Evidence map›Paper›PMID 25703023›Full record

ArticleJournal of neuroscience research2015

Brain changes associated with thromboxane receptor antagonist SQ 29,548 treatment in a mouse model.

Andrew A Rebel, Siri A Urquhart, Kendra L Puig, Atreyi Ghatak, Stephen A Brose, Mikhail Y Golovko, Colin K Combs

Open access · hybridAbstract read
In one paragraph

Article in Journal of neuroscience research, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.3field-weighted citation impact, top 46% 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

1 citing paper in PubMed, 3 citations in OpenAlex.

  1. 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

7 authors at 1 institution in 1 country.

Andrew A RebelDepartment of Biology, University of North Dakota School of Medicine and Health Sciences, Grand Forks, North Dakota.
Siri A UrquhartDepartment of Biology, University of North Dakota School of Medicine and Health Sciences, Grand Forks, North Dakota.
Kendra L PuigDepartment of Basic Sciences, University of North Dakota School of Medicine and Health Sciences, Grand Forks, North Dakota.
Atreyi GhatakDepartment of Basic Sciences, University of North Dakota School of Medicine and Health Sciences, Grand Forks, North Dakota.
Stephen A BroseDepartment of Basic Sciences, University of North Dakota School of Medicine and Health Sciences, Grand Forks, North Dakota.
Mikhail Y GolovkoDepartment of Basic Sciences, University of North Dakota School of Medicine and Health Sciences, Grand Forks, North Dakota.
Colin K CombsDepartment of Basic Sciences, University of North Dakota School of Medicine and Health Sciences, Grand Forks, North Dakota.
University of North Dakota · US

Funding

Research CoresP20GM103442 · NIGMS · UNIVERSITY OF NORTH DAKOTA · PI Donald A. Sens · 2012 to 2026
$53.0M
WORKSHOPS AND EVALUATIONP20RR016471 · NCRR · UNIVERSITY OF NORTH DAKOTA · PI DELORME, EUGENE L. · 2001 to 2011
$31.7M
Pilot Projects CoreP30GM103329 · NIGMS · UNIVERSITY OF NORTH DAKOTA · PI GEIGER, JONATHAN DAVID · 2012 to 2016
$5.1M
APP Regulates Brain and Adipose Changes in ObesityR01AG042819 · NIA · UNIVERSITY OF NORTH DAKOTA · PI COMBS, COLIN K, GOLOVKO, MIKHAIL Y · 2012 to 2016
$1.4M
NCRR NIH HHS P20 RR016471NIA NIH HHS R01 5R01AG042819NIA NIH HHS R01 AG042819NIGMS NIH HHS 5P30 GM103329NIGMS NIH HHS P20 GM103442NIGMS NIH HHS P20GM103442/P20RR016471NIGMS NIH HHS P30 GM103329
6 · The paper itself

Abstract

The purpose of this study was to characterize behavioral and physiological effects of a selective thromboxane (TP) receptor antagonist, SQ 29,548, in the C57Bl/6 mouse model. At 6 months of age, male mice were given either sham or drug i.p. injections for 3 days at a dose of 2 mg/kg each day. On the day after the final injection, mice were subjected to behavioral testing before brain collection. Left hemisphere hippocampi were collected from all mice for protein analysis via Western blot. Right brain hemispheres were fixed and embedded in gelatin and then serially sectioned. The sections were immunostained with anti-c-Fos antibodies. Prostaglandin analysis was performed from remaining homogenized brain samples, minus the hippocampi. Injection of SQ 29,548 decreased selective brain prostaglandin levels compared with sham controls. This correlated with robust increases in limbic-region c-Fos immunoreactivity in the SQ 29,548-injected mice. However, drug-treated mice demonstrated no significant changes in relevant hippocampal protein levels compared with sham treatments, as determined from Western blots. Surprisingly, injection of SQ 29,548 caused mixed changes in parameters of depression and anxiety-like behavior in the mice. In conclusion, the results indicate that administration of peripheral TP receptor antagonists alters brain levels of prostanoids and influences neuronal activity, with only minimal alterations of behavior. Whether the drug affects neurons directly or through a secondary pathway involving endothelium or other tissues remains unclear.

Indexed as

Disease Models, AnimalAnimalsAnxietyBrainBridged Bicyclo Compounds, HeterocyclicDepressionFatty Acids, UnsaturatedHydrazinesMaleMiceMice, Inbred C57BLReceptors, ThromboxaneTreatment OutcomeBridged Bicyclo Compounds, HeterocyclicFatty Acids, UnsaturatedHydrazinesReceptors, ThromboxaneSQ 29548anxietyc-Fosdepressionthromboxanethromboxane receptor

Identifiers

PMID25703023
PMCPMC4478107
OpenAlexW2145114150

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.