Abstracts - Association for Chemoreception Sciences
Abstracts - Association for Chemoreception Sciences
Abstracts - Association for Chemoreception Sciences
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F344 rats on a two-odor discrimination task. Six odorants<br />
(1-propanol, 1-butanol, 1-pentanol, 1-hexanol, 1-heptanol and<br />
1-octanol) were arranged to produce 30 novel odorant pairs<br />
differing between one and five carbon atoms; testing sessions<br />
included presentation of only one randomly assigned pair daily<br />
(200 trials daily). Results showed that, although rats learned<br />
to discriminate between any two odorant pairs, discrimination<br />
accuracy changed systematically with carbon chain length<br />
difference. Error patterns were remarkably consistent across<br />
animals, such that marked increases in misses and false alarms<br />
were indicated <strong>for</strong> pairs differing by one or two carbon atoms.<br />
Across all odorant pairs, these effects were most pronounced<br />
during the first 20 trials. Notably, the greatest degree of<br />
perceptual confusion was displayed <strong>for</strong> two pairs differing by a<br />
single carbon atom, 1-propanol/1-butanol and 1-heptanol/1-<br />
hexanol. These data provide further support <strong>for</strong> carbon chain<br />
length as an important odorant stimulus dimension <strong>for</strong> study of<br />
olfactory receptor interaction (Johnson and Leon, 2000) as well<br />
as demonstrate how hierarchical chemotopic organization of<br />
the olfactory bulb may be reflected perceptually. Furthermore,<br />
development of an animal model using the carbon chain<br />
paradigm may be useful <strong>for</strong> assessing the mechanisms underlying<br />
olfactory dysfunction.<br />
#P210 POSTER SESSION IV:<br />
CHEMICAL SIGNALING AND BEHAVIOR;<br />
ANIMAL BEHAVIOR/PSYCHOPHYSICS;<br />
CHEMOSENSATION AND METABOLISM;<br />
VOMERONSASAL AND CHEMICAL<br />
COMMUNICATION<br />
The Gustatory Stop-Signal Task: A Method <strong>for</strong> Measuring<br />
Taste Quality Discrimination in Mice with Millisecond<br />
Temporal Resolution<br />
Dustin M Graham, David L Hill<br />
UVA/Psychology Charlottesville, VA, USA<br />
There is a lack of consensus regarding the roles of temporal and<br />
spatial coding of taste quality in the gustatory system due in<br />
part to various experimental and analytical differences among<br />
previous studies. Quantitative behavioral analysis can be used<br />
to test <strong>for</strong> the cognitive principle of speed-accuracy tradeoff<br />
(SAT), a hallmark of temporal processing of sensory stimuli.<br />
However, current methods used to study taste perception<br />
in rodents are temporally too slow <strong>for</strong> precise reaction-time<br />
measurements required to test <strong>for</strong> SAT in the gustatory system.<br />
We designed a novel behavioral paradigm, the Gustatory Stop-<br />
Signal Task, in head-restrained mice <strong>for</strong> measuring perceptual<br />
identification of taste stimuli with millisecond temporal<br />
resolution. Using this new paradigm, we will apply threshold<br />
psychophysics to determine if a stimulus-dependent SAT is<br />
present during discrimination of basic tastes. This will provide<br />
crucial behavioral evidence <strong>for</strong> the potential roles of temporal<br />
and spatial coding strategies underlying taste quality coding in<br />
the gustatory system. Additionally, the task can be combined<br />
with advanced physiological techniques, such as visually guided<br />
whole-cell patch-clamp recordings in sub-regions of gustatory<br />
cortex. The gustatory stop-signal task in head-restrained mice<br />
will provide a new foundation to combine precise quantitative<br />
behavioral measurements of taste perception alongside state-ofthe-art<br />
in vivo physiology. Acknowledgements: NIH Grants R01<br />
DC00407 and F32 DC012461 - 01A1<br />
#P211 POSTER SESSION IV:<br />
CHEMICAL SIGNALING AND BEHAVIOR;<br />
ANIMAL BEHAVIOR/PSYCHOPHYSICS;<br />
CHEMOSENSATION AND METABOLISM;<br />
VOMERONSASAL AND CHEMICAL<br />
COMMUNICATION<br />
Free Access to Highly Palatable Food during Adolescence<br />
Increases Anxiety- and Depression-like Behaviors in Males,<br />
but not in Females<br />
Jeong-Won Jahng, Jin-Young Kim, Joo-Young Lee, Jong-Ho Lee<br />
Seoul National University School of Dentistry Seoul, South Korea<br />
We have reported that a long-term access to highly palatable food<br />
(HPF) modulates the hypothalamic-pituitary-adrenal (HPA) axis<br />
response to restraint stress in adult male rats. Psycho-emotional<br />
disorders frequently involve dysfunctions in the HPA axis<br />
activity. In this study, male and female SD rats had free choices<br />
of chocolate cookies as HPF and chow with ad libitum access<br />
from PND 28, and then were subjected to behavioral tests at<br />
youth. Control group received chow only, and food conditions<br />
were continued throughout the whole experimental period. Body<br />
weight gain and daily caloric intake did not differ between HPF<br />
and control groups both in males and females. Total ambulatory<br />
activity was decreased with HPF access in females, but not in<br />
males. However, HPF increased anxiety related behaviors in<br />
males; i.e. increased rostral grooming and decreased the open<br />
arms stay during elevated plus maze test, but did not affect<br />
those indexes in females. Immobility duration during <strong>for</strong>ced<br />
swim test was significantly increased with HPF access in males,<br />
but the increase was not reached to a statistical significance in<br />
females. Stress-induced corticosterone increase was shortened<br />
with HPF access both in males and females. Results suggest that<br />
adolescence free access to highly palatable food may lead to a<br />
dysfunction in the HPA axis activity both in males and females;<br />
however, its psycho-emotional outcome be worse in males.<br />
Acknowledgements: Supported by MOEST(2009K001269 2010-<br />
0003642)<br />
POSTER PRESENTATIONS<br />
<strong>Abstracts</strong> are printed as submitted by the author(s).<br />
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