Abstracts - Association for Chemoreception Sciences
Abstracts - Association for Chemoreception Sciences
Abstracts - Association for Chemoreception Sciences
Create successful ePaper yourself
Turn your PDF publications into a flip-book with our unique Google optimized e-Paper software.
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 />
62