A role for the anterior piriform cortex in early odor preference learning: evidence for multiple olfactory learning structures in the rat pup

cFos activation in the anterior piriform cortex (aPC) occurs in early odor preference learning in rat pups (Roth and Sullivan 2005). Here we provide evidence that the pairing of odor as a conditioned stimulus and β-adrenergic activation in the aPC as an unconditioned stimulus generates early odor pr...

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Bibliographic Details
Published in:Journal of neurophysiology 2013-07, Vol.110 (1), p.141-152
Main Authors: Morrison, Gillian L, Fontaine, Christine J, Harley, Carolyn W, Yuan, Qi
Format: Article
Language:English
Subjects:
Animals
Discrimination Learning - physiology
Female
Long-Term Potentiation - physiology
Male
Olfactory Pathways - growth & development
Olfactory Pathways - physiology
Rats
Rats, Sprague-Dawley
Receptors, Adrenergic, beta - physiology
Receptors, N-Methyl-D-Aspartate - physiology
Smell
Synapses - physiology
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Summary:cFos activation in the anterior piriform cortex (aPC) occurs in early odor preference learning in rat pups (Roth and Sullivan 2005). Here we provide evidence that the pairing of odor as a conditioned stimulus and β-adrenergic activation in the aPC as an unconditioned stimulus generates early odor preference learning. β-Adrenergic blockade in the aPC prevents normal preference learning. Enhancement of aPC cAMP response element-binding protein (CREB) phosphorylation in trained hemispheres is consistent with a role for this cascade in early odor preference learning in the aPC. In vitro experiments suggested theta-burst-mediated long-term potentiation (LTP) at the lateral olfactory tract (LOT) to aPC synapse depends on N-methyl-D-aspartate (NMDA) receptors and can be significantly enhanced by β-adrenoceptor activation, which causes increased glutamate release from LOT synapses during LTP induction. NMDA receptors in aPC are also shown to be critical for the acquisition, but not expression, of odor preference learning, as would be predicted if they mediate initial β-adrenoceptor-promoted aPC plasticity. Ex vivo experiments 3 and 24 h after odor preference training reveal an enhanced LOT-aPC field excitatory postsynaptic potential (EPSP). At 3 h both presynaptic and postsynaptic potentiations support EPSP enhancement while at 24 h only postsynaptic potentiation is seen. LOT-LTP in aPC is excluded by odor preference training. Taken together with earlier work on the role of the olfactory bulb in early odor preference learning, these outcomes suggest early odor preference learning is normally supported by and requires multiple plastic changes at least at two levels of olfactory circuitry.
ISSN:0022-3077
1522-1598
DOI:10.1152/jn.00072.2013