Evidence map›Paper›PMID 20655971›Full record

ArticleProgress in neuro-psychopharmacology & biological psychiatry2010

Effect of chronic fluoxetine treatment on male and female rat erythrocyte and prefrontal cortex fatty acid composition.

Robert K McNamara, Jessica A Able, Therese Rider, Patrick Tso, Ronald Jandacek

Open access · greenAbstract read
In one paragraph

Article in Progress in neuro-psychopharmacology & biological psychiatry, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
0.7field-weighted citation impact, top 31% 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

13 citing papers in PubMed, 21 citations in OpenAlex.

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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

5 authors at 2 institutions in 1 country.

Robert K McNamaraDepartment of Psychiatry, University of Cincinnati College of Medicine, Cincinnati, OH 45267, USA. robert.mcnamara@uc.edu
Jessica A Able
Therese Rider
Patrick Tso
Ronald Jandacek
University of Cincinnati · USUniversity of Cincinnati Medical Center · US

Funding

LIPID, LIPOPROTEIN, AND GLUCOSE METABOLISM COREU24DK059630 · NIDDK · UNIVERSITY OF CINCINNATI · PI TSO, PATRICK · 2001 to 2015
$12.9M
Lipid profile, lipoprotein and apolipoprotein composition, and intestinal fat absorption efficiency in germ-free and conventional miceU2CDK059630 · NIDDK · UNIVERSITY OF CINCINNATI · PI LIU, MIN · 2016 to 2021
$4.9M
Brain Fatty Acid Composition and PKC ActivityR21MH074858 · NIMH · UNIVERSITY OF CINCINNATI · PI MCNAMARA, ROBERT K. · 2006 to 2007
$377k
Omega-3 Fatty Acid Deficient Rat Model of SchizophreniaR21MH073704 · NIMH · UNIVERSITY OF CINCINNATI · PI MCNAMARA, ROBERT K. · 2006 to 2007
$375k
NIDDK NIH HHS DK59630NIDDK NIH HHS U24 DK059630NIDDK NIH HHS U2C DK059630NIMH NIH HHS MH073704NIMH NIH HHS MH074858NIMH NIH HHS R21 MH073704NIMH NIH HHS R21 MH074858
6 · The paper itself

Abstract

Omega-3 (n-3) polyunsaturated fatty acids (PUFA) and fluoxetine (FLX) have additive effects in the treatment of major depressive disorder, and FLX up-regulates genes that regulate fatty acid biosynthesis in vitro. Although these data suggest that FLX may augment n-3 fatty acid biosynthesis, the in vivo effects of FLX treatment on PUFA biosynthesis and peripheral and central membrane compositions are not known. In the present study, male and female rats were treated with FLX (10 mg/kg/day) through their drinking water for 30 days (P60-P90). Plasma FLX and norfluoxetine (NFLX) concentrations were determined by liquid chromatography tandem mass spectrometry, and erythrocyte and prefrontal cortex (PFC) fatty acid composition determined by gas chromatography. To confirm central effects of FLX, serotonin turnover in the PFC was determined by high performance liquid chromatography. Chronic FLX treatment resulted in clinically-relevant plasma FLX concentrations in male and female rats, and significantly decreased serotonin turnover in the PFC. After correcting for multiple comparisons, chronic FLX treatment did not significantly alter erythrocyte fatty acid composition in male or female rats. Chronic FLX treatment significantly and selectively increased docosapentaenoic acid (22:5n-6) in the PFC of female rats, but not in male rats. These preclinical findings do not support the hypothesis that chronic FLX treatment increases n-3 fatty acid biosynthesis or membrane composition.

Indexed as

AnimalsAntidepressive Agents, Second-GenerationBody WeightChromatography, GasChromatography, High Pressure LiquidErythrocytesFatty AcidsFemaleFluoxetineMalePrefrontal CortexRandom AllocationRatsRats, Long-EvansSerotoninAntidepressive Agents, Second-GenerationFatty AcidsFluoxetinenorfluoxetineSerotonin

Identifiers

PMID20655971
PMCPMC2939160
OpenAlexW1963532283

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.