Abstracts - Association for Chemoreception Sciences
Abstracts - Association for Chemoreception Sciences
Abstracts - Association for Chemoreception Sciences
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#9 INDUSTRY SYMPOSIUM:<br />
TASTE AND SMELL IN TRANSLATION:<br />
APPLICATIONS FROM BASIC RESEARCH<br />
Insights from olfactory receptor screening<br />
Joel Mainland<br />
Monell Chemical Senses Center, Philadelphia PA 19104 USA<br />
A major advances in the taste field in recent decades was the<br />
identification of receptors that mediate taste. Expression of these<br />
receptors in heterologous cell-based assays has allowed scientists<br />
in both academia and industry to screen <strong>for</strong> novel taste agonists,<br />
antagonists, and modifiers. Similar studies in olfactory receptors<br />
have lagged behind the taste field due to the size of the receptor<br />
family as well as difficulties in expressing the receptors in<br />
heterologous cells. In this talk we will explore the current state of<br />
the science in olfactory receptor screening, relationships between<br />
odorant structure and odor quality, and the identification of<br />
agonists, antagonists and modifiers <strong>for</strong> olfactory receptors.<br />
#10 INDUSTRY SYMPOSIUM:<br />
TASTE AND SMELL IN TRANSLATION:<br />
APPLICATIONS FROM BASIC RESEARCH<br />
Mechanisms of olfactory adaptation<br />
Haiqing Zhao<br />
Johns Hopkins University, Baltimore MD 21218 USA<br />
Olfactory receptor cells exhibit reduced sensitivity upon<br />
prolonged or repeated odor exposure––a phenomenon known as<br />
adaptation. Adaptation at the cellular level is thought to underlie,<br />
at least in part, the perceptual desensitization of an odor<br />
over time. In vertebrates, several calcium-dependent feedback<br />
mechanisms have been proposed to account <strong>for</strong> adaption of<br />
olfactory receptor cells. Recent studies using molecular genetic<br />
approaches that allow selective disruption of these calciumdependent<br />
mechanisms have provide new insight into how<br />
olfactory adaptation may occur.<br />
#12 PRESIDENTIAL SYMPOSIUM:<br />
GUT PEPTIDE INTERACTIONS BETWEEN<br />
TASTE, FEEDING, AND REWARD<br />
Bariatric surgery and appetite<br />
Carel Le Roux<br />
Experimental Pathology, UCD Conway Institute, School of Medicine<br />
and Medical Science, University College Dublin, Ireland<br />
A good model to investigate appetite reduction in humans and<br />
rodents with associated major weight loss is bariatric surgery.<br />
Gastric bypass, but not gastric banding caused increased<br />
postprandial PYY and GLP-1 favouring enhanced satiety.<br />
An early and exaggerated insulin response mediates improved<br />
glycaemic control. The rodent model of bypass showed elevated<br />
PYY, GLP-1 and gut hypertrophy compared with sham-operated<br />
rats. Moreover, exogenous PYY reduced food intake while<br />
blockade of endogenous PYY increased food intake.<br />
A prospective follow-up human study of gastric bypass showed<br />
progressively increasing PYY, enteroglucagon, and GLP-1<br />
responses associated with enhanced satiety. Blocking these<br />
responses in animal and human models leads to increased food<br />
intake. Thus, following gastric bypass, a pleiotrophic endocrine<br />
response may contribute to improved glycaemic control,<br />
appetite reduction, and long-term lowering of body weight.<br />
We have shown that changes occur in the sensory, reward<br />
and physiological domains of taste that may mechanistically<br />
contribute to the alterations in food preferences after gastric<br />
bypass. The sustained nature of weight loss, reduced appetite<br />
and shifts in food preferences may be explained by gut adaptation<br />
and chronic hormone elevation.<br />
#13 PRESIDENTIAL SYMPOSIUM:<br />
GUT PEPTIDE INTERACTIONS BETWEEN<br />
TASTE, FEEDING, AND REWARD<br />
Common Mechanisms of Alimentary Chemosensation:<br />
Implications <strong>for</strong> Taste, Ingestion and Glucose Homeostasis<br />
Steven D. Munger 1,2<br />
1<br />
University of Maryland School of Medicine, Department of Anatomy<br />
and Neurobiology Baltimore, MD, USA, 2 University of Maryland<br />
School of Medicine, Department of Medicine Baltimore, MD, USA<br />
The last two decades has seen a growing recognition that a<br />
common molecular toolkit is employed along the length of the<br />
alimentary canal to detect and respond to nutrients. For example,<br />
many of the same proteins that are critical <strong>for</strong> recognizing sweet,<br />
bitter and umami taste stimuli in the mouth, including T1R and<br />
T2R taste receptors and the transduction proteins a-gustducin<br />
and TRPM5, are found throughout the gastrointestinal (GI) tract<br />
and associated organs. Similarly, taste buds express a number of<br />
neuropeptides that are perhaps best understood in other systems<br />
as endocrine factors that impact nutrient metabolism and/or<br />
ingestive behaviors. A better understanding of the molecular<br />
mechanisms that couple nutrient detection to peptide secretion in<br />
gustatory and GI tissues could lead to the identification of new<br />
pharmacological targets <strong>for</strong> impacting ingestion, satiety, nutrient<br />
assimilation or glycemic control. I will discuss our recent studies<br />
in rodents, including animals deficient in specific taste receptor<br />
subunits or receiving Roux-en-Y gastric bypass, that provide<br />
new insights into the mechanisms of nutrient response in the<br />
mouth and gut and the role of these mechanisms in taste coding,<br />
post-ingestive nutrient response, and the regulation of glucose<br />
homeostasis. Acknowledgements: NIDCD (DC010110), Tate &<br />
Lyle Americas, Ajinomoto Amino Acid Research Program<br />
ORAL ABSTRACTS<br />
<strong>Abstracts</strong> are printed as submitted by the author(s).<br />
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