To identify the mechanisms which mediate the psychosocially induced suppression of the stress hormone cortisol in socially subordinate, reproductively suppressed female marmosets. RESULTS Chronic suppression or elevation of the stress hormone cortisol is often associated with neuropsychiatric disorders in humans. As a possible model for these endocrine disturbances, we have been investigating the causes of chronic cortisol suppression in socially subordinate, reproductively suppressed female marmosets. To date, we have examined (1) baseline adrenocorticotrophic hormone (ACTH) levels, to determine whether cortisol suppression is caused by reduced pituitary stimulation of the adrenal cortex; (2) ACTH and cortisol responses to dexamethasone, a synthetic glucocorticoid, to determine whether subordinate females exhibit enhanced sensitivity to glucocorticoid negative feedback; and (3) cortisol responses to exogenous ACTH, to determine whether cortisol suppression is associated with reduced adrenal sensitivity. Results thus far indicate that neither baseline plasma ACTH levels nor the pituitary and adrenocortical responses to dexamethasone differ between groups. Howev er, subordinate females show a blunted adrenocortical response to exogenous ACTH. These results suggest that reduced adrenocortical responsiveness is an important component of adrenocortical suppression in subordinate females. FUTURE DIRECTIONS We will continue to investigate the physiological, biochemical, and molecular mechanisms of adrenocortical suppression in subordinate female marmosets as a model of adrenocortical dysregulation in human neuropsychiatric disorders. KEY WORDS dominance, subordination, ovarian cycle, adrenal cortex, adrenocorticotrophic hormone, glucocorticoids FUNDING NIMH MH53709-01 PUBLICATIONS Saltzman, W., N.J. Schultz-Darken, F.H. Wegner, D.J. Wittwer, and D.H. Abbott. 1998. Suppression of cortisol levels in subordinate female marmosets Reproductive and social contributions. Hormones and Behavior 33:58-74. [J] Abbott, D.H., W. Saltzman, N.J. Schultz-Darken, and P.L. Tannenbaum. 1998. Adaptations to subordinate status in female marmoset monkeys. Comparative Biochemistry and Physiology Part C 119:261-274. [J]

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
Primate Research Center Grants (P51)
Project #
5P51RR000167-41
Application #
6454351
Study Section
Project Start
2001-05-01
Project End
2002-04-30
Budget Start
Budget End
Support Year
41
Fiscal Year
2001
Total Cost
Indirect Cost
Name
University of Wisconsin Madison
Department
Type
DUNS #
161202122
City
Madison
State
WI
Country
United States
Zip Code
53715
Kang, HyunJun; Mesquitta, Walatta-Tseyon; Jung, Ho Sun et al. (2018) GATA2 Is Dispensable for Specification of Hemogenic Endothelium but Promotes Endothelial-to-Hematopoietic Transition. Stem Cell Reports 11:197-211
Rhoads, Timothy W; Burhans, Maggie S; Chen, Vincent B et al. (2018) Caloric Restriction Engages Hepatic RNA Processing Mechanisms in Rhesus Monkeys. Cell Metab 27:677-688.e5
Ellis-Connell, Amy L; Balgeman, Alexis J; Zarbock, Katie R et al. (2018) ALT-803 Transiently Reduces Simian Immunodeficiency Virus Replication in the Absence of Antiretroviral Treatment. J Virol 92:
Park, Mi Ae; Jung, Ho Sun; Slukvin, Igor (2018) Genetic Engineering of Human Pluripotent Stem Cells Using PiggyBac Transposon System. Curr Protoc Stem Cell Biol 47:e63
Ellis, Amy; Balgeman, Alexis; Rodgers, Mark et al. (2017) Characterization of T Cells Specific for CFP-10 and ESAT-6 in Mycobacterium tuberculosis-Infected Mauritian Cynomolgus Macaques. Infect Immun 85:
Rodrigues, Michelle A (2017) Female Spider Monkeys (Ateles geoffroyi) Cope with Anthropogenic Disturbance Through Fission-Fusion Dynamics. Int J Primatol 38:838-855
Buechler, Connor R; Bailey, Adam L; Lauck, Michael et al. (2017) Genome Sequence of a Novel Kunsagivirus (Picornaviridae: Kunsagivirus) from a Wild Baboon (Papio cynocephalus). Genome Announc 5:
Wu, Hong; Whritenour, Jessica; Sanford, Jonathan C et al. (2017) Identification of MHC Haplotypes Associated with Drug-induced Hypersensitivity Reactions in Cynomolgus Monkeys. Toxicol Pathol 45:127-133
Shackman, A J; Fox, A S; Oler, J A et al. (2017) Heightened extended amygdala metabolism following threat characterizes the early phenotypic risk to develop anxiety-related psychopathology. Mol Psychiatry 22:724-732
Kalin, Ned H (2017) Mechanisms underlying the early risk to develop anxiety and depression: A translational approach. Eur Neuropsychopharmacol 27:543-553

Showing the most recent 10 out of 528 publications