Evidence map›Paper›PMID 22699904›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2012

Changing neuroestrogens within the auditory forebrain rapidly transform stimulus selectivity in a downstream sensorimotor nucleus.

Luke Remage-Healey, Narendra R Joshi

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed
6.1field-weighted citation impact, top 2% 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

52 citing papers in PubMed, 83 citations in OpenAlex.

  1. Article
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  6. A neural circuit perspective on brain aromatase.Frontiers in neuroendocrinology · 2022
    Review
  7. Non-sensory Influences on Auditory Learning and Plasticity.Journal of the Association for Research in Otolaryngology : JARO · 2022
    Review
  8. Article
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  12. Article
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  19. On the role of brain aromatase in females: why are estrogens produced locally when they are available systemically?Journal of comparative physiology. A, Neuroethology, sensory, neural, and behavioral physiology · 2018
    Review
  20. 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

2 authors at 1 institution in 1 country.

Luke Remage-HealeyNeuroscience and Behavior Program, Center for Neuroendocrine Studies, University of Massachusetts, Amherst, Massachusetts 01003, USA. healey@cns.umass.edu
Narendra R Joshi
University of Massachusetts Amherst · US

Funding

Modulation of forebrain circuits by local neurosteroid productionR00NS066179 · NINDS · UNIVERSITY OF MASSACHUSETTS AMHERST · PI REMAGE-HEALEY, LUKE R · 2010 to 2012
$721k
Modulation of forebrain circuits by local neurosteroid productionK99NS066179 · NINDS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI REMAGE-HEALEY, LUKE R · 2009 to 2010
$98k
NINDS NIH HHS K99 NS066179NINDS NIH HHS K99/R00 NS066179NINDS NIH HHS R00 NS066179
6 · The paper itself

Abstract

The activity of sensory circuits is shaped by neuromodulators, which can have downstream consequences for both sensorimotor integration and behavioral output. Recent evidence indicates that brain-derived estrogens ("neuroestrogens") can act as local circuit modulators in the songbird auditory forebrain. Specifically, neuroestrogens fluctuate in the auditory caudomedial nidopallium (NCM) during social interactions and in response to song stimuli. Within minutes of elevation, neuroestrogens also enhance auditory response properties of NCM neurons, and acute blockade of estrogen production in NCM disrupts behavioral song preferences. Here, we test the hypothesis that fluctuating neuroestrogens within NCM influence stimulus selectivity in a downstream sensorimotor nucleus (HVC, used as a proper name) that receives indirect auditory input from NCM. Dual extracellular recordings coupled with retrodialysis delivery show that song selectivity in HVC is rapidly enhanced by increasing neuroestrogens in NCM in adult males. Conversely, inhibiting neuroestrogen production in NCM causes a rapid decline in song selectivity in HVC, demonstrating the endogenous nature of this modulatory network. In contrast, HVC selectivity is unaffected by neuroestrogen delivery to either nearby caudomedial mesopallium or into HVC itself, indicating that neuroestrogen actions are restricted to NCM. In juvenile males, identical neuroestrogen treatment in NCM also does not alter HVC selectivity, consistent with a developmental maturation of the auditory network. Lastly, the rapid actions of estrogens leading to enhanced HVC selectivity appear to be mediated by membrane-bound receptors in NCM. These findings indicate that steroid-dependent modulation of sensory processing is not locally restricted and can be transmitted transynaptically to influence downstream sensorimotor and premotor targets.

Indexed as

Acoustic StimulationAction PotentialsAge FactorsAnimalsAromatase InhibitorsAuditory PathwaysAuditory PerceptionBiotinEstradiolFadrozoleFinchesMaleMicrodialysisNeuronsProsencephalonVocalization, AnimalAromatase InhibitorsBiotinEstradiolFadrozole

Identifiers

PMID22699904
PMCPMC3380542
OpenAlexW2062114293

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.