Givaudan-Roure Lecture - Association for Chemoreception Sciences
Givaudan-Roure Lecture - Association for Chemoreception Sciences
Givaudan-Roure Lecture - Association for Chemoreception Sciences
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61 Poster [ ] Olfaction: Animal Behavior<br />
NOT ONLY - BUT ALSO -ADRENOCEPTORS ARE INVOLVED<br />
IN EARLY ODOR PREFERENCE LEARNING IN THE RAT<br />
Mclean J.H. 1, Mccann J. 2, Darby-King A. 1, Harley C.W. 2 1Basic<br />
Medical <strong>Sciences</strong>, Memorial University of Newfoundland, St. John's,<br />
Newfoundland, Canada; 2Psychology, Memorial University of<br />
Newfoundland, St. John's, Newfoundland, Canada<br />
Early preference olfactory learning is important <strong>for</strong> the survival of<br />
infant rats because they need to associate the odor of the mother with<br />
reward (food). In the neonate, tactile stimulation activates the locus<br />
coeruleus (Nakamura et al., 1987) in the brain stem. Noradrenergic<br />
(NE) neurons in the locus coeruleus (LC) have a strong axonal<br />
projection to the olfactory bulb (Shipley et al., 1985; McLean and<br />
Shipley, 1989; McLean et al., 1991). When NE activation is paired<br />
with odor in the neonate, preference <strong>for</strong> the odor (learning) takes place<br />
(Sullivan et al., 2000;Sullivan et al., 1991;Sullivan et al., 1989;Price et<br />
al., 1998;Langdon et al., 1997). The LC β-adrenergic input has been<br />
shown to be necessary and sufficient <strong>for</strong> preference acquisition to occur<br />
in rats up to around postnatal day 10. Surprisingly, despite observations<br />
that α-adrenoceptors are present (Day et al. 1997, Winzer Serhan et al,<br />
1997) and functional (Hayar et al. 2001) in the olfactory bulb, there is<br />
relatively little known about their function in behavior. In this study, we<br />
tested the hypothesis that α-adrenoceptors have roles similar to the βadrenoceptors<br />
in early olfactory learning. In this set of experiments we<br />
showed that activation of the α1-adrenoceptors was sufficient to induce<br />
early preference learning in the rat while the α2-adrenoceptor agonists<br />
did not show an effect. The α-adrenoceptors acted in a dose-dependent<br />
manner similar to the β-adrenoceptors in early odor preference learning.<br />
This work is supported by a grant from CIHR-CEDA Regional<br />
Partnership<br />
62 Poster [ ] Olfaction: Animal Behavior<br />
THE EFFECT OF CONCENTRATION AND CONDITIONING<br />
ON ODORANT DISCRIMINATION BY THE HONEYBEE<br />
Fussnecker B.L. 1, Carlton M. 1, Wright G. 2, Smith B.H. 1 1Entomology,<br />
Ohio State University, Columbus, OH; 2Mathematical Biosciences<br />
Institute, Ohio State University, columbus, OH<br />
Naturally occurring odors used by animals <strong>for</strong> mate recognition, food<br />
identification and other purposes must be detected at concentrations that<br />
vary across several orders of magnitude. Olfactory systems must<br />
there<strong>for</strong>e have the capacity to represent odors over a large range of<br />
concentrations regardless of dramatic changes in odor salience. The<br />
stability of the representation of an odor relative to other odors across<br />
concentration has not been extensively evaluated. We tested the ability<br />
of honeybees to discriminate pure odorants across a range of<br />
concentrations at and above their detection threshold. We also<br />
examined how their ability to discriminate among odors changed as a<br />
function of the number of times they had encountered an odorant in<br />
association with an appetitive reward. Our study showed that<br />
discrimination among odorants was a function both of the concentration<br />
and the number of experiences a subject has with an odorant. We<br />
hypothesize that this arises from two separate mechanisms in the<br />
olfactory system.<br />
16<br />
63 Poster [ ] Olfaction: Animal Behavior<br />
DILTIAZEM ADMINISTERED NASALLY DECREASES FOOD<br />
INTAKE AND ATTENUATES WEIGHT GAIN IN RATS<br />
Maher T.J. 1, Amer A. 1, Adams C. 2, Chen W. 3, Weinrich K. 3<br />
1Massachusetts College of Pharmacy and Health <strong>Sciences</strong>, Boston, MA;<br />
2Compellis Pharmaceuticals, Somerville, MA; 3Longwood<br />
Pharmaceuticals, Inc., Boston, MA<br />
Energy intake is continuously influenced by many complex<br />
endogenous neurochemical systems located both centrally and<br />
peripherally, in addition to numerous external environmental stimuli,<br />
such as olfaction. As the processing of odorant in<strong>for</strong>mation by many<br />
olfactory neurons is mediated via Ca2+-currents through Ca2+<br />
channels, a novel approach at influencing the ingestive behaviors of<br />
animals might there<strong>for</strong>e involve altering olfactory acuity via Ca2+<br />
channel blockade. The present study tested the ability of a Ca2+<br />
channel blocker, diltiazem (D), to alter food intake in rats made<br />
hyperphagic. D was delivered using the intranasal (i.n.), intraperitoneal<br />
(i.p.) and oral (p.o.) routes of administration. Male Sprague Dawley rats<br />
maintained in a reversed-lighting environment, which had been fooddeprived<br />
<strong>for</strong> 4hrs at the beginning of the dark cycle, were administered<br />
different doses of D or vehicle (V) and the amount of food consumed<br />
was measured. While food intake at 1, 2 and 4 hrs post D administration<br />
was significantly decreased in a dose-dependent manner after i.n.<br />
administration, neither the i.p. nor p.o. routes significantly affected food<br />
intake. In another experiment, rats were trained to eat their daily meal<br />
during the first 4hrs at the onset of the dark cycle. Once acclimated to<br />
this schedule, daily treatment <strong>for</strong> 14 days with i.n. D or V prior to food<br />
introduction resulted in a dose-dependent attenuation of weight gain.<br />
Together these studies suggest that i.n. administration of D possesses<br />
significant anorectic activity that may have utility in influencing energy<br />
intake. Additional studies are needed to determine the exact<br />
mechanisms and sites of action of i.n. administered D.<br />
64 Poster [ ] Olfaction: Animal Behavior<br />
KV1.3-TARGETED GENE-DELETION INCREASES<br />
METABOLIC FUNCTION AND OLFACTORY ABILITY<br />
Thompson R.N. 1, Perkins R.M. 1, Parsons A.D. 2, Overton M. 2, Fadool<br />
D. 1 1Dept. Biological Sci, Prog. in Neurosci., Florida State University,<br />
Tallahassee, FL; 2Dept Nutrition, Food, & Exer Sci, Prog. in Neurosci.,<br />
Florida State University, Tallahassee, FL<br />
Mice with gene-targeted deletion (KO) of the voltage-dependent K<br />
channel, Kv1.3, have smaller glomeruli and thus were behaviorally<br />
phenotyped to understand the channel´s contribution to olfaction. Mice<br />
were monitored (8d) in environmental chambers where data are<br />
computer-acquired every 30 seconds. KO animals were found to have<br />
abnormal ingestive behaviors yet equivalent daily caloric/water intake;<br />
KOs ate more intermittently and drank larger volumes less frequently.<br />
KO animals had slightly increased metabolism and locomotor activity<br />
in the dark cycle and weighed less than aged-matched wildtype mice.<br />
KO mice were not anosmic, in fact, retrieval time to recover a hidden<br />
food item was twice as fast as that observed <strong>for</strong> wildtype mice. Odor<br />
habituation trials using complex mixtures and single alcohols indicated<br />
that KO mice can discriminate molecules differing by only 1 carbon.<br />
Food-restricted mice were trained to dig <strong>for</strong> a hidden reward paired<br />
with an odorant using a two-choice paradigm to determine odorant<br />
threshold ability. KO mice per<strong>for</strong>med the paired task more quickly and<br />
at concentrations 1,000 to 10,000 fold less than that by wildtype mice.<br />
While these tasks are influenced by memory, both genotypes per<strong>for</strong>med<br />
equivalently in object recognition testing and test of motivation <strong>for</strong><br />
object exploration. This unusual set of behaviors in the Kv1.3 KO mice<br />
suggest that Kv1.3 serves additional roles beyond shaping the resting<br />
potential. Supported by NIH DC03387(NIDCD) and NIH HL-56732.