-mail: Email: laurentg@cco.caltech.edu).

Our inferences about brain mechanisms underlying perception rely on whether it is possible for the brain to 'reconstruct' a stimulus from the information contained in the spike trains from many neurons1, 2, 3, 4, 5. How the brain actually accomplishes this reconstruction remains largely unknown. Oscillatory and synchronized activities in the brain of mammals have been correlated with distinct behavioural states or the execution of complex cognitive tasks6, 7, 8, 9, 10, 11 and are proposed to participate in the 'binding' of individual features into more complex percepts12, 13, 14,. But if synchronization is indeed relevant, what senses it? In insects, oscillatory synchronized activity in the early olfactory system seems to be necessary for fine odour discrimination15 and enables the encoding of information about a stimulus in spike times relative to the oscillatory 'clock'16. Here we study the decoding of these coherent oscillatory signals. We identify a population of neurons downstream from the odour-activated, synchronized neuronal assemblies. These downstream neurons show odour responses whose specificity is degraded when their inputs are desynchronized. This degradation of selectivity consists of the appearance of responses to new odours and a loss ofdiscrimination of spike trains evoked by different odours. Suchloss of information is never observed in the upstream neurons whose activity is desynchronized. These results indicate that information encoded in time across ensembles of neurons converges onto single neurons downstream in the pathway.

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