Evidence map›Paper›PMID 22606285›Full record

ArticlePloS one2012

Dysfunction in fatty acid amide hydrolase is associated with depressive-like behavior in Wistar Kyoto rats.

K Yaragudri Vinod, Shan Xie, Delphine Psychoyos, Basalingappa L Hungund, Thomas B Cooper, Shanaz M Tejani-Butt

Open access · goldAbstract read
In one paragraph

Article in PloS one, 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
6.2field-weighted citation impact, top 3% 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, 92 citations in OpenAlex.

  1. Review
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  5. Supplementation withFrontiers in immunology · 2024
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  12. The Ups and Downs of Endocannabinoid Signaling in Chronic Pain-Induced Depression.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2022
    Article
  13. Review
  14. Article
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  20. D3 dopamine receptors and a missense mutation of fatty acid amide hydrolase linked in mouse and men: implication for addiction.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2020
    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

6 authors at 4 institutions in 1 country.

K Yaragudri VinodDivision of Analytical Psychopharmacology, Nathan Kline Institute for Psychiatric Research, Orangeburg, New York, United States of America. vyaragudri@nki.rfmh.org
Shan Xie
Delphine Psychoyos
Basalingappa L Hungund
Thomas B Cooper
Shanaz M Tejani-Butt
Nathan Kline Institute for Psychiatric Research · USNew York Psychoanalytic Society and Institute · USTexas A&M Health Science Center · USUniversity of the Sciences · US

Funding

Teratogenic Effects of Marijuana in Developing Chick CNSF32DA021977 · NIDA · TEXAS A&M UNIVERSITY HEALTH SCIENCE CTR · PI PSYCHOYOS, DELPHINE · 2008 to 2010
$178k
Role of the Endocannabinoid System in the Neurobiology of Depressive BehaviorR03MH085079 · NIMH · NATHAN S. KLINE INSTITUTE FOR PSYCH RES · PI YARAGUDRI, VINOD K · 2009 to 2010
$158k
NIDA NIH HHS DA021977NIDA NIH HHS F32 DA021977NIMH NIH HHS MH085079NIMH NIH HHS R03 MH085079
6 · The paper itself

Abstract

backgroundWhile the etiology of depression is not clearly understood at the present time, this mental disorder is thought be a complex and multifactorial trait with important genetic and environmental contributing factors. METHODOLOGY/PRINCIPAL

findingsThe role of the endocannabinoid (eCB) system in depressive behavior was examined in Wistar Kyoto (WKY) rat strain, a genetic model of depression. Our findings revealed selective abnormalities in the eCB system in the brains of WKY rats compared to Wistar (WIS) rats. Immunoblot analysis indicated significantly higher levels of fatty acid amide hydrolase (FAAH) in frontal cortex and hippocampus of WKY rats with no alteration in the level of N-arachidonyl phosphatidyl ethanolamine specific phospholipase-D (NAPE-PLD). Significantly higher levels of CB1 receptor-mediated G-protein coupling and lower levels of anandamide (AEA) were found in frontal cortex and hippocampus of WKY rats. While the levels of brain derived neurotropic factor (BDNF) were significantly lower in frontal cortex and hippocampus of WKY rats compared to WIS rats, pharmacological inhibition of FAAH elevated BDNF levels in WKY rats. Inhibition of FAAH enzyme also significantly increased sucrose consumption and decreased immobility in the forced swim test in WKY rats. CONCLUSIONS/SIGNIFICANCE: These findings suggest a critical role for the eCB system and BDNF in the genetic predisposition to depressive-like behavior in WKY rats and point to the potential therapeutic utility of eCB enhancing agents in depressive disorder.

Indexed as

AmidohydrolasesAnimalsArachidonic AcidsBenzamidesBrainBrain-Derived Neurotrophic FactorCannabinoid Receptor ModulatorsCarbamatesDepressive DisorderDisease Models, AnimalEndocannabinoidsEnzyme InhibitorsFatty Acid Amide HydrolasesFrontal LobeGenetic Predisposition to DiseaseHippocampusAmidohydrolasesanandamideArachidonic AcidsBenzamidesBrain-Derived Neurotrophic FactorCannabinoid Receptor ModulatorsCarbamatescyclohexyl carbamic acid 3'-carbamoylbiphenyl-3-yl esterEndocannabinoidsEnzyme InhibitorsFatty Acid Amide HydrolasesNapepld protein, ratPhospholipase DPolyunsaturated AlkamidesReceptor, Cannabinoid, CB1

Identifiers

PMID22606285
PMCPMC3351478
OpenAlexW1998809338

What OpenQuestion holds

Textmetadata
LicenceCC0
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.