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Network synchronization across the longitudinal axis of the developing rat hippocampus
Siddiq, Bilal S. ; DaRosa, Andrew M. ; Evans, Madeline C. ; Gaudio, Elizabeth C. ; Mysiewicz, Steven C. ; Renna, Catelyn M. (Catie) ; Shamambo, Maleelo (Lelo) ; Velrajan, Srilakshmi (Sri) ; Van Vliet, Trevor ; Yu, Shuliang (Mogy)
Siddiq, Bilal S.
DaRosa, Andrew M.
Evans, Madeline C.
Gaudio, Elizabeth C.
Mysiewicz, Steven C.
Renna, Catelyn M. (Catie)
Shamambo, Maleelo (Lelo)
Velrajan, Srilakshmi (Sri)
Van Vliet, Trevor
Yu, Shuliang (Mogy)
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URCAS, Symposiums, Student research, 2018 Spring, Class of 2020, Class of 2018, Class of 2019, Biology, Department of
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201804_Siddiq_Bilal_Poster_Slidedeck.pdf
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201804_Siddiq_Bilal_Hippocampal Slice Physiology_Figure1.pdf
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Abstract
Epilepsy is a neurological disorder characterized by recurrent seizures. Researching epilepsy
requires animal models, as the brain manipulation required to understand epileptogenic activity
is not possible in humans. Extracellular recordings measure network level activation in slice
models of epilepsy. A magnesium-free solution is often used in slice physiology to increase
excitation, through enhanced glutamate receptor activity. Magnesium blocks the activation of
glutamate receptors via binding near the pore region. Magnesium also lowers calcium’s ability to
initiate presynaptic neurotransmitter release. We aim to elucidate the mechanisms of a dorsal neuro-protective system, which reduces the excitability of dorsal hippocampal tissue with age.
While the mechanisms underlying the magnesium-free model are well established, the effects of
this model across the longitudinal axis of the hippocampus and throughout development have not
been clearly characterized. We studied the effects of the magnesium-free model through
extracellular field recordings of CA1 pyramidal neurons from dorsal and ventral hippocampal
slices throughout development, and found young, dorsal hippocampal tissue to be the most
excitable. Additionally, our data suggests the effect of no magnesium is minimal in ventral
slices. These data support the theory of the dorsal protection system being critical in the
reduction of excitability seen with age.