253 Poster Central Olfaction and Chemical EcologyIONIC MECHANISMS REGULATING INTRINSIC BURSTINGIN MOUSE OLFACTORY BULB EXTERNAL TUFTED CELLSLiu S. 1 , Shipley M.T. 1 1 Anatomy and Neurobiology, University ofMaryland at Baltimore, Baltimore, MDExternal tufted (ET) cells in olfactory bulb glomeruli receivemonosynaptic olfactory nerve (ON) input and excite periglomerular andshort axon cells thus forming the basic glomerular local circuit. ET cellsexhibit spontaneous bursting at the range of frequency (1-8 Hz) whichspans the range of rodent sniffing frequencies. Thus ET cellsspontaneously drive the glomerular circuit in a range of frequenciesideally matched to the periodic sampling of odorant stimuli. ET cellbursting is mediated by intrinsic conductances. A persistent Na + current(I NaP ) active near resting membrane potential is required for burstgeneration but the mechanisms that regulate the duration of a burst, itstermination and the inter-burst interval are unknown. The threshold foraction potentials in mouse ET cells is ~-44 mV. When the membrane isdepolarized to intermediate levels (~ -38 mV) a Ca 2+ spike is generated.NiCl 2 (1 mM) and NNC55-0396 (50 µM), a selective T-type calciumchannel blocker, completely abolished this low-voltage activatedcalcium spike and Ca 2+ current. We hypothesized that activation of T-type Ca 2+ channels might activate Ca 2+ -activated K current, whichterminates bursts by re-polarizing the membrane. Consistent with this,ET cells exhibit large-conductance calcium-dependent potassium (BK)currents which were blocked by iberiotoxin (IBTX, 200 nM), a selectiveBK channel blocker. Furthermore, IBTX significantly broadens theevoked burst duration. These results support the hypothesis that the T-type calcium channel plays a critical role in the burst firing activity ofET cells by activating BK channels, which contribute to the terminationof the burst. Supported by NIH NIDCD DC 36940 & DC 02173.254 Poster Central Olfaction and Chemical EcologyBINARAL INTERACTION MODULATES OLFACTORY BULBRESPONSES TO ODORANT HISTORYSinger B. 1 , Kim S. 2 , Zochowski M. 2 1 Neuroscience Graduate Program,University of Michigan, Ann Arbor, MI; 2 Department of Physics,University of Michigan, Ann Arbor, MIWhile odorant-evoked oscillations in the vertebrate olfactory bulbhave been studied extensively, information about which neural circuitsgenerate and modulate them has been missing. In particular, it is unclearto what extent oscillations are a product of the olfactory bulb alone, or ifthey reflect coactivation of the olfactory bulb and other central odorprocessingregions. Using voltage-sensitive dye imaging, we show thatpaired-pulse odorant presentations with interstimulus intervals of 2-5 shad dramatic and diverse effects on the DC depolarization andoscillations that occur in the turtle olfactory bulb. If the same odorant ispresented on each pulse, the DC depolarization is depressed while thepower of the low-latency 14 Hz oscillation is enhanced in response tothe second stimulation. If different odorants are presented on the firstand second pulse, then all components of the response are depressed.These effects are present if both pulses are delivered to the same naris,or if the first pulse is delivered contralaterally to the second. Thesimilarity of uninaral and binaral effects suggest that the historydependentmodulation of the olfactory bulb response is mediated bybrain structures sending bilateral projections to both olfactory bulbs.This work was supported by a UM Research Incentives Grant (M.Z.).B.H.S is supported by NIH T32-GM007863 and T32-DC00011.255 Poster Central Olfaction and Chemical EcologyMULTI-SINGLE UNIT AND LOCAL FIELD OSCILLATORYDYNAMICS FROM IN-VIVO BRAIN STIMULATIONFOCUSED ON PARALLEL CONNECTIONS BETWEEN THEANTERIOR AND POSTERIOR PIRIFORM CORTICES ANDTHE ENTORHINAL CORTEXHermer-Vazquez R. 1 , Hermer-Vazquez L. 1 1 Psychology, University ofFlorida, Gainesville, FLA major question in neuroscience concerns the computationaladvantages of parallel processing in the brain. The olfactory-limbiccircuitry contains multiple examples of parallel inputs from multipleareas onto a single upstream center. The current study was undertakento determine the neural correlates of olfactory information flow betweentwo output sites in the piriform to the medial entorhinal cortex. Thisposter focuses on stage 1 of these ongoing experiments, conducted inthe anesthetized preparation. Our prior results from recordingsimultaneously from multiple nodes within the olfactory-motor circuitduring a GO/NO-GO olfactory task found the importance of transientfrequency modulation and spike inhibitory activity in predicting trialoutcome. Our hypothesis states that specific frequency bands from thetato gamma facilitate both the transfer of an artificial stimulus pulse or astimulus odor, in a site-specific manner, from the posterior and anteriorpiriform to distinct laminar layers of the medial entorhinal cortex. Weused grid microelectrode wires for anterior and posterior piriformstimulation and vertical silicon multisite electrodes for recording currentsources in the entorhinal cortex layers. Results currently indicate wehave detected layer-specific long lasting complex waveforms generatedby one or both piriform sites to the entorhinal, with distinct frequencydepedendent modulation. These results will aid in characterizing howthe flow of information from the periphery, influences feedfowarddynamics as exemplified by the parallel inputs from the piriform to theentorhinal cortices.256 Poster Central Olfaction and Chemical EcologyNEUROMODULATORY ROLE FOR POST-SYNAPTICDENSITY 95 (PSD-95) IN THE OLFACTORY BULBMarks D.R. 1 , Fadool D. 2 1 Neuroscience, Florida State University,Tallahassee, FL; 2 Biological Science, Neuroscience, and MolecularBiophysics, Florida State University, Tallahassee, FLPrevious work by our laboratory has demonstrated a pivotal role forthe voltage-gated Shaker potassium channel (Kv1.3) highly expressedin the olfactory bulb (OB) in acuity, threshold, and odorantdiscrimination. The insulin receptor (IR) kinase and the adaptor protein,PSD-95, are expressed at high levels in the OB whereby PSD-95disrupts insulin-evoked Kv1.3 current suppression in an activitydependantmanner. We now show that all three proteins are co-localizedin the OB, with PSD-95 showing heavy labeling across all neurolaminaincluding the glomeruli. We found that PSD-95 coimmunoiprecipitateswith Kv1.3 as well as the IR kinase, demonstrating a multiple proteinproteininteraction. PSD-95 clusters Kv1.3 in HEK293 cells, as well asclusters the IR kinase, but only in the presence of Kv1.3. A PSD-95mutant lacking the SH 3 and guanylate kinase (GK) domain (PSD-95SH 3 ) was constructed, as well as use of previous mutants created by A.El-Husseini (2002) to dissect the interaction of these three proteins.PSD-95 PM (palmitoylation) was also used to demonstrate that PSD-95may be involved in the trafficking and distribution of Kv1.3. Wepropose a model of interaction of Kv1.3, IR kinase, and PSD-95 whereKv1.3 channels are bound by PDZ domains 1 & 2 of PSD-95 and the IRkinase is bound by the SH 3 domain. These data demonstrate that PSD-95 may influence the excitability of synaptic connections in the OB viaK channel interaction and subsequent modulation. Supported by NIHDC03387 (NIDCD).64
257 Poster Central Olfaction and Chemical EcologyDIFFERENCES IN ODOR RESPONSES BETWEEN ANTERIORAND POSTERIOR PIRIFORM CORTEXIllig K.R. 1 , Kay R. 1 1 Psychology, University of Virginia,Charlottesville, VASingle pyramidal cells in piriform cortex respond to a large numberof structurally dissimlar odors, can distinguish between highly similarodorant compounds, and develop responses to non-olfactorycomponents of an odor-guided behavioral task. Together with observedanatomical features (e.g., Illig, 2005, J. Comp. Neurol. 488: 224-231),such complexity of responding suggests an information processingscheme in piriform cortex that combines convergent information fromthe olfactory bulb, amygdala and prefrontal cortex. To gain a betterunderstanding of these processes, we recorded responses of singleneurons in the anterior (APC) and posterior (PPC) piriform cortex to abroad range of structurally varied odorants. Of particular interest wasthe degree to which responses in these two areas differed, given theirdifferences in anatomical and functional organization. Results indicatethat APC cells display selectivity for one or two odors within an odorclass (µ = 1.37 odors), as shown previously. Interestingly, single cellsdisplayed such selectivity for multiple classes of odors (e.g., aldehydesand ketones), and such responses were related in complex ways toodorant structures. Results in PPC include evidence for an active,dynamic tuning of odor specificity within an odor trial, and apreferrential response by individual cells for multiple distinct odorswithin an odor class. Neither of these response characteristics werefound in APC. Taken together, these results point to separate,complimentary processing of odor information in APC and PPC.Supported by NIH Grant 05557 from NIDCD (KRI)258 Poster Central Olfaction and Chemical EcologyEXPERIENCE-DEPENDENT ADAPTATION OF SENSORYSYNAPSES IN THE OLFACTORY BULBTyler W.J. 1 , Murthy V.N. 1 1 Molecular & Cellular Biology, HarvardUniversity, Cambridge, MAExperience-dependent changes in neural circuits have traditionallybeen investigated in brain regions several synapses downstream of thesensory organ. Whether sensory experience can alter peripheral sensorysynapses remains largely unknown. In many animals, including rodents,synaptic processing of odor information initially occurs in glomeruli ofthe olfactory bulb. Here, we find that unilateral naris occlusion inneonatal rats results in the strengthening of primary synapses made byolfactory sensory neurons. Sensory information continues to beamplified through the circuit in deprived animals, as second-orderexcitatory synapses between neurons in the glomerular region were alsofound to be stronger. The increase in synaptic strength, triggered bysensory deprivation, is mediated by coordinated changes in both preandpostsynaptic properties. Our observations demonstrate that sensoryexperience can modify synaptic strength at the very first site ofinformation transfer between the environment and an organism. Thismodification may possibly serve as a mechanism for homeostatic gaincontrol in odor processing. Support: NIH and Klingenstein Fund.259 Poster Central Olfaction and Chemical EcologyTRANSIENT BETA-FREQUENCY SPIKING COUPLINGOLFACTORY AND MOTOR SITES DURING OLFACTORY S+RECOGNITIONHermer-Vazquez L. 1 , Hermer-Vazquez R. 1 1 Psychology, University ofFlorida, Gainesville, FLIn previous work, we demonstrated that olfactory and motor brainregions display synchronous, transient (
- Page 1 and 2:
1 Symposium Chemosensory Receptors
- Page 3 and 4:
9 Symposium Chemosensory Receptors
- Page 5 and 6:
17 Givaudan LectureFISHING FOR NOVE
- Page 7 and 8:
25 Symposium Impact of Odorant Meta
- Page 10 and 11:
37 Poster Peripheral Olfaction and
- Page 12 and 13:
45 Poster Peripheral Olfaction and
- Page 14 and 15: 53 Poster Peripheral Olfaction and
- Page 16 and 17: 61 Poster Peripheral Olfaction and
- Page 18 and 19: 69 Poster Peripheral Olfaction and
- Page 20 and 21: 77 Poster Peripheral Olfaction and
- Page 22 and 23: 85 Poster Peripheral Olfaction and
- Page 24 and 25: 93 Poster Chemosensory Coding and C
- Page 26 and 27: 101 Poster Chemosensory Coding and
- Page 28 and 29: 109 Poster Chemosensory Coding and
- Page 30 and 31: 117 Poster Chemosensory Coding and
- Page 32 and 33: 125 Poster Chemosensory Coding and
- Page 34 and 35: 133 Poster Chemosensory Coding and
- Page 36 and 37: sniffing behavior. Furthermore, we
- Page 38 and 39: 149 Slide Chemosensory Coding and C
- Page 40 and 41: 157 Slide Taste ChemoreceptionHTAS2
- Page 42 and 43: 165 Poster Multimodal, Chemosensory
- Page 44 and 45: 173 Poster Multimodal, Chemosensory
- Page 46 and 47: 181 Poster Multimodal, Chemosensory
- Page 48 and 49: 189 Poster Multimodal, Chemosensory
- Page 50 and 51: 197 Poster Multimodal, Chemosensory
- Page 52 and 53: 205 Poster Multimodal, Chemosensory
- Page 54 and 55: 213 Poster Multimodal, Chemosensory
- Page 56 and 57: 221 Poster Multimodal, Chemosensory
- Page 58 and 59: 229 Slide Molecular Genetic Approac
- Page 60 and 61: 237 Poster Central Olfaction and Ch
- Page 62 and 63: 245 Poster Central Olfaction and Ch
- Page 66 and 67: 261 Poster Central Olfaction and Ch
- Page 68 and 69: 269 Poster Central Olfaction and Ch
- Page 70 and 71: 277 Poster Central Olfaction and Ch
- Page 72 and 73: 285 Poster Central Olfaction and Ch
- Page 74 and 75: 293 Poster Central Olfaction and Ch
- Page 76 and 77: 301 Slide Central OlfactionOLFACTOR
- Page 78 and 79: 309 Poster Chemosensory Molecular G
- Page 80 and 81: 317 Poster Chemosensory Molecular G
- Page 82 and 83: 325 Poster Chemosensory Molecular G
- Page 84 and 85: 333 Poster Chemosensory Molecular G
- Page 86 and 87: 341 Poster Chemosensory Molecular G
- Page 88 and 89: 349 Poster Chemosensory Molecular G
- Page 90 and 91: 357 Poster Chemosensory Molecular G
- Page 92 and 93: 365 Poster Chemosensory Molecular G
- Page 94 and 95: 373 Symposium Olfactory Bulb Comput
- Page 96 and 97: 381 Symposium Presidential: Why Hav
- Page 98 and 99: 389 Poster Central Taste and Chemos
- Page 100 and 101: 397 Poster Central Taste and Chemos
- Page 102 and 103: 405 Poster Central Taste and Chemos
- Page 104 and 105: 413 Poster Central Taste and Chemos
- Page 106 and 107: 421 Poster Central Taste and Chemos
- Page 108 and 109: 429 Poster Central Taste and Chemos
- Page 110 and 111: 437 Symposium Neural Dynamics and C
- Page 112 and 113: 445 Poster Developmental, Neurogene
- Page 114 and 115:
453 Poster Developmental, Neurogene
- Page 116 and 117:
461 Poster Developmental, Neurogene
- Page 118 and 119:
469 Poster Developmental, Neurogene
- Page 120 and 121:
477 Poster Developmental, Neurogene
- Page 122 and 123:
485 Poster Developmental, Neurogene
- Page 124 and 125:
493 Poster Developmental, Neurogene
- Page 126 and 127:
501 Poster Developmental, Neurogene
- Page 128 and 129:
Brody, Carlos, 438Brown, R. Lane, 3
- Page 130 and 131:
Gilbertson, Timothy Allan, 63, 64,
- Page 132 and 133:
Klouckova, Iveta, 150Klyuchnikova,
- Page 134 and 135:
Ni, Daofeng, 93Nichols, Zachary, 35
- Page 136 and 137:
Sorensen, Peter W., 23, 288, 289Sou
- Page 138:
Zeng, Musheng, 466Zeng, Shaoqun, 26