Synaptic Organization of Anterior Olfactory Nucleus Inputs to Piriform Cortex

Odors activate distributed ensembles of neurons within the piriform cortex, forming cortical representations of odor thought to be essential to olfactory learning and behaviors. This odor response is driven by direct input from the olfactory bulb, but is also shaped by a dense network of associative or intracortical inputs to piriform, which may enhance or constrain the cortical odor representation. With optogenetic techniques, it is possible to functionally isolate defined inputs to piriform cortex and assess their potential to activate or inhibit piriform pyramidal neurons. The anterior olfactory nucleus (AON) receives direct input from the olfactory bulb and sends an associative projection to piriform cortex that has potential roles in the state-dependent processing of olfactory behaviors. Here, we provide a detailed functional assessment of the AON afferents to piriform in male and female C57Bl/6J mice. We confirm that the AON forms glutamatergic excitatory synapses onto piriform pyramidal neurons; and while these inputs are not as strong as piriform recurrent collaterals, they are less constrained by disynaptic inhibition. Moreover, AON-to-piriform synapses contain a substantial NMDAR-mediated current that prolongs the synaptic response at depolarized potentials. These properties of limited inhibition and slow NMDAR-mediated currents result in strong temporal summation of AON inputs within piriform pyramidal neurons, and suggest that the AON could powerfully enhance activation of piriform neurons in response to odor. SIGNIFICANCE STATEMENT Odor information is transmitted from olfactory receptors to olfactory bulb, and then to piriform cortex, where ensembles of activated neurons form neural representations of the odor. While these ensembles are driven by primary bulbar afferents, and shaped by intracortical recurrent connections, the potential for another early olfactory area, the anterior olfactory nucleus (AON), to contribute to piriform activity is not known. Here, we use optogenetic circuit-mapping methods to demonstrate that AON inputs can significantly activate piriform neurons, as they are coupled to NMDAR currents and to relatively modest disynaptic inhibition. The AON may enhance the piriform odor response, encouraging further study to determine the states or behaviors through which AON potentiates the cortical response to odor.

[1]  Bartlett W. Mel,et al.  NMDA spikes mediate amplification of inputs in the rat piriform cortex , 2018, eLife.

[2]  K. Bolding,et al.  Recurrent cortical circuits implement concentration-invariant odor coding , 2018, Science.

[3]  L F Abbott,et al.  A transformation from temporal to ensemble coding in a model of piriform cortex , 2018, eLife.

[4]  Thomas Deneux,et al.  Odor identity coding by distributed ensembles of neurons in the mouse olfactory cortex , 2017, eLife.

[5]  Melanie A Woodin,et al.  Top-down modulation of olfactory-guided behaviours by the anterior olfactory nucleus pars medialis and ventral hippocampus , 2016, Nature Communications.

[6]  A. Meyer-Lindenberg,et al.  Oxytocin Enhances Social Recognition by Modulating Cortical Control of Early Olfactory Processing , 2016, Neuron.

[7]  V. Murthy,et al.  Functional Properties of Cortical Feedback Projections to the Olfactory Bulb , 2012, Neuron.

[8]  Jeffry S. Isaacson,et al.  Cortical Feedback Control of Olfactory Bulb Circuits , 2012, Neuron.

[9]  Venkatesh N. Murthy,et al.  Optophysiological analysis of associational circuits in the olfactory cortex , 2012, Front. Neural Circuits.

[10]  Norimitsu Suzuki,et al.  Microcircuits Mediating Feedforward and Feedback Synaptic Inhibition in the Piriform Cortex , 2012, The Journal of Neuroscience.

[11]  S. Siegelbaum,et al.  Recurrent Circuitry Dynamically Shapes the Activation of Piriform Cortex , 2011, Neuron.

[12]  Jeffry S. Isaacson,et al.  A Major Role for Intracortical Circuits in the Strength and Tuning of Odor-Evoked Excitation in Olfactory Cortex , 2011, Neuron.

[13]  P. Brunjes,et al.  The mouse olfactory peduncle , 2011, The Journal of comparative neurology.

[14]  Dan D. Stettler,et al.  Driving Opposing Behaviors with Ensembles of Piriform Neurons , 2011, Cell.

[15]  Karl Deisseroth,et al.  Optogenetics in Neural Systems , 2011, Neuron.

[16]  Michael D. Ehlers,et al.  Neural Circuit Mechanisms for Pattern Detection and Feature Combination in Olfactory Cortex , 2011, Neuron.

[17]  Norimitsu Suzuki,et al.  Two Layers of Synaptic Processing by Principal Neurons in Piriform Cortex , 2011, The Journal of Neuroscience.

[18]  Jeffry S. Isaacson,et al.  From Dendrite to Soma: Dynamic Routing of Inhibition by Complementary Interneuron Microcircuits in Olfactory Cortex , 2010, Neuron.

[19]  J. Bekkers,et al.  Inhibitory neurons in the anterior piriform cortex of the mouse: Classification using molecular markers , 2010, The Journal of comparative neurology.

[20]  Norimitsu Suzuki,et al.  Distinctive classes of GABAergic interneurons provide layer-specific phasic inhibition in the anterior piriform cortex. , 2010, Cerebral cortex.

[21]  Dan D. Stettler,et al.  Representations of Odor in the Piriform Cortex , 2009, Neuron.

[22]  J. Isaacson,et al.  Odor Representations in Olfactory Cortex: “Sparse” Coding, Global Inhibition, and Oscillations , 2009, Neuron.

[23]  K. Svoboda,et al.  The subcellular organization of neocortical excitatory connections , 2009, Nature.

[24]  N. Schoppa,et al.  GABAergic Circuits Control Input–Spike Coupling in the Piriform Cortex , 2008, The Journal of Neuroscience.

[25]  Norimitsu Suzuki,et al.  Neural Coding by Two Classes of Principal Cells in the Mouse Piriform Cortex , 2006, The Journal of Neuroscience.

[26]  Lawrence C Katz,et al.  Synaptic Integration of Olfactory Information in Mouse Anterior Olfactory Nucleus , 2006, The Journal of Neuroscience.

[27]  Kurt R Illig,et al.  Differences in chemo‐ and cytoarchitectural features within pars principalis of the rat anterior olfactory nucleus suggest functional specialization , 2006, The Journal of comparative neurology.

[28]  Feng Zhang,et al.  Channelrhodopsin-2 and optical control of excitable cells , 2006, Nature Methods.

[29]  Kevin M. Franks,et al.  Strong Single-Fiber Sensory Inputs to Olfactory Cortex: Implications for Olfactory Coding , 2006, Neuron.

[30]  Peter Hegemann,et al.  Multiple photocycles of channelrhodopsin. , 2005, Biophysical journal.

[31]  K. Deisseroth,et al.  Millisecond-timescale, genetically targeted optical control of neural activity , 2005, Nature Neuroscience.

[32]  K. R. Illig Projections from orbitofrontal cortex to anterior piriform cortex in the rat suggest a role in olfactory information processing , 2005, The Journal of comparative neurology.

[33]  J. Isaacson,et al.  Synapse-Specific Downregulation of NMDA Receptors by Early Experience: A Critical Period for Plasticity of Sensory Input to Olfactory Cortex , 2005, Neuron.

[34]  L. Haberly,et al.  Parallel-distributed processing in olfactory cortex: new insights from morphological and physiological analysis of neuronal circuitry. , 2001, Chemical senses.

[35]  L. Haberly,et al.  New Features of Connectivity in Piriform Cortex Visualized by Intracellular Injection of Pyramidal Cells Suggest that “Primary” Olfactory Cortex Functions Like “Association” Cortex in Other Sensory Systems , 2000, The Journal of Neuroscience.

[36]  J. Miller,et al.  GFPcre fusion vectors with enhanced expression. , 1999, Analytical biochemistry.

[37]  M. Cattarelli,et al.  Intrinsic association fiber system of the piriform cortex: A quantitative study based on a cholera toxin B subunit tracing in the rat , 1996, The Journal of comparative neurology.

[38]  L. Haberly,et al.  NMDA-dependent induction of long-term potentiation in afferent and association fiber systems of piriform cortex in vitro , 1990, Brain Research.

[39]  M. Luskin,et al.  The topographic organization of associational fibers of the olfactory system in the rat, including centrifugal fibers to the olfactory bulb , 1983, The Journal of comparative neurology.

[40]  L. Haberly,et al.  Association and commissural fiber systems of the olfactory cortex of the rat II. Systems originating in the olfactory peduncle , 1978, The Journal of comparative neurology.

[41]  L. Haberly,et al.  Association and commissural fiber systems of the olfactory cortex of the rat. I. Systems originating in the piriform cortex and adjacent areas , 1978, The Journal of comparative neurology.

[42]  K. R. Illig,et al.  Contralateral projections of the rat anterior olfactory nucleus , 2009, The Journal of comparative neurology.

[43]  Pavel Osten,et al.  Stereotaxic gene delivery in the rodent brain , 2007, Nature Protocols.

[44]  L. Haberly,et al.  Membrane currents evoked by afferent fiber stimulation in rat piriform cortex. I. Current source-density analysis. , 1993, Journal of neurophysiology.