Our most significant accomplishments in the last four years can be briefly summarized: (1) We have shown that worms alter their behavior depending on food quality. They seek high-quality food by altering their locomotion. This behavior is plastic, in that it is modified by past experience and hunger. (2) We have worked out a molecular pathway that is induced by starvation, and that leads to changed feeding behavior. We call this the hunger pathway, operationally defining hunger as an internal state that satisfies two criteria: ) it is brought on by starvation, and (2) it causes an increase in feeding and food-seeking behavior. (3) We lave found a new behavior that resembles satiety in vertebrates. When fed an excess of high-quality food, worms (apparently) become full: they stop eating, slow down, and appear to fall asleep. Together, these discoveries have given us insight into a broad question of great significance, whose existence we were barely even aware of 4 years ago: how is appetite controlled? There are few universal truths in biology, but the following is a candidate: All organisms must adapt to the quality and quantity of food available in their environment. Human responses to food evolved in an environment where high-calorie food was scarce and precious. In our novel, nutritionally rich environment, improper control of appetite contributes to diseases from anorexia to the current epidemic of obesity. We propose, in the years of extended funding, to continue our investigation of this new problem of appetite ;ontrol.
Our specific aims are:
Aim 1 : Upstream mechanisms in hunger signaling.
Aim 2 : Downstream effects of hunger signaling.
Aims 1 and 2 focus on hunger signaling. The core hunger signaling pathway in pharyngeal muscle extends from the muscarinic acetylcholine receptor GAR-3 to the MAP kinase MPK-1. We call this a hunger pathway because (1) it is activated by starvation, and (2) it has physiological and behavioral effects that allow the animals to cope. This raises two obvious questions:
Aim 1 :What is upstream of the muscarinic receptor? How is the pathway activated by starvation? Aim 2: What is downstream of MPK-1? How does activation of the pathway change physiology and behavior? Aim 3: Cellular and molecular mechanisms of food preference.
Aim 3 will focus on food preference. Here we will focus on a single question: by what cellular and molecular mechanisms is high-quality food distinguished from low? A genetic screen will identify genes necessary for food preference. Calcium imaging will test the hypothesis that specific interneurons in the locomotory circuit respond to food quality.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Method to Extend Research in Time (MERIT) Award (R37)
Project #
7R37HL046154-22
Application #
8230551
Study Section
Special Emphasis Panel (NSS)
Program Officer
Wang, Lan-Hsiang
Project Start
1991-04-05
Project End
2014-02-28
Budget Start
2012-03-01
Budget End
2013-02-28
Support Year
22
Fiscal Year
2012
Total Cost
$295,010
Indirect Cost
$97,679
Name
Virginia Commonwealth University
Department
Physiology
Type
Schools of Medicine
DUNS #
105300446
City
Richmond
State
VA
Country
United States
Zip Code
23298
Artyukhin, Alexander B; Yim, Joshua J; Cheong Cheong, Mi et al. (2015) Starvation-induced collective behavior in C. elegans. Sci Rep 5:10647
Steciuk, Mark; Cheong, Mi; Waite, Christopher et al. (2014) Regulation of synaptic transmission at the Caenorhabditis elegans M4 neuromuscular junction by an antagonistic relationship between two calcium channels. G3 (Bethesda) 4:2535-43
Avery, Leon (2014) A model of the effect of uncertainty on the C elegans L2/L2d decision. PLoS One 9:e100580
Cheong, Mi Cheong; Lee, Hyoung-Joo; Na, Keun et al. (2013) NSBP-1 mediates the effects of cholesterol on insulin/IGF-1 signaling in Caenorhabditis elegans. Cell Mol Life Sci 70:1623-36
Song, Bo-Mi; Faumont, Serge; Lockery, Shawn et al. (2013) Recognition of familiar food activates feeding via an endocrine serotonin signal in Caenorhabditis elegans. Elife 2:e00329
Straud, Sarah; Lee, Inhwan; Song, Bomi et al. (2013) The jaw of the worm: GTPase-activating protein EAT-17 regulates grinder formation in Caenorhabditis elegans. Genetics 195:115-25
Fang-Yen, Christopher; Gabel, Christopher V; Samuel, Aravinthan D T et al. (2012) Laser microsurgery in Caenorhabditis elegans. Methods Cell Biol 107:177-206
Avery, Leon; You, Young-Jai (2012) C. elegans feeding. WormBook :1-23
You, Young-Jai; Avery, Leon (2012) Appetite Control: worm's-eye-view. Animal Cells Syst (Seoul) 16:351-356
Raizen, David; Song, Bo-Mi; Trojanowski, Nick et al. (2012) Methods for measuring pharyngeal behaviors. WormBook :1-13

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