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Exposure to early life stress regulates Bdnf expression in SERT mutant rats in an anatomically selective fashion
Authors:Francesca Calabrese  Rick H. A. van der Doelen  Gianluigi Guidotti  Giorgio Racagni  Tamas Kozicz  Judith R. Homberg  Marco A. Riva
Affiliation:1. Department of Pharmacological and Biomolecular Sciences, Università degli Studi di Milano, Milan, Italy;2. Department of Anatomy, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, Nijmegen, The Netherlands;3. Department of Cognitive Neuroscience, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, Nijmegen, The Netherlands
Abstract:Although the causes of psychiatric disorders are not fully understood, it is well established that mental illness originates from the interaction between genetic and environmental factors. In this regard, compelling evidence demonstrates that depression can be the consequence of altered, and often maladaptive, response to adversities during pre‐ and early post‐natal life. In this study, we investigated the impact of chronic maternal separation (MS) on the expression of the neurotrophin brain‐derived neurotrophic factor (BDNF) in serotonin transporter (SERT) knockout rats in the ventral and dorsal hippocampus as well as the ventromedial and dorsomedial prefrontal cortex (PFC). We found that both SERT deletion and the MS led to an overall reduction in Bdnf expression in the ventral hippocampus and the ventromedial PFC, whereas in the dorsal hippocampus and in the dorsomedial PFC, we observed a significant increase in the neurotrophin gene expression after MS exposure, specifically in the heterozygous SERT rats. In summary, we show that the modulation of Bdnf expression in SERT mutant rats exposed to MS reflects the complex functional consequences of this gene–environment interaction with a clear distinction between the ventral and the dorsal subfields of the hippocampus and of the PFC.
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Keywords:maternal separation  neurotrophin  serotonin  ventral and dorsal hippocampus/prefrontal cortex
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