Researchers found that disrupting
maternal care of mice produced changes in levels of hundreds of genes regulated by the transcription factor
orthodenticle homeobox 2 (OTX2) in the VTA brain reward center. The good news was that although early
stress could establish the groundwork for later depression, that priming could
be undone by intervention at the right moment. Professor Eric
J. Nestler, who led the mouse study, explained that this “mouse paradigm will
be useful for understanding the molecular correlates of increased risk of
depression resulting from early life stress and could pave the way to look for
such sensitive windows in human studies. The ultimate translational goal of
this research is to aid treatment discoveries relevant to individuals who
experienced childhood stress and trauma.”
http://science.sciencemag.org/content/356/6343/1185
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