A high-fat diet is associated with the development of obesity seen in experimental animals and, in all likelihood, plays a role in the epidemic of obesity seen in affluent nations. The long term objectives of this research proposal are to understand the mechanisms which underlie the development of obesity in rats eating a high-fat diet and to develop strategies to prevent this form of obesity. This research project has focused on two strains of rats, one of which develops obesity when eating a high-fat diet, called SENSITIVE rats and a second strain which is RESISTANT to developing obesity while eating the same high-fat diet. This difference in response to a high-fat diet implies that the mechanisms controlling energy balance differ between these two strains and suggests that through manipulation of these mechanisms, energy balance might be altered. The clinical implications of such a finding are manifest. The general hypothesis of this proposal is that switching from a low to a high-fat diet activates signals in the RESISTANT rats which are integrated in the brain to maintain energy balance by reducing food intake and/or by increasing energy expenditure. The overall approach is based on the concept that energy balance is a regulated system with afferent feed-back signals about the state of nutrient stores and a central integrating system for translating messages into efferent signals which regulate food intake and energy expenditure. The hypothesis that the effects of 3-hydroxybutyrate act as an afferent signal will be tested by manipulating hepatic portal levels. The central integration of information connected with the switch from a low- to a high-fat diet will be examined by lesioning separate hypothalamic nuclei and by recording the ambient local concentration of the neurotransmitters serotonin and norepineplirine. The final set of studies will examine the effect of infusing beta-agonists into the central nervous system or peripherally to test the hypothesis that activation of central or peripheral adrenergic receptors might prevent the development of obesity in rats eating a high-fat diet.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project (R01)
Project #
5R01DK032089-11
Application #
3230573
Study Section
Nutrition Study Section (NTN)
Project Start
1982-08-01
Project End
1994-07-31
Budget Start
1992-08-01
Budget End
1993-07-31
Support Year
11
Fiscal Year
1992
Total Cost
Indirect Cost
Name
Louisiana State University A&M Col Baton Rouge
Department
Type
Organized Research Units
DUNS #
075050765
City
Baton Rouge
State
LA
Country
United States
Zip Code
70803
King, Bruce M; Primeaux, Stefany D; Zadeh, Mohammad L et al. (2011) Olfactory bulbectomy impairs the feeding response to 2-deoxy-D-glucose in rats. Brain Res 1367:207-12
Barnes, Maria J; Argyropoulos, George; Bray, George A (2010) Preference for a high fat diet, but not hyperphagia following activation of mu opioid receptors is blocked in AgRP knockout mice. Brain Res 1317:100-7
Barnes, Maria J; Primeaux, Stefany D; Bray, George A (2008) Food deprivation increases the mRNA expression of micro-opioid receptors in the ventral medial hypothalamus and arcuate nucleus. Am J Physiol Regul Integr Comp Physiol 295:R1385-90
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Primeaux, Stefany D; Tong, Melissa; Holmes, Gregory M (2007) Effects of chronic spinal cord injury on body weight and body composition in rats fed a standard chow diet. Am J Physiol Regul Integr Comp Physiol 293:R1102-9
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Primeaux, Stefany D; Wilson, Steven P; Cusick, Michael C et al. (2005) Effects of altered amygdalar neuropeptide Y expression on anxiety-related behaviors. Neuropsychopharmacology 30:1589-97
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White, Christy L; Ishihara, Yuri; Dotson, Travis L et al. (2004) Effect of a beta-3 agonist on food intake in two strains of rats that differ in susceptibility to obesity. Physiol Behav 82:489-96

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