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Givaudan-Roure Lecture - Association for Chemoreception Sciences

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69 Slide [ ] Trigeminal <strong>Chemoreception</strong><br />

FATTY ACIDS INHIBIT DELAYED RECTIFYING K<br />

CHANNELS IN ISOLATED TRIGEMINAL NEURONS.<br />

Gilbertson T.A. 1, Klein J.T. 1, Farmer-George M. 1, Hansen D.R. 1, Simon<br />

S.A. 2 1Biology & Center <strong>for</strong> Integrated BioSystems, Utah State<br />

University, Logan, UT; 2Anesthesiology, Duke University, Durham, NC<br />

Chemosensory cues <strong>for</strong> fat have been shown to be mediated by fatty<br />

acids (FA) acting directly on subtypes of delayed rectifying K (DRK)<br />

channels in taste receptor cells (TRCs). Since it is generally believed<br />

that texture is important <strong>for</strong> oral fat recognition and that texture<br />

perception is mediated, at least in part, by trigeminal (TG) innervation,<br />

we have examined the effects of fatty acids (0.1-10 µM) on isolated rat<br />

TG neurons using whole-cell patch clamp recording. TG ganglia were<br />

removed and individual TG neurons were isolated by enzymatic<br />

methods and placed into culture <strong>for</strong> 24-72 h. Patch recordings were<br />

made be<strong>for</strong>e, during and after application of a variety of fatty acids<br />

including saturated (SFA), monounsaturated (MUFA) and<br />

polyunsaturated (PUFA) <strong>for</strong>ms. Similar to our results in TRCs, PUFAs<br />

caused a reversible, time-dependent inhibition of DRK channels in TG<br />

neurons, consistent with an open-channel block leading to cell<br />

activation. In contrast to fungi<strong>for</strong>m TRCs, which respond specifically to<br />

PUFAs, TG neurons were much less specific and responded to a variety<br />

of fatty acid types, including some MUFA and SFA, in a similar<br />

fashion. Thus, FA effects on DRK channels may not only mediate the<br />

taste of fat, but may also contribute to the perception of its textural<br />

properties via activation of oral TG fibers. Currently, we are using<br />

quantitative PCR to compare the expression of DRK channels in TG<br />

neurons with TRCs to determine the source of the FA specificity<br />

differences. Supported by NIH DK59611(TAG), DC01065 (SAS).<br />

70 Symposium [ ] Receptors: Choosing Genes, Targeting<br />

Axons, Detecting Chemicals<br />

PERCEPTION OF CHEMICAL CUES AND NAVIGATION IN C.<br />

ELEGANS<br />

Bargmann C.I. 1 1Anatomy, University of Cali<strong>for</strong>nia, San Francisco,<br />

San Francisco, CA<br />

Behavior arises from the interplay between the environment and<br />

intrinsic properties of neurons and neural circuits. To understand how<br />

the genetics and development of the nervous system contribute to<br />

specific behaviors, we are studying olfactory system in the nematode C.<br />

elegans. C. elegans senses hundreds of different compounds,<br />

discriminates between them, and generates different behaviors in<br />

response to different odors. It is possible to define the specific neurons<br />

that generate these behaviors, since the C. elegans nervous system<br />

consists of just 302 neurons that have reproducible functions,<br />

morphologies and synaptic connections. Previous studies have<br />

generated an understanding of the methods by which animals detect and<br />

respond to a single sensory stimulus. In C. elegans, odors are detected<br />

by over 1000 G protein-coupled odorant receptors. Individual olfactory<br />

neurons express multiple receptor genes, allowing a few cells to detect<br />

many odors. A given sensory neuron is primarily dedicated to a single<br />

behavioral task, such as attraction or repulsion. We are now asking how<br />

animals navigate through complex sensory environments using multiple<br />

odors or sensory inputs. For these studies, we have focused on complex<br />

natural stimuli that should be present in the soil environment, such as<br />

different bacterial foods, natural physical stimuli, and other animals<br />

(social groups). C. elegans shows unexpected sophistication in its<br />

behavior when it faces ecologically relevant challenges like pathogenic<br />

bacteria or metabolic stress. Using the wiring diagram, we are<br />

identifying the circuits <strong>for</strong> navigation behavior and asking how sensory<br />

inputs regulate those circuits.<br />

18<br />

71 Symposium [ ] Receptors: Choosing Genes, Targeting<br />

Axons, Detecting Chemicals<br />

THE BIOLOGY OF SWEET, BITTER AND UMAMI TASTE<br />

Zuker C.S. 1 1Section of Neurobiology, University of Cali<strong>for</strong>nia, San<br />

Diego, La Jolla, CA<br />

72 Symposium [ ] Receptors: Choosing Genes, Targeting<br />

Axons, Detecting Chemicals<br />

INTERNAL REPRESENTATIONS OF THE OLFACTORY<br />

WORLD<br />

Wang J. 1, Wong A.M. 2, Axel R. 3 1Neurobiology and Behavior,<br />

Columbia University, New York, NY; 2Department of Biochemistry and<br />

Molecular Biophysics, Columbia University, New YOrk, NY;<br />

3Biochemistry and Molecular Biophysics, Columbia University, New<br />

York, NY<br />

Olfactory perception requires the recognition of a vast repertoire of<br />

odorants in the periphery and central neural mechanisms that allow the<br />

discrimination of odors. The organization of the peripheral olfactory<br />

system appears remarkably similar in fruit flies and mammals. The<br />

convergence of like axons into discrete glomerular structures provides<br />

an anatomic map in the antennal lobe. How does the anatomic map<br />

translate into a functional map? We have developed a sensitive imaging<br />

system in the Drosophila brain that couples two-photon microscopy<br />

with the specific expression of the calcium-sensitive fluorescent<br />

protein, G-CaMP, to examine neural activity. At natural odor<br />

concentrations, each odor elicits a distinct and sparse pattern of activity<br />

that is conserved in different flies. We have combined Ca2+ imaging<br />

with electrical recordings to demonstrate the faithful propagation of the<br />

glomerular map by projection neurons that innervate the protocerebrum.<br />

The quality of an odor may there<strong>for</strong>e be reflected by defined spatial<br />

patterns of activity, first in the antennal lobe and ultimately in higher<br />

olfactory centers. We have identified a spatially invariant sensory map<br />

in the fly protocerebrum that is divergent and no longer exhibits the<br />

insular segregation of like axons observed in the antennal lobe. This<br />

organization provides the opportunity <strong>for</strong> the integration of multiple<br />

glomerular inputs by hierarchical cell assemblies in the protocerebrum.

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