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Resilience to anhedonia-passive coping induced by early life experience is linked to a long-lasting reduction of Ih current in VTA dopaminergic neurons
Author(s) -
Sebastian Luca D’Addario,
Matteo Di Segni,
Ada Ledonne,
Rosamaria Piscitelli,
Lucy Babicola,
Alessandro Martini,
Elena Spoleti,
Camilla Mancini,
Donald Ielpo,
Francesca R. D’Amato,
Diego Andolina,
Davide Ragozzino,
Nicola Biagio Mercuri,
Carlo Cifani,
Massimiliano Renzi,
Ezia Guatteo,
Rossella Ventura
Publication year - 2021
Publication title -
neurobiology of stress
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.481
H-Index - 33
ISSN - 2352-2895
DOI - 10.1016/j.ynstr.2021.100324
Subject(s) - dopaminergic , ventral tegmental area , anhedonia , neuroscience , psychology , dopamine , midbrain , social defeat , chronic stress , central nervous system
Exposure to aversive events during sensitive developmental periods can affect the preferential coping strategy adopted by individuals later in life, leading to either stress-related psychiatric disorders, including depression, or to well-adaptation to future adversity and sources of stress, a behavior phenotype termed “resilience”. We have previously shown that interfering with the development of mother-pups bond with the Repeated Cross Fostering (RCF) stress protocol can induce resilience to depression-like phenotype in adult C57BL/6J female mice. Here, we used patch-clamp recording in midbrain slice combined with both in vivo and ex vivo pharmacology to test our hypothesis of a link between electrophysiological modifications of dopaminergic neurons in the intermediate Ventral Tegmental Area (VTA) of RCF animals and behavioral resilience. We found reduced hyperpolarization-activated (Ih) cation current amplitude and evoked firing in VTA dopaminergic neurons from both young and adult RCF female mice. In vivo, VTA-specific pharmacological manipulation of the Ih current reverted the pro-resilient phenotype in adult early-stressed mice or mimicked behavioral resilience in adult control animals. This is the first evidence showing how pro-resilience behavior induced by early events is linked to a long-lasting reduction of Ih current and excitability in VTA dopaminergic neurons.

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