| Literature DB >> 33802338 |
Namhun Lee1, Se-Jong Oh1, Jang-Woo Park2, Kyung-Rok Nam1, Kyung-Jun Kang1, Kyo-Chul Lee1, Yong-Jin Lee1, June-Seek Choi3, Jeong-Ho Seok4, Jae-Yong Choi1,5.
Abstract
Early life stress (ELS) is strongly associated with psychiatric disorders such as anxiety, depression, and schizophrenia in adulthood. To date, biological, behavioral, and structural aspects of ELS have been studied extensively, but their functional effects remain unclear. Here, we examined NeuroPET studies of dopaminergic, glutamatergic, and serotonergic systems in ELS animal models. Maternal separation and restraint stress were used to generate single or complex developmental trauma. Body weights of animals exposed to single trauma were similar to those of control animals; however, animals exposed to complex trauma exhibited loss of body weight when compared to controls. In behavioral tests, the complex developmental trauma group exhibited a decrease in time spent in the open arm of the elevated plus-maze and an increase in immobility time in the forced swim test when compared to control animals. In NeuroPET studies, the complex trauma group displayed a reduction in brain uptake values when compared to single trauma and control groups. Of neurotransmitter systems analyzed, the rate of decrease in brain uptake was the highest in the serotonergic group. Collectively, our results indicate that developmental trauma events induce behavioral deficits, including anxiety- and depressive-like phenotypes and dysfunction in neurotransmitter systems.Entities:
Keywords: early life stress; neurotransmission; positron emission tomography; trauma
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Year: 2021 PMID: 33802338 PMCID: PMC7959121 DOI: 10.3390/ijms22052522
Source DB: PubMed Journal: Int J Mol Sci ISSN: 1422-0067 Impact factor: 5.923