Evidence map›Paper›PMID 22641180›Full record

ArticleMolecular psychiatry2013

A new perspective for schizophrenia: TAAR1 agonists reveal antipsychotic- and antidepressant-like activity, improve cognition and control body weight.

F G Revel, J-L Moreau, B Pouzet, R Mory, A Bradaia, D Buchy, V Metzler, S Chaboz, K Groebke Zbinden, G Galley and 9 more

Abstract read
PubMed Publisher
In one paragraph

Article in Molecular psychiatry, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 140 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
140citing papers in PubMed, 4 pooled it
5.1field-weighted citation impact, top 4% 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

140 citing papers in PubMed, 4 syntheses or guidelines pooled it, 285 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Pooled it
  5. Effect of TAAR1/5-HTTranslational psychiatry · 2021
    Trial
  6. Schizophrenia: from mechanism to therapy.Science China. Life sciences · 2026
    Review
  7. Article
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  9. Article
  10. Preclinical development of [European journal of nuclear medicine and molecular imaging · 2026
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80 more citing papers are in PubMed but not listed here.

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

19 authors at 2 institutions in 2 countries.

F G RevelNeuroscience Research, Pharmaceuticals Division, F. Hoffmann-La Roche, Basel, Switzerland.
J-L Moreau
B Pouzet
R Mory
A Bradaia
D Buchy
V Metzler
S Chaboz
K Groebke Zbinden
G Galley
R D Norcross
D Tuerck
A Bruns
S R Morairty
T S Kilduff
T L Wallace
C Risterucci
J G Wettstein
M C Hoener
Roche (Switzerland) · CHSRI International · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Schizophrenia is a chronic, severe and highly complex mental illness. Current treatments manage the positive symptoms, yet have minimal effects on the negative and cognitive symptoms, two prominent features of the disease with critical impact on the long-term morbidity. In addition, antipsychotic treatments trigger serious side effects that precipitate treatment discontinuation. Here, we show that activation of the trace amine-associated receptor 1 (TAAR1), a modulator of monoaminergic neurotransmission, represents a novel therapeutic option. In rodents, activation of TAAR1 by two novel and pharmacologically distinct compounds, the full agonist RO5256390 and the partial agonist RO5263397, blocks psychostimulant-induced hyperactivity and produces a brain activation pattern reminiscent of the antipsychotic drug olanzapine, suggesting antipsychotic-like properties. TAAR1 agonists do not induce catalepsy or weight gain; RO5263397 even reduced haloperidol-induced catalepsy and prevented olanzapine from increasing body weight and fat accumulation. Finally, TAAR1 activation promotes vigilance in rats and shows pro-cognitive and antidepressant-like properties in rodent and primate models. These data suggest that TAAR1 agonists may provide a novel and differentiated treatment of schizophrenia as compared with current medication standards: TAAR1 agonists may improve not only the positive symptoms but also the negative symptoms and cognitive deficits, without causing adverse effects such as motor impairments or weight gain.

Indexed as

Analysis of VarianceAnimalsAntipsychotic AgentsAttentionBenzodiazepinesBody WeightCocaineConditioning, OperantDepressionDisease Models, AnimalDopamine Uptake InhibitorsElectroencephalographyHallucinogensHaloperidolHumansMacaca fascicularisAntipsychotic AgentsBenzodiazepinesCocaineDopamine Uptake InhibitorsHallucinogensHaloperidolL 687414OlanzapineOxazolesPhencyclidinePhenethylaminesPyrrolidinonesReceptors, G-Protein-CoupledRO5166017Trace Amine-Associated ReceptorsTritium

Identifiers

PMID22641180
OpenAlexW2011355421

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.