Abstracts - Association for Chemoreception Sciences
Abstracts - Association for Chemoreception Sciences
Abstracts - Association for Chemoreception Sciences
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P O S T E R S<br />
connexin proteins. The OB also exhibits circadian rhythms of<br />
both electrical activity and odor sensitivity, but the cellular<br />
mechanisms underlying these rhythms are unknown. Many<br />
circadian rhythms are under the influence of the daily rhythm of<br />
melatonin released by the pineal gland. Recent data suggest that<br />
melatonin regulates the expression of connexin 43 in myometrial<br />
cells and this contributes to synchronous rhythmic contractions<br />
of the uterus during childbirth. Collectively, these data led to the<br />
hypothesis that melatonin may contribute to the circadian activity<br />
of the OB by regulating gap junction expression and enhancing<br />
synchronous activity. To test this hypothesis, neonatal OB cells,<br />
grown in primary culture, were treated with 3 nM melatonin and<br />
connexin expression was examined by immunofluorescence.<br />
Connexin 43, in control tissue, was expressed primarily at the<br />
borders of contact between astrocytes. In contrast, melatonintreated<br />
astrocytes displayed increased connexin 43 expression,<br />
which included a diffuse cellular expression pattern in addition to<br />
expression at cell-to-cell borders. These results suggest that<br />
melatonin may contribute to the circadian activity of the OB by<br />
enhancing electrical coupling via increased gap junction<br />
expression. Molecular analyses of these effects, and the effects of<br />
melatonin on connexins 36 and 45, are also being examined.<br />
Acknowledgements: Supported in part by the FSU Department of<br />
Biological Science and Program in Neuroscience<br />
#P40 POSTER SESSION I: TASTE IMAGING &<br />
PSYCHOPHYSICS; CENTRAL TASTE;<br />
MULTIPLE MODALITIES; CENTRAL &<br />
PERIPHERAL OLFACTION<br />
Odors eliciting Fear: a Conditioning Approach to Idiopathic<br />
Environmental Intolerance<br />
Patricia Bulsing 1 , Arne Leer 2 , Monique A Smeets 2 ,<br />
Marcel van den Hout 2<br />
1<br />
Unilever Vlaardingen, Netherlands, 2 Utrecht University Utrecht,<br />
Netherlands<br />
Individuals with Idiopathic Environmental Intolerance (IEI) seem<br />
to fear odorous chemicals. To determine whether IEI can be<br />
conceived of as an “odor phobia”, we tested whether odors can<br />
elicit stress responses (1); and whether odors, after association<br />
with fear compared to be<strong>for</strong>e, are evaluated as less pleasant<br />
(2) and avoided more (3). Method: Using differential classical<br />
conditioning paradigm, an odor (either rotten egg as CS+<br />
[CS: Conditioned Stimulus] and peach as CS-, or vice versa), were<br />
conditioned to an electrical shock as Unconditioned Stimulus<br />
(US). The acquisition phase consisted of 6 presentations of the<br />
CS+ followed by electrical shock and 6 presentations of the CSalone.<br />
The extinction phase consisted of 6 CS+ and 6 CS- trials,<br />
with no US. Stress response was assessed via Skin Conductance<br />
Response (SCR); pleasantness via rating scales; avoidance via<br />
sniffing. Results: SCR increased significantly to both odors, but<br />
stress to rotten egg did not extinguish (1); a significant (p =.03)<br />
change in pleasantness during acquisition was encountered, with<br />
the CS+ being liked less after conditioning (2); sniffing volume<br />
associated with the CS+ decreased immediately after the first<br />
trial(s), but reduction in volume was not significant over 6 trials<br />
(3). Discussion: The finding that odors can be conditioned to<br />
stress responses, leading to reduced liking <strong>for</strong> these odors, support<br />
a fear conditioning conception of IEI. However, the absence of<br />
extinction and avoidance of the CS+ are problematic in the light<br />
of the theory and additional research is needed, especially since<br />
extinction would be the treatment of choice in view of the theory.<br />
Acknowledgements: NWO Vidi 452-03-334<br />
#P41 POSTER SESSION I: TASTE IMAGING &<br />
PSYCHOPHYSICS; CENTRAL TASTE;<br />
MULTIPLE MODALITIES; CENTRAL &<br />
PERIPHERAL OLFACTION<br />
Species specific regulation of the olfactory bulb<br />
dopaminergic phenotype<br />
Kasturi Banerjee 1 , Shivraj Bhosle 1 , Harriet Baker 1,2 ,<br />
John W. Cave 1,2<br />
1<br />
Burke Medical Research Institute White Plains, NY, USA,<br />
2<br />
Weill Cornell Medical College New York, NY, USA<br />
Our previous studies indicated that the transcription factor ER81<br />
regulates tyrosine hydroxylase (TH) expression in the mouse<br />
olfactory bulb (OB) by directly binding to the TH proximal<br />
promoter. A recent study suggested ER81 also regulates<br />
expression of other genes necessary <strong>for</strong> the dopaminergic<br />
phenotype by a molecular mechanism similar to TH, and this<br />
ER81-dependent differentiation of the dopaminergic neuronal<br />
phenotype is conserved from nematodes to mammals. However, a<br />
phylogenetic analysis of genomic DNA sequences corresponding<br />
to promoter regions <strong>for</strong> several dopaminergic genes in mammals<br />
revealed that the reported binding sites that mediate ER81<br />
regulation of the dopaminergic phenotype are not conserved.<br />
Chromatin immunoprecipitation (ChIP) experiments with mouse<br />
OB tissue suggested that ER81 binds to several proximal<br />
promoter regions of many dopaminergic genes, but ChIP<br />
experiments with OB tissue from dog indicate that orthologous<br />
regions of these genes are not bound by ER81. Focusing on the<br />
expression of TH, which is the rate-limiting enzyme in dopamine<br />
biosynthesis, electromobility gel shift assays showed that<br />
recombinantly expressed ER81 can bind the TH promoter from<br />
rodents, but not humans. Transcription assays comparing human<br />
and rat TH promoters in a cultured murine OB cell line also<br />
suggested that there is species-specific regulation of TH. Together,<br />
our findings suggest that there are species-specific molecular<br />
mechanisms that regulate differentiation of OB dopaminergic<br />
phenotype. However, these findings do not exclude the possibility<br />
that there is also a conserved molecular differentiation pathway<br />
that functions in combination with the species-specific<br />
mechanisms. Acknowledgements: NIH DC008955<br />
#P42 POSTER SESSION I: TASTE IMAGING &<br />
PSYCHOPHYSICS; CENTRAL TASTE;<br />
MULTIPLE MODALITIES; CENTRAL &<br />
PERIPHERAL OLFACTION<br />
The olfactory capabilities of mice with long-term unilateral<br />
naris occlusion (UNO) and contralateral bulbectomy (bulb-x)<br />
Cathy J Angely, David M Coppola<br />
Department of Biology, Randolph Macon College Ashland, VA,<br />
USA<br />
UNO has been the most common method of effecting stimulus<br />
deprivation in studies of olfactory plasticity. However, despite the<br />
large corpus on the effects of this manipulation dating back to the<br />
19th century, little is known about its behavioral sequela. Here we<br />
report the results of classical olfactory habituation and<br />
discrimination studies on adult mice that had undergone unilateral<br />
bulb-x and contralateral naris occlusion perinatally. The olfactory<br />
per<strong>for</strong>mance of UNO mice was compared to matched controls<br />
that had unilateral bulb-x but intact nares. Both experiments<br />
employed a masking protocol in which after successful<br />
dishabituation or discrimination to pure odors (0.1% isoamyl<br />
40 | AChemS <strong>Abstracts</strong> 2010 <strong>Abstracts</strong> are printed as submitted by the author(s)