The role of """"""""stress"""""""" in the modulation of immunity has recently come under intensive investigation. However, """"""""stress"""""""" is a highly ambiguous term and many of the stress manipulations in the laboratory bear little or no relation to stress as encountered in nature. This research application takes the novel approach of using the biologically relevant stress resulting from agonistic encounters and aggressive interactions between mice in a social conflict paradigm to gain an understanding of the mechanisms and interrelationships governing stress induced modulation of the immune system. Results from immunological experiments will form the basis for selection of experimental groups to be used for endocrinological analysis in order to identify presumably important pathways of endocrine mediation of immunity. Immunological responsiveness will be assessed through the in vivo and in vitro use of specific and non-specific immune stimulants, flow cytometer cell analysis and measurement of immunoregulatory molecules. Endocrinological analysis will include selective ablation of endocrine function by surgical, pharmacological and immunoneutralization techniques. Based on results obtained from the above, experiments will be designed to specifically test the degree to which immunological and endocrinological systems interact in response to the stress of social conflict. This research design will thus allow for a direct cause and effect relationship between the immune and endocrine systems to be examined. As such, this proposal seeks to address whether a biologically relevant stress can modulate immunological competence. This information may therefore be applicable to the study of Acquired Immune Deficiency Syndrome (AIDS), since it has been suggested that the progression of AIDS may be dependent, in part, on altered interactions between the endocrine and immune systems resulting from the psychological stress that is experienced by its victims.

Agency
National Institute of Health (NIH)
Institute
National Institute of Mental Health (NIMH)
Type
First Independent Research Support & Transition (FIRST) Awards (R29)
Project #
1R29MH045246-01
Application #
3475239
Study Section
Neurosciences Research Review Committee (BPN)
Project Start
1988-09-01
Project End
1993-08-31
Budget Start
1988-09-01
Budget End
1989-08-31
Support Year
1
Fiscal Year
1988
Total Cost
Indirect Cost
Name
Minnesota State University, Mankato
Department
Type
Schools of Arts and Sciences
DUNS #
City
Mankato
State
MN
Country
United States
Zip Code
56001
Nguyen, K T; Lyte, M (1997) Norepinephrine-induced growth and alteration of molecular fingerprints in Escherichia coli O157:H7. Adv Exp Med Biol 412:265-7
Lyte, M; Arulanandam, B; Nguyen, K et al. (1997) Norepinephrine induced growth and expression of virulence associated factors in enterotoxigenic and enterohemorrhagic strains of Escherichia coli. Adv Exp Med Biol 412:331-9
Lyte, M (1993) The role of microbial endocrinology in infectious disease. J Endocrinol 137:343-5
Salak, J L; McGlone, J J; Lyte, M (1993) Effects of in vitro adrenocorticotrophic hormone, cortisol and human recombinant interleukin-2 on porcine neutrophil migration and luminol-dependent chemiluminescence. Vet Immunol Immunopathol 39:327-37
Lyte, M; Ernst, S (1993) Alpha and beta adrenergic receptor involvement in catecholamine-induced growth of gram-negative bacteria. Biochem Biophys Res Commun 190:447-52
Lyte, M; Ernst, S (1992) Catecholamine induced growth of gram negative bacteria. Life Sci 50:203-12
Lyte, M (1992) The role of catecholamines in gram-negative sepsis. Med Hypotheses 37:255-8
Lyte, M; Ernst, S; Driemeyer, J et al. (1991) Strain-specific enhancement of splenic T cell mitogenesis and macrophage phagocytosis following peripheral axotomy. J Neuroimmunol 31:1-8
Lyte, M; Nelson, S G; Thompson, M L (1990) Innate and adaptive immune responses in a social conflict paradigm. Clin Immunol Immunopathol 57:137-47
Lyte, M; Nelson, S G; Baissa, B (1990) Examination of the neuroendocrine basis for the social conflict-induced enhancement of immunity in mice. Physiol Behav 48:685-91