Evidence map›Paper›PMID 23152302›Full record

ArticleSynapse (New York, N.Y.)2013

Columnar distribution of catecholaminergic neurons in the ventrolateral periaqueductal gray and their relationship to efferent pathways.

Shelby K Suckow, Emily L Deichsel, Susan L Ingram, Michael M Morgan, Sue A Aicher

Abstract read
In one paragraph

Article in Synapse (New York, N.Y.), 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.0field-weighted citation impact, top 25% 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

23 citing papers in PubMed, 35 citations in OpenAlex.

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  14. Functional Involvement of Human Periaqueductal Gray and Other Midbrain Nuclei in Cognitive Control.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2019
    Article
  15. Article
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  17. Central Amygdala Circuits Mediate Hyperalgesia in Alcohol-Dependent Rats.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2018
    Article
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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

5 authors at 2 institutions in 1 country.

Shelby K SuckowDepartment of Physiology and Pharmacology, Oregon Health and Science University, Portland, Oregon 97223, USA.
Emily L Deichsel
Susan L Ingram
Michael M Morgan
Sue A Aicher
Oregon Health & Science University · USWashington State University Vancouver · US

Funding

Ultrastructure and Single Particle Microscopy CoreP30NS061800 · NINDS · OREGON HEALTH & SCIENCE UNIVERSITY · PI AICHER, SUE A · 2009 to 2020
$6.6M
Psychostimulants induce long-term changes in nociception.R01DA027625 · NIDA · WASHINGTON STATE UNIVERSITY · PI AICHER, SUE A, INGRAM, SUSAN L · 2009 to 2013
$2.3M
Confocal MicroscopeS10RR016858 · NCRR · OREGON HEALTH AND SCIENCE UNIVERSITY · PI WELSH, JOHN P · 2002 to 2002
$500k
NCRR NIH HHS RR016858NCRR NIH HHS S10 RR016858NIDA NIH HHS DA02765NIDA NIH HHS R01 DA027625NINDS NIH HHS P30 NS061800NINDS NIH HHS P30 NS091800
6 · The paper itself

Abstract

The periaqueductal gray (PAG) is a critical brain region involved in opioid analgesia and provides efferents to descending pathways that modulate nociception. In addition, the PAG contains ascending pathways to regions involved in the regulation of reward, including the substantia nigra (SN) and the ventral tegmental area (VTA). SN and VTA contain dopaminergic neurons that are critical for the maintenance of positive reinforcement. Interestingly, the PAG is also reported to contain a population of dopaminergic neurons. In this study, the distribution of catecholaminergic neurons within the ventrolateral (vl) PAG was examined using immunocytochemical methods. In addition, the catecholaminergic PAG neurons were examined to determine whether these neurons are integrated into ascending (VTA, SN) and descending rostral ventral medulla (RVM) efferent pathways from this region. The immunocytochemical analysis determined that catecholaminergic neurons in the PAG are both dopaminergic and noradrenergic and these neurons have a distinct rostrocaudal distribution within the ventrolateral column of PAG. Dopaminergic neurons were concentrated rostrally and were significantly smaller than noradrenergic neurons. Combined immunocytochemistry and tract tracing methods revealed that catecholaminergic neurons are distinct from, but closely associated with, both ascending and descending efferent projection neurons. Finally, by electron microscopy, catecholaminergic neurons showed close dendritic appositions with other neurons in PAG, suggesting a possible nonsynaptic mechanism for regulation of PAG output by these neurons. In conclusion, our data indicate that there are two populations of catecholaminergic neurons in the vlPAG that form dendritic associations with both ascending and descending efferents suggesting a possible nonsynaptic modulation of vlPAG neurons.

Indexed as

AnimalsCatecholaminesEfferent PathwaysMaleMedulla OblongataNeuronsPeriaqueductal GrayRatsRats, Sprague-DawleyVentral Tegmental AreaCatecholamines

Identifiers

PMID23152302
PMCPMC3553663
OpenAlexW2003691211

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.