Evidence map›Paper›PMID 33060181›Full record

RevieweNeuro

Prenatal Opioid Exposure Enhances Responsiveness to Future Drug Reward and Alters Sensitivity to Pain: A Review of Preclinical Models and Contributing Mechanisms.

Gregory G Grecco, Brady K Atwood

Open access · goldAbstract readReview
In one paragraph

Review in eNeuro. 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
5.2field-weighted citation impact, top 5% 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, 32 citations in OpenAlex.

  1. Article
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  9. GABA system as the cause and effect in early development.Neuroscience and biobehavioral reviews · 2024
    Review
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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

2 authors at 1 institution in 1 country.

Gregory G GreccoDepartment of Pharmacology and Toxicology, Indiana University School of Medicine, Indianapolis, IN 46202.ORCID 0000-0002-0700-8633
Brady K AtwoodDepartment of Pharmacology and Toxicology, Indiana University School of Medicine, Indianapolis, IN 46202 bkatwood@iu.edu.ORCID 0000-0002-7441-2724
University School · US

Funding

Indiana Medical Scientist/Engineer Training ProgramT32GM077229 · NIGMS · INDIANA UNIVERSITY INDIANAPOLIS · PI GASTON, BENJAMIN, HERBERT, BRITTNEY-SHEA · 2008 to 2022
$6.0M
Synapse-specific interactions between ethanol and opioid receptor-mediated synaptic depression in dorsal striatum: ADRD suppR01AA027214 · NIAAA · INDIANA UNIVERSITY INDIANAPOLIS · PI ATWOOD, BRADY · 2018 to 2022
$2.5M
The Impact of Fetal Methadone Exposure on Alcohol-Related Behavior and Alcohol-Induced Changes in the StriatumF30AA028687 · NIAAA · INDIANA UNIVERSITY INDIANAPOLIS · PI GRECCO, GREGORY GIOVANNI · 2020 to 2023
$173k
NIAAA NIH HHS F30 AA028687NIAAA NIH HHS R01 AA027214NIGMS NIH HHS T32 GM077229
6 · The paper itself

Abstract

The opioid crisis has resulted in an unprecedented number of neonates born with prenatal opioid exposure (POE); however, the long-term effects of POE on offspring behavior and neurodevelopment remain relatively unknown. The advantages and disadvantages of the various preclinical POE models developed over the last several decades are discussed in the context of clinical and translational relevance. Although considerable and important variability exists among preclinical models of POE, the examination of these preclinical models has revealed that opioid exposure during the prenatal period contributes to maladaptive behavioral development as offspring mature including an altered responsiveness to rewarding drugs and increased pain response. The present review summarizes key findings demonstrating the impact of POE on offspring drug self-administration (SA), drug consumption, the reinforcing properties of drugs, drug tolerance, and other reward-related behaviors such as hypersensitivity to pain. Potential underlying molecular mechanisms which may contribute to this enhanced addictive phenotype in POE offspring are further discussed with special attention given to key brain regions associated with reward including the striatum, prefrontal cortex (PFC), ventral tegmental area (VTA), hippocampus, and amygdala. Improvements in preclinical models and further areas of study are also identified which may advance the translational value of findings and help address the growing problem of POE in clinical populations.

Indexed as

Analgesics, OpioidPharmaceutical PreparationsFemaleHumansInfant, NewbornPainPregnancyRewardVentral Tegmental AreaAnalgesics, OpioidPharmaceutical Preparationsaddictionanimal modelsfetal opioidgestationpregnancyprenatal opioid

Identifiers

PMID33060181
PMCPMC7768284
OpenAlexW3093109231

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.