Evidence map›Paper›PMID 19067354›Full record

ArticleThe Journal of comparative neurology2009

Avian nucleus retroambigualis: cell types and projections to other respiratory-vocal nuclei in the brain of the zebra finch (Taeniopygia guttata).

J M Wild, M F Kubke, R Mooney

Open access · greenAbstract read
In one paragraph

Article in The Journal of comparative neurology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
2.5field-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

25 citing papers in PubMed, 48 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. A feedforward inhibitory premotor circuit for auditory-vocal interactions in zebra finches.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  8. Article
  9. Review
  10. Review
  11. Article
  12. Article
  13. Article
  14. Auditory-vocal mirroring in songbirds.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2014
    Review
  15. Review
  16. Article
  17. Article
  18. Coding rate and duration of vocalizations of the frog, Xenopus laevis.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2012
    Article
  19. Shared developmental and evolutionary origins for neural basis of vocal-acoustic and pectoral-gestural signaling.Proceedings of the National Academy of Sciences of the United States of America · 2012
    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

3 authors at 2 institutions in 2 countries.

J M WildDepartment of Anatomy, Faculty of Medical and Health Sciences, University of Auckland, Auckland, New Zealand. jm.wild@auckland.ac.nz
M F Kubke
R Mooney
University of Auckland · NZDuke University · US

Funding

SYNAPTIC AND CELLULAR MECHANISMS OF AVIAN SONG LEARNINGR01DC002524 · NIDCD · DUKE UNIVERSITY · PI MOONEY, RICHARD D · 1995 to 2014
$4.1M
Sensorimotor control of the oropharynx and esophagusR01NS029467 · NINDS · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI SUTHERS, RODERICK ATKINS · 1991 to 2014
$3.3M
Cellular Mechanisms of Vocal-Respiratory IntegrationR01DC004691 · NIDCD · DUKE UNIVERSITY · PI MOONEY, RICHARD D. · 2001 to 2005
$1.2M
NIDCD NIH HHS R01 DC002524NIDCD NIH HHS R01 DC004691NIDCD NIH HHS R01DC04691NINDS NIH HHS R01 NS029467
6 · The paper itself

Abstract

In songbirds song production requires the intricate coordination of vocal and respiratory muscles under the executive influence of the telencephalon, as for speech in humans. In songbirds the site of this coordination is suspected to be the nucleus retroambigualis (RAm), because it contains premotor neurons projecting upon both vocal motoneurons and spinal motoneurons innervating expiratory muscles, and because it receives descending inputs from the telencephalic vocal control nucleus robustus archopallialis (RA). Here we used tract-tracing techniques to provide a more comprehensive account of the projections of RAm and to identify the different populations of RAm neurons. We found that RAm comprises diverse projection neuron types, including: 1) bulbospinal neurons that project, primarily contralaterally, upon expiratory motoneurons; 2) a separate group of neurons that project, primarily ipsilaterally, upon vocal motoneurons in the tracheosyringeal part of the hypoglossal nucleus (XIIts); 3) neurons that project throughout the ipsilateral and contralateral RAm; 4) another group that sends reciprocal, ascending projections to all the brainstem sources of afferents to RAm, namely, nucleus parambigualis, the ventrolateral nucleus of the rostral medulla, nucleus infra-olivarus superior, ventrolateral parabrachial nucleus, and dorsomedial nucleus of the intercollicular complex; and 5) a group of relatively large neurons that project their axons into the vagus nerve. Three morphological classes of RAm cells were identified by intracellular labeling, the dendritic arbors of which were confined to RAm, as defined by the terminal field of RA axons. Together the ascending and descending projections of RAm confirm its pivotal role in the mediation of respiratory-vocal control.

Indexed as

Vocalization, AnimalAnimalsBrainCell ShapeFinchesHumansMaleNeural PathwaysNeuronsRespiratory CenterSpinal Cord

Identifiers

PMID19067354
PMCPMC2673955
OpenAlexW2058412944

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.