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Abstracts - Association for Chemoreception Sciences

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allows visualization and quantification of the interneuron cell<br />

bodies throughout the bulbar layers of the AOB (Krosnowski<br />

et al, 2012). We found significant differences in the number of<br />

cholinergic interneurons in the anterior and posterior glomerular<br />

layer (GL) and the external plexi<strong>for</strong>m layer (EPL), with the<br />

highest numbers of cholinergic interneurons in the anterior GL<br />

and posterior EPL. In the posterior EPL, we also noted a high<br />

density of GFP+ cells <strong>for</strong>ming a ring around the outer edges<br />

of the layer, thus creating a heavy GFP+ population along<br />

the border between the anterior and posterior AOB. We then<br />

examined the possible role of ChAT interneurons in the AOB<br />

using adult male mice exposed to either bedding from a mated<br />

pair or to a male aggressor mouse. We monitored the activity<br />

marker, c-fos, in these regions and found significantly higher<br />

levels of activation of ChAT-expressing cells in the EPL in both<br />

exposure groups when compared to activation in control mice,<br />

suggesting that this population may serve a role in the processing<br />

of social odor cues. Thus, we have identified a significant<br />

cholinergic interneuron population in the AOB that varies<br />

significantly in the anterior and posterior regions. Thus, our data<br />

supports the idea that the anterior and posterior AOB process<br />

sensory in<strong>for</strong>mation differently and suggests that this cholinergic<br />

interneuron population may serve to process olfactory<br />

in<strong>for</strong>mation in a region specific manner. Acknowledgements:<br />

Supported by research grants NIH/NIDCD 009269, 012831 and<br />

ARRA administrative supplement to WL<br />

#P87 POSTER SESSION II:<br />

OLFACTION DEVELOPMENT; TASTE CNS;<br />

NEUROIMAGING; OLFACTION CNS<br />

Suppression of <strong>Association</strong> Synapses in Piri<strong>for</strong>m Cortex<br />

During Post-Training Sleep Impairs Odor Memory Selectivity<br />

Dylan C Barnes 1,2 , Donald A Wilson 1,2,3<br />

1<br />

Graduate Center CUNY New York City, NY, USA, 2 Nathan Kline<br />

Institute Orangeburg, NY, USA, 3 NYU Langone Medical Center New<br />

York City, NY, USA<br />

Slow wave sleep (SWS) is characterized by slow-wave<br />

oscillations in neocortex, as well as sharp waves (SPW) in<br />

both the hippocampus and piri<strong>for</strong>m cortex (PCX). Neural<br />

activity during SWS is hypothesized to contribute to memory<br />

consolidation through “replay” of waking activity patterns. For<br />

example, we have demonstrated that imposed replay of odorevoked<br />

activity in the olfactory system during SWS enhances<br />

subsequent memory of that odor. Neurons co-activated by an<br />

odor are hypothesized to become linked into a cohesive ensemble<br />

through strengthening of association synapses. Replay of odor<br />

evoked ensemble activity during SWS may help strengthen<br />

these connections and improve memory and memory acuity.<br />

Here, we tested the hypothesis of that association fiber activity<br />

during SWS facilitates replay and memory of recently learned<br />

odors by infusing baclofen (or saline) into the PCX during posttraining<br />

sleep. Baclofen is a GABA-B receptor agonist that has<br />

been shown to selectively depress association fiber synapses.<br />

Rats were chronically implanted with bilateral cannulae and<br />

a recording electrode in the anterior PCX. After recovery, rats<br />

were differentially conditioned with CS+ odor/footshock and<br />

CS- odor stimuli. During the 4 hours immediately post-training,<br />

animals were placed in a sleeping chamber and bilaterally<br />

infused with either baclofen or saline. Local field potential<br />

and EMG activity were recorded during conditioning,<br />

post-training sleep, and test periods. On test day, 24 hours<br />

following conditioning, freezing responses to the CS+, CSand<br />

other odors were examined. Preliminary behavioral results<br />

suggest that post-training PCX baclofen infusions do not<br />

impair memory <strong>for</strong> the CS+ but reduce odor acuity/enhance<br />

generalization of the odor-fear response. Acknowledgements:<br />

F31-DC012284 to D.C.B. and R01-DC003906 from the<br />

NIDCD to D.A.W.<br />

#P88 POSTER SESSION II:<br />

OLFACTION DEVELOPMENT; TASTE CNS;<br />

NEUROIMAGING; OLFACTION CNS<br />

Cholinergic modulation of glomerular odor sensitivity<br />

in the olfactory bulb<br />

Mounir Bendahmane, M Cameron Ogg, Max L Fletcher<br />

University of Tennessee Health Science Center Memphis, TN, USA<br />

In the olfactory system, many studies have shown that<br />

cholinergic input to the olfactory bulb is not only involved in<br />

learning and memory but also detection and discrimination.<br />

In this study we used calcium imaging to explore the cholinergic<br />

effect on OB postsynaptic glomerular odor responses. Using mice<br />

expressing GCaMP2 in M/T cells, we studied the modulation<br />

of dorsal surface glomerular odor concentration-response<br />

curves via HDB (horizontal limb of the diagonal band of Broca)<br />

stimulation or OB cholinergic pharmacological manipulation.<br />

Overall, we find that increased cholinergic OB activation through<br />

HDB stimulation or cholinergic-uptake blocker application<br />

increases the sensitivity of individual glomerular odor responses<br />

by shifting the odor concentration-response curve to the left and<br />

decreasing the EC50 by up to one log unit in odor concentration.<br />

This effect was observed <strong>for</strong> all glomeruli tested regardless<br />

of baseline odor sensitivity or odorant used. OB application<br />

of a muscarinic antagonist completely blocks these shifts,<br />

suggesting that the increased sensitivity observed is primarily<br />

driven by muscarinic activation. We are now exploring the<br />

cholinergic effects on individual OB cell types using two-photon<br />

microscopy to further address these effects at the single cell level.<br />

Acknowledgements: NIH R03 DC009853 and the Pew Scholars<br />

Program in the Biomedical <strong>Sciences</strong>.<br />

POSTER PRESENTATIONS<br />

<strong>Abstracts</strong> are printed as submitted by the author(s).<br />

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