ut this was always the first trial. For the entire norming sample, small, but statistically significant, declines in taste intensity with age were observed <strong>for</strong> each of the four trials (Pearson correlations from -0.1 to -0.2, p
were phenotyped <strong>for</strong> detection thresholds <strong>for</strong> sweet (sucrose), savory (monosodium glutamate), and salty (NaCl) taste using age-appropriate psychophysical testings, dietary habits, blood pressure and obesity. Preliminary analyses revealed that the detection threshold <strong>for</strong> sucrose, salt, and MSG are similar to that previously reported in adults and there were no differences observed between normal weight children and obese children in the detection thresholds <strong>for</strong> any of these basic tastes. In normalweight, but not obese children, salt detection thresholds were positively correlated with systolic blood pressure. As a group, the greater the waist circumference, the lower the sucrose detection threshold (the more sensitive the child was to sucrose) (p=0.02). No such relationships existed <strong>for</strong> salt or MSG in children. Whether the lower detection thresholds <strong>for</strong> sucrose are associated with stronger rein<strong>for</strong>cing value of sweet foods, as has been observed in adults, and understanding the link between salt taste thresholds and blood pressure, are important areas <strong>for</strong> future research. Acknowledgements: This project was funded by an investigator-initiated grant from Ajinomoto, Inc. #P235 POSTER SESSION V: HUMAN TASTE PSYCHOPHYSICS; OLFACTION RECEPTORS; TASTE DEVELOPMENT Statistical Analysis of Factors Previously Described as Significant in the Ability to Taste Propylthiouracil Yields Roles <strong>for</strong> Age, Sex and Tas2r38 Haplotype, but not Fungi<strong>for</strong>m Papillae Density Nicole L. Garneau, Tiffany Derr Denver Museum of Nature & Science Denver, CO, USA The Genetics of Taste research study at the Denver Museum of Nature & Science is in a unique position to collect samples from a diverse population across a wide age range. Using this large population sample we set out to establish the scientific credibility of our community-based laboratory by replicating four previously reported statistically significant factors in the ability to taste propylthiouracil; 1)Age, 2)Sex, 3)Tas2r38 haplotype, and 4)Fungi<strong>for</strong>m papillae density. Using regression analysis and the Student T-test we can replicate the role of age and sex in taste score (gLMS following a propylthiouracil taste test). Similarly, the presence of at least one dominant allele <strong>for</strong> the Tas2r38 gene is a significant predictor of taste. Finally, in order to decrease subjectivity, we developed a dichotomous key <strong>for</strong> objective analysis of fungi<strong>for</strong>m papillae density. Using this method we did not find that increased papillae density correlates to an increased propylthiouracil taste score. In conclusion, the ability to replicate the significance of age, sex and Tas2r38 haplotype, as well as the development of objective methodology <strong>for</strong> papillae analysis, all demonstrate the ability <strong>for</strong> citizen-scientists in a communitybased laboratory to collect, prepare and analyze data that can contribute to the field of chemoreception. In addition, we submit that using standardized methodology <strong>for</strong> fungi<strong>for</strong>m papillae density allows <strong>for</strong> a more objective analysis of morphological data. Using this methodology we find no relationship between fungi<strong>for</strong>m papillae density and propylthiouracil score in our data set. This data contradicts previously published studies and suggests that fungi<strong>for</strong>m papillae density may not be as reliable a metric <strong>for</strong> classifying taster status as previously thought. Acknowledgements: This work was supported by volunteer citizen-scientists at the Denver Museum of Nature & Science, and through support from 2008-2012 from R25 RR025066 NIH NCRR SEPA. #P236 POSTER SESSION V: HUMAN TASTE PSYCHOPHYSICS; OLFACTION RECEPTORS; TASTE DEVELOPMENT The effects of temperature on sequential and mixture interactions between sucrose and saccharin Barry G Green 1,2 , Danielle Nachtigal 1 1 The John B. Pierce Laboratory New Haven, CT, USA, 2 Yale University School of Medicine New Haven, CT, USA The sweet taste of sucrose and saccharin has been shown to depend on stimulation of the T1R2-T1R3 receptor, but it is also clear that these two stimuli interact with the receptor in different ways. Most recently it was found that self-adaptation is temperature-dependent <strong>for</strong> sucrose but not <strong>for</strong> saccharin (Green & Nachtigal, 2012), and a previous study showed that high concentrations of saccharin can block the sweetness of sucrose (and of itself) and evoke a sweet water taste (Galindo-Cusperino et al, 2006). The aim of the present study was to determine if temperature modulates the ability of sucrose to cross-adapt saccharin and/or of saccharin to block the sweetness of sucrose and produce a sweet water taste. Subjects rated the sweetness and bitterness of 0.42 M sucrose, 3.2 mM saccharin, 100 mM saccharin, or binary mixtures of sucrose and the 2 concentrations of saccharin, with and without pre-exposure to themselves or each of the other stimuli. The variables of interest were the duration of pre-exposure (3 or 10 s) and solution temperature (37° or 21°C). The stimuli were sampled by dipping the tongue tip into the solutions, and intensity ratings were made on the gLMS be<strong>for</strong>e the tongue was retracted back into the mouth. The results confirmed the previous findings and showed that (1) the magnitude of sweet water taste (after exposure to 100 mM saccharin) is temperature-dependent, and (2) surprisingly, preexposure to sucrose <strong>for</strong> 3 or 10 sec appeared to counteract the ability of 100 mM saccharin to block sweetness, independent of temperature. These results support the hypothesis that sucrose and saccharin bind to at least 2 different sites on the T1R2-T1R3 receptor and raise new questions about the factors that can affect excitatory and inhibitory interactions between these sites. Acknowledgements: Supported in part by NIH grant DC005002 POSTER PRESENTATIONS <strong>Abstracts</strong> are printed as submitted by the author(s). 121
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AChemS Association for Chemorecepti
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Table of Contents 2013 AChemS Meeti
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2013 Annual Meeting Exhibitors EXHI
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2013 Awardees We are pleased to ann
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Oral Abstracts #1 GIVAUDAN LECTURE:
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#9 INDUSTRY SYMPOSIUM: TASTE AND SM
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#17 PLATFORM PRESENTATIONS: OLFACTI
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maintenance; demonstrate a contribu
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self renew, as well as produce post
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#35 SYMPOSIUM: NEW APPROACHES TO PH
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auditory cues anticipating the gene
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#46 PLATFORM PRESENTATIONS: TASTE P
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#51 SYMPOSIUM: EXPERIENCE DRIVEN PL
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#57 SYMPOSIUM: THE NEW ‘FACES’
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Poster Presentations #P1 POSTER SES
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For patients not involved in litiga
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show increased high-fat food avidit
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suggest that latency of the N1 OERP
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#P23 POSTER SESSION I: MULTIMODAL R
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#P28 POSTER SESSION I: MULTIMODAL R
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and/or bitter taste are expressed n
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#P39 POSTER SESSION I: MULTIMODAL R
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the mOR-EG receptor and MUPP1 and i
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odor responses. Recently, transient
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women; mean age 23.4 years; range 2
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#P61 POSTER SESSION II: OLFACTION D
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#P65 POSTER SESSION II: OLFACTION D
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#P70 POSTER SESSION II: OLFACTION D
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axons into the olfactory bulb where
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with the latency of quinine-induced
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allows visualization and quantifica
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via iontophoretic injection in the
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pharmacological inhibition of synap
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#P102 POSTER SESSION II: OLFACTION
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