421 Poster Central Taste and <strong>Chemosensory</strong> BehaviorINHIBITION OF MUSCARINIC ACETYLCHOLINERECEPTORS ALTERS PERFORMANCE OF MICE IN ANODOR DISCRIMINATION TASKSchutzman J. 1 , Clevenger A.C. 1 , Doucette W. 1 , Caldwell S. 2 , SalcedoE. 2 , Restrepo D. 2 1 Neuroscience Program, University of ColoradoHealth Sciences Center, Aurora, CO; 2 Cell and Developmental Biology,University of Colorado Health Sciences Center, Aurora, COThe olfactory bulb (OB) is heavily innervated by cholinergic fibersoriginating in the horizontal limb of the diagonal band of Broca, andacetylcholine (ACh) has been postulated to modulate OB processingthereby affecting the ability to distinguish structurally similar odorants(Linster,C. and Cleland,T.A., Neural Netw. 15, 709-717, 2002). In thispreliminary study we have altered the function of nicotinic andmuscarinic ACh receptors either through drug infusion into the OB, orby using a mouse defective for the α7 ACh receptor. Mice wereimplanted with bilateral cannulae allowing direct drug injection intoeach OB. Immediately following drug injection, mice were tested on ago-no go odor discrimination task in which one odor was rewarded.Mice treated with scopolamine, an inhibitor of muscarinic receptors,displayed a delay in attaining criterion compared to controls. Incontrast, mice treated with mecamylamine, a nicotinic receptorinhibitor, did not display differences from controls in the go-no go task.In order to determine whether mice defective for the α7 ACh receptorhave a deficiency in discrimination threshold, we used a MaximumLikelihood Parameter Estimation by Sequential Testing (MLPEST)procedure (Clevenger and Restrepo, Chem. Senses. 31:9-26, 2006). Wedid not find any differences between α7 knockouts and controls. Furtherstudies are being performed to determine whether the thresholdmeasured using MLPEST is different in α7 knockouts and controlswhen the mice are subjected to extensive training. Supported by NIHgrant MH068582 (DR), F30 DC 5740 (AC) and a NARSAD EsselInvestigator award (DR)422 Poster Central Taste and <strong>Chemosensory</strong> BehaviorSPEED-ACCURACY TRADEOFF IN OLFACTIONRinberg D. 1 , Koulakov A. 2 , Gelperin A. 1 1 Monell Chemical SensesCenter, Philadelphia, PA; 2 Freeman Building, Cold Spring HarborLaboratory, Cold Spring Harbor, NYThe basic psychophysical principle of speed accuracy tradeoff (SAT)has been used to understand key aspects of neuronal informationprocessing in vision and audition, but has not yet been reported inolfaction. We present the first direct observation of SAT in olfactionand resolve a seeming controversy between results obtained inreaction-time experiments by Uchida and Mainen (Nat. Neurosci., 6,1224, 2003) and Abraham, Spors, et al. (Neuron, 44, 865, 2004). Wedeveloped a behavioral paradigm for mice in which both the time ofodor exposure and the difficulty of the odor discrimination task werecontrolled by the experimenter. The mouse was trained to keep its nosein the odor sampling port during odor delivery until an auditory signalindicated the availability of water reward in one of two water ports. Theodor stimulus indicated whether reward was available in the left or rightwater port. The difficulty of the task was varied by presenting more orless similar pairs of mixtures.. We found that longer enforced odorexposure (from 200–1200 msec) led to more accurate odordiscrimination (from 60 to 95%), even beyond the level at which miceperformed voluntarily, in the reaction-time paradigm developed for ratsby Uchida and Mainen (2003). The presence of SAT in olfactionprovides strong evidence for temporal integration in olfaction andconstrains the applicability of different models of olfactory informationprocessing. Supported by the Army Research Office and the WhitehallFoundation.423 Poster Central Taste and <strong>Chemosensory</strong> BehaviorROLE OF CHOLINERGIC MODULATION IN THE MAINOLFACTORY BULB IN RATS FOR OLFACTORY ACUITYAND DISCRIMINATION LEARNINGFerreti C. 1 , Mandairon N. 1 , McNamara A. 2 , Stack C. 1 , Linster C. 11 Cornell University, Ithaca, NY; 2 Neurobiology and Behavior, CornellUniversity, Ithaca, NYThe objective of this study was to investigate the specific role ofcholinergic modulation in olfactory bulb processing. We tested the roleof cholinergic modulation in the olfactory bulb of cannulated rats bybilateral injections of vehicle (6 µL saline), the cholinergic antagonistsscopolamine (20 µg and 100 µg), the nicotinic antagonist MLA (20 µgand 100 µg), a combination of both drugs, or the cholinesteraseinhibitor neostigmine (dosage) 20 minutes before the behavioral tasks.We tested the role of cholinergic modulation on spontaneous odordiscrimination in the absence of reward conditioning using a habituationtask. A second test involved a olfactory discrimination task in which aodor-reward association has to be formed. We found that spontaneousdiscrimination between chemically related odorants was impaired whennicotinic, but not muscarinic receptors were blocked in the olfactorybulb. Additionally, the spontaneous discrimination between very similarodorants was enhanced when cholinergic modulation was increased.Interestingly, no effect of modulating the action of acetylcholine in theolfactory bulb was seen when rats were trained on a forced choice, twoodor discrimination task. Supported by the Marie Curie Foundation(NM) and NIDCD grant DC005130 (CL).424 Poster Central Taste and <strong>Chemosensory</strong> BehaviorBROAD ACTIVATION OF THE OLFACTORY BULBPRODUCES LONG-LASTING CHANGES IN ODORPERCEPTION IN RATSMandairon N. 1 , Kiselycznyk C.L. 2 , Stack C. 1 , Ferreti C. 1 , Linster C. 11 Cornell University, Ithaca, NY; 2 Neurobiology and Behavior, CornellUniversity, Ithaca, NYA number of electrophysiological experiments have shown that odorexposure alone, unaccompanied by behavioral training, changes theresponse patterns of neurons in the olfactory bulb (Buonviso & Chaput,2000; Buonviso, Gervais, Chalansonnet, & Chaput, 1998; Montag-Sallaz & Buonviso, 2002; Wilson et al., 1985). As a consequence ofthese changes, across mitral cells in the olfactory bulb, individual odorsshould be better discriminated due to previous exposure. We havepreviously shown that a daily 60 minute exposures to odorants duringtwo weeks enhance rats´ ability to discriminate between chemicallysimilar odorants in a relative odor-unspecific manner (Mandairon et al.,1996). Here we first show that the perception of test odorants is onlymodulated by enrichment with odorants that activate at least partiallyoverlapping regions of the olfactory bulb. Second, we show that a broadactivation of olfactory bulb neurons by daily local infusion of NMDAinto both olfactory bulbs enhances the discrimination betweenchemically related odorants in a manner similar to the effect of dailyexposure to odorants. The results strongly suggest that (1) changes inolfactory processing are responsible for the observed modulation ofodor perception and (2) increased activity in the olfactory bulb networkis sufficient to produce these changes. Funded by the Curie Foundation,France (ML).106
425 Poster Central Taste and <strong>Chemosensory</strong> BehaviorSNIFFING PATTERNS OF RATS DURING LEARNING ANDPERFORMANCE OF ODOR DISCRIMINATION TASKSWesson D.W. 1 , Verhagen J.V. 1 , Wachowiak M. 1 1 Biology, BostonUniversity, Boston, MAOdor sampling (sniffing) is a dynamic behavior. Most earlier studieshave focused on sniffing strictly in the context of odor discrimination.In this study, we monitored sniffing behavior continuously in ratslearning and performing odor discriminations under two differentbehavioral paradigms and asked how sniffing relates to odordiscrimination as well as to other behavioral parameters. In bothparadigms, rats were habituated to head restraint and trained to performa simple lick-no-lick two odor discrimination. Sniffing, measured asintranasal pressure transients, was monitored during task acquisitionand performance. In paradigm 1, the test odorant was presented after arandom intertrial interval, with no other associated cues, while inparadigm 2 the rat was allowed to initiate each trial by pressing a barafter a tone was presented. In paradigm 1, rats sniffed at a fairlyconsistent slow frequency of 1–2 Hz. Surprisingly, sniff frequency didnot increase around the time of odor presentation. Presenting a novelodorant as a CS- induced high frequency (6–10 Hz) sniffing whichhabituated within 1–2 trials despite continued successful performance ofthe task. In paradigm 2, rats consistently showed bouts of fast sniffing.Fast sniffing began immediately following the tone and just precedingbar press, but ceased as soon as odor presentation began. Odordiscrimination difficulty did not influence the likelihood or duration offast sniffing. Thus, fast sniffing is more strongly associated with theexpectation of or search for an odor stimulus than with thediscrimination of the odor itself. Funded by NIDCD DC06441.426 Poster Central Taste and <strong>Chemosensory</strong> BehaviorOLFACTORY SENSITIVITY FOR ENANTIOMERS ANDTHEIR RACEMIC MIXTURES—A COMPARATIVE STUDY INMICE AND SPIDER MONKEYSJoshi D. 1 , Voelkl M. 2 , Shepherd G.M. 1 , Laska M. 1 1 Neurobiology, YaleUniversity, New Haven, CT; 2 Medical Psychology, University ofMunich, Munich, GermanyEnantiomers appear to be particularly valuable tools to assess odorstructure-activity relationships. Using an operant conditioningparadigm, we determined olfactory detection thresholds for the opticalantipodes of carvone and limonene as well as for their racemic mixturesin CD-1 mice. We found that (a) with few exceptions the mice wereable to detect all six stimuli at concentrations below 1 ppm, (b) allanimals were more sensitive for (–)-limonene compared to (+)-limonene, whereas no systematic difference in sensitivity was observedfor the optical antipodes of carvone, and (c) racemic mixtures of bothlimonene and carvone were not perceived at lower concentrationscompared to the single compounds. Also using an operant conditioningparadigm, five spider monkeys were tested in parallel. We found that(a) the spider monkeys were at least as sensitive for all six stimuli as themice, (b) all animals were more sensitive for (+)-limonene compared to(–)-limonene, whereas no systematic difference in sensitivity wasobserved for (+)- and (–)-carvone, and (c) racemic mixtures of bothlimonene and carvone were perceived at lower concentrations comparedto the single compounds. Possible reasons underlying the differentpatterns of sensitivity found with mice and spider monkeys arediscussed. GMS is supported by NIH grant (5 R01 DC00086-38) andthe Human Brain Project.427 Poster Central Taste and <strong>Chemosensory</strong> BehaviorBRIEF STIMULUS PRESENTATIONS PERMIT GUSTATORYDETECTION OF LINOLEIC ACID BUT NOT OLEIC ACID INRATSPittman D.W. 1 , Adamson A. 1 , Bramlett M. 1 , Evans S. 1 , Gasque L. 1 ,Lister R. 1 1 Psychology, Wofford College, Spartanburg, SCWe have shown that Sprague-Dawley rats can detect and avoid bothlinoleic and oleic acid during 15-min 2-bottle preference testingfollowing a conditioned taste aversion pairing. This study characterizedthe ability of rats to detect a variety of concentrations (44, 88, 176 µM)of linoleic, oleic, and lauric acid following a conditioned taste aversionpairing with either 88 µM linoleic or oleic acid as the conditionedstimulus. Furthermore, the role of the chorda tympani nerve wasexamined through bilateral transections in a subset of the subjects. Alltesting was conducted in the Davis Rig using 30-s stimulus durations.Rats with intact gustatory systems and a conditioned stimulus of 88 µMlinoleic acid showed significant (F 1,160 = 20.230; p < 0.01) avoidance of44, 88, and 176 µM linoleic acid and a slight generalized avoidance ofoleic acid at the 88 and 176 µM concentrations with no avoidance oflauric acid. There was a significant effect of chorda tympani nervetransection (F 1.160 = 10.381; p < 0.01) eliminating the avoidance of oleicacid and 44 µM linoleic acid with a diminished avoidance of linoleicacid at 88 and 176 µM concentrations. Rat with intact gustatory systemsand a conditioned stimulus of 88 µM oleic acid did not demonstrate anyavoidance of linoleic, oleic, or lauric acid. Based on the current studyand our previous findings, it appears that the chorda tympani nerveplays a role in the selective detection of linoleic acid but not oleic acid.Furthermore, there appears to be another mechanism of free fatty aciddetection that may be based on olfactory or post-ingestive cues.428 Poster Central Taste and <strong>Chemosensory</strong> BehaviorSALT DISCRIMINATION IN RATS WITH CROSS-REGENERATED LINGUAL GUSTATORY NERVESBlonde G. 1 , Jiang E. 1 , Garcea M. 1 , Spector A.C. 1 1 Department ofPsychology and Center for Smell and Taste, University of Florida,Gainesville, FLBecause chorda tympani nerve (CT) transection in rats severelydisrupts their performance in salt discrimination tasks, butglossopharyngeal nerve (GL) transection does not, we tested whetherrats with either the CT cross-regenerated to the posterior tongue or theGL cross-regenerated to the anterior tongue would be competent on aNaCl vs. KCl discrimination using a two-response operant procedure.In both groups of rats with cross-regenerated nerves, overallperformance decreased significantly relative to before surgery.Performance was also significantly lower than rats with intact ornormally regenerated CT nerves, and no better than rats with bilateralCT transection. With further postsurgical testing, some rats in allgroups improved their performance, seemingly learning a newdiscrimination. Amiloride treatment significantly decreasedperformance in all groups both pre- and postsurgically. Functionalconnectivity in the cross-regenerated nerves was confirmedelectrophysiologically in a subset of animals and regeneration in allanimals was verified histologically. These results suggest that neithercross-regeneration condition emulates the normally regenerated CTwith regard to this task. It is possible that the cross-regenerated nervesare capable of providing discriminable signals generated by these salttaste stimuli, however the contribution of the greater superficial petrosalnerve to the performance cannot be dismissed. We thank Drs. ScottHerness and Susan Travers for their help with the electrophysiology.Supported by NIH R01-DC01628.107
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