Objectives The objective of this study is to examine the long-term effects of early social experience on behavior, cognitive function, HPA axis regulation, and psychobiological responses to stress in differentially-reared monkeys. ABSTRACT:As a joint cooperative venture between the MacArthur Foundation and the Asher Center, we have been conducting a number of follow-up studies on an existing cohort of rhesus monkeys that were exposed to variations in early experience as part of previous studies funded by the MacArthur Foundation Research Network on Depression. This cohort is comprised of monkeys that were generated from conditions in which their early experience was varied as part of a program of research entitled """"""""Primate Models of Depression"""""""" (""""""""PMOD""""""""). In the original study, forty-eight rhesus monkeys were reared under two different social conditions from infancy, and later were either exposed or not exposed to stress in conjunction with pharmacologic treatments during the late infancy period (balanced across rearing groups). Animals in the altered early rearing group (peer-reared) were found to differ from controls (mother-reared) in their behavioral, hormonal and neurobiological profiles during the infancy and juvenile period. Follow-up studies have documented that behavioral, psychobiological and cognitive differences between the respective groups of monkeys persist into young adulthood. Keywords early experience, neurobiological development, HPA axis, biogenic amines, cognition, abnormal behavior

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
Primate Research Center Grants (P51)
Project #
5P51RR000167-36
Application #
5219954
Study Section
Project Start
Project End
Budget Start
Budget End
Support Year
36
Fiscal Year
1996
Total Cost
Indirect Cost
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