Evidence map›Paper›PMID 30291632›Full record

ArticleThe Journal of comparative neurology2019

Seasonal changes in neuronal turnover in a forebrain nucleus in adult songbirds.

Tracy A Larson, Nivretta M Thatra, Daren Hou, Rachael A Hu, Eliot A Brenowitz

Abstract read
In one paragraph

Article in The Journal of comparative neurology, 2019. 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
2.2field-weighted citation impact, top 13% 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, 16 citations in OpenAlex.

  1. Article
  2. Article
  3. Adult neurogenesis is necessary for functional regeneration of a forebrain neural circuit.Proceedings of the National Academy of Sciences of the United States of America · 2024
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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

5 authors at 1 institution in 1 country.

Tracy A LarsonDepartment of Biology, University of Washington, Seattle, Washington.ORCID 0000-0001-6973-5433
Nivretta M ThatraDepartment of Biology, University of Washington, Seattle, Washington.
Daren HouDepartment of Psychology, University of Washington, Seattle, Washington.
Rachael A HuDepartment of Biology, University of Washington, Seattle, Washington.
Eliot A BrenowitzDepartment of Biology, University of Washington, Seattle, Washington.ORCID 0000-0002-1920-923X
University of Washington · US

Funding

TRAINING IN MOLECULAR AND CELLULAR BIOLOGYT32GM007270 · NIGMS · UNIVERSITY OF WASHINGTON · PI RAIBLE, DAVID W · 1985 to 2020
$21.0M
Intellectual and Developmental Disabilities Research CenterU54HD083091 · NICHD · UNIVERSITY OF WASHINGTON · PI DOHERTY, DANIEL · 2014 to 2019
$7.9M
COMPARATIVE STUDIES OF VOCAL CONTROLR01MH053032 · NIMH · UNIVERSITY OF WASHINGTON · PI BRENOWITZ, ELIOT A · 1995 to 2015
$5.3M
Hormones and Brain ProtectionR01NS075331 · NINDS · UNIVERSITY OF WASHINGTON · PI BRENOWITZ, ELIOT A · 2012 to 2016
$1.6M
NICHD NIH HHS U54 HD083091NIGMS NIH HHS T32 GM007270NIMH NIH HHS R01 MH053032NINDS NIH HHS R01 NS075331
6 · The paper itself

Abstract

Neuronal death and replacement, or neuronal turnover, in the adult brain are one of many fundamental processes of neural plasticity. The adult avian song control circuit provides an excellent model for exploring mature neuronal death and replacement by new neurons. In the song control nucleus, HVC of adult male Gambel's white-crowned sparrows (Zonotrichia leucophrys gambelli) nearly 68,000 neurons are added each breeding season and die during the subsequent nonbreeding season. To accommodate large seasonal differences in HVC neuron number, the balance between neuronal addition and death in HVC must differ between seasons. To determine whether maintenance of new HVC neurons changes within and between breeding and nonbreeding conditions, we pulse-labeled two different cohorts of new HVC neurons under both conditions and quantified their maintenance. We show that the maintenance of new HVC neurons, as well as new nonneuronal cells, was higher at the onset of breeding conditions than at the onset of nonbreeding conditions. Once a steady-state HVC volume and neuronal number were attained in either breeding or nonbreeding conditions, neuronal and nonneuronal maintenance were similarly low. We found that new neuronal number correlated with a new nonneuronal number within each cohort of new neurons. Together, these data suggest that sex steroids promote the survival of an initial population of new neurons and nonneuronal cells entering HVC. However, once HVC is fully grown or regressed, neuronal and nonneuronal cell turnover is regulated by a common mechanism likely independent of direct sex steroid signaling.

Indexed as

SeasonsAgingAnimalsCell DeathMaleNeurogenesisNeuronal PlasticityNeuronsProsencephalonSparrowsadult neurogenesisanti-BrdU (RRID: AB_2536432)anti-NeuN (RRID: AB_2532109)degenerationneuronal deathseasonal plasticitysongbirdsteroid hormonetestosterone

Identifiers

PMID30291632
PMCPMC6333494
OpenAlexW2894768691

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.