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Oliver H Miller

3 papers in the library · publishing 2014-2025

Papers

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Genome-Wide Translatome Analysis Following Low-Dose Ketamine to Reveal Novel Targets for Antidepressant Treatment.

Synapse November 1, 2025 Oliver H Miller, Nils Grabole, Isabelle Wells et al.

Low-dose ketamine is an efficacious antidepressant for treatment-resistant unipolar and bipolar depressed patients. Major depressive disorder patients receiving a single infusion report elevated mood within 2 h, and ketamine's antidepressant effects have been observed as long as 7 days posttreatment. In light of this remarkable observation, efforts have been undertaken to "reverse-translate"...

DOI: 10.1002/syn.70033 (opens in new tab) Full text (opens in new tab) Ketamine antidepressant Molecular mechanisms Vipr2 target discovery Targeted depression treatment

Synaptic Regulation of a Thalamocortical Circuit Controls Depression-Related Behavior.

Cell Reports August 22, 2017 Oliver H Miller, Andreas Bruns, Imen Ben Ammar et al.

The NMDA receptor (NMDAR) antagonist ketamine elicits a long-lasting antidepressant response in patients with treatment-resistant depression. Understanding how antagonism of NMDARs alters synapse and circuit function is pivotal to developing circuit-based therapies for depression. Using virally induced gene deletion, ex vivo optogenetic-assisted circuit analysis, and in vivo chemogenetics and...

GluN2B-containing NMDA receptors regulate depression-like behavior and are critical for the rapid antidepressant actions of ketamine

Elife October 23, 2014 Oliver H Miller, Ling-Ling Yang, Chih-Chieh Wang et al.

A single, low dose of the NMDA receptor antagonist ketamine produces rapid antidepressant actions in treatment-resistant depressed patients. Understanding the cellular mechanisms underlying this will lead to new therapies for treating major depression. NMDARs are heteromultimeric complexes formed through association of two GluN1 and two GluN2 subunits. We show that in vivo deletion of GluN2B,...