TY - JOUR
T1 - Primate Early Life Stress Leads to Long-Term Mild Hippocampal Decreases in Corticosteroid Receptor Expression
AU - Arabadzisz, Dimitrula
AU - Diaz-Heijtz, Rochellys
AU - Knuesel, Irene
AU - Weber, Elisabeth
AU - Pilloud, Sonia
AU - Dettling, Andrea C.
AU - Feldon, Joram
AU - Law, Amanda J.
AU - Harrison, Paul J.
AU - Pryce, Christopher R.
N1 - Funding Information:
This research was funded by the Swiss Federal Institute of Technology (ETH) Zurich, the Swiss National Science Foundation (SNSF) National Center for Competence in Research (NCCR) , Swiss Etiological Study of Adjustment and Mental Health , Grant 51A240–104890 , the NCCR Neural Plasticity and Repair , a SNSF Project Grant 31-67791.02 , and the Wellcome Trust , United Kingdom. We are extremely grateful to Jean-Marc Fritschy for providing laboratory facilities; Corinne Sidler, Mary Walker, and Helen Gordon-Andrews for their expert technical assistance; and Sandor Vizi for helpful and stimulating discussion.
PY - 2010/6/1
Y1 - 2010/6/1
N2 - Background: Expression of mineralocorticoid receptor (MR) and glucocorticoid receptor (GR) genes are moderately reduced in several brain regions in depression. These reductions could be partly due to early life stress (ELS), which predicts emotional disorders. Controlled primate studies are important to test whether ELS sufficient to induce long-term emotional changes also induces long-term altered MR and/or GR brain expression. Methods: In the common marmoset, ELS of daily 30-120-min social isolation across month-1 resulted in some long-term changes in homeostasis and emotional behavior. In some of these same subjects, the aim of this study was to use marmoset-specific riboprobes to determine whether ELS produced long-term effects on brain MR and GR gene expression. Results: At adolescence, relative to control subjects, ELS marmosets exhibited mildly reduced messenger RNA signal for both MR (-15%, p = .05) and GR (-13%, p = .02) in hippocampus-primarily CA1-2-but not in prefrontal cortex, other cortical regions, or hypothalamus. Conclusions: In adolescent marmoset monkey brains, reduced hippocampal expression of MR and GR are consistent chronic-indicators of ELS. It is unlikely that these chronic, mild, specific reductions were acute-mediators of the observed long-term emotional effects of ELS. However, they do suggest involvement of hippocampal MR/GR in the neurodevelopmental effects of ELS.
AB - Background: Expression of mineralocorticoid receptor (MR) and glucocorticoid receptor (GR) genes are moderately reduced in several brain regions in depression. These reductions could be partly due to early life stress (ELS), which predicts emotional disorders. Controlled primate studies are important to test whether ELS sufficient to induce long-term emotional changes also induces long-term altered MR and/or GR brain expression. Methods: In the common marmoset, ELS of daily 30-120-min social isolation across month-1 resulted in some long-term changes in homeostasis and emotional behavior. In some of these same subjects, the aim of this study was to use marmoset-specific riboprobes to determine whether ELS produced long-term effects on brain MR and GR gene expression. Results: At adolescence, relative to control subjects, ELS marmosets exhibited mildly reduced messenger RNA signal for both MR (-15%, p = .05) and GR (-13%, p = .02) in hippocampus-primarily CA1-2-but not in prefrontal cortex, other cortical regions, or hypothalamus. Conclusions: In adolescent marmoset monkey brains, reduced hippocampal expression of MR and GR are consistent chronic-indicators of ELS. It is unlikely that these chronic, mild, specific reductions were acute-mediators of the observed long-term emotional effects of ELS. However, they do suggest involvement of hippocampal MR/GR in the neurodevelopmental effects of ELS.
KW - Corticosteroid receptor
KW - depression
KW - early life stress
KW - hippocampus
KW - marker
KW - neurodevelopment
KW - neuropathology
KW - primate
UR - http://www.scopus.com/inward/record.url?scp=77951879471&partnerID=8YFLogxK
U2 - 10.1016/j.biopsych.2009.12.016
DO - 10.1016/j.biopsych.2009.12.016
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C2 - 20132928
AN - SCOPUS:77951879471
SN - 0006-3223
VL - 67
SP - 1106
EP - 1109
JO - Biological Psychiatry
JF - Biological Psychiatry
IS - 11
ER -