Evidence map›Paper›PMID 17920665›Full record

ArticlePharmacology, biochemistry, and behavior2008

5-HT6 receptor antagonist reversal of emotional learning and prepulse inhibition deficits induced by apomorphine or scopolamine.

Ellen S Mitchell, John F Neumaier

Abstract read
In one paragraph

Article in Pharmacology, biochemistry, and behavior, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.8field-weighted citation impact, top 32% 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

10 citing papers in PubMed, 30 citations in OpenAlex.

  1. Review
  2. Striatal 5-HT6 Receptors Regulate Cocaine Reinforcement in a Pathway-Selective Manner.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2016
    Article
  3. Article
  4. Potentiation of GluN2C/D NMDA receptor subtypes in the amygdala facilitates the retention of fear and extinction learning in mice.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2014
    Article
  5. Article
  6. Article
  7. Article
  8. Article
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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

2 authors at 1 institution in 1 country.

Ellen S MitchellUniversity of Washington, Box 359911, Harborview Medical Center, 325 9th Ave, Seattle, WA 98104, USA.
John F Neumaier
University of Washington · US

Funding

GENETIC APPROACHES TO AGING RESEARCHT32AG000057 · NIA · UNIVERSITY OF WASHINGTON · PI RABINOVITCH, PETER S · 1985 to 2019
$14.2M
The Role of Serotonin Receptors In Brain Reward CircuitsR01DA016432 · NIDA · UNIVERSITY OF WASHINGTON · PI NEUMAIER, JOHN F · 2003 to 2010
$2.3M
NIA NIH HHS AG000057NIA NIH HHS T32 AG000057NIDA NIH HHS DA16432NIDA NIH HHS R01 DA016432
6 · The paper itself

Abstract

5-HT6 receptors have been implicated in consolidation of visuospatial and reward-based learning tasks. Since 5-HT6 receptors may be important in modulation of sensory gating which is often affected in schizophrenic patients, we tested whether Ro 4368554, a 5-HT6 selective antagonist at a dose of 10 mg/kg, could reverse the loss of prepulse inhibition from apomorphine or scopolamine. In addition, we also tested whether Ro 4368554 altered fear conditioning using fear potentiated startle, a model for emotional learning. Prepulse inhibition of startle was disrupted by apomorphine (0.5 mg/kg) when prepulse emissions were 5 dB above background but not above 15 dB, while scopolamine (0.5 mg/kg) caused disruption at both prepulse levels. Scopolamine-mediated disruption was not reversed by Ro 4368854 but apomorphine-mediated disruption was significantly ameliorated by 5-HT6 inhibition. For fear potentiated startle, scopolamine and/or Ro 4368554 were administered before two daily fear conditioning sessions; rats were tested on the following day. Rats that received scopolamine displayed no fear potentiated startle but Ro 4368554 reversed this scopolamine deficit. Additionally, we mapped Fos induction in rats treated with scopolamine and/or Ro 4368554; scopolamine increased Fos expression in the central nucleus of the amygdala and this was attenuated by Ro 4368554. In summary, we have demonstrated the efficacy of 5-HT6 antagonists in modulating sensory gating and fear conditioning, and thus may be of therapeutic use for schizophrenia-related disorders.

Indexed as

AmygdalaAnimalsApomorphineDopamine AgonistsEmotionsFearGenes, fosImmunohistochemistryIndolesLearningMaleMaze LearningMuscarinic AntagonistsPiperazinesRatsRats, Sprague-DawleyApomorphineDopamine AgonistsIndolesMuscarinic AntagonistsPiperazinesReceptors, SerotoninRo4368554Scopolamineserotonin 6 receptorSerotonin Antagonists

Identifiers

PMID17920665
PMCPMC2322863
OpenAlexW2153200821

What OpenQuestion holds

Textmetadata
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.