Our long-term objectives are to quantify relationships among diet and blood amino acid (AA) concentrations associated with specific alterations in brain, liver, and muscle AA pools and changes in food intake and choice. Individual objectives are to determine: 1) quantitative relationships among diet and blood AA concentrations that lead to competition among groups of AA for uptake into tissues and result in predictable changes in tissue, especially brain, AA and neurotransmitter pools; 2) relationships between changes in brain and other tissue AA pools and in feeding behavior; 3) influences of dietary and hormonal treatments on these relationships. Rats will receive diets containing specific competitors for transport of AA; tissue AA concentrations will be determined in order to measure in vivo relationships between diet and specific changes in tissue AA pools. Neurotransmitter concentrations will be measured where selective changes occur in concentrations of brain AA precursors of neurotransmitters. Food intake/choice will be monitored (computerized system) under conditions known to alter brain or liver AA pools. Competition for AA transport into skeletal muscle will be examined in vitro in soleus muscle. Rats with lesions of the area postrema will be used to test if dietary AA may depress food intake because of malaise (learned aversions). Plasma CCK and GH will be determined in rats fed different amounts of protein. Vagotomized rats will be used to test if diet-induced depressions in food intake may be related to changes in liver AA which provides a signal via the vagus. Brain protein synthesis will be examined in vitro in an already developed system; effects of selective changes in brain AA pools on protein synthesis will be studied. Results will contribute to knowledge of regulation of tissue AA concentrations and how these may be modified selectively. Such information is essential for: 1) optimizing treatments for hepatic, renal, and genetic diseases causing impairment of AA regulatory systems; 2) understanding significance of abnormal blood AA patterns observed during use of enteral or parenteral preparations; 3) providing basic information for understanding and developing treatments for patients with behavioral aberrations and for assessing the validity of claims for effects of diet on behavior of """"""""normal"""""""" individuals.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project (R01)
Project #
2R01DK010747-21
Application #
3224711
Study Section
Nutrition Study Section (NTN)
Project Start
1976-09-01
Project End
1989-03-31
Budget Start
1987-04-01
Budget End
1988-03-31
Support Year
21
Fiscal Year
1987
Total Cost
Indirect Cost
Name
University of Wisconsin Madison
Department
Type
Earth Sciences/Resources
DUNS #
161202122
City
Madison
State
WI
Country
United States
Zip Code
53715
Tews, J K; Repa, J J; Harper, A E (1992) Protein selection by rats adapted to high or moderately low levels of dietary protein. Physiol Behav 51:699-712
Tews, J K; Repa, J J; Harper, A E (1991) Branched-chain and other amino acids in tissues of rats fed leucine-limiting amino acid diets containing norleucine. J Nutr 121:364-78
Eisenstein, R S; Harper, A E (1991) Relationship between protein intake and hepatic protein synthesis in rats. J Nutr 121:1581-90
Tovar, A R; Tews, J K; Torres, N et al. (1991) Neutral amino acid transport into rat skeletal muscle: competition, adaptive regulation, and effects of insulin. Metabolism 40:410-9
Tackman, J M; Tews, J K; Harper, A E (1990) Dietary disproportions of amino acids in the rat: effects on food intake, plasma and brain amino acids and brain serotonin. J Nutr 120:521-33
Anderson, S A; Tews, J K; Harper, A E (1990) Dietary branched-chain amino acids and protein selection by rats. J Nutr 120:52-63
Tews, J K; Repa, J J; Harper, A E (1990) Norleucine: a branched-chain amino acid analog affecting feeding behavior of rats. Pharmacol Biochem Behav 35:911-21
Harper, A E; Peters, J C (1989) Protein intake, brain amino acid and serotonin concentrations and protein self-selection. J Nutr 119:677-89
Tovar, A; Tews, J K; Torres, N et al. (1988) Some characteristics of threonine transport across the blood-brain barrier of the rat. J Neurochem 51:1285-93
Tews, J K; Repa, J J; Harper, A E (1988) Induction of conditioned taste aversion in rats by GABA or other amino acids. Physiol Behav 42:591-7