Evidence map›Paper›PMID 26795091›Full record

ArticleBehavioural brain research2016

Serotonergic activation of locomotor behavior and posture in one-day old rats.

Hillary E Swann, R Blaine Kempe, Ashley M Van Orden, Michele R Brumley

Open access · greenAbstract read
In one paragraph

Article in Behavioural brain research, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.6field-weighted citation impact, top 33% 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

2 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. Perinatal effects of scorpion venoms: maternal and offspring development.The journal of venomous animals and toxins including tropical diseases · 2017
    Review
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.

Hillary E SwannIdaho State University, Department of Psychology, Pocatello, ID, United States.
R Blaine KempeIdaho State University, Department of Psychology, Pocatello, ID, United States.
Ashley M Van OrdenIdaho State University, Department of Psychology, Pocatello, ID, United States.
Michele R BrumleyIdaho State University, Department of Psychology, Pocatello, ID, United States. Electronic address: brummich@isu.edu.
Idaho State University · US

Funding

Women's health: interplay of maternal diet and key demographics on neurological health in the rural frontier and remote WestP20GM103408 · NIGMS · UNIVERSITY OF IDAHO · PI Carolyn Hovde Bohach · 2012 to 2026
$59.8M
Experiential modulation of action patterns in the developing ratR15HD062980 · NICHD · IDAHO STATE UNIVERSITY · PI BRUMLEY, MICHELE R. · 2010 to 2010
$165k
NICHD NIH HHS 1R15HD062980-01NICHD NIH HHS R15 HD062980NIGMS NIH HHS P20 GM103408NIGMS NIH HHS P20GM103408
6 · The paper itself

Abstract

The purpose of this study was to determine what dose of quipazine, a serotonergic agonist, facilitates air-stepping and induces postural control and patterns of locomotion in newborn rats. Subjects in both experiments were 1-day-old rat pups. In Experiment 1, pups were restrained and tested for air-stepping in a 35-min test session. Immediately following a 5-min baseline, pups were treated with quipazine (1.0, 3.0, or 10.0 mg/kg) or saline (vehicle control), administered intraperitoneally in a 50 μL injection. Bilateral alternating stepping occurred most frequently following treatment with 10.0 mg/kg quipazine, however the percentage of alternating steps, interlimb phase, and step period were very similar between the 3.0 and 10.0 mg/kg doses. For interlimb phase, the forelimbs and hindlimbs maintained a near perfect anti-phase pattern of coordination, with step period averaging about 1s. In Experiment 2, pups were treated with 3.0 or 10.0 mg/kg quipazine or saline, and then were placed on a surface (open field, unrestrained). Both doses of quipazine resulted in developmentally advanced postural control and locomotor patterns, including head elevation, postural stances, pivoting, crawling, and a few instances of quadrupedal walking. The 3.0 mg/kg dose of quipazine was the most effective at evoking sustained locomotion. Between the 2 experiments, behavior exhibited by the rat pup varied based on testing environment, emphasizing the role that environment and sensory cues exert over motor behavior. Overall, quipazine administered at a dose of 3.0 mg/kg was highly effective at promoting alternating limb coordination and inducing locomotor activity in both testing environments.

Indexed as

Analysis of VarianceAnimalsAnimals, NewbornDose-Response Relationship, DrugExtremitiesFemaleLocomotionMalePosturePsychomotor PerformanceQuipazineRatsRats, Sprague-DawleySerotoninSerotonin Receptor AgonistsTime FactorsQuipazineSerotoninSerotonin Receptor AgonistsInterlimb coordinationLocomotionNeonatal ratPostureQuipazineStepping

Identifiers

PMID26795091
PMCPMC4769103
OpenAlexW2235340399

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.