Early Parental Deprivation in the Marmoset Monkey Produces Long-Term Changes in Hippocampal Expression of Genes Involved in Synaptic Plasticity and Implicated in Mood Disorder

被引:49
作者
Law, Amanda J. [1 ,2 ]
Pei, Qi [1 ]
Walker, Mary [1 ]
Gordon-Andrews, Helen [1 ]
Weickert, Cyndi Shannon [2 ,4 ]
Feldon, Joram [3 ]
Pryce, Christopher R. [3 ]
Harrison, Paul J. [1 ]
机构
[1] Univ Oxford, Warneford Hosp, Dept Psychiat, Oxford OX3 7JX, England
[2] NIMH, Clin Brain Disorders Branch, Bethesda, MD 20892 USA
[3] Swiss Fed Inst Technol, Lab Behav Neurobiol, Schwerzenbach, Switzerland
[4] Univ New S Wales, Prince Wales Res Inst, Schizophrenia Res Lab, Randwick, NSW, Australia
基金
英国惠康基金; 美国国家科学基金会;
关键词
depression; GAP-43; hippocampus; mRNA; 5-HT1A receptor; VGAT; RECEPTOR MESSENGER-RNA; POSITRON-EMISSION-TOMOGRAPHY; EARLY-LIFE STRESS; MAJOR DEPRESSIVE DISORDER; VESICULAR GLUTAMATE TRANSPORTER; NEUROTROPHIC FACTOR; BIPOLAR DISORDER; MATERNAL SEPARATION; RAT HIPPOCAMPUS; NEUROPSYCHIATRIC DISORDERS;
D O I
10.1038/npp.2008.106
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
In mood disorder, early stressors including parental separation are vulnerability factors, and hippocampal involvement is prominent. In common marmoset monkeys, daily parental deprivation during infancy produces a prodepressive state of increased basal activity and reactivity in stress systems and mild anhedonia that persists at least to adolescence. Here we examined the expression of eight genes, each implicated in neural plasticity and in the pathophysiology of mood disorder, in the hippocampus of these same adolescent marmosets, relative to their normally reared sibling controls. We also measured hippocampal volume. Early deprivation led to decreases in hippocampal growth-associated protein-43 (GAP-43) mRNA, serotonin 1A receptor (5-HT1AR) mRNA and binding ([H-3]WAY100635), and to increased vesicular GABA transporter mRNA. Brain-derived neurotrophic factor (BDNF), synaptophysin, vesicular glutamate transporter 1 (VGluT1), microtubule-associated protein-2, and spinophilin transcripts were unchanged. There were some correlations with in vivo biochemical and behavioral indices, including VGluT1 mRNA with reward-seeking behavior, and serotonin 1A receptor mRNA with CSF cortisol. Early deprivation did not affect hippocampal volume. We conclude that early deprivation in a nonhuman primate, in the absence of subsequent stressors, has a long-term effect on the hippocampal expression of genes implicated in synaptic function and plasticity. The reductions in GAP-43 and serotonin 1A receptor expressions are comparable with findings in mood disorder, supporting the possibility that the latter reflect an early developmental contribution to disease vulnerability. Equally, the negative results suggest that other features of mood disorder, such as decreased hippocampal volume and BDNF expression, are related to different aspects of the pathophysiological process.
引用
收藏
页码:1381 / 1394
页数:14
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