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Impaired Bidirectional Synaptic Plasticity in Juvenile Offspring Following Prenatal Ethanol Exposure
Author(s) -
Fontaine Christine J.,
Pinar Cristina,
Yang Waisley,
Pang Angela F.,
Suesser Konrad E.,
Choi James S. J.,
Christie Brian R.
Publication year - 2019
Publication title -
alcoholism: clinical and experimental research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.267
H-Index - 153
eISSN - 1530-0277
pISSN - 0145-6008
DOI - 10.1111/acer.14170
Subject(s) - long term potentiation , perforant path , offspring , dentate gyrus , synaptic plasticity , hippocampal formation , ltp induction , long term depression , hippocampus , stimulus (psychology) , juvenile , neuroscience , perforant pathway , medicine , endocrinology , psychology , biology , pregnancy , nmda receptor , ampa receptor , receptor , psychotherapist , genetics
Background The hippocampus is particularly vulnerable to the teratogenic effects of prenatal ethanol exposure (PNEE), and hippocampal structural and functional deficits are thought to contribute to the learning and memory deficits that are a hallmark feature of fetal alcohol spectrum disorders. Methods Sprague Dawley dams were exposed to a liquid diet that contained EtOH (35.5% EtOH‐derived calories) throughout gestation, and then, PNEE juvenile (P21‐28) male and female offspring were used for in vitro electrophysiological recordings. We examined long‐term potentiation (LTP), long‐term depression (LTD), and depotentiation in the medial perforant path input to the dentate gyrus (DG) to determine the impact of PNEE on the dynamic range of bidirectional synaptic plasticity in both sexes. Results PNEE reduced the responsiveness of the DGs of male but not in female offspring, and this effect was no longer apparent when GABAergic signaling was inhibited. There was also a sex‐specific LTD impairment in males, but increasing the duration of the conditioning stimulus could overcome this deficit. The magnitude of LTP was also reduced, but in both sexes following PNEE. This appears to be an increase in the threshold for induction, not in capacity, as the level of LTP induced in PNEE animals was increased to control levels when additional conditioning stimuli were administered. Conclusions These data are the first to describe, in a single study, the impact of PNEE on the dynamic range of bidirectional synaptic plasticity in the juvenile DG in both males and in females. The data suggest that PNEE increases the threshold for LTP in the DG in both sexes, but produces a sex‐specific increase in the threshold for LTD in males These alterations reduce the dynamic range for synaptic plasticity in both sexes.