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  Dysregulation of the mesoprefrontal dopamine circuit mediates an early-life stress-induced synaptic imbalance in the prefrontal cortex

Oh, W. C., Rodríguez, G., Asede, D., Jung, K., Hwang, I.-W., Ogelman, R., et al. (2021). Dysregulation of the mesoprefrontal dopamine circuit mediates an early-life stress-induced synaptic imbalance in the prefrontal cortex. Cell Reports, (5). Retrieved from https://www.cell.com/article/S2211124721004058/pdf.

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Genre: Zeitschriftenartikel
Alternativer Titel : Cell Reports

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 Urheber:
Oh, Won Chan1, Autor
Rodríguez, Gabriela1, Autor
Asede, Douglas1, Autor
Jung, Kanghoon1, Autor
Hwang, In-Wook1, Autor
Ogelman, Roberto1, Autor
Bolton, McLean M.1, Autor
Kwon, Hyung-Bae1, Autor
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1external, ou_persistent22              

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Schlagwörter: Animals, Male, Mice, synaptic plasticity, dopamine, Prefrontal Cortex, two-photon microscopy, Dopamine, early-life stress, excitatory synapse, inhibitory synapse, PFC, VTA
 Zusammenfassung: Stress adversely affects an array of cognitive functions. Although stress-related disorders are often addressed in adulthood, far less is known about how early-life stress (ELS) affects the developing brain in early postnatal periods. Here we show that ELS, induced by maternal separation, leads to synaptic alteration of layer 2/3 pyramidal neurons in the prefrontal cortex (PFC) of mice. We find that layer 2/3 neurons show increased excitatory synapse numbers following ELS and that this is accompanied by hyperexcitability of PFC-projecting dopamine (DA) neurons in the ventral tegmental area. Notably, excitatory synaptic change requires local signaling through DA D2 receptors. In vivo pharmacological treatment with a D2 receptor agonist in the PFC of control mice mimics the effects of ELS on synaptic alterations. Our findings reveal a neuromodulatory mechanism underlying ELS-induced PFC dysfunction, and this mechanism may facilitate a more comprehensive understanding of how ELS leads to mental disorders.

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 Datum: 2021
 Publikationsstatus: Erschienen
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Titel: Cell Reports
  Alternativer Titel : Cell Rep
Genre der Quelle: Zeitschrift
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Seiten: 109074 Band / Heft: (5) Artikelnummer: - Start- / Endseite: - Identifikator: ISBN: 2211-1247