The proposed research will develop a comparative primate model to study the effects of stress on immune responses. Although it is generally acknowledged that stress can compromise resistance to disease, further research is still needed to determine how different types of stress influence specific aspects of immune responses. In addition, better animal models are needed in this field because of marked species differences and the difficulties inherent in generating stress paradigms that are comparable to human situations. We propose to study two primate species, the squirrel monkey and the rhesus monkey, because they offer two dramatically different physiological systems for evaluating the relationship between psychoendocrine activation and immune responses. The endocrinological and immunological consequences of a non-invasive stress occurring under natural circumstances will be investigated. For the young infant and lactating female, we propose to utilize the varying degrees of stress that can be reliably evoked by different types of mother-infant separation. In the adult, we propose to evaluate the effects of disturbances in ongoing social relations: the response to isolation, the xenophobic response to unfamiliar conspecifics, and the agitation involved in establishing new social relations. Stress will be assessed by measuring changes in circulating levels of plasma cortisol and by alterations in behavior. Immune competence will be measured in control and stressed individuals by measuring (1) immunoglobulin levels; (2) antibody response to specific challenge; (3) level of hemolytic complement (CH50) as well as complement components C4 and C3; (4) macrophage function as indicated by chemiluminescence; (5) T cell function as indicated by measurement of 'active' response to mitogen stimulation and inducibility of specific T cell responsiveness to antigen stimulation; (6) natural killer cell activity.

Agency
National Institute of Health (NIH)
Institute
National Institute of Mental Health (NIMH)
Type
Research Project (R01)
Project #
7R01MH041659-01
Application #
3380407
Study Section
Biopsychology Study Section (BPO)
Project Start
1985-09-01
Project End
1986-09-29
Budget Start
1985-09-01
Budget End
1986-09-29
Support Year
1
Fiscal Year
1985
Total Cost
Indirect Cost
Name
University of Wisconsin Madison
Department
Type
Schools of Arts and Sciences
DUNS #
161202122
City
Madison
State
WI
Country
United States
Zip Code
53715
Coe, Christopher L; Lulbach, Gabriele R; Schneider, Mary L (2002) Prenatal disturbance alters the size of the corpus callosum in young monkeys. Dev Psychobiol 41:178-85
Coe, Christopher L; Kramer, Marian; Kirschbaum, Clemens et al. (2002) Prenatal stress diminishes the cytokine response of leukocytes to endotoxin stimulation in juvenile rhesus monkeys. J Clin Endocrinol Metab 87:675-81
Coe, C L; Ershler, W B (2001) Intrinsic and environmental influences on immune senescence in the aged monkey. Physiol Behav 73:379-84
Price, K C; Coe, C L (2000) Maternal constraint on fetal growth patterns in the rhesus monkey (Macaca mulatta): the intergenerational link between mothers and daughters. Hum Reprod 15:452-7
Coe, C L; Lubach, G R (2000) Prenatal influences on neuroimmune set points in infancy. Ann N Y Acad Sci 917:468-77
Coe, C L; Crispen, H R (2000) Social stress in pregnant squirrel monkeys (Saimiri boliviensis peruviensis) differentially affects placental transfer of maternal antibody to male and female infants. Health Psychol 19:554-9
Price, K C; Hyde, J S; Coe, C L (1999) Matrilineal transmission of birth weight in the rhesus monkey (Macaca mulatta) across several generations. Obstet Gynecol 94:128-34
Reyes, T M; Fabry, Z; Coe, C L (1999) Brain endothelial cell production of a neuroprotective cytokine, interleukin-6, in response to noxious stimuli. Brain Res 851:215-20
Bailey, M T; Coe, C L (1999) Maternal separation disrupts the integrity of the intestinal microflora in infant rhesus monkeys. Dev Psychobiol 35:146-55
Bailey, M T; Karaszewski, J W; Lubach, G R et al. (1999) In vivo adaptation of attenuated Salmonella typhimurium results in increased growth upon exposure to norepinephrine. Physiol Behav 67:359-64

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