Evidence map›Paper›PMID 21779782›Full record

ArticlePsychopharmacology2012

Antidepressant-like properties of oral riluzole and utility of incentive disengagement models of depression in mice.

Shannon L Gourley, Jonathan W Espitia, Gerard Sanacora, Jane R Taylor

Open access · greenAbstract read
In one paragraph

Article in Psychopharmacology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
2.3field-weighted citation impact, top 13% 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

43 citing papers in PubMed, 84 citations in OpenAlex.

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  13. BDNF Augmentation Using Riluzole Reverses Doxorubicin-Induced Decline in Cognitive Function and Neurogenesis.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2023
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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

4 authors at 1 institution in 1 country.

Shannon L GourleyDepartment of Psychiatry, Division of Molecular Psychiatry, Yale University, New Haven, CT 06511, USA. shannon.l.gourley@emory.edu
Jonathan W Espitia
Gerard Sanacora
Jane R Taylor
Yale University · US

Funding

Interdisciplinary Research on Stress, Self-Control & AddictionUL1DE019586 · NIDCR · YALE UNIVERSITY · PI SINHA, RAJITA · 2008 to 2011
$5.0M
COGNITIVE DYSFUNCTION AFTER CHRONIC PCP, THC AND COCAINER01DA011717 · NIDA · YALE UNIVERSITY · PI TAYLOR, JANE R · 1998 to 2014
$3.4M
Incentive Motivation in Addiction: PKA MechanismsR01DA015222 · NIDA · YALE UNIVERSITY · PI TAYLOR, JANE R · 2003 to 2013
$2.7M
Effects of Stress and Glutamatergic Agents on Glutamate Cycling and BehaviorR01MH081211 · NIMH · YALE UNIVERSITY · PI SANACORA, GERARD · 2009 to 2013
$1.8M
Stress-Induced Compulsive Behaviors: CRF Regulation (#3 of 14)RL1AA017537 · NIAAA · YALE UNIVERSITY · PI TAYLOR, JANE R · 2007 to 2011
$1.0M
Role of amygdalostriatal CREB activity in persistent depressive-like behaviorF31MH079680 · NIMH · YALE UNIVERSITY · PI GOURLEY, SHANNON LEIGH · 2007 to 2008
$35k
NIAAA NIH HHS AA017537NIAAA NIH HHS RL1 AA017537NIDA NIH HHS R01 DA011717NIDA NIH HHS R01 DA015222NIDCR NIH HHS UL1 DE019586NIDCR NIH HHS UL1-DE19586NIMH NIH HHS F31 MH079680NIMH NIH HHS MH079680NIMH NIH HHS MH081211NIMH NIH HHS R01 MH081211
6 · The paper itself

Abstract

rationaleThe neuroprotective agent riluzole has antidepressant-like properties in humans, but its mechanisms of action are unclear. Despite the increasing utility of transgenic and knockout mice in addressing such issues, previous studies aimed at characterizing biochemical mechanisms have been conducted in rats.

objectivesWe sought to optimize an oral riluzole administration protocol with antidepressant-like consequences in C57BL/6 mice, a common background strain in genetically modified mice.

methodsRiluzole (6-60 μg/ml) was dissolved in tap water and replaced regular drinking water for up to 3 weeks; sensitivity to tail suspension, forced swimming, and the locomotor response to extinction training in a model of "incentive disengagement" were tested. Peripheral and central effects of long-term 60-μg/ml treatment were also evaluated.

resultsRiluzole had dose-dependent antidepressant-like effects in the forced swim test, and like chronic fluoxetine, exerted antidepressant-like actions in an adaptation of the "incentive disengagement" model at the highest concentration tested. This 60-μg/ml concentration also restored hippocampal brain-derived neuroptrophic factor (BDNF) expression after chronic corticosteroid exposure and increased glutamate glial transporter 1 (GLT-1, or EAAT2) expression without significantly affecting baseline locomotor activity, thymus and adrenal gland weights, or blood serum corticosterone. The lowest 6-μg/ml concentration increased locomotor activity, potentially consistent with an anxiolytic-like effect.

conclusionsRiluzole's therapeutic potential for treating mood disorders may involve GLT-1 and BDNF, and we suggest this protocol could be used to further characterize its precise long-term biochemical mechanisms of action in animal models of depression.

Indexed as

Disease Models, AnimalMotivationAdministration, OralAnimalsAntidepressive AgentsBrain-Derived Neurotrophic FactorDepressionDose-Response Relationship, DrugExcitatory Amino Acid Transporter 2MaleMiceMice, Inbred C57BLRiluzoleAntidepressive AgentsBrain-Derived Neurotrophic FactorExcitatory Amino Acid Transporter 2RiluzoleSlc1a2 protein, mouse

Identifiers

PMID21779782
PMCPMC3674097
OpenAlexW2076406171

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.