sniffing behavior. Furthermore, we recommend against use of RIP.141 Poster <strong>Chemosensory</strong> Coding and ClinicalOLFACTORY DETECTION THRESHOLDS IN HUNGER ANDSATIETYSchreder T. 1 , Albrecht J. 1 , Rzeznicka A. 1 , Schöpf V. 1 , Anzinger A. 1 ,Demmel M. 1 , Pollatos O. 1 , Kopietz R. 1 , Linn J. 1 , Wiesmann M. 1 1 Dept.of Neuroradiology, University of Munich, Munich, GermanyObjectives: Several investigators reported the existence of foodrelatedchanges in olfactory sensitivity but the findings are highlydiverse. We investigated whether olfactory detection thresholds arecorrelated with food intake. Methods: Using the Sniffin´ Sticks,sensitivity to the non-food odor n-butanol and the food-odor isoamylacetate was assessed when hungry (overnight fast) and satiated (after astandardized breakfast, 668 ± 135 calories) in twenty-four femalesubjects with normal olfactory function. Results and Conclusions: Wefound no consistent pattern of changes in olfactory detection thresholdsrelated to food intake (n-butanol 10.2 ± 1.9 vs. 10.3 ± 1.9, isoamylacetate 11.4 ± 2.5 vs. 12.5 ± 2.7). Ratings regarding valence and arousalof the subjects as well as ratings of pleasantness (n-butanol 5.96 ± 2.07vs. 6.08 ± 2.06, isoamyl acetate 2.29 ± 1.00 vs. 2.67 ± 1.13) andintensity of the odors (n-butanol 7.63 ± 1.21 vs. 7.38 ± 1.47, isoamylacetate 7.13 ± 1.70 vs. 7.13 ± 1.36) did not differ significantly betweenhunger and satiety. In summary, we could not find any evidence thatfood intake has effects on olfactory function in healthy subjects.142 Poster <strong>Chemosensory</strong> Coding and ClinicalLATERALIZATION OF ODOR IDENTIFICATIONGudziol V. 1 , Zahnert T. 2 , Hummel C. 2 1 Dresden Medical School,Dresden, Germany; 2 Department of Otorhinolaryngology, University ofDresden Medical School, Germany, Dresden, GermanyAims of the present study were (1) to investigate the frequency oflateralized differences in olfactory function and (2) to correlate the selfassessment of olfactory sensitivity with the results from measuredolfactory function. To this end all participants rated their olfactorysensitivity as “complete loss,” “bad,” “normal,” “good,” or “excellent.”Odor identification of over 1700 subjects (652 women, 1063 men) wasobtained with a 12-item test from the “Sniffin´ Sticks” test battery. Allodors were applied to each nostril in a randomized order while thecontralateral nostril was closed. Group analyses revealed that selfassessment of olfactory sensitivity correlated well with the results of theolfactory screening test (r1715 = 0.51; p < 0.001). On an individuallevel, however, ratings of olfactory sensitivity exhibited significantdifferences from the results of olfactory testing. Ninety-three percent ofhealthy subjects (n = 479) demonstrated a side difference of three orless points. In patients with nasal symptoms (n = 1236) this figure was86%. Lateralized differences were largest in subjects with decreasedolfactory function. In conclusion, lateralized differences in odoridentification are no rare finding.143 Poster <strong>Chemosensory</strong> Coding and ClinicalTHE CLINICAL CHARACTERISTICS AND PATHOGENESISOF DYSOSMIAMiwa T. 1 , Tsukatani T. 1 , Furukawa M. 1 1 Otorhinolaryngology,Kanazawa University, Kanazawa, JapanThe majority of patients having problems with smell sensationcomplain of hyposmia or anosmia. Although many of these patients alsohave dysosmia, a distorted olfactory sensation, the clinicalcharacteristics and pathogenesis of dysosmia remains obscure. In thisstudy, 308 patients who came to our clinic were analyzed to determinethe status of their dysosmia using clinical records and questionnaires.The most common cause of their olfactory disturbance wasnasosinusitis, however the incidence of dysosmia was not very high.More than 50% of the patients having a sensorineural olfactorydisturbance such as post upper respiratory infection (URI) or headinjury complained of olfactory distortion. The onset and sensation ofdysosmia was different for patients with post URI compared to headinjury. The 83% of the patients with post URI reported that they felt adifferent odor from the original odor and 46% of post URI patientscould only experience a limited number of odor sensations. Thesesensations started several months from the onset of the olfactorydisturbance. On the other hand, the rate of patients reporting distortedsmell sensation in the absence of an odor stimulus was higher inpatients with head injury than for post URI. Based on these results andrecent discoveries regarding odor recognition mechanisms, wehypothesize the following underlying causes of dysosmia for post URIand head injury. In post URI dysosmia is likely to occur due to themisdirection of regenerating axons, while for posttraumatic olfactorydisturbances the cause is more likely to be due to damage in olfactoryregions of the brain.144 Poster <strong>Chemosensory</strong> Coding and ClinicalTHE HEDONIC DATABASE OF SMELL-FRANKONIA(HEDOS-F) – AN ANALYSIS OF GENDER DIFFERENCESThuerauf N. 1 , Reulbach U. 1 , Lunkenheimer J. 1 , Spannenberger R. 1 ,Vassiliadu A. 2 , Markovic K. 1 1 Department of Psychiatry andPsychotherapy, University of Erlangen-Nürnberg, Erlangen, Bavaria,Germany; 2 Department of Neurology, University of Erlangen-Nürnberg,Erlangen, Bavaria, GermanyThe Sniffin Stick Test has been employed widely in order to assessolfactory function in health and disease. The hedonic evaluation of thetest odors still remains to be investigated. Thus, the aims of our projectwere (1) to collect hedonic and intensity estimates in a large humanpopulation and (2) to install a hedonic database suited to analyse theinfluence on hedonic and intensity estimates of the following factors:age, gender, site of stimulation, threshold, odor discrimation andidentification. 201 volunteers participated in our study (mean age: 42.0± 16.3, minimum age: 19 years, maximum age: 83 years, males: 103,females: 98). We executed the Sniffin Stick Test and registeredintensity and hedonic estimates using an analogue rating scale. Theoverall hedonic estimate for all odors was 12.5 ± 18.4 (right) and 11.5 ±17.4 (left) (unpleasantness/pleasantness scale: -100 to +100) indicatingthat the test is relatively balanced. The statistical analysis of genderdifferences revealed significant differences for the odors `orange´,`lemon´, `clove´, `turpentine´, `apple´, `pineapple´, `rose´, `fish´ (Mann-Whitney-U-Test) indicating a gender specific emotional evaluation ofthese odors. Our results also demonstrate that the Sniffin Stick Test caneasily be extended by assessing intensity and hedonic estimates creatinga useful tool for investigating the emotional aspects of smell.36
145 Poster <strong>Chemosensory</strong> Coding and ClinicalTHE HEDONIC DATABASE OF SMELL-FRANCONIA(HEDOS-F)—THE INFLUENCE OF AGE ON THE HEDONICESTIMATES OF ODORSMarkovic K. 1 , Reulbach U. 1 , Lunkenheimer J. 1 , Vassiliadu A. 2 ,Spannenberger R. 1 , Thuerauf N. 1 1 Department of Psychiatry andPsychotherapy, University of Erlangen-Nürnberg, Erlangen, Bavaria,Germany; 2 Department of Neurology, University of Erlangen-Nürnberg,Erlangen, Bavaria, GermanyNumerous studies have been conducted collecting normative valuesdependent on age for the three major components of the Sniffin StickTest. Especially for the elderly a significant loss of olfactory functioncould be demonstrated. Less is known about the influence of age on thehedonic evaluation of the standard odors of the test. Thus, the aim ofour project was to analyse the influence of age on the hedonic andintensity estimates of a large human population. Data were provided bythe Hedonic Database of Smell-Franconia (HeDoS-F) consisting of 201single data sets with the parameters age, gender, odor threshold, odordiscrimination, oder identification, intensity estimates, hedonicestimates and site of odor presentation (mean age: 42.0 ± 16.3,minimum age: 19, maximum age: 83, males: 103, females: 98). Thestatistcal analysis of the hedonic and intensity estimates was calculatedfor 6 age intervals (ANOVA; Kruskal-Wallis-Test / for single odors).The relative scaling for `unpleasantness / pleasantness´ was -100 to+100 visual analogue rating units (VARU). We found a statisticallysignificant influence of age on the relative values of the overall hedonicestimates whereas the absolute values of hedonic estimates and theintensity estimates were not age dependent. Our results demonstrate thathedonic estimates depend on age while the intensity evaluation of odorsis relatively stable over the entire life span.146 Poster <strong>Chemosensory</strong> Coding and ClinicalWITHDRAWN147 Poster <strong>Chemosensory</strong> Coding and ClinicalIDENTIFICATION OF NEUROTROPHIC FACTORS BDNF, NT-3, AND NT-4 IN HUMAN SALIVAMilewski A.L. 1 , Utermohlen V. 1 1 Division of Nutritional Sciences,Cornell University, Ithaca, NYBrain-derived neurotrophic factor (BDNF), neurotrophin-3 (NT-3),neurotrophin-4 (NT-4), and nerve growth factor (NGF) are structurallyrelated polypeptides necessary for the survival and maintenance ofmany types of central and peripheral innervating neurons. In rodentlingual epithelium, BDNF and NT-4 are crucial for the innervation ofgustatory tissue, while NT-3 supports the innervation of somatosensorytissue. Though initially thought to function only as target-derivedfactors, these proteins and their receptors are expressed to a certainextent in rodent and human lingual tissue, suggesting additionalautocrine or paracrine trophic effects. Of these proteins, NGF is foundin rodent salivary glands and was recently discovered in human saliva.This study was undertaken to determine if BDNF, NT-3, and NT-4 arealso present in human saliva. SDS-PAGE/Western blot analysis ofsalivary samples from 14 male subjects was conducted using polyclonalantibodies against each protein. This method revealed the presence ofall three proteins in saliva, in both pro- and mature forms. This suggeststhat the salivary glands may be releasing the proteins to promotesurvival of the lingual epithelial cells. This is supported by previousfindings in rodents that removal of the salivary glands can lead to adecrease in fungiform papillae and taste bud number. Alternatively, thegustatory and somatosensory cells themselves might be the source, inwhich case the proteins may be acting in an autocrine or paracrinefunction. This work was supported by an NIH training grant.148 Poster <strong>Chemosensory</strong> Coding and ClinicalMETABOLOMIC ANALYSES OF HUMAN SKIN: AGE ANDDISEASE BIOMARKERSGallagher M. 1 , Preti G. 1 , Fakharzadeh S.S. 2 , Leyden J.J. 2 , SpielmanA.I. 3 , Willse A. 4 1 Monell Chemical Senses Center, Philadelphia, PA;2 Dermatology, Univ of Pennsylvania, Philadelphia, PA; 3 Basic Science& Craniofacial Biology, New York Univ, New York, NY; 4 Statistics &Quantitative Sciences, Pacific Northwest National Lab, Richland, WASkin odorants should change with age, differ with gender and mayprovide biomarkers of abnormal changes.We performed comprehensivemetabolomic analyses of skin constituents from 23 healthy humansubjects to identify volatile metabolites and assess how they varybetween subjects. Understanding the natural variation of metabolitesfrom healthy subjects provides a baseline from which to assessabnormalities and diagnose disease. Skin metabolites were collected bySolid-Phase-Microextraction (SPME) and solvent extraction andanalyzed via gas chromatography/mass spectrometry (GC/MS). Skinsecretions were also probed for the presence of human odor-bindingproteins. Qualitatively, most individuals yielded similar constituents:both exogenous and endogenous components were seen. SPME-GC/MS analyses revealed the presence of C 8 -C 12 aldehydes and C 8 -C 12ketones in almost every subject´s volatiles. Analysis of the GC/MS datacollected by solvent extraction primarily showed the presence of largeamounts of C 12 to C 18 acids, and squalene. Extract data also suggestsome quantitative and perhaps qualitative differences between youngand older subjects. In addition, we analyzed the co-expression patternsof metabolites to identify sets of metabolites that are potentially coregulated.Western blot analysis demonstrated the presence of apocrinesecretion odor-binding proteins in all age groups and genders. Bycharacterizing the nature and abundance of skin-derived components inhealthy individuals, this study provides a database of normalconstituents against which comparisons can be made with similarsamples obtained from individuals with basal cell and other skincarcinomas. Supported in part by NIH grant T32 DC00014.37
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