Obesity accounts for significant morbidity in the USA and Western societies in general. Consumption of excess calories is a major contributing factor to the development of obesity. Consequently, understanding the neural controls of food intake is an important consideration for dealing with the development of obesity. Clearly, people eat in response to a variety of stimuli - physiological, environmental, emotional and social. However, the termination of food intake usually involves sensory signals from the viscera. Viscerosensory signals from the stomach and intestine provide important direct control of food intake. For example, both mechanical stimulation of the stomach, and chemical stimulation of the intestine provide negative feedback that contributes to termination of food intake (satiation). Although vagal sensory neurons are known to carry both gastric mechanosensitive and intestinal chemosensitive signals to the brain, nothing is known about the neurotransmitters and receptors that communicate these signals from the vagus, to and through the brain. Recently the applicant demonstrated that ionotropic, N-methyl-D-aspartate receptors (NMDA receptors) participate in termination of food intake. Additional observations suggest that NMDA receptors may specifically participate in satiety signaled by viscerosensory feedback. In support of this suggestion, preliminary results are presented indicating that NMDA receptors involved in termination of feeding are located in the dorsal hindbrain, where vagal sensory fibers from the gastrointestinal tract terminate. These results raise the intriguing possibility that NMDA receptors participate in receipt and/or integration of viscerosensory satiety signals within the first few central synapses. Accordingly, the overall goal of the experiments proposed in this application is to identify the nature of viscerosensory satiety signals, mediated by NMDA receptors and to locate the anatomical site(s) at which NMDA receptor participation in satiety occurs. In this work we will use intracranial injection technology will be used in combination with physiological manipulations of the gastrointestinal tract to locate the site of NMDA receptor participation in satiation and to analyze the physiological signals mediated by NMDA receptors in the rat.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project (R01)
Project #
5R01DK052849-02
Application #
2906055
Study Section
Special Emphasis Panel (ZRG2-BPO (01))
Program Officer
Yanovski, Susan Z
Project Start
1998-08-01
Project End
2001-07-31
Budget Start
1999-08-01
Budget End
2000-07-31
Support Year
2
Fiscal Year
1999
Total Cost
Indirect Cost
Name
Washington State University
Department
Veterinary Sciences
Type
Schools of Veterinary Medicine
DUNS #
041485301
City
Pullman
State
WA
Country
United States
Zip Code
99164
Campos, Carlos A; Ritter, Robert C (2015) NMDA-type glutamate receptors participate in reduction of food intake following hindbrain melanocortin receptor activation. Am J Physiol Regul Integr Comp Physiol 308:R1-9
Zhao, Huan; Peters, James H; Zhu, Mingyan et al. (2015) Frequency-dependent facilitation of synaptic throughput via postsynaptic NMDA receptors in the nucleus of the solitary tract. J Physiol 593:111-25
Campos, Carlos A; Shiina, Hiroko; Ritter, Robert C (2014) Central vagal afferent endings mediate reduction of food intake by melanocortin-3/4 receptor agonist. J Neurosci 34:12636-45
Campos, Carlos A; Shiina, Hiroko; Silvas, Michael et al. (2013) Vagal afferent NMDA receptors modulate CCK-induced reduction of food intake through synapsin I phosphorylation in adult male rats. Endocrinology 154:2613-25
Campos, Carlos A; Wright, Jason S; Czaja, Krzysztof et al. (2012) CCK-induced reduction of food intake and hindbrain MAPK signaling are mediated by NMDA receptor activation. Endocrinology 153:2633-46
Gallaher, Z R; Ryu, V; Herzog, T et al. (2012) Changes in microglial activation within the hindbrain, nodose ganglia, and the spinal cord following subdiaphragmatic vagotomy. Neurosci Lett 513:31-6
Zhang, Jingchuan; Ritter, Robert C (2012) Circulating GLP-1 and CCK-8 reduce food intake by capsaicin-insensitive, nonvagal mechanisms. Am J Physiol Regul Integr Comp Physiol 302:R264-73
Ritter, Robert C (2011) A tale of two endings: modulation of satiation by NMDA receptors on or near central and peripheral vagal afferent terminals. Physiol Behav 105:94-9
Wright, Jason; Campos, Carlos; Herzog, Thiebaut et al. (2011) Reduction of food intake by cholecystokinin requires activation of hindbrain NMDA-type glutamate receptors. Am J Physiol Regul Integr Comp Physiol 301:R448-55
Ruiter, Marieke; Duffy, Patricia; Simasko, Steven et al. (2010) Increased hypothalamic signal transducer and activator of transcription 3 phosphorylation after hindbrain leptin injection. Endocrinology 151:1509-19

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