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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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