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Olusegun J. Ariwodola

Researcher at Wake Forest University

Publications -  24
Citations -  1065

Olusegun J. Ariwodola is an academic researcher from Wake Forest University. The author has contributed to research in topics: Neurotransmission & Inhibitory postsynaptic potential. The author has an hindex of 17, co-authored 24 publications receiving 957 citations.

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Ethanol Potentiation of GABAergic Synaptic Transmission May Be Self-Limiting: Role of Presynaptic GABAB Receptors

TL;DR: It is demonstrated that, at perisomatic synapses in the rat hippocampus, ethanol enhances presynaptic GABAB autoreceptor function and that this interaction reduces the overall potentiating effect of ethanol at these synapses, suggesting that an interaction between ethanol and presynptic GABABAutoreceptor activity regulates the ethanol sensitivity of GABAergic synapses.
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Functional characterization of des-IGF-1 action at excitatory synapses in the CA1 region of rat hippocampus.

TL;DR: This characterization of the acute actions of des-IGF-1 at hippocampal excitatory synapses may provide insight into the mechanism by which long-term increases in plasma IGF-1 impart cognitive benefits in aged rats.
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Increased Basolateral Amygdala Pyramidal Cell Excitability May Contribute to the Anxiogenic Phenotype Induced by Chronic Early-Life Stress.

TL;DR: It is discovered that early-life stress decreases the activity of a specific class of potassium channels and increases the intrinsic excitability of BLA neurons and present evidence that enhancing the function of these channels normalizes BLA excitability and attenuates anxiety-like behaviors.
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Alcohol potently inhibits the kainate receptor-dependent excitatory drive of hippocampal interneurons.

TL;DR: EtOH increases excitability of pyramidal neurons indirectly by inhibiting the KA-R-dependent drive of γ-aminobutyric acid (GABA)ergic interneurons, and it is postulated that this effect may explain, in part, some of the paradoxical excitatory actions of this widely abused substance.
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Locomotor Sensitization to Ethanol Impairs NMDA Receptor-Dependent Synaptic Plasticity in the Nucleus Accumbens and Increases Ethanol Self-Administration

TL;DR: It is suggested that disruption of accumbal core NMDA receptor-dependent plasticity may represent a synaptic correlate associated with ethanol-induced locomotor sensitization and increased propensity to consume ethanol.