75 and 39 of 80 PbN cells were activated after the ipsilateral andcontralateral DMX stimulation, respectively. Among theseactivated cells, only 7 cells were inhibited. All inhibitoryresponses were evoked after contralateral DMX stimulation.The effect of activation of the DMX on taste-driven responsesof the PN cells was examined on 20 PbN cells that were excited,and all seven cells that were inhibited after the DMX stimulation.The DMX stimulation enhanced or inhibited the taste-evokedactivities in all cells tested, parallel to the type of inputs whichthey received from the DMX. These results suggest that tasteresponsiveneurons in the PbN receive convergent input fromthe DMX and that DMX activation modulates taste responsesof these cells.#P40 Poster session I: Chemosensory disorders,models and aging/Central chemosensory circuitsTaste Responsive Multipolar and Elongated Neurons inHamster Nucleus of the Solitary Tract (NST) ProjectDifferentially to Targets in the Brainstem: An In-VivoIntracellular Recording, Labeling, and Tracing StudyCheng-Xiang Li 1 , Qiuhong Yang 1 , Cheng-Shu Li 2 , David V.Smith 1 , Robert S. Waters 11University of Tennessee Health Science Center Memphis, TN,USA, 2 Southern Illinois University Carbondale, IL, USANeurons in the rostral part of the nucleus of the solitary tract(NST) have been described morphologically as multipolar,elongated (fusi<strong>for</strong>m), and ovoid. Attempts, including our own,to relate neuronal structure (cell size, shape, and/or dendriticconfiguration) to function (taste specific input, firingcharacteristics) have met with limited success. One avenue, stillunexplored is whether classes of NST neurons project to differenttargets in the brainstem. To address this possibility, we recordedthe activity of taste responsive neurons in NST, labeled thoseneurons with biocytin, and traced their projections to targetregions in the brainstem. We recorded responses to lingualstimulation with anodal current and to tastants that includedsucrose, NaCl, citric acid, and quinine. Recorded cells werelabeled with 2% biocytin, and the animal maintained <strong>for</strong> aminimum of 2.5 hrs to allow <strong>for</strong> axonal transport. Hamsters wereanesthetized and then perfused with saline followed by 4%para<strong>for</strong>maldehyde. Brains were removed, sectioned at 100 µmthickness in a horizontal or sagittal plane, stained withcytochrome oxidase and/or Nissl to visualize brainstem nucleiand labeled cells. Data were taken from ten unambiguouslylabeled neurons, which were examined <strong>for</strong> taste input, firingproperties, and reconstructed using Neurolucida. Our resultssuggest that elongated cells (n=3) project exclusively to thehypoglossal nucleus while multipolar (n=7) project toparabrachial nucleus, reticular <strong>for</strong>mation and/or trigeminalsensorimotor nuclei. These results obtained from a limitednumber of labeled cells suggest that NST cell morphology mayrelate, in part, to their efferent target(s).#P41 Poster session I: Chemosensory disorders,models and aging/Central chemosensory circuitsAnalysis of Spike Train Variability in Chemosensory NeuronsWithin the Rat Geniculate GanglionAlexandre A Nikonov 1 , Vernon Lawhern 2 , Robert J Contreras 111Department of Psychology and Program in Neuroscience, FSUTallahassee, FL, USA, 2 Department of Statistics, FSU Tallahassee,FL, USASensory neurons encode in<strong>for</strong>mation by using the number ofspikes and /or the precise timing of these spikes. Here, weexamined the coefficient of variation (CV) of the inter-spikeinterval distribution of GG neurons after application of the basictaste stimuli. In anesthetized male rats, we recorded single-cell5-s responses from 17 narrowly tuned (8 to sucrose; 9 to MSG)and 15 broadly tuned (7 NaCl-best; 8 citric acid-best)neurons. Broadly tuned neurons responded robustly to 10 mMcitric acid and 100 mM KCl indicating input from Type III,presynaptic cells in fungi<strong>for</strong>m taste buds, while narrowly tunedneurons were unresponsive to these two stimuli indicating inputfrom Type II, receptor cells. Narrowly tuned neurons had anaverage spontaneous rate of 0.3± 0.2 spikes/s, response latency of0.6 ± 0.3s, and response frequency of 8.5 ± 3.2 spikes/s. Their CVdropped gradually from 0.8 be<strong>for</strong>e stimulation to 0.5 after thestart of the response and remained stable thereafter during thestimulation time. Broadly tuned neurons had an averagespontaneous rate of 2.3 ± 0.6 spikes/s, a response latency of 1.5±0.7s, and response frequency of 12 ± 3.2spikes/s. Their CVdecreased from 0.9 be<strong>for</strong>e stimulation to an intermediate low andachieving a distinct minimum of 0.4 3-s after stimulus applicationand lasting a few hundred milliseconds. These temporal dischargepatterns were specific to some chemical stimuli or mixtures ofthem. Analysis of patterns of activity across many neurons willhelp us understand how GG neurons code taste in<strong>for</strong>mation.#P42 Poster session I: Chemosensory disorders,models and aging/Central chemosensory circuitsNeuron Survival and Central Terminal Field PersistenceDespite Limited Peripherial Regeneration of the InjuredChorda Tympani Nerve in Adult RatsRebecca Reddaway, David L. HillUniversity of Virginia Charlottesville, VA, USAUnilateral chorda tympani nerve transection (CTX) producespersistent morphological and physiological changes in theperipheral and central taste systems despite functionalregeneration of the injured nerve in adult rats. To betterunderstand changes resulting from CTX, we focused experimentson the injured CT nerve. Primary sensory neuron death andtransganglionic degeneration are typical consequences of sensorynerve transection and are often attributed to the loss of trophicsupport from peripheral target organs. However in the tastesystem where the peripheral targets (taste buds) are constantlyturning-over, there is potential <strong>for</strong> an attenuated peripheraltrophic dependence. The current study uses fluorescent retrogradetracers to measure CT cell numbers in the geniculate ganglia andnerve terminal field volumes in the rostral nucleus of the solitarytract (rNTS) following nerve injury. Two different fluorescentlabels, the first (DiI) applied at the time of CTX and the second(Micro-Emerald) at 14, 60, 90, or 120 post-CTX, were used tomeasure 1) the total number of CT neurons surviving CTXP O S T E R S<strong>Abstracts</strong> | 39
and 2) the number of CT neurons with regenerated peripheralaxons. Transgangionically transported fluorescent label allows usto compare the volume of vestigial and functional CT nerveterminal field post-CTX. Our results indicate that CT cells do notdie following CTX, despite attenuated regeneration of peripheralaxons. In addition, measures of labeled CT terminal fields in therNTS indicate 1) a lack of degeneration, and 2) a reduction incentral axons that are functionally connected to peripheraltargets. Such measures will be useful <strong>for</strong> understanding injuryinducedchanges seen in experimental animal populations andtaste abnormalities seen in human patients after CT nerve injury.#P43 Poster session I: Chemosensory disorders,models and aging/Central chemosensory circuitsA Network Model of Taste Processing in the Nucleus of theSolitary TractA.M. Rosen 1 , H. Sichtig 2 , J.D. Schaffer 2,3 , P.M. Di Lorenzo 11Dept. of Psychology, Binghamton University Binghamton, NY,USA, 2 Dept. of Bioengineering, Binghamton UniversityBinghamton, NY, USA, 3 Philips Research, North Am.Briarcliff Manor, NY, USAThough the functional architecture of many primary sensorynuclei has been well characterized, the organization of the nucleusof the solitary tract (NTS), the first central relay <strong>for</strong> gustation,remains a mystery. Here, we used electrophysiological datarecorded from single cells in the NTS to in<strong>for</strong>m a network modelof taste processing. Previous studies have revealed that stimulationof the chorda tympani (CT) nerve initiates two <strong>for</strong>ms ofinhibitory influences in separate groups of NTS cells. These <strong>for</strong>msof inhibition differed in time course and were correlated withdistinct NTS taste response properties. That is, one inhibitoryinfluence peaked early, decayed rapidly and was associated withshort latency responses to CT stimulation and narrow tuningacross tastants. Conversely, the second inhibitory influencepeaked late, decayed slowly and was seen in cells with longlatency responses to CT stimulation and broad tuning. Based onthese data, we designed a model of the NTS consisting of discretecell assemblies with a projection neuron and two different typesof inhibitory interneuron. Each cell assembly is reciprocallyconnected to every other and is characterized by a distinct profileof sensitivity across tastants. Input to the network of integrateand-firemodel neurons was based on recordings from the CTnerve. Responses to taste stimulation as well as paired-pulse CTstimulation were simulated. The network dynamics of the NTSmodel operated in a “winner-take-all” fashion, where differencesin the stimulus sensitivities between assemblies enhanceddiscrimination between taste qualities. We propose that suchdynamics may account <strong>for</strong> the coherence in across neuronpatterns of NTS responses between similar tastants.#P44 Poster session I: Chemosensory disorders,models and aging/Central chemosensory circuitsLinoleic acid does not enhance chorda tympani nerveresponses to sucrose, citric acid and quinine hydrochlorideJennifer M Strat<strong>for</strong>d, Robert J ContrerasFlorida State University Department of Psychology and Programin Neuroscience Tallahassee, FL, USAPrevious studies suggest that the chorda tympani nerve (CT) isimportant in carrying fat taste in<strong>for</strong>mation to the central nervoussystem, as bilateral transection of the CT (CTX) raises the tastediscrimination threshold <strong>for</strong> the free fatty acid, linoleic acid (LA).Surprisingly, the CT is unresponsive to lingual application of LAalone. However, electrophysiological studies of isolated tastereceptors have shown that LA inhibits delayed rectifyingpotassium channels, presumably broadening action potentials,and augmenting responses to other taste stimuli (Gilbertson et al,1997). Thus, the contribution of the CT in this process maydepend upon the presence of other taste stimuli. In this regard,we previously found that co- application of LA and eithermonosodium glutamate (MSG) or sodium chloride (NaCl)elicited greater CT responses than did either MSG or NaClpresented alone (Strat<strong>for</strong>d et al, 2008). In the present study, werecorded CT electrophysiological activity in response to tastemixtures of LA and sucrose (SUC), citric acid (CA), or quininehydrochloride (QHCl) in anesthetized male rats. Unlike theeffects observed with MSG and NaCl, we found that the additionof LA did not alter CT responses to SUC, CA and QHCl.However, CT is weakly responsive to SUC, CA and QHCl inrats. There<strong>for</strong>e, CT whole nerve recordings may lack thesensitivity to detect small changes in CT responses to these tastestimuli. It is more probable, however, that LA may affect CTresponses to MSG and NaCl only, perhaps by specificallymodulating gustatory processing of Na+- which is found in bothMSG and NaCl. This possibility may be explored in futurestudies using a pharmacological antagonist of epithelial sodiumchannels or a non sodium salt, such as potassium chloride.#P45 Poster session I: Chemosensory disorders,models and aging/Central chemosensory circuitsImprovement of olfactory function in patients treated<strong>for</strong> chronic rhinosinositis is related to increasing olfactorybulb volumeVolker Gudziol, Dorothee BuschhüterSmell and Taste Centre Dresden, GermanyAim of the present study was to investigate whether the humanolfactory bulb (OB) volume increases after short-term treatmentof olfactory function. Nineteen patients with chronicrhinosinositis with polyps were investigated. All patients receivedfunctional endoscopic sinus surgery. In addition, 18 volunteerswithout history and endoscopic signs of chronic rhinosinositiswere also investigated. Measurements were per<strong>for</strong>med on 2occasions separated by 3 months in patients and 4 month incontrols. Olfactory function was evaluated in great detailseparately <strong>for</strong> each nostril; MR scans of the OB wereper<strong>for</strong>med. Volumetric measures of the OB were based onplanimetric manual contouring. In healthy controls the OBvolume was not significantly different between the twomeasurements. In contrast, OB volume in patients increasedsignificantly from initial 64.5 ± 13.9mm³ to 70.0 ± 15.3mm³40 | AChemS <strong>Abstracts</strong> <strong>2009</strong>
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eta, ENAC gamma), b-actin, PLC-b 2
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educed granule cell spiking. These
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data here from mouse studies using
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in taste bud induction and developm
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trends in expression of GAP-43, OMP
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four (4 AFC) that they believe is m
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pleasantness (r=.275 p=.006), where
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utyl, hexyl, and octyl benzene). We
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taller compared to wild-type mice.
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animals over the age of P24 were gi
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classify subjects as PROP non-taste
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al 2008. Increases in glucose sensi
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differences in taste receptors is n
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IndexAbaffy, T - 48Abakah, R - P299
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Illig, K - 19, P109Imoto, T - P136I
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Rucker, J - P305Rudenga, K - P315Ru
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AChemS Abstracts 2009 | 135
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Registration7:30 am to 1:00 pm, 6:3
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Notes______________________________
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