Adequate amino acid (AA) nutrition is essential for the health and well being of humans and animals alike. Because AAs have no storage pool, the development of an indispensable amino acid (IAA) deficiency can occur rapidly, particularly if a mild state of protein deficiency already exists. AA deficiencies have been shown to compromise growth and any bodily function that depends on protein synthesis, such as wound healing. In addition, IAA imbalance leads to a well-described anorectic response. Since AA supplements have become fashionable, especially among """"""""health food"""""""" faddists, dieters, and athletes, IAA imbalance should be recognized as a potential health hazard. Moreover, many human diseases are complicated by IAA disproportion. Given the importance of AA nutrition, it is imperative to gain a better understanding of the basic mechanisms by which the responses to IAA deficiency are integrated by the brain. The long term goals of the work in this laboratory are to understand how IAA deficiency is recognized by the body and how this deficiency causes the depression of food intake. The IAA imbalanced diet (1MB) is an excellent nutritional model for these studies, as the biochemical and behavioral responses are robust, rapid and well described. The anterior piriform cortex (APC) of the brain appears to be the chemosensor for IAA deficiency; however, the APC cannot act alone to cause the anorectic response. Thus, the signals generated by the APC must be integrated with other brain areas, likely in the anterior forebrain, to change eating behavior. The goals of this proposal are to determine the circuitry and mechanisms by which the brain integrates the initial response to 1MB. We propose to achieve these goals through the following:
Specific Aim 1, to identify the neural circuit within the forebrain that integrates the sensory signals from the APC and activates other brain areas to initiate the anorectic responses to TMB;
Specific Aim 2, to determine the neurochemical mechanisms that mediate the response to 1MB;
and Specific Aim 3, to determine the order of activation in this neural circuit and the signaling mechanisms.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Project (R01)
Project #
5R01NS033347-06
Application #
6476085
Study Section
Nutrition Study Section (NTN)
Program Officer
Edwards, Emmeline
Project Start
1995-06-01
Project End
2004-11-30
Budget Start
2001-12-01
Budget End
2002-11-30
Support Year
6
Fiscal Year
2002
Total Cost
$222,000
Indirect Cost
Name
University of California Davis
Department
Veterinary Sciences
Type
Schools of Veterinary Medicine
DUNS #
094878337
City
Davis
State
CA
Country
United States
Zip Code
95618
Gietzen, Dorothy W; Aja, Susan M (2012) The brain's response to an essential amino acid-deficient diet and the circuitous route to a better meal. Mol Neurobiol 46:332-48
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Hao, S; Ross-Inta, C M; Gietzen, D W (2010) The sensing of essential amino acid deficiency in the anterior piriform cortex, that requires the uncharged tRNA/GCN2 pathway, is sensitive to wortmannin but not rapamycin. Pharmacol Biochem Behav 94:333-40
Gietzen, Dorothy W; Hao, Shuzhen; Anthony, Tracy G (2007) Mechanisms of food intake repression in indispensable amino acid deficiency. Annu Rev Nutr 27:63-78
Gietzen, Dorothy W; Rogers, Quinton R (2006) Nutritional homeostasis and indispensable amino acid sensing: a new solution to an old puzzle. Trends Neurosci 29:91-9
Sharp, James W; Ross-Inta, Catherine M; Hao, Shuzhen et al. (2006) Co-localization of phosphorylated extracellular signal-regulated protein kinases 1/2 (ERK1/2) and phosphorylated eukaryotic initiation factor 2alpha (eIF2alpha) in response to a threonine-devoid diet. J Comp Neurol 494:485-94
Bellinger, Larry L; Williams, Fred E; Lucente, James et al. (2005) Autonomic efferents affect intake of imbalanced amino acid diets by rats. Pharmacol Biochem Behav 81:24-31
Hao, Shuzhen; Sharp, James W; Ross-Inta, Catherine M et al. (2005) Uncharged tRNA and sensing of amino acid deficiency in mammalian piriform cortex. Science 307:1776-8
Koehnle, Thomas J; Stephens, Angel L; Gietzen, Dorothy W (2004) Threonine-imbalanced diet alters first-meal microstructure in rats. Physiol Behav 81:15-21
Gietzen, Dorothy W; Ross, Catherine M; Hao, Shuzhen et al. (2004) Phosphorylation of eIF2alpha is involved in the signaling of indispensable amino acid deficiency in the anterior piriform cortex of the brain in rats. J Nutr 134:717-23

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