Evidence map›Paper›PMID 26779591›Full record

ArticleThe Journal of comparative neurology2016

Localization of the M2 muscarinic cholinergic receptor in dendrites, cholinergic terminals, and noncholinergic terminals in the rat basolateral amygdala: An ultrastructural analysis.

Jay F Muller, Franco Mascagni, Violeta Zaric, David D Mott, Alexander J McDonald

Open access · greenAbstract read
In one paragraph

Article in The Journal of comparative neurology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.3field-weighted citation impact, top 22% 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

13 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Diverse Spatiotemporal Scales of Cholinergic Signaling in the Neocortex.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2020
    Review
  7. Article
  8. Article
  9. Article
  10. Evidence for MNeuroscience · 2017
    Article
  11. Cholinergic regulation of fear learning and extinction.Journal of neuroscience research · 2017
    Review
  12. The Diversity of Spine Synapses in Animals.Neuromolecular medicine · 2016
    Review
  13. 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

5 authors at 1 institution in 1 country.

Jay F MullerDepartment of Pharmacology, Physiology, and Neuroscience, University of South Carolina School of Medicine, Columbia, South Carolina, 29208.
Franco MascagniDepartment of Pharmacology, Physiology, and Neuroscience, University of South Carolina School of Medicine, Columbia, South Carolina, 29208.
Violeta ZaricDepartment of Pharmacology, Physiology, and Neuroscience, University of South Carolina School of Medicine, Columbia, South Carolina, 29208.
David D MottDepartment of Pharmacology, Physiology, and Neuroscience, University of South Carolina School of Medicine, Columbia, South Carolina, 29208.
Alexander J McDonaldDepartment of Pharmacology, Physiology, and Neuroscience, University of South Carolina School of Medicine, Columbia, South Carolina, 29208.
University of South Carolina · US

Funding

Muscarinic Modulation of the Basolateral AmygdalaR01MH104638 · NIMH · UNIVERSITY OF SOUTH CAROLINA AT COLUMBIA · PI MCDONALD, ALEXANDER JOSEPH, MOTT, DAVID D · 2015 to 2019
$2.3M
Synaptic Organization of the Basolateral AmygdalaR01DA027305 · NIDA · UNIVERSITY OF SOUTH CAROLINA AT COLUMBIA · PI MCDONALD, ALEXANDER JOSEPH · 2009 to 2012
$1.2M
NIDA NIH HHS R01 DA027305NIMH NIH HHS R01 MH104638
6 · The paper itself

Abstract

Activation of M2 muscarinic receptors (M2Rs) in the rat anterior basolateral nucleus (BLa) is critical for the consolidation of memories of emotionally arousing events. The present investigation used immunocytochemistry at the electron microscopic level to determine which structures in the BLa express M2Rs. In addition, dual localization of M2R and the vesicular acetylcholine transporter protein (VAChT), a marker for cholinergic axons, was performed to determine whether M2R is an autoreceptor in cholinergic axons innervating the BLa. M2R immunoreactivity (M2R-ir) was absent from the perikarya of pyramidal neurons, with the exception of the Golgi complex, but was dense in the proximal dendrites and axon initial segments emanating from these neurons. Most perikarya of nonpyramidal neurons were also M2R-negative. About 95% of dendritic shafts and 60% of dendritic spines were M2 immunoreactive (M2R(+) ). Some M2R(+) dendrites had spines, suggesting that they belonged to pyramidal cells, whereas others had morphological features typical of nonpyramidal neurons. M2R-ir was also seen in axon terminals, most of which formed asymmetrical synapses. The main targets of M2R(+) terminals forming asymmetrical (putative excitatory) synapses were dendritic spines, most of which were M2R(+) . The main targets of M2R(+) terminals forming symmetrical (putative inhibitory or neuromodulatory) synapses were unlabeled perikarya and M2R(+) dendritic shafts. M2R-ir was also seen in VAChT(+) cholinergic terminals, indicating a possible autoreceptor role. These findings suggest that M2R-mediated mechanisms in the BLa are very complex, involving postsynaptic effects in dendrites as well as regulating release of glutamate, γ-aminobutyric acid, and acetylcholine from presynaptic axon terminals. J. Comp. Neurol. 524:2400-2417, 2016. © 2016 Wiley Periodicals, Inc.

Indexed as

AnimalsBasolateral Nuclear ComplexCholinergic NeuronsDendritesMalePresynaptic TerminalsRatsRats, Sprague-DawleyReceptor, Muscarinic M2Receptor, Muscarinic M2acetylcholineautoreceptorelectron microscopyimmunocytochemistryRRID:AB_572269RRID:AB_94952vesicular acetylcholine transporter protein

Identifiers

PMID26779591
PMCPMC5094197
OpenAlexW2282518150

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.