Evidence map›Paper›PMID 24275076›Full record

ArticleProgress in neuro-psychopharmacology & biological psychiatry2014

Acute, but not repeated, administration of the neurotensin NTS1 receptor agonist PD149163 decreases conditioned footshock-induced ultrasonic vocalizations in rats.

Adam J Prus, Todd M Hillhouse, Amber L LaCrosse

Abstract read
In one paragraph

Article in Progress in neuro-psychopharmacology & biological psychiatry, 2014. 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
4.8field-weighted citation impact, top 6% 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, 34 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Neurotensin in reward processes.Neuropharmacology · 2020
    Review
  7. Manipulations of Central Amygdala Neurotensin Neurons Alter the Consumption of Ethanol and Sweet Fluids in Mice.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2020
    Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. 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

3 authors at 3 institutions in 1 country.

Adam J PrusPsychology Department, Northern Michigan University, Marquette, MI, USA. Electronic address: aprus@nmu.edu.
Todd M HillhouseDepartment of Psychology, Virginia Commonwealth University, Richmond, VA, USA.
Amber L LaCrosseSchool of Psychology, Arizona State University, Phoenix, AZ, USA.
Arizona State University · USNorthern Michigan University · USVirginia Commonwealth University · US

Funding

Neurotensin Analogs For Neurocognitive Deficits In SchizophreniaR15MH083241 · NIMH · NORTHERN MICHIGAN UNIVERSITY · PI PRUS, ADAM JOSEPH · 2008 to 2009
$207k
NIMH NIH HHS 1R15MH083241-01NIMH NIH HHS R15 MH083241
6 · The paper itself

Abstract

Neurotensin is an endogenous neuropeptide that has significant interactions with monoamine neurotransmitter systems. To date, neurotensin NTS1 receptor agonists, such as PD149163, have been primarily evaluated for the treatment for schizophrenia, drug addiction, and pain. Recently, PD149163 was found to attenuate fear-potentiated startle in rats, an experimental procedure used for screening anxiolytic drugs. The present study sought to assess these findings through testing PD149163 in a conditioned footshock-induced ultrasonic vocalization (USV) model. Conditioning was conducted in male Wistar rats using chambers equipped with shock grid floors and an ultrasonic vocalization detector. PD149163 and the 5-HT1A receptor partial agonist buspirone produced a statistically significant reduction of 22kHz USV counts. The typical antipsychotic haloperidol also reduced 22kHz USV counts, but did so at cataleptic doses. Ten days of repeated administration of PD149163 abolished the inhibitory effects of PD149163 on 22kHz USVs. These findings further support an anxiolytic profile for PD149163. However, tolerance to these effects may limit the utility of these drugs for the treatment of anxiety.

Indexed as

ElectroshockAnimalsAnti-Anxiety AgentsAntipsychotic AgentsBuspironeCatalepsyConditioning, PsychologicalDrug ToleranceFearHaloperidolMaleNeurotensinRatsRats, WistarReceptors, NeurotensinVocalization, AnimalAnti-Anxiety AgentsAntipsychotic AgentsBuspironeHaloperidolNeurotensinneurotensin type 1 receptorPD 149163Receptors, NeurotensinAnxietyBuspironeNeurotensinPD149163Ultrasonic vocalizationUSVVEHVehicle

Identifiers

PMID24275076
PMCPMC3923471
OpenAlexW1972318409

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.