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- W2034808029 abstract "The most commonly reported precipitating factor for seizures is stress. However, the underlying mechanisms whereby stress triggers seizures are not yet fully understood. Here we demonstrate a potential mechanism underlying changes in neuronal excitability in the hippocampus following chronic stress, involving a shift in the reversal potential for GABA (EGABA) associated with a dephosphorylation of the potassium chloride co-transporter, KCC2. Mice subjected to chronic restraint stress (30min/day for 14 consecutive days) exhibit an increase in serum corticosterone levels which is associated with increased susceptibility to seizures induced with kainic acid (20mg/kg). Following chronic stress, but not acute stress, we observe a dephosphorylation of KCC2 residue S940, which regulates KCC2 cell surface expression and function, in the hippocampus. To determine the impact of alterations in KCC2 expression following chronic stress, we performed gramicidin perforated patch recordings to measure changes in EGABA and neuronal excitability of principal hippocampal neurons. We observe a depolarizing shift in EGABA in hippocampal CA1 pyramidal neurons after chronic stress. In addition, there is an increase in the intrinsic excitability of CA1 pyramidal neurons, evident by a shift in the input-output curve which could be reversed with the NKCC1 inhibitor, bumetanide. These data uncover a potential mechanism involving chronic stress-induced plasticity in chloride homeostasis which may contribute to stress-induced seizure susceptibility." @default.
- W2034808029 created "2016-06-24" @default.
- W2034808029 creator A5023589964 @default.
- W2034808029 creator A5042607905 @default.
- W2034808029 date "2015-01-01" @default.
- W2034808029 modified "2023-10-10" @default.
- W2034808029 title "Chronic stress shifts the GABA reversal potential in the hippocampus and increases seizure susceptibility" @default.
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- W2034808029 doi "https://doi.org/10.1016/j.eplepsyres.2014.10.003" @default.
- W2034808029 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/4272449" @default.
- W2034808029 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/25524838" @default.