Exposure to stress elicits behavioral and physiological responses in animals and humans, including changes in food intake and body weight. This proposal will take advantage of a unique animal model of social stress, the Visible Burrow System (VBS). The VBS provides a semi-naturalistic environment in which a dominance hierarchy naturally develops among male rats producing dominant (DOM) and subordinate (SUB) animals that can be easily identified with minimal experimenter intervention. Although significant changes in body weight among the SUB group have been reliably observed, little if anything is known of its etiology. In addition, the long-term consequences of altered body weight regulation resulting from chronic social stress have not been examined in this model. The proposed experiments will lay the groundwork for understanding these and other stress-related conditions in humans and may point to novel therapeutic strategies.
The specific aims are: 1) to test the hypothesis that body weight loss in subordinates during VBS housing is attributable to decreased food intake and/or to increases in energy expenditure, 2) to test the hypothesis that physiological, endocrine and neurochemical changes that are evident following 14 days of chronic stress in the VBS will return to control levels when the animals are allowed to recover outside the VBS. A secondary hypothesis is that SUB will gain weight during recovery preferentially as adipose tissue and DOM will gain weight primarily as lean body mass, 3) to test the hypothesis that multiple, intermittent episodes of social stress produce more severe and enduring changes of brain neurochemistry and energy homeostasis than a single episode.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Predoctoral Individual National Research Service Award (F31)
Project #
5F31NS047791-02
Application #
6874364
Study Section
Special Emphasis Panel (ZRG1-F06 (20))
Program Officer
Mitler, Merrill
Project Start
2004-02-01
Project End
2005-09-30
Budget Start
2005-02-01
Budget End
2005-09-30
Support Year
2
Fiscal Year
2005
Total Cost
$22,943
Indirect Cost
Name
University of Cincinnati
Department
Psychiatry
Type
Schools of Medicine
DUNS #
041064767
City
Cincinnati
State
OH
Country
United States
Zip Code
45221
McEwen, Bruce S; McKittrick, Christina R; Tamashiro, Kellie L K et al. (2015) The brain on stress: Insight from studies using the Visible Burrow System. Physiol Behav 146:47-56
Tamashiro, Kellie L K (2015) Developmental and environmental influences on physiology and behavior--2014 Alan N. Epstein Research Award. Physiol Behav 152:508-15
Yoshimichi, Go; Lo, Chunmin C; Tamashiro, Kellie L K et al. (2012) Effect of peripheral administration of cholecystokinin on food intake in apolipoprotein AIV knockout mice. Am J Physiol Gastrointest Liver Physiol 302:G1336-42
Tamashiro, Kellie L K (2011) Metabolic syndrome: links to social stress and socioeconomic status. Ann N Y Acad Sci 1231:46-55
Ulrich-Lai, Yvonne M; Christiansen, Anne M; Ostrander, Michelle M et al. (2010) Pleasurable behaviors reduce stress via brain reward pathways. Proc Natl Acad Sci U S A 107:20529-34
Tamashiro, Kellie L K; Nguyen, Mary M N; Ostrander, Michelle M et al. (2007) Social stress and recovery: implications for body weight and body composition. Am J Physiol Regul Integr Comp Physiol 293:R1864-74
Tamashiro, Kellie L K; Hegeman, Maria A; Nguyen, Mary M N et al. (2007) Dynamic body weight and body composition changes in response to subordination stress. Physiol Behav 91:440-8
Tamashiro, Kellie L K; Sakai, Randall R; Yamazaki, Yukiko et al. (2007) Developmental, behavioral, and physiological phenotype of cloned mice. Adv Exp Med Biol 591:72-83
Tamashiro, Kellie L K; Hegeman, Maria A; Sakai, Randall R (2006) Chronic social stress in a changing dietary environment. Physiol Behav 89:536-42
Duncan, Elizabeth A; Tamashiro, Kellie L K; Nguyen, Mary M N et al. (2006) The impact of moderate daily alcohol consumption on aggression and the formation of dominance hierarchies in rats. Psychopharmacology (Berl) 189:83-94

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