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Allie J Widman

2 papers in the library · publishing 2018

Papers

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Disinhibition of CA1 pyramidal cells by low-dose ketamine and other antagonists with rapid antidepressant efficacy.

Proceedings of the National Academy of Sciences March 27, 2018 Allie J Widman, Lori L McMahon

Low-dose ketamine, an open-channel N-methyl d-aspartate receptor (NMDAR) antagonist, mediates rapid antidepressant effects in humans that are mimicked in preclinical rodent models. Disinhibition of pyramidal cells via decreased output of fast-spiking GABAergic interneurons has been proposed as a key mechanism that triggers the antidepressant response. Unfortunately, to date, disinhibition has...

DOI: 10.1073/pnas.1718883115 (opens in new tab) Full text (opens in new tab) Gabaergic transmission Disinhibition Excitation/inhibition balance Hippocampal networks +1

Intravascular Ketamine Increases Theta-Burst but Not High Frequency Tetanus Induced LTP at CA3-CA1 Synapses Within Three Hours and Devoid of an Increase in Spine Density.

Frontiers in Synaptic Neuroscience 2018 Allie J Widman, Amy E Stewart, Elise M Erb et al.

In the past 20 years, ketamine has become a promising treatment for Major Depressive Disorder (MDD) due to its rapid and sustain antidepressant effects in patients. A single ketamine treatment causes improvement in depressive symptoms within hours and can last weeks, long after it is eliminated. Previous studies have demonstrated increased synaptic plasticity at CA3-CA1 synapses in hippocampus...