Evidence map›Paper›PMID 32023492›Full record

ReviewBehavioural brain research2020

Ketamine: Leading us into the future for development of antidepressants.

Flavia R Carreno, Daniel J Lodge, Alan Frazer

Open access · greenAbstract readReview
In one paragraph

Review in Behavioural brain research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.9field-weighted citation impact, top 16% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

9 citing papers in PubMed, 15 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Review
  5. Review
  6. Mechanisms associated with the antidepressant-like effects of L-655,708.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2020
    Article
  7. Article
  8. Article
  9. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors at 3 institutions in 1 country.

Flavia R CarrenoDepartment of Pharmacology & Center for Biomedical Neuroscience, University of Texas Health Science Center, San Antonio, TX, United States. Electronic address: Carrenof@uthscsa.edu.
Daniel J LodgeDepartment of Pharmacology & Center for Biomedical Neuroscience, University of Texas Health Science Center, San Antonio, TX, United States; South Texas Veterans Health Care System, Audie L. Murphy Division, United States.
Alan FrazerDepartment of Pharmacology & Center for Biomedical Neuroscience, University of Texas Health Science Center, San Antonio, TX, United States; South Texas Veterans Health Care System, Audie L. Murphy Division, United States.
Murphy Oil Corporation (United States) · USSouth Texas Veterans Health Care System · USThe University of Texas Health Science Center at San Antonio · US

Funding

Regulation of ventral hippocampal system functionR01MH090067 · NIMH · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI LODGE, DANIEL · 2010 to 2019
$3.5M
Novel mechanisms contributing to the antidepressant-like response of pharmacological hippocampal activationR21MH113899 · NIMH · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI CARRENO, FLAVIA · 2018 to 2019
$419k
Selective negative allosteric modulators of alpha 5-GABAA receptors: novel psychotherapeutic drugsI01BX000559 · VA · SOUTH TEXAS VETERANS HEALTH CARE SYSTEM · PI MORILAK, DAVID A · 2011 to 2025
–
BLRD VA I01 BX000559NIMH NIH HHS R01 MH090067NIMH NIH HHS R21 MH113899
6 · The paper itself

Abstract

Numerous randomized double-blind clinical trials have consistently shown that that a single intravenous administration of a subanesthetic dose of ketamine to treatment-resistant depressed patients significantly improved depressive symptomatology rapidly, within two hours, with the effect lasting up to seven days. Despite its very promising effects, ketamine has long been associated with potential for abuse as it can cause psychotropic side effects, such as hallucinations, false beliefs, and severe impairments in judgment and other cognitive processes. Consequently, within the last two decades preclinical research has been carried out aimed at understanding its mechanisms of action and the brain circuits involved in ketamine's antidepressant effects, both of which are discussed in this review. Furthermore, with the hippocampus being a key target for ketamine's beneficial antidepressant effects, we and others have begun to examine behavioral and neurochemical effects of drugs that act selectively on the hippocampus due to the preferential location of their receptor targets. Such drugs are negative allosteric modulators (NAMs) and positive allosteric modulator (PAM) of the α5-GABA

Indexed as

Drug DevelopmentAllosteric RegulationAnimalsAntidepressive AgentsDepressive Disorder, Treatment-ResistantHippocampusHumansKetamineMajor Depressive DisorderMolecular Targeted TherapyNeural PathwaysReceptors, GABA-AReceptors, N-Methyl-D-AspartateReceptors, Opioid, muAntidepressive AgentsGabra5 protein, mouseGabra5 protein, ratKetamineReceptors, GABA-AReceptors, N-Methyl-D-AspartateReceptors, Opioid, muDepressionKetamineNegative allosteric modulatorsReceptorsVentral hippocampusα5-containing GABA(A)

Identifiers

PMID32023492
PMCPMC7890296
OpenAlexW3003505607

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.