Evidence map›Paper›PMID 25206323›Full record

ReviewFrontiers in neural circuits2014

Unraveling the architecture of the dorsal raphe synaptic neuropil using high-resolution neuroanatomy.

Mariano Soiza-Reilly, Kathryn G Commons

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in neural circuits, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.1field-weighted citation impact, top 14% 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

22 citing papers in PubMed, 50 citations in OpenAlex.

  1. Article
  2. Article
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  4. Review
  5. Article
  6. Article
  7. Article
  8. Implication of 5-HT7 receptor in prefrontal circuit assembly and detrimental emotional effects of SSRIs during development.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2020
    Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. The 5-HTPsychopharmacology · 2018
    Article
  14. Q&A: Array tomography.BMC biology · 2018
    Article
  15. Article
  16. Article
  17. Propagation of pathological α-synuclein in marmoset brain.Acta neuropathologica communications · 2017
    Article
  18. Article
  19. Neuronal correlates of depression.Cellular and molecular life sciences : CMLS · 2015
    Review
  20. Dorsal raphe nucleus projecting retinal ganglion cells: Why Y cells?Neuroscience and biobehavioral reviews · 2015
    Review
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

2 authors at 2 institutions in 2 countries.

Mariano Soiza-ReillyInstitut du Fer à Moulin, INSERM, UMR-S 839 Paris, France ; Université Pierre et Marie Curie Paris, France.
Kathryn G CommonsDepartment of Anesthesiology, Perioperative, and Pain Medicine, Boston Children's Hospital Boston, MA, USA ; Department of Anaesthesia, Harvard Medical School Boston, MA, USA.
Boston Children's Hospital · USSorbonne Université · FR

Funding

Topography of Serotonin DysfunctionR01DA021801 · NIDA · BOSTON CHILDREN'S HOSPITAL · PI COMMONS, KATHRYN G · 2007 to 2018
$3.6M
NIDA NIH HHS R01 DA021801
6 · The paper itself

Abstract

The dorsal raphe nucleus (DRN), representing the main source of brain's serotonin, is implicated in the pathophysiology and therapeutics of several mental disorders that can be debilitating and life-long including depression, anxiety and autism. The activity of DRN neurons is precisely regulated, both phasically and tonically, by excitatory glutamate and inhibitory GABAergic axons arising from extra-raphe areas as well as from local sources within the nucleus. Changes in serotonin neurotransmission associated with pathophysiology may be encoded by alterations within this network of regulatory afferents. However, the complex organization of the DRN circuitry remains still poorly understood. Using a recently developed high-resolution immunofluorescence technique called array tomography (AT) we quantitatively analyzed the relative contribution of different populations of glutamate axons originating from different brain regions to the excitatory drive of the DRN. Additionally, we examined the presence of GABA axons within the DRN and their possible association with glutamate axons. In this review, we summarize our findings on the architecture of the rodent DRN synaptic neuropil using high-resolution neuroanatomy, and discuss possible functional implications for the nucleus. Understanding of the synaptic architecture of neural circuits at high resolution will pave the way to understand how neural structure and function may be perturbed in pathological states.

Indexed as

AnimalsDorsal Raphe NucleusFluorescent Antibody Techniquegamma-Aminobutyric AcidGlutamic AcidNeuropilSynapsesTryptophan Hydroxylasegamma-Aminobutyric AcidGlutamic AcidTryptophan Hydroxylaseaxo-axonicglutamate decarboxylase 65synapsesultrathin serial-sectionsvesicular glutamate transporter

Identifiers

PMID25206323
PMCPMC4143723
OpenAlexW2126882894

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.