Evidence map›Paper›PMID 33328864›Full record

ArticleFrontiers in neuroscience2020

Methadone Suppresses Neuronal Function and Maturation in Human Cortical Organoids.

Wei Wu, Hang Yao, Ila Dwivedi, Priscilla D Negraes, Helen W Zhao, Juan Wang, Cleber A Trujillo, Alysson R Muotri, Gabriel G Haddad

Open access · goldAbstract read
In one paragraph

Article in Frontiers in neuroscience, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.1field-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

12 citing papers in PubMed, 23 citations in OpenAlex.

  1. Review
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  5. Synaptic plasticity in human thalamocortical assembloids.bioRxiv : the preprint server for biology · 2024
    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

9 authors at 1 institution in 1 country.

Wei WuDepartment of Pediatrics, School of Medicine, University of California, San Diego, San Diego, CA, United States.
Hang YaoDepartment of Pediatrics, School of Medicine, University of California, San Diego, San Diego, CA, United States.
Ila DwivediDepartment of Pediatrics, School of Medicine, University of California, San Diego, San Diego, CA, United States.
Priscilla D NegraesDepartment of Cellular and Molecular Medicine, Stem Cell Program, Center for Academic Research and Training in Anthropogeny, Kavli Institute for Brain and Mind, University of California, San Diego, San Diego, CA, United States.
Helen W ZhaoDepartment of Pediatrics, School of Medicine, University of California, San Diego, San Diego, CA, United States.
Juan WangDepartment of Pediatrics, School of Medicine, University of California, San Diego, San Diego, CA, United States.
Cleber A TrujilloDepartment of Cellular and Molecular Medicine, Stem Cell Program, Center for Academic Research and Training in Anthropogeny, Kavli Institute for Brain and Mind, University of California, San Diego, San Diego, CA, United States.
Alysson R MuotriDepartment of Pediatrics, School of Medicine, University of California, San Diego, San Diego, CA, United States.
Gabriel G HaddadDepartment of Pediatrics, School of Medicine, University of California, San Diego, San Diego, CA, United States.
University of California, San Diego · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Accumulating evidence has suggested that prenatal exposure to methadone causes multiple adverse effects on human brain development. Methadone not only suppresses fetal neurobehavior and alters neural maturation, but also leads to long-term neurological impairment. Due to logistical and ethical issues of accessing human fetal tissue, the effect of methadone on brain development and its underlying mechanisms have not been investigated adequately and are therefore not fully understood. Here, we use human cortical organoids which resemble fetal brain development to examine the effect of methadone on neuronal function and maturation during early development. During development, cortical organoids that are exposed to clinically relevant concentrations of methadone exhibited suppressed maturation of neuronal function. For example, organoids developed from 12th week till 24th week have an about 7-fold increase in AP firing frequency, but only half and a third of this increase was found in organoids exposed to 1 and 10 μM methadone, respectively. We further demonstrated substantial increases in

Indexed as

cortical organoidion channeliPSCsmethadoneneural functionpatch-clamp

Identifiers

PMID33328864
PMCPMC7719724
OpenAlexW3108156348

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.