Abstract

Adolescence is a time of continued brain maturation, particularly in limbic and cortical regions, which undoubtedly plays a role in the physiological and emotional changes. Juvenile rats repeatedly exposed to prenatal stress (PS) exhibit behavioral features often observed in neuropsychiatric disorders including depression. However, to date the underlying neurological mechanisms are still unclear. In the current study, juvenile offspring rats whose mothers were exposed to PS were evaluated for depression-related behaviors in open field and sucrose preference test. NMDA receptor subunits NR1 and NR2A in the hippocampus, frontal cortex and striatum were assayed by western blotting. The results indicated that PS resulted in several behavioral anomalies in the OFT and sucrose preference test. Moreover, reduced levels of NMDA receptor subunits NR1 and NR2A in the hippocampus, and NR1 in prefrontal cortex and striatum of prenatally stressed juvenile offspring were found. Treatment with MK-801 to pregnant dams could prevent all those changes in the juvenile offspring. Collectivity, these data support the argument that PS to pregnant dams could induce depression-like behavior, which may be involved with abnormal expression of NR1 and NR2A in specific brain regions, and MK-801 may have antidepressant-like effects on the juvenile offspring.

Highlights

  • Depression is a common and serious disorder of adolescence [1]

  • We demonstrated that chronic restraint stress given to pregnant dams could cause depression-like behavior in the juvenile offspring

  • Our present findings suggested that NMDA receptors subunits NR1 and NR2A in a limited region in brain was reduced by Prenatal stress (PS)

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Summary

Introduction

Depression is a common and serious disorder of adolescence [1]. Alterations in glutamate neurotransmission are believed to play a role in the pathophysiology of depression [4]. Brain changes associated with early-onset depression have been reported in the hippocampus, amygdala, caudate nucleus, putamen, and frontal cortex, structures that are extensively interconnected. They comprise a neuroanatomic circuit that has been termed the limbic-corticalstriatal-pallidal-thalamic tract. As the important components of this circuit, hippocampus, frontal cortex and striatum play an important role in the pathophysiology of depression [7,8]

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