Evidence map›Paper›PMID 26041829›Full record

ArticleJournal of neurophysiology2015

Structural and functional characterization of dendritic arbors and GABAergic synaptic inputs on interneurons and principal cells in the rat basolateral amygdala.

Paul M Klenowski, Matthew J Fogarty, Arnauld Belmer, Peter G Noakes, Mark C Bellingham, Selena E Bartlett

Open access · greenAbstract read
In one paragraph

Article in Journal of neurophysiology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
3.0field-weighted citation impact, top 9% 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

24 citing papers in PubMed, 40 citations in OpenAlex.

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  7. Size-dependent differences in mitochondrial volume density in phrenic motor neurons.Journal of applied physiology (Bethesda, Md. : 1985) · 2023
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  11. Vasoactive Intestinal Polypeptide-Immunoreactive Interneurons within Circuits of the Mouse Basolateral Amygdala.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2018
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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

6 authors at 3 institutions in 1 country.

Paul M KlenowskiTranslational Research Institute and Institute for Health and Biomedical Innovation, Queensland University of Technology, Brisbane, Queensland, Australia;
Matthew J FogartySchool of Biomedical Sciences, The University of Queensland, Brisbane, Queensland, Australia; and.
Arnauld BelmerTranslational Research Institute and Institute for Health and Biomedical Innovation, Queensland University of Technology, Brisbane, Queensland, Australia;
Peter G NoakesSchool of Biomedical Sciences, The University of Queensland, Brisbane, Queensland, Australia; and Queensland Brain Institute, The University of Queensland, Brisbane, Queensland, Australia.
Mark C BellinghamSchool of Biomedical Sciences, The University of Queensland, Brisbane, Queensland, Australia; and.
Selena E BartlettTranslational Research Institute and Institute for Health and Biomedical Innovation, Queensland University of Technology, Brisbane, Queensland, Australia; selena.bartlett@qut.edu.au.
University of Queensland · AUQueensland University of Technology · AUTranslational Research Institute · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The basolateral amygdala (BLA) is a complex brain region associated with processing emotional states, such as fear, anxiety, and stress. Some aspects of these emotional states are driven by the network activity of synaptic connections, derived from both local circuitry and projections to the BLA from other regions. Although the synaptic physiology and general morphological characteristics are known for many individual cell types within the BLA, the combination of morphological, electrophysiological, and distribution of neurochemical GABAergic synapses in a three-dimensional neuronal arbor has not been reported for single neurons from this region. The aim of this study was to assess differences in morphological characteristics of BLA principal cells and interneurons, quantify the distribution of GABAergic neurochemical synapses within the entire neuronal arbor of each cell type, and determine whether GABAergic synaptic density correlates with electrophysiological recordings of inhibitory postsynaptic currents. We show that BLA principal neurons form complex dendritic arborizations, with proximal dendrites having fewer spines but higher densities of neurochemical GABAergic synapses compared with distal dendrites. Furthermore, we found that BLA interneurons exhibited reduced dendritic arbor lengths and spine densities but had significantly higher densities of putative GABAergic synapses compared with principal cells, which was correlated with an increased frequency of spontaneous inhibitory postsynaptic currents. The quantification of GABAergic connectivity, in combination with morphological and electrophysiological measurements of the BLA cell types, is the first step toward a greater understanding of how fear and stress lead to changes in morphology, local connectivity, and/or synaptic reorganization of the BLA.

Indexed as

AnimalsBasolateral Nuclear ComplexCell SizeDendritesgamma-Aminobutyric AcidImaging, Three-DimensionalImmunohistochemistryInhibitory Postsynaptic PotentialsInterneuronsMaleMicroscopy, ConfocalPatch-Clamp TechniquesRats, WistarSynapsesTissue Culture Techniquesgamma-Aminobutyric Acidbasolateral amygdaladendritic spinesGABAsynaptic currents

Identifiers

PMID26041829
PMCPMC4725099
OpenAlexW2166906092

What OpenQuestion holds

Textmetadata
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.