Evidence map›Paper›PMID 35593070›Full record

ArticleJournal of neuroscience research2022

NURR1-deficient mice have age- and sex-specific behavioral phenotypes.

Francesca Montarolo, Serena Martire, Francesco Chiara, Sarah Allegra, Silvia De Francia, Eriola Hoxha, Filippo Tempia, Marco Alfonso Capobianco, Antonio Bertolotto

Open access · hybridAbstract read
In one paragraph

Article in Journal of neuroscience research, 2022. 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
1.4field-weighted citation impact, top 21% 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, 14 citations in OpenAlex.

  1. Article
  2. Molecular Screening Reveals De Novo Loss-of-FunctionInternational journal of molecular sciences · 2025
    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

9 authors at 2 institutions in 1 country.

Francesca MontaroloNeuroscience Institute Cavalieri Ottolenghi (NICO), Orbassano, Italy.
Serena MartireNeurology Department and Regional Referring Center of Multiple Sclerosis (CReSM), University Hospital San Luigi Gonzaga, Orbassano, Italy.
Francesco ChiaraDepartment of Biological and Clinical Sciences, University of Turin, AOU San Luigi Gonzaga, Orbassano, Italy.
Sarah AllegraDepartment of Biological and Clinical Sciences, University of Turin, AOU San Luigi Gonzaga, Orbassano, Italy.
Silvia De FranciaDepartment of Biological and Clinical Sciences, University of Turin, AOU San Luigi Gonzaga, Orbassano, Italy.
Eriola HoxhaNeuroscience Institute Cavalieri Ottolenghi (NICO), Orbassano, Italy.
Filippo TempiaNeuroscience Institute Cavalieri Ottolenghi (NICO), Orbassano, Italy.
Marco Alfonso CapobiancoNeuroscience Institute Cavalieri Ottolenghi (NICO), Orbassano, Italy.
Antonio BertolottoNeuroscience Institute Cavalieri Ottolenghi (NICO), Orbassano, Italy.
Neuroscience Institute · ITOspedale San Luigi Gonzaga · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The transcription factor NURR1 is essential to the generation and maintenance of midbrain dopaminergic (mDA) neurons and its deregulation is involved in the development of dopamine (DA)-associated brain disorders, such as Parkinson's disease (PD). The old male NURR1 heterozygous knockout (NURR1-KO) mouse has been proposed as a model of PD due to its altered motor performance that was, however, not confirmed in a subsequent study. Based on these controversial results, we explored the effects of the NURR1 deficiency on locomotor activity, motor coordination, brain and plasma DA levels, blood pressure and heart rate of old mice, also focusing on the potential effect of sex. As a probable consequence of the role of NURR1 in DA pathway, we observed that the old NURR1-KO mouse is characterized by motor impairment, and increased brain DA level and heart rate, independently from sex. However, we also observed an alteration in spontaneous locomotor activity that only affects males. In conclusion, NURR1 deficiency triggers sex- and age-specific alterations of behavioral responses, of DA levels and cardiovascular abnormalities. Further studies in simplified systems will be necessary to dissect the mechanism underlying these observations.

Indexed as

Nuclear Receptor Subfamily 4, Group A, Member 2Parkinson DiseaseAnimalsDopamineDopaminergic NeuronsFemaleMaleMiceMice, KnockoutPhenotypeTranscription FactorsDopamineNuclear Receptor Subfamily 4, Group A, Member 2Transcription Factorsdopaminelocomotionmotor impairmentmurine modelNURR1Parkinson's disease

Identifiers

PMID35593070
PMCPMC9539971
OpenAlexW4280560127

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.