Evidence map›Paper›PMID 30311651›Full record

ArticleThe Journal of comparative neurology2019

Midline thalamic inputs to the amygdala: Ultrastructure and synaptic targets.

Alon Amir, Jean-Francois Paré, Yoland Smith, Denis Paré

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 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

11 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Differential Regulation of Prelimbic and Thalamic Transmission to the Basolateral Amygdala by Acetylcholine Receptors.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2023
    Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. 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

4 authors.

Alon AmirCenter for Molecular and Behavioral Neuroscience, Rutgers University-Newark, Newark, New Jersey.
Jean-Francois ParéDepartment of Neurology, Yerkes National Primate Research Center, Emory University, Atlanta, Georgia.
Yoland SmithDepartment of Neurology, Yerkes National Primate Research Center, Emory University, Atlanta, Georgia.
Denis ParéCenter for Molecular and Behavioral Neuroscience, Rutgers University-Newark, Newark, New Jersey.ORCID 0000-0001-5471-8868

Funding

Yerkes National Primate Research Center Role of type-I IFN in regulating COVID-19 induced inflammation and pathogenesisP51OD011132 · OD · EMORY UNIVERSITY · PI Joon Sup Lee · 2012 to 2026
$167.0M
Midline thalamic control of the amygdalaR01MH107239 · NIMH · RUTGERS THE STATE UNIV OF NJ NEWARK · PI PARE, DENIS · 2015 to 2019
$1.9M
NIH HHS P51 OD011132NIMH NIH HHS R01 MH107239
6 · The paper itself

Abstract

One of the main subcortical inputs to the basolateral nucleus of the amygdala (BL) originates from a group of dorsal thalamic nuclei located at or near the midline, mainly from the central medial (CMT), and paraventricular (PVT) nuclei. Although similarities among the responsiveness of BL, CMT, and PVT neurons to emotionally arousing stimuli suggest that these thalamic inputs exert a significant influence over BL activity, little is known about the synaptic relationships that mediate these effects. Thus, the present study used Phaseolus vulgaris-leucoagglutinin (PHAL) anterograde tracing and electron microscopy to shed light on the ultrastructural properties and synaptic targets of CMT and PVT axon terminals in the rat BL. Virtually all PHAL-positive CMT and PVT axon terminals formed asymmetric synapses. Although CMT and PVT axon terminals generally contacted dendritic spines, a substantial number ended on dendritic shafts. To determine whether these dendritic shafts belonged to principal or local-circuit cells, calcium/calmodulin-dependent protein kinase II (CAMKIIα) immunoreactivity was used as a selective marker of principal BL neurons. In most cases, dendritic shafts postsynaptic to PHAL-labeled CMT and PVT terminals were immunopositive for CaMKIIα. Overall, these results suggest that CMT and PVT inputs mostly target principal BL neurons such that when CMT or PVT neurons fire, little feed-forward inhibition counters their excitatory influence over principal cells. These results are consistent with the possibility that CMT and PVT inputs constitute major determinants of BL activity.

Indexed as

AmygdalaAnimalsCalcium-Calmodulin-Dependent Protein Kinase Type 2DendritesMaleMidline Thalamic NucleiNeuronal Tract-TracersPhytohemagglutininsRats, Sprague-DawleySynapsesCalcium-Calmodulin-Dependent Protein Kinase Type 2leukoagglutinins, plantsNeuronal Tract-TracersPhytohemagglutininsamygdalaCAMKIIαelectron microscopyRRID AB_2313606RRID AB_2313686RRID AB_2336656RRID AB_2637031RRID AB_447192RRID RGD_734476thalamustract-tracing

Identifiers

PMID30311651
PMCPMC6347509

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.