Primate stress research has focused on severe social stress and its pathogenic effects on brain and behavior development. Consequently, few researchers have examined the possibility that mild forms of early social stress promote adaptive outcomes in primate development. Recently, our lab reported that brief, intermittent maternal separations (IS) in squirrel monkey infants subsequently lead to diminished anxiety, prosocial tendencies, enhanced glucocorticoid negative-feedback sensitivity, better spatial memory, and enlarged prefrontal brain regions. Since submitting my original NRSA proposal, I have determined that IS alters mother-infant social behavior at reunions. Also, in an unfamiliar environment, IS infants spend less time clinging to their mothers and more time exploring novel objects than NS infants. Although these data provide compelling evidence that IS triggers adaptations in postnatal development, it is not yet known a) whether IS produces differences in stress hormone responses and behavioral performance on a prefrontal-dependent cognitive task, b) whether the prefrontal enlargement previously identified in adult IS monkeys emerges earlier in postnatal brain development, and c) whether IS produces differences in prefrontal white matter integrity. This proposal delineates a series of experiments designed to answer these questions. Results from these studies will advance our understanding of how mild stressful experiences promote cognitive, emotional, and postnatal brain development. This animal model provides valuable insights on a basic process in human development, insofar as early emotional challenges foster adaptations useful later in life.

Agency
National Institute of Health (NIH)
Institute
National Institute of Mental Health (NIMH)
Type
Postdoctoral Individual National Research Service Award (F32)
Project #
5F32MH066537-03
Application #
6863690
Study Section
Biobehavioral and Behavioral Processes 3 (BBBP)
Program Officer
Curvey, Mary F
Project Start
2003-04-01
Project End
2006-03-31
Budget Start
2005-04-01
Budget End
2006-03-31
Support Year
3
Fiscal Year
2005
Total Cost
$51,548
Indirect Cost
Name
Stanford University
Department
Psychiatry
Type
Schools of Medicine
DUNS #
009214214
City
Stanford
State
CA
Country
United States
Zip Code
94305
Yuen, Kaeli W; Garner, Joseph P; Carson, Dean S et al. (2014) Plasma oxytocin concentrations are lower in depressed vs. healthy control women and are independent of cortisol. J Psychiatr Res 51:30-6
Parker, Karen J; Buckmaster, Christine L; Lindley, Steven E et al. (2012) Hypothalamic-pituitary-adrenal axis physiology and cognitive control of behavior in stress inoculated monkeys. Int J Behav Dev 36:
Parker, Karen J; Hyde, Shellie A; Buckmaster, Christine L et al. (2011) Somatic and neuroendocrine responses to standard and biologically salient acoustic startle stimuli in monkeys. Psychoneuroendocrinology 36:547-56
Lyons, David M; Parker, Karen J; Schatzberg, Alan F (2010) Animal models of early life stress: Implications for understanding resilience. Dev Psychobiol 52:402-10
Parker, Karen J; Kenna, Heather A; Zeitzer, Jamie M et al. (2010) Preliminary evidence that plasma oxytocin levels are elevated in major depression. Psychiatry Res 178:359-62
Lyons, David M; Parker, Karen J; Schatzberg, Alan F (2010) Animal models of early life stress: implications for understanding resilience. Dev Psychobiol 52:616-24
Katz, Maor; Liu, Chunlei; Schaer, Marie et al. (2009) Prefrontal plasticity and stress inoculation-induced resilience. Dev Neurosci 31:293-9
Parker, Karen J; Rainwater, Kimberly L; Buckmaster, Christine L et al. (2007) Early life stress and novelty seeking behavior in adolescent monkeys. Psychoneuroendocrinology 32:785-92
Parker, Karen J; Buckmaster, Christine L; Sundlass, Karan et al. (2006) Maternal mediation, stress inoculation, and the development of neuroendocrine stress resistance in primates. Proc Natl Acad Sci U S A 103:3000-5
Parker, Karen J; Buckmaster, Christine L; Justus, Katharine R et al. (2005) Mild early life stress enhances prefrontal-dependent response inhibition in monkeys. Biol Psychiatry 57:848-55

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