189 Poster Multimodal, <strong>Chemosensory</strong> Measurement,Psychophysical, Clinical Olfactory, and TrigeminalASPARAGUS MALODOR IN URINE—A TRUEPOLYMORPHISM?Pelchat M. 1 , Bykowski C. 1 , Izbicki E. 1 , Reed D. 1 1 Monell ChemicalSenses Center, Philadelphia, PAIt has long been recognized that urine from some individuals whohave eaten asparagus smells like vegetable soup or rotten cabbage.Previous authors have suggested that there are individual differences inproduction of the malodor (e.g. Alison & McWhirter, 1956) or thateverybody produces the odor, but some are insensitive to it (e.g. Lisonet al., 1980). We asked: Are there individual differences in perceptionof asparagus malodor in urine?; Are there individual differences in theproduction of asparagus malodor in urine?; Are there both nonproducersand non-perceivers? 37 adults served as urine donors on twoseparate days. On one day, they ate roasted asparagus and on the otherday they ate bread. They gave a urine sample right before and two hoursafter each snack (4 samples, total). 31 adults were sensory evaluators.Urines from a single donor were evaluated in each session. Evaluatorsperformed a two-alternative forced choice in which their task was toidentify (by smell) the after-asparagus urine (AAU). The AAU wascompared to the before-asparagus urine and the after-bread urine fromthe same donor. We found evidence for individual differences in bothperception and production of asparagus malodor in urine, but at lowerlevels than previously reported: 2/31 evaluators were not able todistinguish the AAU from other samples at a better than chance leveland an additional 2/31 were accurate significantly less of the time thanwere other evaluators. All evaluators with poor discrimination hadotherwise normal olfactory function. For 2/37 urines, the evaluatorswere not able to distinguish the AAU from other samples at a betterthan chance level.190 Poster Multimodal, <strong>Chemosensory</strong> Measurement,Psychophysical, Clinical Olfactory, and TrigeminalWORKING MEMORY FOR ODORSOlsson M.J. 1 , Jonsson F.U. 1 , Moeller P. 2 1 Psychology, UppsalaUniversity, Uppsala, Sweden; 2 Food Science, Sensory Science, RoyalVeterinary and Agricultural University, Fredriksberg C, DenmarkLittle is known about working memory for odors. Dade et al. (2001)compared working memory for odors and faces in a two-back samedifferenttask and found similar levels of performance. Because theodorants in their study were highly identifiable odorants, verbal codingis likely to have supported the memory performance. In our study, usinga similar two-back same-different task, we compared odors that couldbe verbally described to a variable degree. Twenty-two paid participants(16 women), with a mean age of 28.09 (SD = 9.17) judged a series of36 odors. The probability of an odor on trial n to be same as the one ontrial n-2 was .33. Complementary judgments of the odorants´ perceivedintensity, familiarity and verbal category were also required.Preliminary results indicate that memory performance varied with boththe level of familiarity and the level to which the odor could beverbalized, with higher levels yielding higher memory performance.Familiarity and verbalisation on trial n and n-2 were equally importantfor memory performance. (VR-HS:2005-1779)191 Poster Multimodal, <strong>Chemosensory</strong> Measurement,Psychophysical, Clinical Olfactory, and TrigeminalTHE INHIBITION OF STRESS—ODOR CONDITIONINGMaute C. 1 , Sitvarin L. 1 , Petrova M. 1 , Dalton P. 1 1 Monell ChemicalSenses Center, Philadelphia, PAOdors, especially novel ones, are often readily associated withpeople, places and even emotional states. In a series of studies, we havebeen investigating the ability of odors to acquire such learnedassociations to either positive or negative emotions. In the presentstudy, we evaluated the degree to which a negative association betweenan odor and a stressor could be prevented by simply pre-exposing theindividuals to the odor while they were in a non-stressful or relaxingstate. Using a latent inhibition paradigm, individuals were exposed togalbanum on three occasions. On the first two occasions, the odor waspaired with either a stressful public speaking and mathematical task or anon-stressful slideshow. On the final session, individuals were merelyre-exposed to the odor while measures of autonomic arousal andsubjective health and well-being reports were obtained. Individualswho experienced the odor in the non-stressful condition first exhibitedlower levels of autonomic arousal and fewer adverse symptoms in thetest session than did individuals whose first odor experience occurredduring the stressful condition. If novel or salient odors that are likely tobe experienced under stressful or dangerous conditions can be identifiedprior to that event, the findings suggest that the ability of these odors toacquire and potentiate conditioned responses can be reduced by preexposureunder non-stressful conditions. This technique could be usefulfor minimizing the persistence of odor-elicited memories and adverseresponses that are often experienced by disaster relief workers, militarypersonnel and other individuals. Supported by DOD Grant 17-01-1-0782192 Poster Multimodal, <strong>Chemosensory</strong> Measurement,Psychophysical, Clinical Olfactory, and TrigeminalADVERSE EFFECT OF AIR POLLUTION ON OLFACTORYDETECTION OF A CONTAMINATED FOOD BY RESIDENTSOF MEXICO CITYHudson R. 1 , Guarneros M. 2 , Martínez-Gómez M. 3 , Distel H. 4 1 UnivNacional Autónoma de México, Mexico City, Mexico; 2 Univ NacionalAutónoma de México, Mexico; 3 Centro Tlaxcala Biol Conducta, UnivAutónoma de Tlaxcala, Mexico; 4 Univ München, Munich, GermanyRecently we reported that residents of Mexico City (MC; high airpollution) are poorer in detecting, describing and discriminating odorsof beverages than residents of the state of Tlaxcala (Tx; low airpollution). Here we ask if air pollution also affects performance on areal-life task - detecting contamination of a common food. Healthy nonsmokers18-30 years old (MC n = 30, Tx n = 30, equal numbers of menand women) were presented with odorants in squeeze bottles. Whentested with ascending concentrations of stimuli in a 3-way oddballparadigm, Tx subjects detected the odor of orange drink (Tang, Kraft),milk (Nido, Nestlé), and dimethyldisulfide (D) at significantly lowerconcentrations than MC subjects. When presented with milk in itscommercially recommended concentration but mixed with increasingconcentrations of D (a component of "off" milk), Tx subjects detectedthe presence of D and provided descriptions and negative hedonicjudgements at significantly lower concentrations than MC subjects.Also, while Tx subjects began to respond negatively to D at the samelow concentration whether presented alone or in milk, MC subjects firstresponded negatively to it in milk at significantly higher concentrations,that is, detection of D was masked by milk odor to some extent in MCbut not in Tx subjects. Thus, air pollution may affect an olfactoryfunction as basic as judging the edibility of foods.48
193 Poster Multimodal, <strong>Chemosensory</strong> Measurement,Psychophysical, Clinical Olfactory, and TrigeminalPATHOPHYSIOLOGY OF THE OLFACTORYNEUROEPITHELIUM IN A MURINE MODEL OF ALLERGICRHINITISEpstein V.A. 1 , Robinson A.M. 1 , Bryce P.J. 2 , Conley D.B. 1 , Kern R.C. 11 Otolaryngology-HNS, Northwestern University, Chicago, IL; 2 Allergy-Immunology, Northwestern University, Chicago, ILBackground: Olfactory dysfunction is present in 15-20% of patientssuffering from allergic rhinitis, but the specific pathophysiology ispoorly understood. Traditionally, smell deficits in patients withsinonasal disease have been attributed to diminished airflow to theolfactory cleft. Recent studies however, have demonstratedinflammatory changes in the olfactory epithelium (OE) and increasedapoptosis of olfactory sensory neurons (OSNs) in patients with chronicrhinosinusitis and anosmia. The effect of inflammation in allergicrhinitis alone has not been examined. Objective: This study examinesthe effect of allergy on the OE and OSN apoptosis employing a murinemodel of allergic rhinitis. Methods: 7 to 8-week old C57BL/6 micewere sensitized by means of intranasal application of a protein extractof Aspergillus fumigatus three times a week for three weeks, rested forone week, and then challenged either acutely or chronically with thesame allergen. The olfactory neuroepithelium of these mice and wildtypecontrols was assessed for immunohistochemical evidence ofapoptosis and inflammation. Results: Sensitized mice in both the acuteand chronic groups had significantly greater eosinophil infiltration ofthe OE and activation of the apoptotic effector enzyme Caspase-3 ascompared to the wild-type control. The chronically exposed groupdemonstrated the greatest apoptotic activity, while the acute group had amore intense inflammatory influx. Conclusion: Taken together thisdata supports the hypothesis that the olfactory deficits in patients withallergic rhinitis may be the result of inflammatory changes resulting inOSN apoptosis within the OE. Supported by the Department ofOtolaryngology-HNS.194 Poster Multimodal, <strong>Chemosensory</strong> Measurement,Psychophysical, Clinical Olfactory, and TrigeminalNEURONAL AND INFLAMMATORY CHANGES IN NASALTISSUES OF CHRONIC RHINOSINUSITIS PATIENTSYee K.K. 1 , Ozdener M.H. 1 , Cowart B.J. 1 , Pribitkin E.A. 2 , Rawson N.E. 11 Monell Chemical Senses Center, Philadelphia, PA; 2 Otolaryngology,Thomas Jefferson University, Philadelphia, PAOur on-going project examines the impact of inflammation on theolfactory mucosa (OM) due to chronic rhinosinusitis (CRS) pre- andpost-treatment. Nasal lavages were collected and evaluated for thepresence of inflammatory cells and level changes in specificinterleukins and chemokines via cytokine array. Morphologicalcharacteristics of the OM from biopsies were analyzed by quantitativemeasurements and alterations of neuronal cells were assessed byimmunocytochemistry. We observed both similar and uniqueinflammatory, morphological and neuronal changes across CRS patientsand within individuals before and after treatment. Cytokine arrayresults yield specific chemokine patterns. OM histopathology revealscellular proliferation based on Ki67 immunoreactivity (Ki67-ir) andOMP-ir neurons in most samples; however, there are alterations incellular structure and anatomical distribution. We also observed adeficit of ck18-ir supporting cells (SCs) in biopsies with the most severeinflammatory pathology and keratinization of the superficial epithelium.The absence of a normal SC population in CRS OM is a previouslyunreported phenomenon, and may indicate that these cells areparticularly susceptible to inflammation-related damage. These initialfindings provide an insight into the complex changes induced bychronic inflammation on the OM. Psychophysical and clinical datacollected from these patients will enable correlation of molecular andpatient outcome measures. Funded in part by NIH DC006760 andDC000014.195 Poster Multimodal, <strong>Chemosensory</strong> Measurement,Psychophysical, Clinical Olfactory, and TrigeminalLASER SCANNING MICROSCOPY OF THE NASAL MUCOSA:A PRELIMINARY, EX VIVO STUDYPau H. 1 , Stachs O. 2 , Stave J. 2 , Guthoff R. 2 , Witt M. 3 , Just T. 41 Otorhinolaryngology, University of Rostock, Rostock, Mecklenburg-West Pomerania, Germany; 2 Ophthalmology, University of Rostock,Rostock, Mecklenburg-West Pomerania, Germany; 3 University ofTechnology, Dresden, Dresden, Saxony, Germany; 4 University ofRostock, Rostock, Mecklenburg-West Pomerania, GermanyA confocal microscopic approach was performed to establish and todifferentiate between chronic inflammation and hyperplasia of the nasalmucosa without inflammation. Aim of this study was to assess thepotential use of laser scanning microscopy (LSM) for in vivo diagnosisof nasal diseases. Nineteen specimens (2 different regions of the middleturbinate) of 10 patients with chronic rhinosinusitis (CRS) wereinvestigated using LSM. The findings were compared with both, thecorresponding histopathological sections and hyperplastic nasal mucosaobtained from patients who underwent turbinate surgery (12 specimensof 7 patients). The following criteria were used for characterization ofinflammation: thickness of the epithelium, motility of the kinocilia ofthe respiratory epithelium within 20 minutes after biopsy andidentification of inflammatory cells. LSM enables differentiationbetween respiratory and squamous and olfactory epithelium,respectively. The cilia of the respiratory epithelium and the directedmucous transport can be observed ex vivo. LSM exhibited differencesfor the parameter “inflammation cells” and “thickness of theepithelium” being highest in CRS compared to hyperplasia. Amonglymphocytes, koilocytes were identified in CRS. They are characterizedby their swollen ballooned appearance combined with a vacuolatedcytoplasm. Further investigations are needed to assess the potential roleof this technology to evaluate nasal mucosa in vivo.196 Poster Multimodal, <strong>Chemosensory</strong> Measurement,Psychophysical, Clinical Olfactory, and TrigeminalTHE RELATIONSHIP BETWEEN HUMAN NASAL ANATOMYAND OLFACTORY ABILITYHanson R.E. 1 , Hornung D.E. 1 , Leopold D.A. 2 1 St. Lawrence University,Canton, NY; 2 Univeristy of Nebraska Medical Center, Omaha, NEThe nasal airspace of 6 subjects was delineated from T1-weightedcoronal MRIs under 4 conditions (pre dilator, post nasal dilator, 4 hoursafter dilator application and following dilator removal). As expected,the nasal dilator increased the overall size of the nasal cavity comparedto the undilated condition, with increases seen in both the nasal valveregion and in the more posterior bony regions. The changes seen in thenasal valve area suggest wearing a dilator directs more incoming airtoward the upper part of the nose. The increase in volume seen in thebony region generally results in a widening of the area around themiddle turbinate with some increase in the early anterior section of thearea around the superior turbinate. These changes in the bony region arelikely reflexive (i.e. initiated as a result of the dilation of the nasal valveregion) and are more pronounced 4 hours after dilation as compared towhat is observed immediately after dilator application. The relationshipbetween these changes and laminar and turbulent flow in the variousparts of the nose is still not clear, but, at the least, nasal dilators wouldseem to proportionally increase airflow to the airspace around theolfactory receptors. This change in airflow patterns is certainly part ofthe explanation of the decrease in olfactory threshold, increase inmagnitude estimation and better identification seen when wearing nasaldilators. The results of the present study give added support to the useof nasal dilators for better describing the relationship between nasalanatomy and olfactory ability.49
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