Evidence map›Paper›PMID 22104138›Full record

ArticleSchizophrenia research2012

The role of endogenous neurotensin in psychostimulant-induced disruption of prepulse inhibition and locomotion.

Ricardo Cáceda, Elisabeth B Binder, Becky Kinkead, Charles B Nemeroff

Abstract read
In one paragraph

Article in Schizophrenia research, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.2field-weighted citation impact, top 50% 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

6 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. 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

4 authors at 1 institution in 1 country.

Ricardo CácedaDepartment of Psychiatry and Behavioral Sciences, Emory University School of Medicine, Suite 4000 WMB, 101 Woodruff Circle, Atlanta, GA 30322, USA. rcaceda@med.miami.edu
Elisabeth B Binder
Becky Kinkead
Charles B Nemeroff
Emory University · US

Funding

NEUROTENSIN--AN ENDOGENOUS NEUROLEPTIC-LIKE PEPTIDER01MH039415 · NIMH · EMORY UNIVERSITY · PI KINKEAD, BECKY L · 1985 to 2010
$3.7M
NEUROTENSIN, AN ENDOGENOUS NEUROLEPTIC-LIKE PEPTIDER37MH039415 · NIMH · EMORY UNIVERSITY · PI NEMEROFF, CHARLES B · 1987 to 1994
–
NIMH NIH HHS MH39415NIMH NIH HHS R01 MH039415
6 · The paper itself

Abstract

The neuropeptide neurotensin (NT) is closely associated with dopaminergic and glutamatergic systems in the rat brain. Central injection of NT into the nucleus accumbens (NAcc) or peripheral administration of NT receptor agonists, reduces many of the behavioral effects of psychostimulants. However, the role of endogenous NT in the behavioral effects of psychostimulants (e.g. DA agonists and NMDA receptor antagonists) remains unclear. Using a NTR antagonist, SR142948A, the current studies were designed to examine the role of endogenous NT in DA receptor agonist- and NMDA receptor antagonist-induced disruption of prepulse inhibition of the acoustic startle response (PPI), locomotor hyperactivity and brain-region specific c-fos mRNA expression. Adult male rats received a single i.p. injection of SR142948A or vehicle followed by D-amphetamine, apomorphine or dizocilpine challenge. SR142948A had no effect on baseline PPI, but dose-dependently attenuated d-amphetamine- and dizocilpine-induced PPI disruption and enhanced apomorphine-induced PPI disruption. SR142948A did not significantly affect either baseline locomotor activity or stimulant-induced hyperlocomotion. Systemic SR142948A administration prevented c-fos mRNA induction in mesolimbic terminal fields (prefrontal cortex, lateral septum, NAcc, ventral subiculum) induced by all three psychostimulants implicating the VTA as the site for NT modulation of stimulant-induced PPI disruption. Further characterization of the NT system may be valuable to find clinical useful compounds for schizophrenia and drug addiction.

Indexed as

Acoustic StimulationAdamantaneAmphetamineAnalysis of VarianceAnimalsApomorphineBehavior, AnimalCentral Nervous System StimulantsDose-Response Relationship, DrugGait Disorders, NeurologicGene Expression RegulationImidazolesMaleNeurotensinProto-Oncogene Proteins c-fosPsychomotor PerformanceAdamantaneAmphetamineApomorphineCentral Nervous System StimulantsImidazolesNeurotensinProto-Oncogene Proteins c-fosReceptors, NeurotensinRNA, MessengerSR 142948A

Identifiers

PMID22104138
PMCPMC3595536
OpenAlexW2122720413

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.