Evidence map›Paper›PMID 27864939›Full record

ArticleThe Journal of comparative neurology2017

GABAergic innervation of the ciliary ganglion in macaque monkeys - A light and electron microscopic study.

Miriam Barnerssoi, Paul J May, Anja K E Horn

Open access · greenAbstract read
In one paragraph

Article in The Journal of comparative neurology, 2017. 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
0.3field-weighted citation impact, top 38% 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, 10 citations in OpenAlex.

  1. Fatigue and Arousal Modulations Revealed by Saccade and Pupil Dynamics.International journal of environmental research and public health · 2022
    Article
  2. Article
  3. Review
  4. Article
  5. Neural basis of location-specific pupil luminance modulation.Proceedings of the National Academy of Sciences of the United States of America · 2018
    Article
  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

3 authors at 2 institutions in 2 countries.

Miriam BarnerssoiInstitute of Anatomy and Cell Biology I, Ludwig-Maximilian Universität, Munich, Germany.
Paul J MayDepartments of Neurobiology and Anatomical Sciences, Ophthalmology, and Neurology, University of Mississippi Medical Center, Jackson, MS, 39216.
Anja K E HornInstitute of Anatomy and Cell Biology I, Ludwig-Maximilian Universität, Munich, Germany.
Ludwig-Maximilians-Universität München · DEUniversity of Mississippi Medical Center · US

Funding

MIDBRAIN CIRCUITRY FOR NEURONAL CONTROL OF GAZER01EY014263 · NEI · UNIVERSITY OF MISSISSIPPI MEDICAL CENTER · PI GAMLIN, PAUL DOUGLAS, MAY, PAUL J · 2003 to 2018
$5.2M
NEI NIH HHS R01 EY014263
6 · The paper itself

Abstract

The vertebrate ciliary ganglion (CG) is a relay station in the parasympathetic pathway activating the iris sphincter and ciliary muscle to mediate pupillary constriction and lens accommodation, respectively. While the postganglionic motoneurons in the CG are cholinergic, as are their inputs, there is evidence from avian studies that GABA may also be involved. Here, we used light and electron microscopic methods to examine the GABAergic innervation of the CG in Macaca fascicularis monkeys. Immunohistochemistry for the gamma aminobutyric acid synthesizing enzyme glutamic acid decarboxylase (GAD) and choline acetyltransferase (ChAT) revealed that all CG neurons are contacted by ChAT-positive terminals. A subpopulation of 17.5% of CG neurons was associated with terminal boutons expressing GAD-immunoreactivity in addition. Double-labeling for GAD and synaptophysin confirmed that these were synaptic terminals. Electron microscopic analysis in conjunction with GABA-immunogold staining showed that (1) GAD-positive terminals mainly target dendrites and spines in the perisomatic neuropil of CG neurons; (2) GABA is restricted to a specific terminal type, which displays intermediate features lying between classically excitatory and inhibitory endings; and (3) if a CG neuron is contacted by GABA-positive terminals, virtually all perisomatic terminals supplying it show GABA immunoreactivity. The source of this GABAergic input and whether GABA contributes to a specific CG function remains to be investigated. Nevertheless, our data indicate that the innervation of the ciliary ganglion is more complex than previously thought, and that GABA may play a neuromodulatory role in the control of lens or pupil function. J. Comp. Neurol. 525:1517-1531, 2017. © 2016 Wiley Periodicals, Inc.

Indexed as

AnimalsFluorescent Antibody TechniqueGABAergic NeuronsGanglia, ParasympatheticImmunohistochemistryMacaca fascicularisMaleMicroscopy, Electron, TransmissioncotransmissionlensparasympatheticpupilRRID:AB_2079751RRID:AB_2199013RRID: AB_47765RRID:AB_90715RRID:SCR_003070RRID:SCR_014199RRID:SCR_014235

Identifiers

PMID27864939
PMCPMC5808918
OpenAlexW2551496458

What OpenQuestion holds

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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.