Summary Sensory perception is not a simple feed-forward process and higher brain areas can actively modulate information processing in “lower” areas. We used optogenetic methods to examine how cortical feedback projections affect circuits in the first olfactory processing stage, the olfactory bulb. Selective activation of back projections from the anterior olfactory nucleus/cortex (AON) revealed functional glutamatergic synaptic connections on several types of bulbar interneurons. Unexpectedly, AON axons also directly depolarized mitral cells, enough to elicit spikes reliably in a time window of a few milliseconds. Mitral cells received strong disynaptic inhibition, a third of which arises in the glomerular layer. Activating feedback axons in vivo led to suppression of spontaneous as well as odor-evoked activity of mitral cells, sometimes preceded by a temporally-precise increase in firing probability. Our study indicates that cortical feedback can shape the activity of bulbar output neurons by enabling precisely timed spikes and enforcing broad inhibition to suppress background activity.

In odorant-rich environments, animals must be able to detect specific odorants of interest against variable backgrounds. However, several studies have suggested that both humans and rodents are very poor at analyzing the components of odorant mixtures, leading to the idea that olfaction is a synthetic sense in which mixtures are perceived holistically. We have developed a behavioral task to directly measure the ability of mice to perceive mixture components and found that mice can be easily trained to detect target odorants embedded in unpredictable and variable mixtures. We imaged the responses of olfactory bulb glomeruli to the individual odors used in the task in mice expressing the Ca++ indicator GCaMP3 in olfactory receptor neurons. By relating behavioral performance to the glomerular response patterns, we found that the difficulty of segregating the target from the background was strongly dependent on the extent of overlap between the representations of the target and the background odors by olfactory receptors. Our study indicates that the olfactory system has powerful analytic abilities that are constrained by the limits of combinatorial neural representation of odorants at the level of the olfactory receptors.

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The olfactory system, like other sensory systems, can detect specific stimuli of interest amidst complex, varying backgrounds. To gain insight into the neural mechanisms underlying this ability, we imaged responses of mouse olfactory bulb glomeruli to mixtures. We used this data to build a model of mixture responses that incorporated nonlinear interactions and trial-to-trial variability and explored potential decoding mechanisms that can mimic mouse performance when given glomerular responses as input. We find that a linear decoder with sparse weights could match mouse performance using just a small subset of the glomeruli (~15). However, when such a decoder is trained only with single odors, it generalizes poorly to mixture stimuli due to nonlinear mixture responses. We show that mice similarly fail to generalize, suggesting that they learn this segregation task discriminatively by adjusting task-specific decision boundaries without taking advantage of a demixed representation of odors.

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